Fabio Macciardi

Title(s)Professor, Psychiatry and Human Behavior
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(949) 824-4424
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    1. Genetic polymorphism data support a relationship between schizophrenia and microsatellite variability in PLA2G4A in Northern Europeans not Han Chinese. Am J Med Genet B Neuropsychiatr Genet. 2021 Dec 09. Hudson CJ, Groh AMR, Macciardi F, Hudson RC. PMID: 34889025.
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    2. Sparse deep neural networks on imaging genetics for schizophrenia case-control classification. Hum Brain Mapp. 2021 Jun 01; 42(8):2556-2568. Chen J, Li X, Calhoun VD, Turner JA, van Erp TGM, Wang L, Andreassen OA, Agartz I, Westlye LT, Jönsson E, Ford JM, Mathalon DH, Macciardi F, O'Leary DS, Liu J, Ji S. PMID: 33724588; PMCID: PMC8090768.
      View in: PubMed   Mentions: 2     Fields:    
    3. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cereb Cortex. 2021 03 05; 31(4):1873-1887. Tilot AK, Khramtsova EA, Liang D, Grasby KL, Jahanshad N, Painter J, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Liu S, Brotman SM, Thompson PM, Medland SE, Macciardi F, Stranger BE, Davis LK, Fisher SE, Stein JL. PMID: 33290510; PMCID: PMC7945014.
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    4. Plasma Sphingomyelins in Late-Onset Alzheimer's Disease. J Alzheimers Dis. 2021; 83(3):1161-1171. Fote G, Wu J, Mapstone M, Macciardi F, Fiandaca MS, Federoff HJ. PMID: 34397408.
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    5. Functional impairment of cortical AMPA receptors in schizophrenia. Schizophr Res. 2020 Jun 05. Zeppillo T, Schulmann A, Macciardi F, Hjelm BE, Föcking M, Sequeira PA, Guella I, Cotter D, Bunney WE, Limon A, Vawter MP. PMID: 32513544; PMCID: PMC7718399.
      View in: PubMed   Mentions: 2     Fields:    
    6. Metabolic correlates of prevalent mild cognitive impairment and Alzheimer's disease in adults with Down syndrome. Alzheimers Dement (Amst). 2020; 12(1):e12028. Mapstone M, Gross TJ, Macciardi F, Cheema AK, Petersen M, Head E, Handen BL, Klunk WE, Christian BT, Silverman W, Lott IT, Schupf N, Alzheimer's Biomarkers Consortium–Down Syndrome (ABC-DS) Investigators. PMID: 32258359; PMCID: PMC7131985.
      View in: PubMed   Mentions: 4  
    7. The genetic architecture of the human cerebral cortex. Science. 2020 03 20; 367(6484). Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, Agartz I, Alhusaini S, Almeida MAA, Alnæs D, Amlien IK, Andersson M, Ard T, Armstrong NJ, Ashley-Koch A, Atkins JR, Bernard M, Brouwer RM, Buimer EEL, Bülow R, Bürger C, Cannon DM, Chakravarty M, Chen Q, Cheung JW, Couvy-Duchesne B, Dale AM, Dalvie S, de Araujo TK, de Zubicaray GI, de Zwarte SMC, den Braber A, Doan NT, Dohm K, Ehrlich S, Engelbrecht HR, Erk S, Fan CC, Fedko IO, Foley SF, Ford JM, Fukunaga M, Garrett ME, Ge T, Giddaluru S, Goldman AL, Green MJ, Groenewold NA, Grotegerd D, Gurholt TP, Gutman BA, Hansell NK, Harris MA, Harrison MB, Haswell CC, Hauser M, Herms S, Heslenfeld DJ, Ho NF, Hoehn D, Hoffmann P, Holleran L, Hoogman M, Hottenga JJ, Ikeda M, Janowitz D, Jansen IE, Jia T, Jockwitz C, Kanai R, Karama S, Kasperaviciute D, Kaufmann T, Kelly S, Kikuchi M, Klein M, Knapp M, Knodt AR, Krämer B, Lam M, Lancaster TM, Lee PH, Lett TA, Lewis LB, Lopes-Cendes I, Luciano M, Macciardi F, Marquand AF, Mathias SR, Melzer TR, Milaneschi Y, Mirza-Schreiber N, Moreira JCV, Mühleisen TW, Müller-Myhsok B, Najt P, Nakahara S, Nho K, Olde Loohuis LM, Orfanos DP, Pearson JF, Pitcher TL, Pütz B, Quidé Y, Ragothaman A, Rashid FM, Reay WR, Redlich R, Reinbold CS, Repple J, Richard G, Riedel BC, Risacher SL, Rocha CS, Mota NR, Salminen L, Saremi A, Saykin AJ, Schlag F, Schmaal L, Schofield PR, Secolin R, Shapland CY, Shen L, Shin J, Shumskaya E, Sønderby IE, Sprooten E, Tansey KE, Teumer A, Thalamuthu A, Tordesillas-Gutiérrez D, Turner JA, Uhlmann A, Vallerga CL, van der Meer D, van Donkelaar MMJ, van Eijk L, van Erp TGM, van Haren NEM, van Rooij D, van Tol MJ, Veldink JH, Verhoef E, Walton E, Wang M, Wang Y, Wardlaw JM, Wen W, Westlye LT, Whelan CD, Witt SH, Wittfeld K, Wolf C, Wolfers T, Wu JQ, Yasuda CL, Zaremba D, Zhang Z, Zwiers MP, Artiges E, Assareh AA, Ayesa-Arriola R, Belger A, Brandt CL, Brown GG, Cichon S, Curran JE, Davies GE, Degenhardt F, Dennis MF, Dietsche B, Djurovic S, Doherty CP, Espiritu R, Garijo D, Gil Y, Gowland PA, Green RC, Häusler AN, Heindel W, Ho BC, Hoffmann WU, Holsboer F, Homuth G, Hosten N, Jack CR, Jang M, Jansen A, Kimbrel NA, Kolskår K, Koops S, Krug A, Lim KO, Luykx JJ, Mathalon DH, Mather KA, Mattay VS, Matthews S, Mayoral Van Son J, McEwen SC, Melle I, Morris DW, Mueller BA, Nauck M, Nordvik JE, Nöthen MM, O'Leary DS, Opel N, Martinot MP, Pike GB, Preda A, Quinlan EB, Rasser PE, Ratnakar V, Reppermund S, Steen VM, Tooney PA, Torres FR, Veltman DJ, Voyvodic JT, Whelan R, White T, Yamamori H, Adams HHH, Bis JC, Debette S, Decarli C, Fornage M, Gudnason V, Hofer E, Ikram MA, Launer L, Longstreth WT, Lopez OL, Mazoyer B, Mosley TH, Roshchupkin GV, Satizabal CL, Schmidt R, Seshadri S, Yang Q, Alzheimer’s Disease Neuroimaging Initiative, CHARGE Consortium, EPIGEN Consortium, IMAGEN Consortium, SYS Consortium, Parkinson’s Progression Markers Initiative, Alvim MKM, Ames D, Anderson TJ, Andreassen OA, Arias-Vasquez A, Bastin ME, Baune BT, Beckham JC, Blangero J, Boomsma DI, Brodaty H, Brunner HG, Buckner RL, Buitelaar JK, Bustillo JR, Cahn W, Cairns MJ, Calhoun V, Carr VJ, Caseras X, Caspers S, Cavalleri GL, Cendes F, Corvin A, Crespo-Facorro B, Dalrymple-Alford JC, Dannlowski U, de Geus EJC, Deary IJ, Delanty N, Depondt C, Desrivières S, Donohoe G, Espeseth T, Fernández G, Fisher SE, Flor H, Forstner AJ, Francks C, Franke B, Glahn DC, Gollub RL, Grabe HJ, Gruber O, Håberg AK, Hariri AR, et al. PMID: 32193296; PMCID: PMC7295264.
      View in: PubMed   Mentions: 56     Fields:    Translation:Humans
    8. ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. Transl Psychiatry. 2020 03 20; 10(1):100. Thompson PM, Jahanshad N, Ching CRK, Salminen LE, Thomopoulos SI, Bright J, Baune BT, Bertolín S, Bralten J, Bruin WB, Bülow R, Chen J, Chye Y, Dannlowski U, de Kovel CGF, Donohoe G, Eyler LT, Faraone SV, Favre P, Filippi CA, Frodl T, Garijo D, Gil Y, Grabe HJ, Grasby KL, Hajek T, Han LKM, Hatton SN, Hilbert K, Ho TC, Holleran L, Homuth G, Hosten N, Houenou J, Ivanov I, Jia T, Kelly S, Klein M, Kwon JS, Laansma MA, Leerssen J, Lueken U, Nunes A, Neill JO, Opel N, Piras F, Piras F, Postema MC, Pozzi E, Shatokhina N, Soriano-Mas C, Spalletta G, Sun D, Teumer A, Tilot AK, Tozzi L, van der Merwe C, Van Someren EJW, van Wingen GA, Völzke H, Walton E, Wang L, Winkler AM, Wittfeld K, Wright MJ, Yun JY, Zhang G, Zhang-James Y, Adhikari BM, Agartz I, Aghajani M, Aleman A, Althoff RR, Altmann A, Andreassen OA, Baron DA, Bartnik-Olson BL, Marie Bas-Hoogendam J, Baskin-Sommers AR, Bearden CE, Berner LA, Boedhoe PSW, Brouwer RM, Buitelaar JK, Caeyenberghs K, Cecil CAM, Cohen RA, Cole JH, Conrod PJ, De Brito SA, de Zwarte SMC, Dennis EL, Desrivieres S, Dima D, Ehrlich S, Esopenko C, Fairchild G, Fisher SE, Fouche JP, Francks C, Frangou S, Franke B, Garavan HP, Glahn DC, Groenewold NA, Gurholt TP, Gutman BA, Hahn T, Harding IH, Hernaus D, Hibar DP, Hillary FG, Hoogman M, Hulshoff Pol HE, Jalbrzikowski M, Karkashadze GA, Klapwijk ET, Knickmeyer RC, Kochunov P, Koerte IK, Kong XZ, Liew SL, Lin AP, Logue MW, Luders E, Macciardi F, Mackey S, Mayer AR, McDonald CR, McMahon AB, Medland SE, Modinos G, Morey RA, Mueller SC, Mukherjee P, Namazova-Baranova L, Nir TM, Olsen A, Paschou P, Pine DS, Pizzagalli F, Rentería ME, Rohrer JD, Sämann PG, Schmaal L, Schumann G, Shiroishi MS, Sisodiya SM, Smit DJA, Sønderby IE, Stein DJ, Stein JL, Tahmasian M, Tate DF, Turner JA, van den Heuvel OA, van der Wee NJA, van der Werf YD, van Erp TGM, van Haren NEM, van Rooij D, van Velzen LS, Veer IM, Veltman DJ, Villalon-Reina JE, Walter H, Whelan CD, Wilde EA, Zarei M, Zelman V, ENIGMA Consortium. PMID: 32198361; PMCID: PMC7083923.
      View in: PubMed   Mentions: 46     Fields:    Translation:Humans
    9. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Mol Psychiatry. 2020 10; 25(10):2455-2467. Bigdeli TB, Genovese G, Georgakopoulos P, Meyers JL, Peterson RE, Iyegbe CO, Medeiros H, Valderrama J, Achtyes ED, Kotov R, Stahl EA, Abbott C, Azevedo MH, Belliveau RA, Bevilacqua E, Bromet EJ, Byerley W, Carvalho CB, Chapman SB, DeLisi LE, Dumont AL, O'Dushlaine C, Evgrafov OV, Fochtmann LJ, Gage D, Kennedy JL, Kinkead B, Macedo A, Moran JL, Morley CP, Dewan MJ, Nemesh J, Perkins DO, Purcell SM, Rakofsky JJ, Scolnick EM, Sklar BM, Sklar P, Smoller JW, Sullivan PF, Macciardi F, Marder SR, Gur RC, Gur RE, Braff DL, Consortium on the Genetics of Schizophrenia (COGS) Investigators, Nicolini H, Escamilla MA, Vawter MP, Sobell JL, Malaspina D, Lehrer DS, Buckley PF, Rapaport MH, Knowles JA, Genomic Psychiatry Cohort (GPC) Consortium, Fanous AH, Pato MT, McCarroll SA, Pato CN. PMID: 31591465; PMCID: PMC7515843.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    10. Dentate gyrus volume deficit in schizophrenia. Psychol Med. 2020 06; 50(8):1267-1277. Nakahara S, Turner JA, Calhoun VD, Lim KO, Mueller B, Bustillo JR, O'Leary DS, McEwen S, Voyvodic J, Belger A, Mathalon DH, Ford JM, Macciardi F, Matsumoto M, Potkin SG, van Erp TGM. PMID: 31155012; PMCID: PMC7068799.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    11. A method for building a genome-connectome bipartite graph model. J Neurosci Methods. 2019 05 15; 320:64-71. Yu Q, Chen J, Du Y, Sui J, Damaraju E, Turner JA, van Erp TGM, Macciardi F, Belger A, Ford JM, McEwen S, Mathalon DH, Mueller BA, Preda A, Vaidya J, Pearlson GD, Calhoun VD. PMID: 30902651; PMCID: PMC6504548.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    12. Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity. Curr Biol. 2019 Mar 04; 29(5):895. Gunz P, Tilot AK, Wittfeld K, Teumer A, Shapland CY, van Erp TGM, Dannemann M, Vernot B, Neubauer S, Guadalupe T, Fernández G, Brunner HG, Enard W, Fallon J, Hosten N, Völker U, Profico A, Di Vincenzo F, Manzi G, Kelso J, St Pourcain B, Hublin JJ, Franke B, Pääbo S, Macciardi F, Grabe HJ, Fisher SE. PMID: 30836076; PMCID: PMC6526943.
      View in: PubMed   Mentions: 3     Fields:    
    13. Transposable Elements. Curr Top Behav Neurosci. 2019; 42:221-246. Guffanti G, Bartlett A, DeCrescenzo P, Macciardi F, Hunter R. PMID: 31605305.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    14. Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1. Schizophr Bull. 2019 01 01; 45(1):222-232. Chen J, Calhoun VD, Lin D, Perrone-Bizzozero NI, Bustillo JR, Pearlson GD, Potkin SG, van Erp TGM, Macciardi F, Ehrlich S, Ho BC, Sponheim SR, Wang L, Stephen JM, Mayer AR, Hanlon FM, Jung RE, Clementz BA, Keshavan MS, Gershon ES, Sweeney JA, Tamminga CA, Andreassen OA, Agartz I, Westlye LT, Sui J, Du Y, Turner JA, Liu J. PMID: 29474680; PMCID: PMC6293216.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    15. Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity. Curr Biol. 2019 01 07; 29(1):120-127.e5. Gunz P, Tilot AK, Wittfeld K, Teumer A, Shapland CY, van Erp TGM, Dannemann M, Vernot B, Neubauer S, Guadalupe T, Fernández G, Brunner HG, Enard W, Fallon J, Hosten N, Völker U, Profico A, Di Vincenzo F, Manzi G, Kelso J, St Pourcain B, Hublin JJ, Franke B, Pääbo S, Macciardi F, Grabe HJ, Fisher SE. PMID: 30554901; PMCID: PMC6380688.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimals
    16. Reply to: New Meta- and Mega-analyses of Magnetic Resonance Imaging Findings in Schizophrenia: Do They Really Increase Our Knowledge About the Nature of the Disease Process? Biol Psychiatry. 2019 04 01; 85(7):e35-e39. van Erp TGM, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, Pearlson GD, Yao N, Fukunaga M, Hashimoto R, Okada N, Yamamori H, Clark VP, Mueller BA, de Zwarte SMC, Ophoff RA, van Haren NEM, Andreassen OA, Gurholt TP, Gruber O, Kraemer B, Richter A, Calhoun VD, Crespo-Facorro B, Roiz-Santiañez R, Tordesillas-Gutiérrez D, Loughland C, Catts S, Fullerton JM, Green MJ, Henskens F, Jablensky A, Mowry BJ, Pantelis C, Quidé Y, Schall U, Scott RJ, Cairns MJ, Seal M, Tooney PA, Rasser PE, Cooper G, Shannon Weickert C, Weickert TW, Hong E, Kochunov P, Gur RE, Gur RC, Ford JM, Macciardi F, Mathalon DH, Potkin SG, Preda A, Fan F, Ehrlich S, King MD, De Haan L, Veltman DJ, Assogna F, Banaj N, de Rossi P, Iorio M, Piras F, Spalletta G, Pomarol-Clotet E, Kelly S, Ciufolini S, Radua J, Murray R, Marques TR, Simmons A, Borgwardt S, Schönborn-Harrisberger F, Riecher-Rössler A, Smieskova R, Alpert KI, Bertolino A, Bonvino A, Di Giorgio A, Neilson E, Mayer AR, Yun JY, Cannon DM, Lebedeva I, Tomyshev AS, Akhadov T, Kaleda V, Fatouros-Bergman H, Flyckt L, Karolinska Schizophrenia Project, Rosa PGP, Serpa MH, Zanetti MV, Hoschl C, Skoch A, Spaniel F, Tomecek D, McIntosh AM, Whalley HC, Knöchel C, Oertel-Knöchel V, Howells FM, Stein DJ, Temmingh HS, Uhlmann A, Lopez-Jaramillo C, Dima D, Faskowitz JI, Gutman BA, Jahanshad N, Thompson PM, Turner JA. PMID: 30470561; PMCID: PMC7041557.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    17. Novel Bioinformatics Approach Identifies Transcriptional Profiles of Lineage-Specific Transposable Elements at Distinct Loci in the Human Dorsolateral Prefrontal Cortex. Mol Biol Evol. 2018 10 01; 35(10):2435-2453. Guffanti G, Bartlett A, Klengel T, Klengel C, Hunter R, Glinsky G, Macciardi F. PMID: 30053206; PMCID: PMC6188555.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    18. Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility. Oncotarget. 2018 Sep 25; 9(75):34079-34089. Ciceri S, Gamba B, Corbetta P, Mondini P, Terenziani M, Catania S, Nantron M, Bianchi M, D'Angelo P, Torri F, Macciardi F, Collini P, Di Martino M, Melchionda F, Di Cataldo A, Spreafico F, Radice P, Perotti D, AIEOP study group. PMID: 30344923; PMCID: PMC6183341.
      View in: PubMed   Mentions: 8     Fields:    
    19. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395). Brainstorm Consortium, Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A, Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel H, Owen MJ, Mead S, Passmore P, Morgan K, Nöthen MM, Rossor M, Lupton MK, Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A, Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Kurth T, Ligthart L, Terwindt GM, Freilinger T, Ran C, Gordon SD, Borck G, Adams HHH, Lehtimäki T, Wedenoja J, Buring JE, Schürks M, Hrafnsdottir M, Hottenga JJ, Penninx B, Artto V, Kaunisto M, Vepsäläinen S, Martin NG, Montgomery GW, Kurki MI, Hämäläinen E, Huang H, Huang J, Sandor C, Webber C, Muller-Myhsok B, Schreiber S, Salomaa V, Loehrer E, Göbel H, Macaya A, Pozo-Rosich P, Hansen T, Werge T, Kaprio J, Metspalu A, Kubisch C, Ferrari MD, Belin AC, van den Maagdenberg AMJM, Zwart JA, Boomsma D, Eriksson N, Olesen J, Chasman DI, Nyholt DR, Avbersek A, Baum L, Berkovic S, Bradfield J, Buono RJ, Catarino CB, Cossette P, De Jonghe P, Depondt C, Dlugos D, Ferraro TN, French J, Hjalgrim H, Jamnadas-Khoda J, Kälviäinen R, Kunz WS, Lerche H, Leu C, Lindhout D, Lo W, Lowenstein D, McCormack M, Møller RS, Molloy A, Ng PW, Oliver K, Privitera M, Radtke R, Ruppert AK, Sander T, Schachter S, Schankin C, Scheffer I, Schoch S, Sisodiya SM, Smith P, Sperling M, Striano P, Surges R, Thomas GN, Visscher F, Whelan CD, Zara F, Heinzen EL, Marson A, Becker F, Stroink H, Zimprich F, Gasser T, Gibbs R, Heutink P, Martinez M, Morris HR, Sharma M, Ryten M, Mok KY, Pulit S, Bevan S, Holliday E, Attia J, Battey T, Boncoraglio G, Thijs V, Chen WM, Mitchell B, Rothwell P, Sharma P, Sudlow C, Vicente A, Markus H, Kourkoulis C, Pera J, Raffeld M, Silliman S, Boraska Perica V, Thornton LM, Huckins LM, William Rayner N, Lewis CM, Gratacos M, Rybakowski F, Keski-Rahkonen A, Raevuori A, Hudson JI, Reichborn-Kjennerud T, Monteleone P, Karwautz A, Mannik K, Baker JH, O'Toole JK, Trace SE, Davis OSP, Helder SG, Ehrlich S, Herpertz-Dahlmann B, Danner UN, van Elburg AA, Clementi M, Forzan M, Docampo E, Lissowska J, Hauser J, Tortorella A, Maj M, Gonidakis F, Tziouvas K, Papezova H, Yilmaz Z, Wagner G, Cohen-Woods S, Herms S, Julià A, Rabionet R, Dick DM, Ripatti S, Andreassen OA, Espeseth T, Lundervold AJ, Steen VM, Pinto D, Scherer SW, Aschauer H, Schosser A, Alfredsson L, Padyukov L, Halmi KA, Mitchell J, Strober M, Bergen AW, Kaye W, Szatkiewicz JP, Cormand B, Ramos-Quiroga JA, Sánchez-Mora C, Ribasés M, Casas M, Hervas A, Arranz MJ, Haavik J, Zayats T, Johansson S, Williams N, Dempfle A, Rothenberger A, Kuntsi J, Oades RD, Banaschewski T, Franke B, Buitelaar JK, Arias Vasquez A, Doyle AE, Reif A, Lesch KP, Freitag C, Rivero O, Palmason H, Romanos M, Langley K, Rietschel M, Witt SH, Dalsgaard S, Børglum AD, Waldman I, Wilmot B, Molly N, Bau CHD, Crosbie J, Schachar R, et al. PMID: 29930110; PMCID: PMC6097237.
      View in: PubMed   Mentions: 327     Fields:    Translation:Humans
    20. Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Schizophr Res. 2018 11; 201:393-399. Nakahara S, Medland S, Turner JA, Calhoun VD, Lim KO, Mueller BA, Bustillo JR, O'Leary DS, Vaidya JG, McEwen S, Voyvodic J, Belger A, Mathalon DH, Ford JM, Guffanti G, Macciardi F, Potkin SG, van Erp TGM. PMID: 29907492; PMCID: PMC6252137.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    21. Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium. Biol Psychiatry. 2018 11 01; 84(9):644-654. van Erp TGM, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, Pearlson GD, Yao N, Fukunaga M, Hashimoto R, Okada N, Yamamori H, Bustillo JR, Clark VP, Agartz I, Mueller BA, Cahn W, de Zwarte SMC, Hulshoff Pol HE, Kahn RS, Ophoff RA, van Haren NEM, Andreassen OA, Dale AM, Doan NT, Gurholt TP, Hartberg CB, Haukvik UK, Jørgensen KN, Lagerberg TV, Melle I, Westlye LT, Gruber O, Kraemer B, Richter A, Zilles D, Calhoun VD, Crespo-Facorro B, Roiz-Santiañez R, Tordesillas-Gutiérrez D, Loughland C, Carr VJ, Catts S, Cropley VL, Fullerton JM, Green MJ, Henskens FA, Jablensky A, Lenroot RK, Mowry BJ, Michie PT, Pantelis C, Quidé Y, Schall U, Scott RJ, Cairns MJ, Seal M, Tooney PA, Rasser PE, Cooper G, Shannon Weickert C, Weickert TW, Morris DW, Hong E, Kochunov P, Beard LM, Gur RE, Gur RC, Satterthwaite TD, Wolf DH, Belger A, Brown GG, Ford JM, Macciardi F, Mathalon DH, O'Leary DS, Potkin SG, Preda A, Voyvodic J, Lim KO, McEwen S, Yang F, Tan Y, Tan S, Wang Z, Fan F, Chen J, Xiang H, Tang S, Guo H, Wan P, Wei D, Bockholt HJ, Ehrlich S, Wolthusen RPF, King MD, Shoemaker JM, Sponheim SR, De Haan L, Koenders L, Machielsen MW, van Amelsvoort T, Veltman DJ, Assogna F, Banaj N, de Rossi P, Iorio M, Piras F, Spalletta G, McKenna PJ, Pomarol-Clotet E, Salvador R, Corvin A, Donohoe G, Kelly S, Whelan CD, Dickie EW, Rotenberg D, Voineskos AN, Ciufolini S, Radua J, Dazzan P, Murray R, Reis Marques T, Simmons A, Borgwardt S, Egloff L, Harrisberger F, Riecher-Rössler A, Smieskova R, Alpert KI, Wang L, Jönsson EG, Koops S, Sommer IEC, Bertolino A, Bonvino A, Di Giorgio A, Neilson E, Mayer AR, Stephen JM, Kwon JS, Yun JY, Cannon DM, McDonald C, Lebedeva I, Tomyshev AS, Akhadov T, Kaleda V, Fatouros-Bergman H, Flyckt L, Karolinska Schizophrenia Project, Busatto GF, Rosa PGP, Serpa MH, Zanetti MV, Hoschl C, Skoch A, Spaniel F, Tomecek D, Hagenaars SP, McIntosh AM, Whalley HC, Lawrie SM, Knöchel C, Oertel-Knöchel V, Stäblein M, Howells FM, Stein DJ, Temmingh HS, Uhlmann A, Lopez-Jaramillo C, Dima D, McMahon A, Faskowitz JI, Gutman BA, Jahanshad N, Thompson PM, Turner JA. PMID: 29960671; PMCID: PMC6177304.
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    22. Plasma metabolomic biomarkers accurately classify acute mild traumatic brain injury from controls. PLoS One. 2018; 13(4):e0195318. Fiandaca MS, Mapstone M, Mahmoodi A, Gross T, Macciardi F, Cheema AK, Merchant-Borna K, Bazarian J, Federoff HJ. PMID: 29677216; PMCID: PMC5909890.
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    23. Mitochondrial variability in the Mediterranean area: a complex stage for human migrations. Ann Hum Biol. 2018 Feb; 45(1):5-19. De Angelis F, Scorrano G, Martínez-Labarga C, Scano G, Macciardi F, Rickards O. PMID: 29382277.
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    24. Toward Reproducible Results from Targeted Metabolomic Studies: Perspectives for Data Pre-processing and a Basis for Analytic Pipeline Development. Curr Top Med Chem. 2018; 18(11):883-895. Gross T, Mapstone M, Miramontes R, Padilla R, Cheema AK, Macciardi F, Federoff HJ, Fiandaca MS. PMID: 29992885.
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    25. Systems healthcare: a holistic paradigm for tomorrow. BMC Syst Biol. 2017 Dec 19; 11(1):142. Fiandaca MS, Mapstone M, Connors E, Jacobson M, Monuki ES, Malik S, Macciardi F, Federoff HJ. PMID: 29258513; PMCID: PMC5738174.
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    26. Epigenetic mechanisms and associated brain circuits in the regulation of positive emotions: A role for transposable elements. J Comp Neurol. 2016 10 15; 524(15):2944-54. Gaudi S, Guffanti G, Fallon J, Macciardi F. PMID: 27224878.
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    27. LINE1 insertions as a genomic risk factor for schizophrenia: Preliminary evidence from an affected family. Am J Med Genet B Neuropsychiatr Genet. 2016 06; 171(4):534-45. Guffanti G, Gaudi S, Klengel T, Fallon JH, Mangalam H, Madduri R, Rodriguez A, DeCrescenzo P, Glovienka E, Sobell J, Klengel C, Pato M, Ressler KJ, Pato C, Macciardi F. PMID: 26990047.
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    28. Chromosomal anomalies at 1q, 3, 16q, and mutations of SIX1 and DROSHA genes underlie Wilms tumor recurrences. Oncotarget. 2016 Feb 23; 7(8):8908-15. Spreafico F, Ciceri S, Gamba B, Torri F, Terenziani M, Collini P, Macciardi F, Radice P, Perotti D. PMID: 26802027; PMCID: PMC4891013.
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    29. Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium. Mol Psychiatry. 2016 Apr; 21(4):585. van Erp TG, Hibar DP, Rasmussen JM, Glahn DC, Pearlson GD, Andreassen OA, Agartz I, Westlye LT, Haukvik UK, Dale AM, Melle I, Hartberg CB, Gruber O, Kraemer B, Zilles D, Donohoe G, Kelly S, McDonald C, Morris DW, Cannon DM, Corvin A, Machielsen MW, Koenders L, de Haan L, Veltman DJ, Satterthwaite TD, Wolf DH, Gur RC, Gur RE, Potkin SG, Mathalon DH, Mueller BA, Preda A, Macciardi F, Ehrlich S, Walton E, Hass J, Calhoun VD, Bockholt HJ, Sponheim SR, Shoemaker JM, van Haren NE, Pol HE, Ophoff RA, Kahn RS, Roiz-Santiañez R, Crespo-Facorro B, Wang L, Alpert KI, Jönsson EG, Dimitrova R, Bois C, Whalley HC, McIntosh AM, Lawrie SM, Hashimoto R, Thompson PM, Turner JA. PMID: 26283641; PMCID: PMC5751698.
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    30. Huntington's disease cerebrospinal fluid seeds aggregation of mutant huntingtin. Mol Psychiatry. 2015 Nov; 20(11):1286-93. Tan Z, Dai W, van Erp TG, Overman J, Demuro A, Digman MA, Hatami A, Albay R, Sontag EM, Potkin KT, Ling S, Macciardi F, Bunney WE, Long JD, Paulsen JS, Ringman JM, Parker I, Glabe C, Thompson LM, Chiu W, Potkin SG. PMID: 26100538; PMCID: PMC4718563.
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    31. Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium. Mol Psychiatry. 2016 Apr; 21(4):547-53. van Erp TG, Hibar DP, Rasmussen JM, Glahn DC, Pearlson GD, Andreassen OA, Agartz I, Westlye LT, Haukvik UK, Dale AM, Melle I, Hartberg CB, Gruber O, Kraemer B, Zilles D, Donohoe G, Kelly S, McDonald C, Morris DW, Cannon DM, Corvin A, Machielsen MW, Koenders L, de Haan L, Veltman DJ, Satterthwaite TD, Wolf DH, Gur RC, Gur RE, Potkin SG, Mathalon DH, Mueller BA, Preda A, Macciardi F, Ehrlich S, Walton E, Hass J, Calhoun VD, Bockholt HJ, Sponheim SR, Shoemaker JM, van Haren NE, Hulshoff Pol HE, Pol HE, Ophoff RA, Kahn RS, Roiz-Santiañez R, Crespo-Facorro B, Wang L, Alpert KI, Jönsson EG, Dimitrova R, Bois C, Whalley HC, McIntosh AM, Lawrie SM, Hashimoto R, Thompson PM, Turner JA. PMID: 26033243; PMCID: PMC4668237.
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    32. Ablation of D2 autoreceptors causes epigenetic reprogramming of cortical neurons. Mol Psychiatry. 2014 Nov; 19(11):1153. Brami-Cherrier K, Anzalone A, Ramos M, Forne I, Macciardi F, Imhof A, Borrelli E. PMID: 25346033.
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    33. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry. 2015 Jan; 172(1):82-93. Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, Illmann C, McGrath LM, Mayerfeld C, Arepalli S, Barlassina C, Barr CL, Bellodi L, Benarroch F, Berrió GB, Bienvenu OJ, Black DW, Bloch MH, Brentani H, Bruun RD, Budman CL, Camarena B, Campbell DD, Cappi C, Silgado JC, Cavallini MC, Chavira DA, Chouinard S, Cook EH, Cookson MR, Coric V, Cullen B, Cusi D, Delorme R, Denys D, Dion Y, Eapen V, Egberts K, Falkai P, Fernandez T, Fournier E, Garrido H, Geller D, Gilbert DL, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Grünblatt E, Hardy J, Heiman GA, Hemmings SM, Herrera LD, Hezel DM, Hoekstra PJ, Jankovic J, Kennedy JL, King RA, Konkashbaev AI, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Lupoli S, Macciardi F, Maier W, Manunta P, Marconi M, McCracken JT, Mesa Restrepo SC, Moessner R, Moorjani P, Morgan J, Muller H, Murphy DL, Naarden AL, Nurmi E, Ochoa WC, Ophoff RA, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner T, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosário MC, Rosenberg D, Ruhrmann S, Sabatti C, Salvi E, Sampaio AS, Samuels J, Sandor P, Service SK, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Turiel M, Valencia Duarte AV, Vallada H, Veenstra-VanderWeele J, Walitza S, Wang Y, Weale M, Weiss R, Wendland JR, Westenberg HG, Shugart YY, Hounie AG, Miguel EC, Nicolini H, Wagner M, Ruiz-Linares A, Cath DC, McMahon W, Posthuma D, Oostra BA, Nestadt G, Rouleau GA, Purcell S, Jenike MA, Heutink P, Hanna GL, Conti DV, Arnold PD, Freimer NB, Stewart SE, Knowles JA, Cox NJ, Pauls DL. PMID: 25158072; PMCID: PMC4282594.
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    34. Imaging genetics approaches to identify mechanisms in severe mental illness. Biol Psychiatry. 2014 Sep 15; 76(6):436-7. Potkin SG, Macciardi F, van Erp TG. PMID: 25149350.
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    35. Epigenetic reprogramming of cortical neurons through alteration of dopaminergic circuits. Mol Psychiatry. 2014 Nov; 19(11):1193-200. Brami-Cherrier K, Anzalone A, Ramos M, Forne I, Macciardi F, Imhof A, Borrelli E. PMID: 25023144; PMCID: PMC4211954.
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    36. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. J Am Acad Child Adolesc Psychiatry. 2014 Aug; 53(8):910-9. McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, Gallagher P, Fagerness JA, Barr CL, Bellodi L, Benarroch F, Bienvenu OJ, Black DW, Bloch MH, Bruun RD, Budman CL, Camarena B, Cath DC, Cavallini MC, Chouinard S, Coric V, Cullen B, Delorme R, Denys D, Derks EM, Dion Y, Rosário MC, Eapen V, Evans P, Falkai P, Fernandez TV, Garrido H, Geller D, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Grünblatt E, Heiman GA, Hemmings SM, Herrera LD, Hounie AG, Jankovic J, Kennedy JL, King RA, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Lochner C, Lowe TL, Lyon GJ, Macciardi F, Maier W, McCracken JT, McMahon W, Murphy DL, Naarden AL, Neale BM, Nurmi E, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Reus VI, Richter MA, Riddle M, Robertson MM, Rosenberg D, Rouleau GA, Ruhrmann S, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Tischfield JA, Vallada H, Veenstra-VanderWeele J, Walitza S, Wang Y, Wendland JR, Shugart YY, Miguel EC, Nicolini H, Oostra BA, Moessner R, Wagner M, Ruiz-Linares A, Heutink P, Nestadt G, Freimer N, Petryshen T, Posthuma D, Jenike MA, Cox NJ, Hanna GL, Brentani H, Scherer SW, Arnold PD, Stewart SE, Mathews CA, Knowles JA, Cook EH, Pauls DL, Wang K, Scharf JM. PMID: 25062598; PMCID: PMC4218748.
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    37. The perfect neuroimaging-genetics-computation storm: collision of petabytes of data, millions of hardware devices and thousands of software tools. Brain Imaging Behav. 2014 Jun; 8(2):311-22. Dinov ID, Petrosyan P, Liu Z, Eggert P, Zamanyan A, Torri F, Macciardi F, Hobel S, Moon SW, Sung YH, Jiang Z, Labus J, Kurth F, Ashe-McNalley C, Mayer E, Vespa PM, Van Horn JD, Toga AW, Alzheimer’s Disease Neuroimaging Initiative. PMID: 23975276; PMCID: PMC3933453.
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    38. Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers. Brain Imaging Behav. 2014 Jun; 8(2):183-207. Shen L, Thompson PM, Potkin SG, Bertram L, Farrer LA, Foroud TM, Green RC, Hu X, Huentelman MJ, Kim S, Kauwe JS, Li Q, Liu E, Macciardi F, Moore JH, Munsie L, Nho K, Ramanan VK, Risacher SL, Stone DJ, Swaminathan S, Toga AW, Weiner MW, Saykin AJ, Alzheimer’s Disease Neuroimaging Initiative. PMID: 24092460; PMCID: PMC3976843.
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    39. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav. 2014 Jun; 8(2):153-82. Thompson PM, Stein JL, Medland SE, Hibar DP, Vasquez AA, Renteria ME, Toro R, Jahanshad N, Schumann G, Franke B, Wright MJ, Martin NG, Agartz I, Alda M, Alhusaini S, Almasy L, Almeida J, Alpert K, Andreasen NC, Andreassen OA, Apostolova LG, Appel K, Armstrong NJ, Aribisala B, Bastin ME, Bauer M, Bearden CE, Bergmann O, Binder EB, Blangero J, Bockholt HJ, Bøen E, Bois C, Boomsma DI, Booth T, Bowman IJ, Bralten J, Brouwer RM, Brunner HG, Brohawn DG, Buckner RL, Buitelaar J, Bulayeva K, Bustillo JR, Calhoun VD, Cannon DM, Cantor RM, Carless MA, Caseras X, Cavalleri GL, Chakravarty MM, Chang KD, Ching CR, Christoforou A, Cichon S, Clark VP, Conrod P, Coppola G, Crespo-Facorro B, Curran JE, Czisch M, Deary IJ, de Geus EJ, den Braber A, Delvecchio G, Depondt C, de Haan L, de Zubicaray GI, Dima D, Dimitrova R, Djurovic S, Dong H, Donohoe G, Duggirala R, Dyer TD, Ehrlich S, Ekman CJ, Elvsåshagen T, Emsell L, Erk S, Espeseth T, Fagerness J, Fears S, Fedko I, Fernández G, Fisher SE, Foroud T, Fox PT, Francks C, Frangou S, Frey EM, Frodl T, Frouin V, Garavan H, Giddaluru S, Glahn DC, Godlewska B, Goldstein RZ, Gollub RL, Grabe HJ, Grimm O, Gruber O, Guadalupe T, Gur RE, Gur RC, Göring HH, Hagenaars S, Hajek T, Hall GB, Hall J, Hardy J, Hartman CA, Hass J, Hatton SN, Haukvik UK, Hegenscheid K, Heinz A, Hickie IB, Ho BC, Hoehn D, Hoekstra PJ, Hollinshead M, Holmes AJ, Homuth G, Hoogman M, Hong LE, Hosten N, Hottenga JJ, Hulshoff Pol HE, Hwang KS, Jack CR, Jenkinson M, Johnston C, Jönsson EG, Kahn RS, Kasperaviciute D, Kelly S, Kim S, Kochunov P, Koenders L, Krämer B, Kwok JB, Lagopoulos J, Laje G, Landen M, Landman BA, Lauriello J, Lawrie SM, Lee PH, Le Hellard S, Lemaître H, Leonardo CD, Li CS, Liberg B, Liewald DC, Liu X, Lopez LM, Loth E, Lourdusamy A, Luciano M, Macciardi F, Machielsen MW, Macqueen GM, Malt UF, Mandl R, Manoach DS, Martinot JL, Matarin M, Mather KA, Mattheisen M, Mattingsdal M, Meyer-Lindenberg A, McDonald C, McIntosh AM, McMahon FJ, McMahon KL, Meisenzahl E, Melle I, Milaneschi Y, Mohnke S, Montgomery GW, Morris DW, Moses EK, Mueller BA, Muñoz Maniega S, Mühleisen TW, Müller-Myhsok B, Mwangi B, Nauck M, Nho K, Nichols TE, Nilsson LG, Nugent AC, Nyberg L, Olvera RL, Oosterlaan J, Ophoff RA, Pandolfo M, Papalampropoulou-Tsiridou M, Papmeyer M, Paus T, Pausova Z, Pearlson GD, Penninx BW, Peterson CP, Pfennig A, Phillips M, Pike GB, Poline JB, Potkin SG, Pütz B, Ramasamy A, Rasmussen J, Rietschel M, Rijpkema M, Risacher SL, Roffman JL, Roiz-Santiañez R, Romanczuk-Seiferth N, Rose EJ, Royle NA, Rujescu D, Ryten M, Sachdev PS, Salami A, Satterthwaite TD, Savitz J, Saykin AJ, Scanlon C, Schmaal L, Schnack HG, Schork AJ, Schulz SC, Schür R, Seidman L, Shen L, Shoemaker JM, Simmons A, Sisodiya SM, Smith C, Smoller JW, Soares JC, Sponheim SR, Sprooten E, Starr JM, Steen VM, Strakowski S, Strike L, Sussmann J, Sämann PG, Teumer A, Toga AW, Tordesillas-Gutierrez D, Trabzuni D, Trost S, Turner J, Van den Heuvel M, van der Wee NJ, van Eijk K, van Erp TG, van Haren NE, van 't Ent D, van Tol MJ, Valdés Hernández MC, Veltman DJ, Versace A, Völzke H, Walker R, Walter H, Wang L, Wardlaw JM, Weale ME, Weiner MW, Wen W, Westlye LT, Whalley HC, Whelan CD, White T, Winkler AM, Wittfeld K, Woldehawariat G, Wolf C, Zilles D, Zwiers MP, Thalamuthu A, Schofield PR, Freimer NB, Lawrence NS, Drevets W, Alzheimer’s Disease Neuroimaging Initiative, EPIGEN Consortium, IMAGEN Consortium, Saguenay Youth St. PMID: 24399358; PMCID: PMC4008818.
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    40. Transposable elements and psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet. 2014 Apr; 165B(3):201-16. Guffanti G, Gaudi S, Fallon JH, Sobell J, Potkin SG, Pato C, Macciardi F. PMID: 24585726.
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    41. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genet. 2013 Oct; 9(10):e1003864. Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, Bloch MH, Blom RM, Bruun RD, Budman CL, Camarena B, Campbell D, Cappi C, Cardona Silgado JC, Cath DC, Cavallini MC, Chavira DA, Chouinard S, Conti DV, Cook EH, Coric V, Cullen BA, Deforce D, Delorme R, Dion Y, Edlund CK, Egberts K, Falkai P, Fernandez TV, Gallagher PJ, Garrido H, Geller D, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Haddad S, Heiman GA, Hemmings SM, Hounie AG, Illmann C, Jankovic J, Jenike MA, Kennedy JL, King RA, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Macciardi F, McCracken JT, McGrath LM, Mesa Restrepo SC, Moessner R, Morgan J, Muller H, Murphy DL, Naarden AL, Ochoa WC, Ophoff RA, Osiecki L, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner TJ, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosàrio MC, Rosenberg D, Rouleau GA, Ruhrmann S, Ruiz-Linares A, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Valencia Duarte AV, Vallada H, Van Nieuwerburgh F, Veenstra-Vanderweele J, Walitza S, Wang Y, Wendland JR, Westenberg HG, Shugart YY, Miguel EC, McMahon W, Wagner M, Nicolini H, Posthuma D, Hanna GL, Heutink P, Denys D, Arnold PD, Oostra BA, Nestadt G, Freimer NB, Pauls DL, Wray NR, Stewart SE, Mathews CA, Knowles JA, Cox NJ, Scharf JM. PMID: 24204291; PMCID: PMC3812053.
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    67. Adducin- and ouabain-related gene variants predict the antihypertensive activity of rostafuroxin, part 2: clinical studies. Sci Transl Med. 2010 Nov 24; 2(59):59ra87. Lanzani C, Citterio L, Glorioso N, Manunta P, Tripodi G, Salvi E, Carpini SD, Ferrandi M, Messaggio E, Staessen JA, Cusi D, Macciardi F, Argiolas G, Valentini G, Ferrari P, Bianchi G. PMID: 21106941.
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    68. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010 Nov; 42(11):937-48. Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Lango Allen H, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, Heid IM, Steinthorsdottir V, Stringham HM, Weedon MN, Wheeler E, Wood AR, Ferreira T, Weyant RJ, Segrè AV, Estrada K, Liang L, Nemesh J, Park JH, Gustafsson S, Kilpeläinen TO, Yang J, Bouatia-Naji N, Esko T, Feitosa MF, Kutalik Z, Mangino M, Raychaudhuri S, Scherag A, Smith AV, Welch R, Zhao JH, Aben KK, Absher DM, Amin N, Dixon AL, Fisher E, Glazer NL, Goddard ME, Heard-Costa NL, Hoesel V, Hottenga JJ, Johansson A, Johnson T, Ketkar S, Lamina C, Li S, Moffatt MF, Myers RH, Narisu N, Perry JR, Peters MJ, Preuss M, Ripatti S, Rivadeneira F, Sandholt C, Scott LJ, Timpson NJ, Tyrer JP, van Wingerden S, Watanabe RM, White CC, Wiklund F, Barlassina C, Chasman DI, Cooper MN, Jansson JO, Lawrence RW, Pellikka N, Prokopenko I, Shi J, Thiering E, Alavere H, Alibrandi MT, Almgren P, Arnold AM, Aspelund T, Atwood LD, Balkau B, Balmforth AJ, Bennett AJ, Ben-Shlomo Y, Bergman RN, Bergmann S, Biebermann H, Blakemore AI, Boes T, Bonnycastle LL, Bornstein SR, Brown MJ, Buchanan TA, Busonero F, Campbell H, Cappuccio FP, Cavalcanti-Proença C, Chen YD, Chen CM, Chines PS, Clarke R, Coin L, Connell J, Day IN, den Heijer M, Duan J, Ebrahim S, Elliott P, Elosua R, Eiriksdottir G, Erdos MR, Eriksson JG, Facheris MF, Felix SB, Fischer-Posovszky P, Folsom AR, Friedrich N, Freimer NB, Fu M, Gaget S, Gejman PV, Geus EJ, Gieger C, Gjesing AP, Goel A, Goyette P, Grallert H, Grässler J, Greenawalt DM, Groves CJ, Gudnason V, Guiducci C, Hartikainen AL, Hassanali N, Hall AS, Havulinna AS, Hayward C, Heath AC, Hengstenberg C, Hicks AA, Hinney A, Hofman A, Homuth G, Hui J, Igl W, Iribarren C, Isomaa B, Jacobs KB, Jarick I, Jewell E, John U, Jørgensen T, Jousilahti P, Jula A, Kaakinen M, Kajantie E, Kaplan LM, Kathiresan S, Kettunen J, Kinnunen L, Knowles JW, Kolcic I, König IR, Koskinen S, Kovacs P, Kuusisto J, Kraft P, Kvaløy K, Laitinen J, Lantieri O, Lanzani C, Launer LJ, Lecoeur C, Lehtimäki T, Lettre G, Liu J, Lokki ML, Lorentzon M, Luben RN, Ludwig B, MAGIC, Manunta P, Marek D, Marre M, Martin NG, McArdle WL, McCarthy A, McKnight B, Meitinger T, Melander O, Meyre D, Midthjell K, Montgomery GW, Morken MA, Morris AP, Mulic R, Ngwa JS, Nelis M, Neville MJ, Nyholt DR, O'Donnell CJ, O'Rahilly S, Ong KK, Oostra B, Paré G, Parker AN, Perola M, Pichler I, Pietiläinen KH, Platou CG, Polasek O, Pouta A, Rafelt S, Raitakari O, Rayner NW, Ridderstråle M, Rief W, Ruokonen A, Robertson NR, Rzehak P, Salomaa V, Sanders AR, Sandhu MS, Sanna S, Saramies J, Savolainen MJ, Scherag S, Schipf S, Schreiber S, Schunkert H, Silander K, Sinisalo J, Siscovick DS, Smit JH, Soranzo N, Sovio U, Stephens J, Surakka I, Swift AJ, Tammesoo ML, Tardif JC, Teder-Laving M, Teslovich TM, Thompson JR, Thomson B, Tönjes A, Tuomi T, van Meurs JB, van Ommen GJ, Vatin V, Viikari J, Visvikis-Siest S, Vitart V, Vogel CI, Voight BF, Waite LL, Wallaschofski H, Walters GB, Widen E, Wiegand S, Wild SH, Willemsen G, Witte DR, Witteman JC, Xu J, Zhang Q, Zgaga L, Ziegler A, Zitting P, Beilby JP, Farooqi IS, Hebebrand J, Huikuri HV, James AL, Kähönen M, Levinson DF, Macciardi F, Nieminen MS, Ohlsson C, Palmer LJ, Ridker PM, Stumvoll M, Beckmann JS, Boeing H, Boerwinkle E, Boomsma DI, Caulfield MJ, Chanock SJ, Collins FS, Cupples LA, Smith GD, Erdmann J, Froguel P, Grönberg H, Gyllensten U, Hall P, Hansen T, Harris TB, Hattersley AT, Hayes RB, Heinrich J, Hu FB, Hveem K, Illig T, Jarvelin MR, Kaprio J, Karpe F, Khaw KT, Kiemeney LA, Krude H, Laakso M, Lawlor DA, Metspalu A, Munroe PB, Ouwehand WH, Pedersen O, Penninx BW, et al. PMID: 20935630; PMCID: PMC3014648.
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    69. Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. Nat Genet. 2010 Aug; 42(8):658-60. Liu X, Invernizzi P, Lu Y, Kosoy R, Lu Y, Bianchi I, Podda M, Xu C, Xie G, Macciardi F, Selmi C, Lupoli S, Shigeta R, Ransom M, Lleo A, Lee AT, Mason AL, Myers RP, Peltekian KM, Ghent CN, Bernuzzi F, Zuin M, Rosina F, Borghesio E, Floreani A, Lazzari R, Niro G, Andriulli A, Muratori L, Muratori P, Almasio PL, Andreone P, Margotti M, Brunetto M, Coco B, Alvaro D, Bragazzi MC, Marra F, Pisano A, Rigamonti C, Colombo M, Marzioni M, Benedetti A, Fabris L, Strazzabosco M, Portincasa P, Palmieri VO, Tiribelli C, Croce L, Bruno S, Rossi S, Vinci M, Prisco C, Mattalia A, Toniutto P, Picciotto A, Galli A, Ferrari C, Colombo S, Casella G, Morini L, Caporaso N, Colli A, Spinzi G, Montanari R, Gregersen PK, Heathcote EJ, Hirschfield GM, Siminovitch KA, Amos CI, Gershwin ME, Seldin MF. PMID: 20639880; PMCID: PMC3150510.
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    70. Role of UBE3A and ATP10A genes in autism susceptibility region 15q11-q13 in an Italian population: a positive replication for UBE3A. Psychiatry Res. 2011 Jan 30; 185(1-2):33-8. Guffanti G, Strik Lievers L, Bonati MT, Marchi M, Geronazzo L, Nardocci N, Estienne M, Larizza L, Macciardi F, Russo S. PMID: 20609483.
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    71. Identifying gene regulatory networks in schizophrenia. Neuroimage. 2010 Nov 15; 53(3):839-47. Potkin SG, Macciardi F, Guffanti G, Fallon JH, Wang Q, Turner JA, Lakatos A, Miles MF, Lander A, Vawter MP, Xie X. PMID: 20600988; PMCID: PMC3055795.
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    72. Pilot study on schizophrenia in Sardinia. Hum Hered. 2010; 70(2):92-6. Ott J, Macciardi F, Shen Y, Carta MG, Murru A, Triunfo R, Robledo R, Rinaldi A, Contu L, Siniscalco M. PMID: 20558996; PMCID: PMC7077084.
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    73. Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort. Neurobiol Aging. 2010 Aug; 31(8):1355-63. Lakatos A, Derbeneva O, Younes D, Keator D, Bakken T, Lvova M, Brandon M, Guffanti G, Reglodi D, Saykin A, Weiner M, Macciardi F, Schork N, Wallace DC, Potkin SG, Alzheimer's Disease Neuroimaging Initiative. PMID: 20538375; PMCID: PMC2918801.
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    74. Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence. FASEB J. 2010 Aug; 24(8):3066-82. Torri F, Akelai A, Lupoli S, Sironi M, Amann-Zalcenstein D, Fumagalli M, Dal Fiume C, Ben-Asher E, Kanyas K, Cagliani R, Cozzi P, Trombetti G, Strik Lievers L, Salvi E, Orro A, Beckmann JS, Lancet D, Kohn Y, Milanesi L, Ebstein RB, Lerer B, Macciardi F. PMID: 20371615.
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    75. Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene. Am J Hum Genet. 2010 Jan; 86(1):72-6. Volpi L, Roversi G, Colombo EA, Leijsten N, Concolino D, Calabria A, Mencarelli MA, Fimiani M, Macciardi F, Pfundt R, Schoenmakers EF, Larizza L. PMID: 20004881; PMCID: PMC2801743.
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    76. alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy. J Mol Med (Berl). 2010 Feb; 88(2):203-17. Ferrandi M, Cusi D, Molinari I, Del Vecchio L, Barlassina C, Rastaldi MP, Schena FP, Macciardi F, Marcantoni C, Roccatello D, Peters LL, Armelloni S, Min L, Giardino L, Mattinzoli D, Camisasca C, Palazzo F, Manunta P, Ferrari P, Bianchi G. PMID: 19838659; PMCID: PMC2832889.
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    77. Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. PLoS One. 2009 Aug 07; 4(8):e6501. Potkin SG, Guffanti G, Lakatos A, Turner JA, Kruggel F, Fallon JH, Saykin AJ, Orro A, Lupoli S, Salvi E, Weiner M, Macciardi F, Alzheimer's Disease Neuroimaging Initiative. PMID: 19668339; PMCID: PMC2719581.
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    78. Diverse evolutionary histories for beta-adrenoreceptor genes in humans. Am J Hum Genet. 2009 Jul; 85(1):64-75. Cagliani R, Fumagalli M, Pozzoli U, Riva S, Comi GP, Torri F, Macciardi F, Bresolin N, Sironi M. PMID: 19576569; PMCID: PMC2706968.
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    79. A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum Mol Genet. 2009 Apr 15; 18(8):1524-32. Chiò A, Schymick JC, Restagno G, Scholz SW, Lombardo F, Lai SL, Mora G, Fung HC, Britton A, Arepalli S, Gibbs JR, Nalls M, Berger S, Kwee LC, Oddone EZ, Ding J, Crews C, Rafferty I, Washecka N, Hernandez D, Ferrucci L, Bandinelli S, Guralnik J, Macciardi F, Torri F, Lupoli S, Chanock SJ, Thomas G, Hunter DJ, Gieger C, Wichmann HE, Calvo A, Mutani R, Battistini S, Giannini F, Caponnetto C, Mancardi GL, La Bella V, Valentino F, Monsurrò MR, Tedeschi G, Marinou K, Sabatelli M, Conte A, Mandrioli J, Sola P, Salvi F, Bartolomei I, Siciliano G, Carlesi C, Orrell RW, Talbot K, Simmons Z, Connor J, Pioro EP, Dunkley T, Stephan DA, Kasperaviciute D, Fisher EM, Jabonka S, Sendtner M, Beck M, Bruijn L, Rothstein J, Schmidt S, Singleton A, Hardy J, Traynor BJ. PMID: 19193627; PMCID: PMC2664150.
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    80. Developing a genomic-based point-of-care diagnostic system for rheumatoid arthritis and multiple sclerosis. Annu Int Conf IEEE Eng Med Biol Soc. 2009; 2009:827-30. Kalatzis FG, Giannakeas N, Exarchos TP, Lorenzelli L, Adami A, Decarli M, Lupoli S, Macciardi F, Markoula S, Georgiou I, Fotiadis DI. PMID: 19964246.
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    81. Genome-wide strategies for discovering genetic influences on cognition and cognitive disorders: methodological considerations. Cogn Neuropsychiatry. 2009; 14(4-5):391-418. Potkin SG, Turner JA, Guffanti G, Lakatos A, Torri F, Keator DB, Macciardi F. PMID: 19634037; PMCID: PMC3037334.
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    82. Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia. Mol Psychiatry. 2009 Apr; 14(4):416-28. Potkin SG, Turner JA, Fallon JA, Lakatos A, Keator DB, Guffanti G, Macciardi F. PMID: 19065146; PMCID: PMC3254586.
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    83. A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. Schizophr Bull. 2009 Jan; 35(1):96-108. Potkin SG, Turner JA, Guffanti G, Lakatos A, Fallon JH, Nguyen DD, Mathalon D, Ford J, Lauriello J, Macciardi F, FBIRN. PMID: 19023125; PMCID: PMC2643953.
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    84. Association study of brain-derived neurotrophic factor (BDNF) and LIN-7 homolog (LIN-7) genes with adult attention-deficit/hyperactivity disorder. . 2008 Sep 05; 147B(6):945-51. Lanktree M, Squassina A, Krinsky M, Strauss J, Jain U, Macciardi F, Kennedy JL, Muglia P. PMID: 18286632.
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    85. SNPLims: a data management system for genome wide association studies. BMC Bioinformatics. 2008 Mar 26; 9 Suppl 2:S13. Orro A, Guffanti G, Salvi E, Macciardi F, Milanesi L. PMID: 18387201; PMCID: PMC2323662.
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    86. Conceptual basis and methodology of the SOPHIA study. Pharmacogenomics. 2007 Nov; 8(11):1497-509. Glorioso N, Argiolas G, Filigheddu F, Troffa C, Cocco F, Bulla E, Bulla P, Zaninello R, Degortes S, Pitzoi S, Frau F, Fadda S, Pinna Parpaglia P, Bernini G, Bardini M, Fallo F, Malatino L, Regolisti G, Ferri C, Cusi D, Sciacqua A, Perticone F, Degli Esposti E, Baraccani C, Parati G, Veglio F, Mulatero P, Williams TA, Macciardi F, Stancanelli B, Study Group on Cardiovascular Pharmacogenomics of Italian Society of Hypertension. PMID: 18034615.
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    87. Context dependency of the salt intake: left ventricular hypertrophy connection. J Hypertens. 2007 Aug; 25(8):1569-72. Macciardi F, Cusi D. PMID: 17620949.
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    88. Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension. Hum Mol Genet. 2007 Jul 01; 16(13):1630-8. Barlassina C, Dal Fiume C, Lanzani C, Manunta P, Guffanti G, Ruello A, Bianchi G, Del Vecchio L, Macciardi F, Cusi D. PMID: 17510212.
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    89. Interleukin 18 gene polymorphisms predict risk and outcome of Alzheimer's disease. J Neurol Neurosurg Psychiatry. 2007 Aug; 78(8):807-11. Bossù P, Ciaramella A, Moro ML, Bellincampi L, Bernardini S, Federici G, Trequattrini A, Macciardi F, Spoletini I, Di Iulio F, Caltagirone C, Spalletta G. PMID: 17299019; PMCID: PMC2117732.
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    90. Association analyses of the DAOA/G30 and D-amino-acid oxidase genes in schizophrenia: further evidence for a role in schizophrenia. Neuromolecular Med. 2007; 9(2):169-77. Shinkai T, De Luca V, Hwang R, Müller DJ, Lanktree M, Zai G, Shaikh S, Wong G, Sicard T, Potapova N, Trakalo J, King N, Matsumoto C, Hori H, Wong AH, Ohmori O, Macciardi F, Nakamura J, Kennedy JL. PMID: 17627036.
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    91. AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia. Eur J Hum Genet. 2006 Oct; 14(10):1111-9. Amann-Zalcenstein D, Avidan N, Kanyas K, Ebstein RP, Kohn Y, Hamdan A, Ben-Asher E, Karni O, Mujaheed M, Segman RH, Maier W, Macciardi F, Beckmann JS, Lancet D, Lerer B. PMID: 16773125.
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    92. Lack of association between the corticotrophin-releasing hormone receptor 2 gene and panic disorder. Psychiatr Genet. 2006 Jun; 16(3):93-7. Tharmalingam S, King N, De Luca V, Rothe C, Koszycki D, Bradwejn J, Macciardi F, Kennedy JL. PMID: 16691126.
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    93. PP2A-Bgamma subunit and KCNQ2 K+ channels in bipolar disorder. Pharmacogenomics J. 2007 Apr; 7(2):123-32. Borsotto M, Cavarec L, Bouillot M, Romey G, Macciardi F, Delaye A, Nasroune M, Bastucci M, Sambucy JL, Luan JJ, Charpagne A, Jouët V, Léger R, Lazdunski M, Cohen D, Chumakov I. PMID: 16733521.
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    94. The 460Trp allele of alpha-adducin increases carotid intima-media thickness in young adult males. J Hypertens. 2006 Apr; 24(4):697-703. Sarzani R, Cusi D, Salvi F, Barlassina C, Macciardi F, Pietrucci F, Cola G, Catalini R, Dal Fiume C, Dessì-Fulgheri P, Rappelli A. PMID: 16531798.
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    95. Association of the Val158Met catechol O-methyltransferase genetic polymorphism with panic disorder. Neuropsychopharmacology. 2006 Oct; 31(10):2237-42. Rothe C, Koszycki D, Bradwejn J, King N, Deluca V, Tharmalingam S, Macciardi F, Deckert J, Kennedy JL. PMID: 16525418.
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    96. The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23. Mol Psychiatry. 2006 Feb; 11(2):119-21. Amann D, Avidan N, Kanyas K, Kohn Y, Hamdan A, Ben-Asher E, Macciardi F, Beckmann JS, Lancet D, Lerer B. PMID: 16189505.
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    97. Association of the putative susceptibility gene, transient receptor potential protein melastatin type 2, with bipolar disorder. . 2006 Jan 05; 141B(1):36-43. Xu C, Macciardi F, Li PP, Yoon IS, Cooke RG, Hughes B, Parikh SV, McIntyre RS, Kennedy JL, Warsh JJ. PMID: 16252251.
      View in: PubMed   Mentions: 24  Translation:HumansCells
    98. Imaging phenotypes and genotypes in schizophrenia. Neuroinformatics. 2006; 4(1):21-49. Turner JA, Smyth P, Macciardi F, Fallon JH, Kennedy JL, Potkin SG. PMID: 16595857.
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    99. Dopamine D2 receptor gene variants and quantitative measures of positive and negative symptom response following clozapine treatment. Eur Neuropsychopharmacol. 2006 May; 16(4):248-59. Hwang R, Shinkai T, Deluca V, Macciardi F, Potkin S, Meltzer HY, Kennedy JL. PMID: 16278074.
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    100. Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions. Mol Psychiatry. 2005 Nov; 10(11):1006-16. D'Amelio M, Ricci I, Sacco R, Liu X, D'Agruma L, Muscarella LA, Guarnieri V, Militerni R, Bravaccio C, Elia M, Schneider C, Melmed R, Trillo S, Pascucci T, Puglisi-Allegra S, Reichelt KL, Macciardi F, Holden JJ, Persico AM. PMID: 16027737.
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    101. Association study of 12 polymorphisms spanning the dopamine D(2) receptor gene and clozapine treatment response in two treatment refractory/intolerant populations. Psychopharmacology (Berl). 2005 Aug; 181(1):179-87. Hwang R, Shinkai T, De Luca V, Müller DJ, Ni X, Macciardi F, Potkin S, Lieberman JA, Meltzer HY, Kennedy JL. PMID: 15830237.
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    102. Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval. Eur J Hum Genet. 2005 Jun; 13(6):763-71. Levi A, Kohn Y, Kanyas K, Amann D, Pae CU, Hamdan A, Segman RH, Avidan N, Karni O, Korner M, Jun TY, Beckmann JS, Macciardi F, Lerer B. PMID: 15812564.
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    103. Combined analysis of 635 patients confirms an age-related association of the serotonin 2A receptor gene with tardive dyskinesia and specificity for the non-orofacial subtype. Int J Neuropsychopharmacol. 2005 Sep; 8(3):411-25. Lerer B, Segman RH, Tan EC, Basile VS, Cavallaro R, Aschauer HN, Strous R, Chong SA, Heresco-Levy U, Verga M, Scharfetter J, Meltzer HY, Kennedy JL, Macciardi F. PMID: 15857569.
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    104. A linkage study between the GABAA beta2 and GABAA gamma2 subunit genes and major psychoses. CNS Spectr. 2005 Jan; 10(1):57-61. Ambrósio AM, Kennedy JL, Macciardi F, King N, Azevedo MH, Oliveira CR, Pato CN. PMID: 15618948.
      View in: PubMed   Mentions:    Fields:    Translation:HumansPHPublic Health
    105. Pharmacogenetics of autoimmune diseases: research issues in the case of Multiple Sclerosis and the role of IFN-beta. J Autoimmun. 2005; 25 Suppl:1-5. Macciardi F, Martinelli Boneschi F, Cohen D. PMID: 16311019.
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    106. Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol Psychiatry. 2004 Dec; 9(12):1111-21. Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, Macciardi F, Tannock R, Lovett MW, Humphries TW, Barr CL. PMID: 15249932.
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    107. The dopamine-4 receptor gene associated with binge eating and weight gain in women with seasonal affective disorder: an evolutionary perspective. Biol Psychiatry. 2004 Nov 01; 56(9):665-9. Levitan RD, Masellis M, Basile VS, Lam RW, Kaplan AS, Davis C, Muglia P, Mackenzie B, Tharmalingam S, Kennedy SH, Macciardi F, Kennedy JL. PMID: 15522250.
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    108. Lack of association or linkage disequilibrium between schizophrenia and polymorphisms in the 5-HT1Dalpha and 5-HT1Dbeta autoreceptor genes: family-based association study. . 2004 Jul 01; 128B(1):1-5. Ambrósio AM, Kennedy JL, Macciardi F, Coelho I, Soares MJ, Oliveira CR, Pato CN. PMID: 15211620.
      View in: PubMed   Mentions: 1  Translation:Humans
    109. Is G6PD A- deficiency associated with recurrent stillbirths in The Gambia? . 2004 Jul 01; 128A(1):104-5. Sirugo G, Schaefer EA, Mendy A, West B, Bailey R, Walraven G, Sabeti P, Macciardi F, Zonta LA. PMID: 15211670.
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    110. Social adjustment and self-esteem of bipolar patients: a multicentric study. J Affect Disord. 2004 Apr; 79(1-3):97-103. Blairy S, Linotte S, Souery D, Papadimitriou GN, Dikeos D, Lerer B, Kaneva R, Milanova V, Serretti A, Macciardi F, Mendlewicz J. PMID: 15023484.
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    111. PedSplit: pedigree management for stratified analysis. Bioinformatics. 2004 Sep 22; 20(14):2315-6. Lanktree MB, VanderBeek L, Macciardi FM, Kennedy JL. PMID: 15059823.
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    112. Nonparametric linkage analysis between schizophrenia and candidate genes of dopaminergic and serotonergic systems. CNS Spectr. 2004 Apr; 9(4):302-8. Ambrósio AM, Kennedy JL, Macciardi F, Coelho I, Soares MJ, Oliveira CR, Pato MT, Pato CN. PMID: 15048055.
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    113. Family association study between DRD2 and DRD3 gene polymorphisms and schizophrenia in a Portuguese population. Psychiatry Res. 2004 Mar 15; 125(3):185-91. Ambrósio AM, Kennedy JL, Macciardi F, Macedo A, Valente J, Dourado A, Oliveira CR, Pato C. PMID: 15051179.
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    114. No evidence of association or linkage disequilibrium between polymorphisms in the 5' upstream and coding regions of the dopamine D4 receptor gene and schizophrenia in a Portuguese population. . 2004 Feb 15; 125B(1):20-4. Ambrósio AM, Kennedy JL, Macciardi F, Barr C, Soares MJ, Oliveira CR, Pato CN. PMID: 14755438.
      View in: PubMed   Mentions: 3  Translation:Humans
    115. Angiotensinogen gene polymorphism, again? J Hypertens. 2003 Oct; 21(10):1815-8. Cusi D, Macciardi F, Barlassina C. PMID: 14508183.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    116. N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia: TDT and case-control analyses. . 2003 May 15; 119B(1):24-7. Martucci L, Wong AH, Trakalo J, Cate-Carter T, Wong GW, Macciardi FM, Kennedy JL. PMID: 12707933.
      View in: PubMed   Mentions: 7  Translation:Humans
    117. Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24. Mol Psychiatry. 2003 May; 8(5):488-98. Lerer B, Segman RH, Hamdan A, Kanyas K, Karni O, Kohn Y, Korner M, Lanktree M, Kaadan M, Turetsky N, Yakir A, Kerem B, Macciardi F. PMID: 12808429.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansCells
    118. Association between the BDNF gene and schizophrenia. Mol Psychiatry. 2003 Feb; 8(2):146-7. Muglia P, Vicente AM, Verga M, King N, Macciardi F, Kennedy JL. PMID: 12610646.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    119. Identification of candidate genes for psychosis in rat models, and possible association between schizophrenia and the 14-3-3eta gene. Mol Psychiatry. 2003 Feb; 8(2):156-66. Wong AH, Macciardi F, Klempan T, Kawczynski W, Barr CL, Lakatoo S, Wong M, Buckle C, Trakalo J, Boffa E, Oak J, Azevedo MH, Dourado A, Coelho I, Macedo A, Vicente A, Valente J, Ferreira CP, Pato MT, Pato CN, Kennedy JL, Van Tol HH. PMID: 12610648.
      View in: PubMed   Mentions: 24     Fields:    Translation:Animals
    120. Evidence that the N-methyl-D-aspartate subunit 1 receptor gene (GRIN1) confers susceptibility to bipolar disorder. Mol Psychiatry. 2003 Feb; 8(2):241-5. Mundo E, Tharmalingham S, Neves-Pereira M, Dalton EJ, Macciardi F, Parikh SV, Bolonna A, Kerwin RW, Arranz MJ, Makoff AJ, Kennedy JL. PMID: 12610658.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    121. Linkage disequilibrium between dopamine D1 receptor gene (DRD1) and bipolar disorder. Biol Psychiatry. 2002 Dec 15; 52(12):1144-50. Ni X, Trakalo JM, Mundo E, Macciardi FM, Parikh S, Lee L, Kennedy JL. PMID: 12488059.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    122. Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc Natl Acad Sci U S A. 2002 Oct 15; 99(21):13675-80. Chumakov I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio M, Abderrahim H, Bougueleret L, Barry C, Tanaka H, La Rosa P, Puech A, Tahri N, Cohen-Akenine A, Delabrosse S, Lissarrague S, Picard FP, Maurice K, Essioux L, Millasseau P, Grel P, Debailleul V, Simon AM, Caterina D, Dufaure I, Malekzadeh K, Belova M, Luan JJ, Bouillot M, Sambucy JL, Primas G, Saumier M, Boubkiri N, Martin-Saumier S, Nasroune M, Peixoto H, Delaye A, Pinchot V, Bastucci M, Guillou S, Chevillon M, Sainz-Fuertes R, Meguenni S, Aurich-Costa J, Cherif D, Gimalac A, Van Duijn C, Gauvreau D, Ouellette G, Fortier I, Raelson J, Sherbatich T, Riazanskaia N, Rogaev E, Raeymaekers P, Aerssens J, Konings F, Luyten W, Macciardi F, Sham PC, Straub RE, Weinberger DR, Cohen N, Cohen D, Ouelette G, Realson J. PMID: 12364586; PMCID: PMC129739.
      View in: PubMed   Mentions: 210     Fields:    Translation:HumansCells
    123. Pharmacogenetics of antidepressant and mood-stabilizing drugs: a review of candidate-gene studies and future research directions. Int J Neuropsychopharmacol. 2002 Sep; 5(3):255-75. Lerer B, Macciardi F. PMID: 12366879.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansAnimals
    124. The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: evidence from a family-based association study. Am J Hum Genet. 2002 Sep; 71(3):651-5. Neves-Pereira M, Mundo E, Muglia P, King N, Macciardi F, Kennedy JL. PMID: 12161822; PMCID: PMC379201.
      View in: PubMed   Mentions: 126     Fields:    Translation:Humans
    125. Moclobemide response in depressed patients: association study with a functional polymorphism in the monoamine oxidase A promoter. Pharmacopsychiatry. 2002 Jul; 35(4):157-8. Müller DJ, Schulze TG, Macciardi F, Ohlraun S, Gross MM, Scherk H, Neidt H, Syagailo YV, Grässle M, Nöthen MM, Maier W, Lesch KP, Rietschel M. PMID: 12163988.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    126. Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism. Neuropsychopharmacology. 2002 Jul; 27(1):105-19. Lerer B, Segman RH, Fangerau H, Daly AK, Basile VS, Cavallaro R, Aschauer HN, McCreadie RG, Ohlraun S, Ferrier N, Masellis M, Verga M, Scharfetter J, Rietschel M, Lovlie R, Levy UH, Meltzer HY, Kennedy JL, Steen VM, Macciardi F. PMID: 12062911.
      View in: PubMed   Mentions: 52     Fields:    Translation:Humans
    127. Autism and the X chromosome: no linkage to microsatellite loci detected using the affected sibling pair method. Am J Med Genet. 2002 Apr 15; 109(1):36-41. Schutz CK, Polley D, Robinson PD, Chalifoux M, Macciardi F, White BN, Holden JJ. PMID: 11932990.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    128. Angiotensin converting enzyme gene insertion/deletion polymorphism: case-control association studies in schizophrenia, major affective disorder, and tardive dyskinesia and a family-based association study in schizophrenia. Am J Med Genet. 2002 Apr 08; 114(3):310-4. Segman RH, Shapira Y, Modai I, Hamdan A, Zislin J, Heresco-Levy U, Kanyas K, Hirschmann S, Karni O, Finkel B, Schlafman M, Lerner A, Shapira B, Macciardi F, Lerer B. PMID: 11920854.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    129. The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach. Br J Dermatol. 2002 Apr; 146(4):601-8. Hillmer AM, Kruse R, Macciardi F, Heyn U, Betz RC, Ruzicka T, Propping P, Nöthen MM, Cichon S. PMID: 11966690.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    130. Psychiatric pharmacogenetics: personalizing psychostimulant therapy in attention-deficit/hyperactivity disorder. Behav Brain Res. 2002 Mar 10; 130(1-2):85-90. Masellis M, Basile VS, Muglia P, Ozdemir V, Macciardi FM, Kennedy JL. PMID: 11864722.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    131. Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European Multicenter Association Study of affective disorders. Am J Med Genet. 2002 Mar 08; 114(2):177-85. Massat I, Souery D, Del-Favero J, Van Gestel S, Serretti A, Macciardi F, Smeraldi E, Kaneva R, Adolfsson R, Nylander PO, Blackwood D, Muir W, Papadimitriou GN, Dikeos D, Oruc L, Segman RH, Ivezic S, Aschauer H, Ackenheil M, Fuchshuber S, Dam H, Jakovljevic M, Peltonen L, Hilger C, Hentges F, Staner L, Milanova V, Jazin E, Lerer B, Van Broeckhoven C, Mendlewicz J. PMID: 11857579.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    132. 5HT1Dbeta Receptor gene implicated in the pathogenesis of Obsessive-Compulsive Disorder: further evidence from a family-based association study. Mol Psychiatry. 2002; 7(7):805-9. Mundo E, Richter MA, Zai G, Sam F, McBride J, Macciardi F, Kennedy JL. PMID: 12192628.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    133. Association between the dopamine transporter gene and posttraumatic stress disorder. Mol Psychiatry. 2002; 7(8):903-7. Segman RH, Cooper-Kazaz R, Macciardi F, Goltser T, Halfon Y, Dobroborski T, Shalev AY. PMID: 12232785.
      View in: PubMed   Mentions: 51     Fields:    Translation:Humans
    134. Reelin gene alleles and susceptibility to autism spectrum disorders. Mol Psychiatry. 2002; 7(9):1012-7. Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson DR, Guidotti AR, Holden JJ. PMID: 12399956.
      View in: PubMed   Mentions: 40     Fields:    Translation:HumansCells
    135. Evidence for linkage disequilibrium between the alpha 7-nicotinic receptor gene (CHRNA7) locus and schizophrenia in Azorean families. Am J Med Genet. 2001 Dec 08; 105(8):669-74. Xu J, Pato MT, Torre CD, Medeiros H, Carvalho C, Basile VS, Bauer A, Dourado A, Valente J, Soares MJ, Macedo AA, Coelho I, Ferreira CP, Azevedo MH, Macciardi F, Kennedy JL, Pato CN. PMID: 11803513.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansCells
    136. Altered TRPC7 gene expression in bipolar-I disorder. Biol Psychiatry. 2001 Oct 15; 50(8):620-6. Yoon IS, Li PP, Siu KP, Kennedy JL, Macciardi F, Cooke RG, Parikh SV, Warsh JJ. PMID: 11690598.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    137. Polymorphism of the serotonin 5-HT1B receptor gene (HTR1B) associated with minimum lifetime body mass index in women with bulimia nervosa. Biol Psychiatry. 2001 Oct 15; 50(8):640-3. Levitan RD, Kaplan AS, Masellis M, Basile VS, Walker ML, Lipson N, Siegel GI, Woodside DB, Macciardi FM, Kennedy SH, Kennedy JL. PMID: 11690602.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    138. Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder. Mol Psychiatry. 2001 Sep; 6(5):579-85. Lerer B, Macciardi F, Segman RH, Adolfsson R, Blackwood D, Blairy S, Del Favero J, Dikeos DG, Kaneva R, Lilli R, Massat I, Milanova V, Muir W, Noethen M, Oruc L, Petrova T, Papadimitriou GN, Rietschel M, Serretti A, Souery D, Van Gestel S, Van Broeckhoven C, Mendlewicz J. PMID: 11526472.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    139. Association study of a promoter polymorphism of UFD1L gene with schizophrenia. Am J Med Genet. 2001 Aug 08; 105(6):529-33. De Luca A, Pasini A, Amati F, Botta A, Spalletta G, Alimenti S, Caccamo F, Conti E, Trakalo J, Macciardi F, Dallapiccola B, Novelli G. PMID: 11496370.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    140. The role of serotonin transporter protein gene in antidepressant-induced mania in bipolar disorder: preliminary findings. Arch Gen Psychiatry. 2001 Jun; 58(6):539-44. Mundo E, Walker M, Cate T, Macciardi F, Kennedy JL. PMID: 11386982.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    141. Genetically determined low maternal serum dopamine beta-hydroxylase levels and the etiology of autism spectrum disorders. Am J Med Genet. 2001 Apr 15; 100(1):30-6. Robinson PD, Schutz CK, Macciardi F, White BN, Holden JJ. PMID: 11337745.
      View in: PubMed   Mentions: 25     Fields:    
    142. Lack of association between schizophrenia and the phospholipase-A(2) genes cPLA2 and sPLA2. Am J Med Genet. 2001 Apr 08; 105(3):246-9. Frieboes RM, Moises HW, Gattaz WF, Yang L, Li T, Liu X, Vetter P, Macciardi F, Hwu HG, Henn F. PMID: 11353443.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    143. Association analysis of G-protein beta 3 subunit gene with altered Ca(2+) homeostasis in bipolar disorder. Mol Psychiatry. 2001 Mar; 6(2):125-6. Corson TW, Li PP, Kennedy JL, Macciardi F, Cooke RG, Parikh SV, Warsh JJ. PMID: 11317211.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    144. Lack of association between serotonin-2A receptor gene (HTR2A) polymorphisms and tardive dyskinesia in schizophrenia. Mol Psychiatry. 2001 Mar; 6(2):230-4. Basile VS, Ozdemir V, Masellis M, Meltzer HY, Lieberman JA, Potkin SG, Macciardi FM, Petronis A, Kennedy JL. PMID: 11317228.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    145. Lack of association between the T-->C 267 serotonin 5-HT6 receptor gene (HTR6) polymorphism and prediction of response to clozapine in schizophrenia. Schizophr Res. 2001 Jan 15; 47(1):49-58. Masellis M, Basile VS, Meltzer HY, Lieberman JA, Sevy S, Goldman DA, Hamblin MW, Macciardi FM, Kennedy JL. PMID: 11163544.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    146. Is the 5-HT(1Dbeta) receptor gene implicated in the pathogenesis of obsessive-compulsive disorder? Am J Psychiatry. 2000 Jul; 157(7):1160-1. Mundo E, Richter MA, Sam F, Macciardi F, Kennedy JL. PMID: 10873927.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    147. Psychiatric epigenetics: a new focus for the new century. Mol Psychiatry. 2000 Jul; 5(4):342-6. Petronis A, Gottesman II, Crow TJ, DeLisi LE, Klar AJ, Macciardi F, McInnis MG, McMahon FJ, Paterson AD, Skuse D, Sutherland GR. PMID: 10889541.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansAnimals
    148. A tumor suppressor locus in familial and sporadic chordoma maps to 1p36. Int J Cancer. 2000 Jul 01; 87(1):68-72. Miozzo M, Dalprà L, Riva P, Volontà M, Macciardi F, Pericotti S, Tibiletti MG, Cerati M, Rohde K, Larizza L, Fuhrman Conti AM. PMID: 10861454.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    149. A functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene: association with tardive dyskinesia in schizophrenia. Mol Psychiatry. 2000 Jul; 5(4):410-7. Basile VS, Ozdemir V, Masellis M, Walker ML, Meltzer HY, Lieberman JA, Potkin SG, Alva G, Kalow W, Macciardi FM, Kennedy JL. PMID: 10889552.
      View in: PubMed   Mentions: 33     Fields:    Translation:Humans
    150. Adult attention deficit hyperactivity disorder and the dopamine D4 receptor gene. Am J Med Genet. 2000 Jun 12; 96(3):273-7. Muglia P, Jain U, Macciardi F, Kennedy JL. PMID: 10898898.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    151. Lack of linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and bipolar disorder. Am J Med Genet. 2000 Jun 12; 96(3):379-83. Mundo E, Walker M, Tims H, Macciardi F, Kennedy JL. PMID: 10898918.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    152. Update on chromosomal locations for psychiatric disorders: report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, California, October 14-18, 1999. Am J Med Genet. 2000 Jun 12; 96(3):434-49. DeLisi LE, Craddock NJ, Detera-Wadleigh S, Foroud T, Gejman P, Kennedy JL, Lendon C, Macciardi F, McKeon P, Mynett-Johnson L, Nurnberger JI, Paterson A, Schwab S, Van Broeckhoven C, Wildenauer D, Crow TJ. PMID: 10898931.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    153. A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorder. Am J Med Genet. 2000 Apr 03; 96(2):136-40. Massat I, Souery D, Lipp O, Blairy S, Papadimitriou G, Dikeos D, Ackenheil M, Fuchshuber S, Hilger C, Kaneva R, Milanova V, Verheyen G, Raeymaekers P, Staner L, Oruc L, Jakovljevic M, Serretti A, Macciardi F, Van Broeckhoven C, Mendlewicz J. PMID: 10893484.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    154. Linkage of mood disorders with D2, D3 and TH genes: a multicenter study. J Affect Disord. 2000 Apr; 58(1):51-61. Serretti A, Macciardi F, Cusin C, Lattuada E, Souery D, Lipp O, Mahieu B, Van Broeckhoven C, Blackwood D, Muir W, Aschauer HN, Heiden AM, Ackenheil M, Fuchshuber S, Raeymaekers P, Verheyen G, Kaneva R, Jablensky A, Papadimitriou GN, Dikeos DG, Stefanis CN, Smeraldi E, Mendlewicz J. PMID: 10760558.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    155. An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus. Am J Hum Genet. 2000 Mar; 66(3):819-29. Vincent JB, Neves-Pereira ML, Paterson AD, Yamamoto E, Parikh SV, Macciardi F, Gurling HM, Potkin SG, Pato CN, Macedo A, Kovacs M, Davies M, Lieberman JA, Meltzer HY, Petronis A, Kennedy JL. PMID: 10712198; PMCID: PMC1288165.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    156. Pharmacogenetics of antipsychotic treatment: lessons learned from clozapine. Biol Psychiatry. 2000 Feb 01; 47(3):252-66. Masellis M, Basile VS, Ozdemir V, Meltzer HY, Macciardi FM, Kennedy JL. PMID: 10682223.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    157. Association of the MscI polymorphism of the dopamine D3 receptor gene with tardive dyskinesia in schizophrenia. Neuropsychopharmacology. 1999 Jul; 21(1):17-27. Basile VS, Masellis M, Badri F, Paterson AD, Meltzer HY, Lieberman JA, Potkin SG, Macciardi F, Kennedy JL. PMID: 10379516.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCTClinical Trials
    158. Chromosome 4 Workshop Summary: Sixth World Congress on Psychiatric Genetics, Bonn, Germany, October 6-10, 1998. Am J Med Genet. 1999 Jun 18; 88(3):224-8. Kennedy JL, Basile VS, Macciardi FM. PMID: 10374735.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    159. Social adjustment and self-esteem in remitted patients with mood disorders. Eur Psychiatry. 1999 Jun; 14(3):137-42. Serretti A, Cavallini MC, Macciardi F, Namia C, Franchini L, Souery D, Lipp O, Bauwens F, Smeraldi E, Mendlewicz J. PMID: 10572338.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    160. Application of pharmacogenetics to psychotic disorders: the first consensus conference. The Consensus Group for Outcome Measures in Psychoses for Pharmacological Studies. Schizophr Res. 1999 May 25; 37(2):191-6. Rietschel M, Kennedy JL, Macciardi F, Meltzer HY. PMID: 10374654.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    161. DNA methylation at the putative promoter region of the human dopamine D2 receptor gene. Neuroreport. 1999 Apr 26; 10(6):1249-55. Popendikyte V, Laurinavicius A, Paterson AD, Macciardi F, Kennedy JL, Petronis A. PMID: 10363934.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    162. No interaction of GABA(A) alpha-1 subunit and dopamine receptor D4 exon 3 genes in symptomatology of major psychoses. Am J Med Genet. 1999 Feb 05; 88(1):44-9. Serretti A, Macciardi F, Cusin C, Lattuada E, Lilli R, Di Bella D, Catalano M, Smeraldi E. PMID: 10050966.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    163. Genetic variants of dopamine receptor D4 and psychopathology. Schizophr Bull. 1999; 25(3):609-18. Serretti A, Macciardi F, Catalano M, Bellodi L, Smeraldi E. PMID: 10478793.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    164. Alcoholism as a complex trait: comparison of genetic models and role of epidemiological risk factors. Genet Epidemiol. 1999; 17 Suppl 1:S247-52. Macciardi F, Morenghi E, Morabito A. PMID: 10597444.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    165. Dopamine receptor D2 Ser/Cys311 variant associated with disorganized symptomatology of schizophrenia. Schizophr Res. 1998 Nov 30; 34(3):207-10. Serretti A, Macciardi F, Smeraldi E. PMID: 9850987.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    166. Self-esteem in remitted patients with mood disorders is not associated with the dopamine receptor D4 and the serotonin transporter genes. Psychiatry Res. 1998 Aug 17; 80(2):137-44. Serretti A, Macciardi F, Di Bella D, Catalano M, Smeraldi E. PMID: 9754692.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    167. Dopamine receptor D4 gene is associated with delusional symptomatology in mood disorders. Psychiatry Res. 1998 Aug 17; 80(2):129-36. Serretti A, Macciardi F, Cusin C, Lattuada E, Lilli R, Smeraldi E. PMID: 9754691.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    168. Serotonin subtype 2 receptor genes and clinical response to clozapine in schizophrenia patients. Neuropsychopharmacology. 1998 Aug; 19(2):123-32. Masellis M, Basile V, Meltzer HY, Lieberman JA, Sevy S, Macciardi FM, Cola P, Howard A, Badri F, Nöthen MM, Kalow W, Kennedy JL. PMID: 9629566.
      View in: PubMed   Mentions: 37     Fields:    Translation:HumansCells
    169. [Genetic studies and their relevance in social psychiatry]. Epidemiol Psichiatr Soc. 1998 May-Aug; 7(2):94-7. Smeraldi E, Macciardi F. PMID: 9763759.
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    170. Tyrosine hydroxylase gene associated with depressive symptomatology in mood disorder. Am J Med Genet. 1998 Mar 28; 81(2):127-30. Serretti A, Macciardi F, Verga M, Cusin C, Pedrini S, Smeraldi E. PMID: 9613850.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    171. Tyrosine hydroxylase gene in linkage disequilibrium with mood disorders. Mol Psychiatry. 1998 Mar; 3(2):169-74. Serretti A, Macciardi F, Cusin C, Verga M, Pedrini S, Smeraldi E. PMID: 9577842.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    172. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Mol Psychiatry. 1998 Mar; 3(2):141-9. Williams J, Spurlock G, Holmans P, Mant R, Murphy K, Jones L, Cardno A, Asherson P, Blackwood D, Muir W, Meszaros K, Aschauer H, Mallet J, Laurent C, Pekkarinen P, Seppala J, Stefanis CN, Papadimitriou GN, Macciardi F, Verga M, Pato C, Azevedo H, Crocq MA, Gurling H, Owen MJ, et al. PMID: 9577838.
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    173. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. Am J Med Genet. 1998 Feb 07; 81(1):24-8. Spurlock G, Williams J, McGuffin P, Aschauer HN, Lenzinger E, Fuchs K, Sieghart WC, Meszaros K, Fathi N, Laurent C, Mallet J, Macciardi F, Pedrini S, Gill M, Hawi Z, Gibson S, Jazin EE, Yang HT, Adolfsson R, Pato CN, Dourado AM, Owen MJ. PMID: 9514583.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    174. Steady state concentrations of the enantiomers of mianserin and desmethylmianserin in poor and in homozygous and heterozygous extensive metabolizers of debrisoquine. Ther Drug Monit. 1998 Feb; 20(1):7-13. Eap CB, Lima CA, Macciardi F, Woggon B, Powell K, Baumann P. PMID: 9485547.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    175. Analysis of depressive symptomatology in mood disorders. Depress Anxiety. 1998; 8(2):80-5. Serretti A, Lattuada E, Cusin C, Macciardi F, Smeraldi E. PMID: 9784982.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    176. GABAA alpha-1 subunit gene not associated with depressive symptomatology in mood disorders. Psychiatr Genet. 1998; 8(4):251-4. Serretti A, Macciardi F, Cusin C, Lattuada E, Lilli R, Di Bella D, Catalano M, Smeraldi E. PMID: 9861645.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    177. Chromosome 4 workshop. Psychiatr Genet. 1998; 8(2):67-71. Kennedy JL, Macciardi FM. PMID: 9686426.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    178. Apolipoprotein E epsilon 4 and clinical phenotype in schizophrenia. Lancet. 1997 Dec 20-27; 350(9094):1857-8. Rietschel M, Krauss H, Müller DJ, Nöthen MM, Macciardi F. PMID: 9428285.
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    179. Dextromethorphan poisoning in an adolescent with genetic cytochrome P450 CYP2D6 deficiency. Therapie. 1997 Nov-Dec; 52(6):607-8. Baumann P, Vlatkovic D, Macciardi F. PMID: 9734115.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    180. No association of the Ser/Cys311 DRD2 molecular variant with schizophrenia using a classical case control study and the haplotype relative risk. Schizophr Res. 1997 May 24; 25(2):117-21. Verga M, Macciardi F, Pedrini S, Cohen S, Smeraldi E. PMID: 9187010.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    181. No association between schizophrenia and the serotonin receptor 5HTR2a in an Italian population. Am J Med Genet. 1997 Feb 21; 74(1):21-5. Verga M, Macciardi F, Cohen S, Pedrini S, Smeraldi E. PMID: 9034001.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    182. Genotypic association between dopamine transporter gene polymorphisms and schizophrenia. Am J Med Genet. 1997 Feb 21; 74(1):53-7. Persico AM, Macciardi F. PMID: 9034007.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    183. The structure of DSM-III-R schizotypal personality disorder diagnosed by direct interviews. Schizophr Bull. 1997; 23(1):83-92. Battaglia M, Cavallini MC, Macciardi F, Bellodi L. PMID: 9050115.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    184. Evidence for an association between the dopamine D3 receptor gene DRD3 and schizophrenia. Hum Hered. 1997 Jan-Feb; 47(1):6-16. Ebstein RP, Macciardi F, Heresco-Levi U, Serretti A, Blaine D, Verga M, Nebamov L, Gur E, Belmaker RH, Avnon M, Lerer B. PMID: 9017973.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    185. A preliminary report of a strong genetic component for thought disorder in normals. A twin study. Neuropsychobiology. 1997; 36(1):13-8. Gambini O, Campana A, Macciardi F, Scarone S. PMID: 9211438.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    186. NCAM and schizophrenia: genetic studies. Mol Psychiatry. 1997 Jan; 2(1):65-9. Vicente AM, Macciardi F, Verga M, Bassett AS, Honer WG, Bean G, Kennedy JL. PMID: 9154219; PMCID: PMC3160977.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    187. Genetic variant near cytosolic phospholipase A2 associated with schizophrenia. Schizophr Res. 1996 Aug 23; 21(2):111-6. Hudson CJ, Kennedy JL, Gotowiec A, Lin A, King N, Gojtan K, Macciardi F, Skorecki K, Meltzer HY, Warsh JJ, Horrobin DF. PMID: 8873778.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    188. No evidence for association of dopamine D2 receptor variant (Ser311/Cys311) with major psychosis. Am J Med Genet. 1996 Jul 26; 67(4):415-7. Sasaki T, Macciardi FM, Badri F, Verga M, Meltzer HY, Lieberman J, Howard A, Bean G, Joffe RT, Hudson CJ, Kennedy JL. PMID: 8837713.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    189. Identification of symptomatologic patterns common to major psychoses: proposal for a phenotype definition. Am J Med Genet. 1996 Jul 26; 67(4):393-400. Serretti A, Macciardi F, Smeraldi E. PMID: 8837708.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    190. Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. Lancet. 1996 May 11; 347(9011):1294-6. Williams J, Spurlock G, McGuffin P, Mallet J, Nöthen MM, Gill M, Aschauer H, Nylander PO, Macciardi F, Owen MJ. PMID: 8622505.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    191. Pharmacokinetic fluvoxamine-clomipramine interaction with favorable therapeutic consequences in therapy-resistant depressive patient. Pharmacopsychiatry. 1996 May; 29(3):108-10. Conus P, Bondolfi G, Eap CB, Macciardi F, Baumann P. PMID: 8738315.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    192. Psychosis and genes with trinucleotide repeat polymorphism. Hum Genet. 1996 Feb; 97(2):244-6. Sasaki T, Billett E, Petronis A, Ying D, Parsons T, Macciardi FM, Meltzer HY, Lieberman J, Joffe RT, Ross CA, McInnis MG, Li SH, Kennedy JL. PMID: 8566962.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    193. The Wisconsin Card Sorting Test (WCST) performance in normal subjects: a twin study. Neuropsychobiology. 1996; 34(1):14-7. Campana A, Macciardi F, Gambini O, Scarone S. PMID: 8884753.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    194. Association study of dopamine D3 receptor gene and schizophrenia. Am J Med Genet. 1995 Dec 18; 60(6):558-62. Kennedy JL, Billett EA, Macciardi FM, Verga M, Parsons TJ, Meltzer HY, Lieberman J, Buchanan JA. PMID: 8825896.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    195. An international two-stage genome-wide search for schizophrenia susceptibility genes. Nat Genet. 1995 Nov; 11(3):321-4. Moises HW, Yang L, Kristbjarnarson H, Wiese C, Byerley W, Macciardi F, Arolt V, Blackwood D, Liu X, Sjögren B, et al. PMID: 7581457.
      View in: PubMed   Mentions: 54     Fields:    Translation:HumansCells
    196. Association study between the dopamine D4 receptor gene and schizophrenia. Am J Med Genet. 1995 Oct 09; 60(5):452-5. Petronis A, Macciardi F, Athanassiades A, Paterson AD, Verga M, Meltzer HY, Cola P, Buchanan JA, Van Tol HH, Kennedy JL. PMID: 8546161.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    197. Association of the alpha-adducin locus with essential hypertension. Hypertension. 1995 Mar; 25(3):320-6. Casari G, Barlassina C, Cusi D, Zagato L, Muirhead R, Righetti M, Nembri P, Amar K, Gatti M, Macciardi F, et al. PMID: 7875756.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    198. An association study between schizophrenia and the dopamine receptor genes DRD3 and DRD4 using haplotype relative risk. Hum Hered. 1994 Nov-Dec; 44(6):328-36. Macciardi F, Verga M, Kennedy JL, Petronis A, Bersani G, Pancheri P, Smeraldi E. PMID: 7860086.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    199. Analysis of the D4 dopamine receptor gene variant in an Italian schizophrenia kindred. Arch Gen Psychiatry. 1994 Apr; 51(4):288-93. Macciardi F, Petronis A, Van Tol HH, Marino C, Cavallini MC, Smeraldi E, Kennedy JL. PMID: 7909222.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    200. d-cycloserine adjuvant therapy to conventional neuroleptic treatment in schizophrenia: an open-label study. J Neural Transm Gen Sect. 1994; 95(2):105-11. Cascella NG, Macciardi F, Cavallini C, Smeraldi E. PMID: 7865165.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    201. A new Italian pedigree with early-onset Alzheimer's disease. J Geriatr Psychiatry Neurol. 1994 Jan-Mar; 7(1):28-32. Rainero I, Bergamini L, Bruni AC, Ferini-Strambi L, Foncin JF, Gei G, Macciardi F, Montesi MP, Pinessi L, Vaula G. PMID: 8192827.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    202. Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease. Neurology. 1993 Nov; 43(11):2275-9. Rogaev EI, Lukiw WJ, Vaula G, Haines JL, Rogaeva EA, Tsuda T, Alexandrova N, Liang Y, Mortilla M, Amaducci L, Bergamini L, Bruni AC, Foncin JF, Macciardi F, Montesi M, Sorbi S, Rainero I, Pinessi L, Polinsky RJ, Frommelt P, Duara R, Lopez R, Pollen D, Gusella JF, Tanzi R, MacLachlan D, Crapper D, St George-Hyslop PH, et al. PMID: 8232942.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    203. New polymorphism for the human serotonin 1D receptor variant (5-HT1D beta) not linked to schizophrenia in five Canadian pedigrees. Hum Hered. 1993 Sep-Oct; 43(5):315-8. Sidenberg DG, Bassett AS, Demchyshyn L, Niznik HB, Macciardi F, Kamble AB, Honer WG, Kennedy JL. PMID: 8104876.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    204. Review of the putative association of dopamine D2 receptor and alcoholism: a meta-analysis. Am J Med Genet. 1993 Jul 15; 48(2):78-82. Pato CN, Macciardi F, Pato MT, Verga M, Kennedy JL. PMID: 8362930.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    205. The power of systematic genealogical study in familial Alzheimer disease. Ital J Neurol Sci. 1993 Apr; 14(3):239-44. Bruni AC, Montesi MP, Rainero I, Ferini-Strambi L, Macciardi F, Pinessi L, Gei G, Fragiacomo D, Bergamini L. PMID: 8314678.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    206. A two-locus model for familial Alzheimer's disease? Genet Epidemiol. 1993; 10(6):437-41. Macciardi F, Cavallini MC. PMID: 8314040.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    207. Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nat Genet. 1992 Dec; 2(4):330-4. St George-Hyslop P, Haines J, Rogaev E, Mortilla M, Vaula G, Pericak-Vance M, Foncin JF, Montesi M, Bruni A, Sorbi S, Rainero I, Pinessi L, Pollen D, Polinsky R, Nee L, Kennedy J, Macciardi F, Rogaeva E, Liang Y, Alexandrova N, Lukiw W, Schlumpf K, Tanzi R, Tsuda T, Farrer L, Cantu JM, Duara R, Amaducci L, Bergamini L, Gusella J, Roses A, Crapper McLachlan D, et al. PMID: 1303289.
      View in: PubMed   Mentions: 86     Fields:    Translation:HumansCells
    208. Influence of education on WCST performances in schizophrenic patients. Int J Neurosci. 1992 Nov-Dec; 67(1-4):105-9. Gambini O, Macciardi F, Abbruzzese M, Scarone S. PMID: 1305626.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    209. A genetic linkage study of schizophrenia to chromosome 5 markers in a northern Italian population. Biol Psychiatry. 1992 Apr 01; 31(7):720-8. Macciardi F, Kennedy JL, Ruocco L, Giuffra L, Carrera P, Marino C, Rinaldi V, Smeraldi E, Ferrari M. PMID: 1599988.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    210. Genetic transmission of migraine without aura: a study of 68 families. Ital J Neurol Sci. 1991 Dec; 12(6):581-4. D'Amico D, Leone M, Macciardi F, Valentini S, Bussone G. PMID: 1783537.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    211. EEG power spectrum profile and structural CNS characteristics in schizophrenia. Biol Psychiatry. 1990 Jun 15; 27(12):1331-4. Gambini O, Colombo C, Macciardi F, Locatelli M, Calabrese G, Sacchetti E, Scarone S. PMID: 2364121.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    212. Amino acid patterns in schizophrenia: some new findings. Psychiatry Res. 1990 Apr; 32(1):63-70. Macciardi F, Lucca A, Catalano M, Marino C, Zanardi R, Smeraldi E. PMID: 2161549.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    213. Alpha reactivity in schizophrenia and in schizophrenic spectrum disorders: demographic, clinical and hemispheric assessment. Int J Psychophysiol. 1989 Mar; 7(1):47-54. Colombo C, Gambini O, Macciardi F, Bellodi L, Sacchetti E, Vita A, Cattaneo R, Scarone S. PMID: 2925464.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    214. Combined measure of smooth pursuit eye movements and ventricle-brain ratio in schizophrenic disorders. Psychiatry Res. 1987 Aug; 21(4):293-301. Smeraldi E, Gambini O, Bellodi L, Sacchetti E, Vita A, di Rosa M, Macciardi F, Cazzullo CL. PMID: 3498178.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    215. Increased concentrations of various amino acids in schizophrenic patients. Evidence for heterozygosity effects? Hum Genet. 1987 Jun; 76(2):138-40. Smeraldi E, Lucca A, Macciardi F, Bellodi L. PMID: 3610144.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    216. Age at onset of affective disorders in Italian and Swedish patients. Acta Psychiatr Scand. 1987 Apr; 75(4):352-7. Smeraldi E, Macciardi F, Holmgren S, Perris H, von Knorring L, Perris C. PMID: 3495957.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    217. Genetic approach to the study of heterogeneity of affective disorders. J Affect Disord. 1987 Mar-Apr; 12(2):105-13. Gasperini M, Orsini A, Bussoleni C, Macciardi F, Smeraldi E. PMID: 2955001.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    218. Genetic modelling in schizophrenia according to HLA typing. Clin Genet. 1986 Sep; 30(3):157-66. Smeraldi E, Macciardi F, Gasperini M, Orsini A, Bellodi L, Fabio G, Morabito A. PMID: 3490934.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    219. The search for genetic homogeneity in affective disorders. J Affect Disord. 1984 Oct; 7(2):99-107. Smeraldi E, Petroccione A, Gasperini M, Macciardi F, Orsini A. PMID: 6238073.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    220. Outcomes on lithium treatment as a tool for genetic studies in affective disorders. J Affect Disord. 1984 Apr; 6(2):139-51. Smeraldi E, Petroccione A, Gasperini M, Macciardi F, Orsini A, Kidd KK. PMID: 6233346.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    221. Factors affecting the distribution of age at onset in patients with affective disorders. J Psychiatr Res. 1982-1983; 17(3):309-17. Smeraldi E, Gasperini M, Macciardi F, Bussoleni C, Morabito A. PMID: 7187692.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    222. Analytic considerations about distribution of age of onset in schizophrenia. Neuropsychobiology. 1982; 8(2):93-101. Bellodi L, Morabito A, Macciardi F, Gasperini M, Benvenuto MG, Grassi G, Marzorati-Spairani C, Smeraldi E. PMID: 7070648.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    223. Possible relationship between outcome in primary affective disorders treated with lithium and family history. Adv Biochem Psychopharmacol. 1982; 32:157-63. Morabito A, Gasperini M, Macciardi F, Smeraldi E. PMID: 7090891.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    224. Genetic implications in assortative mating of affective disorders. Br J Psychiatry. 1981 Mar; 138:236-9. Negri F, Melica AM, Zuliani R, Gasperini M, Macciardi F, Smeraldi E. PMID: 7272616.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
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