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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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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cereb Cortex. 2020 Dec 09. 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.
      View in: PubMed   Mentions: 1     Fields:    
    2. 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.
      View in: PubMed   Mentions:    Fields:    
    3. 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. PMID: 32258359.
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    4. 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, 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, Hartman CA, Hashimoto R, Heinz A, Henskens FA, Hillegers MHJ, Hoekstra PJ, Holmes AJ, Hong LE, Hopkins WD, Hulshoff Pol HE, Jernigan TL, Jönsson EG, Kahn RS, Kennedy MA, Kircher TTJ, Kochunov P, Kwok JBJ, Le Hellard S, Loughland CM, Martin NG, Martinot JL, McDonald C, McMahon KL, Meyer-Lindenberg A, Michie PT, Morey RA, Mowry B, Nyberg L, Oosterlaan J, Ophoff RA, Pantelis C, Paus T, Pausova Z, Penninx BWJH, Polderman TJC, Posthuma D, Rietschel M, Roffman JL, Rowland LM, Sachdev PS, Sämann PG, Schall U, Schumann G, Scott RJ, Sim K, Sisodiya SM, Smoller JW, Sommer IE, St Pourcain B, Stein DJ, et al. PMID: 32193296.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    5. 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. PMID: 32198361.
      View in: PubMed   Mentions: 10     Fields:    
    6. 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, Nicolini H, Escamilla MA, Vawter MP, Sobell JL, Malaspina D, Lehrer DS, Buckley PF, Rapaport MH, Knowles JA, Fanous AH, Pato MT, McCarroll SA, Pato CN. PMID: 31591465.
      View in: PubMed   Mentions: 6     Fields:    
    7. 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.
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    8. 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.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    9. 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.
      View in: PubMed   Mentions: 3     Fields:    
    10. 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: 1     Fields:    Translation:HumansAnimalsCells
    11. Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1. Schizophr Bull. 2019 01 01; 45(1):222-232. PMID: 29474680.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    12. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimals
    13. 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, 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    14. 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.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimalsCells
    15. 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. PMID: 30344923.
      View in: PubMed   Mentions: 7     Fields:    
    16. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395). 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, Loo SK, McGough JJ, Grevet EH, Medland SE, Robinson E, Weiss LA, Bacchelli E, Bailey A, Bal V, Battaglia A, Betancur C, Bolton P, Cantor R, Celestino-Soper P, Dawson G, De Rubeis S, Duque F, Green A, Klauck SM, Leboyer M, Levitt P, Maestrini E, Mane S, De-Luca DM, Parr J, Regan R, Reichenberg A, Sandin S, Vorstman J, Wassink T, Wijsman E, Cook E, Santangelo S, Delorme R, et al. PMID: 29930110.
      View in: PubMed   Mentions: 181     Fields:    Translation:Humans
    17. 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.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    18. 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, 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.
      View in: PubMed   Mentions: 44     Fields:    Translation:Humans
    19. 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.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
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    84. 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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    85. 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.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    86. 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.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    87. 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.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    88. 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.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansCells
    89. 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.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    90. 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.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansAnimalsCells
    91. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    92. 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.
      View in: PubMed   Mentions: 27     Fields:    Translation:Animals
    93. 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.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCellsCTClinical Trials
    94. 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:
    95. 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.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    96. 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.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCTClinical Trials
    97. 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.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansCells
    98. 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.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    99. 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.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    100. 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.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    101. 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
    102. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    103. 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.
      View in: PubMed   Mentions: 47     Fields:    Translation:HumansCellsCTClinical Trials
    104. 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.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    105. 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:
    106. 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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    107. 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.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCTClinical Trials
    108. PedSplit: pedigree management for stratified analysis. Bioinformatics. 2004 Sep 22; 20(14):2315-6. Lanktree MB, VanderBeek L, Macciardi FM, Kennedy JL. PMID: 15059823.
      View in: PubMed   Mentions: 3     Fields:    
    109. 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.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    110. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    111. 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:
    112. 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
    113. 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:
    114. 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: 33     Fields:    Translation:HumansCells
    115. 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
    116. 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: 23     Fields:    Translation:Animals
    117. 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: 34     Fields:    Translation:Humans
    118. 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
    119. 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.
      View in: PubMed   Mentions: 202     Fields:    Translation:HumansCells
    120. 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
    121. 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.
      View in: PubMed   Mentions: 120     Fields:    Translation:Humans
    122. 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
    123. 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: 50     Fields:    Translation:Humans
    124. 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
    125. 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
    126. 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
    127. 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
    128. 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
    129. 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: 18     Fields:    Translation:Humans
    130. 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: 45     Fields:    Translation:Humans
    131. 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: 38     Fields:    Translation:HumansCells
    132. 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: 31     Fields:    Translation:HumansCells
    133. 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
    134. 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
    135. 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: 31     Fields:    Translation:Humans
    136. 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
    137. 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: 27     Fields:    Translation:HumansCells
    138. 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: 22     Fields:    
    139. 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: 3     Fields:    Translation:HumansCells
    140. 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
    141. 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: 14     Fields:    Translation:Humans
    142. 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: 16     Fields:    Translation:Humans
    143. 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: 16     Fields:    Translation:Humans
    144. 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
    145. 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: 20     Fields:    Translation:HumansCells
    146. 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: 32     Fields:    Translation:Humans
    147. 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
    148. 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
    149. 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
    150. 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
    151. 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
    152. 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.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    153. 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
    154. 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: 23     Fields:    Translation:HumansCTClinical Trials
    155. 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
    156. 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
    157. 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
    158. 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: 4     Fields:    Translation:HumansCells
    159. 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
    160. 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
    161. 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
    162. 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
    163. 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
    164. 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
    165. 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: 36     Fields:    Translation:HumansCells
    166. [Genetic studies and their relevance in social psychiatry]. Epidemiol Psichiatr Soc. 1998 May-Aug; 7(2):94-7. Smeraldi E, Macciardi F. PMID: 9763759.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    167. 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: 11     Fields:    Translation:Humans
    168. 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
    169. 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. PMID: 9577838.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    170. 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
    171. 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
    172. 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
    173. 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
    174. Chromosome 4 workshop. Psychiatr Genet. 1998; 8(2):67-71. Kennedy JL, Macciardi FM. PMID: 9686426.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    175. 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.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    176. 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
    177. 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: 7     Fields:    Translation:Humans
    178. 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
    179. 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
    180. 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
    181. 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
    182. 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
    183. 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.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    184. 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: 7     Fields:    Translation:Humans
    185. 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
    186. 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
    187. 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
    188. 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: 8     Fields:    Translation:Humans
    189. 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
    190. 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
    191. 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
    192. 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. PMID: 7581457.
      View in: PubMed   Mentions: 54     Fields:    Translation:HumansCells
    193. 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
    194. 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. PMID: 7875756.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    195. 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
    196. 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: 5     Fields:    Translation:Humans
    197. 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: 14     Fields:    Translation:Humans
    198. 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
    199. 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. PMID: 8232942.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    200. 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
    201. 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
    202. 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: 1     Fields:    Translation:Humans
    203. A two-locus model for familial Alzheimer's disease? Genet Epidemiol. 1993; 10(6):437-41. Macciardi F, Cavallini MC. PMID: 8314040.
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    204. 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. PMID: 1303289.
      View in: PubMed   Mentions: 81     Fields:    Translation:HumansCells
    205. 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
    206. 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
    207. 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
    208. 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
    209. 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
    210. 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: 2     Fields:    Translation:Humans
    211. 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
    212. 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
    213. 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
    214. 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
    215. 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
    216. 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
    217. 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: 6     Fields:    Translation:Humans
    218. 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
    219. 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
    220. 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
    221. 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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