Pamela L Flodman

Title(s)Adjunct Professor, Pediatrics
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(714) 456-5789, (949) 82
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    1. Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader-Willi syndrome: A multicenter study. Clin Genet. 2021 07; 100(1):29-39. Mahmoud R, Leonenko A, Butler MG, Flodman P, Gold JA, Miller JL, Roof E, Dykens E, Driscoll DJ, Kimonis V. PMID: 33615449.
      View in: PubMed   Mentions: 1     Fields:    
    2. Ethnic disparities in the frequency of cancer reported in family histories. J Genet Couns. 2020 06; 29(3):451-459. Maves H, Flodman P, Nathan D, Smith M. PMID: 32222057.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    3. Molecular subtype and growth hormone effects on dysmorphology in Prader-Willi syndrome. Am J Med Genet A. 2020 01; 182(1):169-175. Oldzej J, Manazir J, Gold JA, Mahmoud R, Osann K, Flodman P, Cassidy SB, Kimonis VE. PMID: 31782896.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    4. A comparative study of patients' perceptions of genetic and genomic medicine services in California and Malaysia. J Community Genet. 2019 Jul; 10(3):351-361. Qian E, Thong MK, Flodman P, Gargus J. PMID: 30506521.
      View in: PubMed   Mentions:
    5. Expanded Insights Into Mechanisms of Gene Expression and Disease Related Disruptions. Front Mol Biosci. 2018; 5:101. Smith M, Flodman PL. PMID: 30542652.
      View in: PubMed   Mentions:
    6. The sequenced rat brain transcriptome--its use in identifying networks predisposing alcohol consumption. FEBS J. 2015 Sep; 282(18):3556-78. Saba LM, Flink SC, Vanderlinden LA, Israel Y, Tampier L, Colombo G, Kiianmaa K, Bell RL, Printz MP, Flodman P, Koob G, Richardson HN, Lombardo J, Hoffman PL, Tabakoff B. PMID: 26183165.
      View in: PubMed   Mentions: 29     Fields:    Translation:AnimalsCells
    7. Is the alcohol deprivation effect genetically mediated? Studies with HXB/BXH recombinant inbred rat strains. Alcohol Clin Exp Res. 2014 Jul; 38(7):2148-57. Vanderlinden LA, Saba LM, Printz MP, Flodman P, Koob G, Richardson HN, Hoffman PL, Tabakoff B. PMID: 24961585.
      View in: PubMed   Mentions: 6     Fields:    Translation:Animals
    8. Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis. Genet Med. 2014 Apr; 16(4):302-10. Greenwood J, Flodman P, Osann K, Boyadjiev SA, Kimonis V. PMID: 24071792.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    9. Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology. Genet Med. 2014 Feb; 16(2):164-9. Gold JA, Ruth C, Osann K, Flodman P, McManus B, Lee HS, Donkervoort S, Khare M, Roof E, Dykens E, Miller JL, Driscoll DJ, Butler MG, Heinemann J, Cassidy S, Kimonis VE. PMID: 23928912.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    10. Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors. J Genet Couns. 2013 Jun; 22(3):291-5. Devers PL, Cronister A, Ormond KE, Facio F, Brasington CK, Flodman P. PMID: 23334531.
      View in: PubMed   Mentions: 55     Fields:    Translation:Humans
    11. Mitochondrial and ion channel gene alterations in autism. Biochim Biophys Acta. 2012 Oct; 1817(10):1796-802. Smith M, Flodman PL, Gargus JJ, Simon MT, Verrell K, Haas R, Reiner GE, Naviaux R, Osann K, Spence MA, Wallace DC. PMID: 22538295.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCellsCTClinical Trials
    12. Susceptibility to anthrax lethal toxin-induced rat death is controlled by a single chromosome 10 locus that includes rNlrp1. PLoS Pathog. 2010 May 20; 6(5):e1000906. Newman ZL, Printz MP, Liu S, Crown D, Breen L, Miller-Randolph S, Flodman P, Leppla SH, Moayeri M. PMID: 20502689.
      View in: PubMed   Mentions: 48     Fields:    Translation:AnimalsCells
    13. Genetical genomic determinants of alcohol consumption in rats and humans. BMC Biol. 2009 Oct 27; 7:70. Tabakoff B, Saba L, Printz M, Flodman P, Hodgkinson C, Goldman D, Koob G, Richardson HN, Kechris K, Bell RL, Hübner N, Heinig M, Pravenec M, Mangion J, Legault L, Dongier M, Conigrave KM, Whitfield JB, Saunders J, Grant B, Hoffman PL, WHO/ISBRA Study on State and Trait Markers of Alcoholism . PMID: 19874574.
      View in: PubMed   Mentions: 97     Fields:    Translation:HumansAnimals
    14. Rightward hemispheric asymmetries in auditory language cortex in children with autistic disorder: an MRI investigation. J Neurodev Disord. 2009 Sep; 1(3):205-14. Gage NM, Juranek J, Filipek PA, Osann K, Flodman P, Isenberg AL, Spence MA. PMID: 19816533.
      View in: PubMed   Mentions: 27     Fields:    
    15. Nuclear and mitochondrial genome defects in autisms. Ann N Y Acad Sci. 2009 Jan; 1151:102-32. Smith M, Spence MA, Flodman P. PMID: 19154520.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    16. Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives. J Autoimmun. 2008 Sep; 31(2):160-5. Neuhausen SL, Steele L, Ryan S, Mousavi M, Pinto M, Osann KE, Flodman P, Zone JJ. PMID: 18692362.
      View in: PubMed   Mentions: 31     Fields:    Translation:Humans
    17. A replication of the Autism Diagnostic Observation Schedule (ADOS) revised algorithms. J Am Acad Child Adolesc Psychiatry. 2008 Jun; 47(6):642-651. Gotham K, Risi S, Dawson G, Tager-Flusberg H, Joseph R, Carter A, Hepburn S, McMAHON W, Rodier P, Hyman SL, Sigman M, Rogers S, Landa R, Spence MA, Osann K, Flodman P, Volkmar F, Hollander E, Buxbaum J, Pickles A, Lord C. PMID: 18434924.
      View in: PubMed   Mentions: 103     Fields:    Translation:Humans
    18. Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA). . 2008 Apr 01; 146A(7):833-42. Richter L, Flodman P, Barria von-Bischhoffshausen F, Burch D, Brown S, Nguyen L, Turner J, Spence MA, Bateman JB. PMID: 18302245.
      View in: PubMed   Mentions:
    19. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet. 2007 Mar; 39(3):319-28. Autism Genome Project Consortium , Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Koop F, Langemeijer M, Langemeijer M, Hijmans C, Hijimans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A, Meyer KJ. PMID: 17322880.
      View in: PubMed   Mentions: 579     Fields:    Translation:Humans
    20. Bayesian risk assessment in genetic testing for autosomal dominant disorders with age-dependent penetrance. J Genet Couns. 2007 Feb; 16(1):29-39. Ogino S, Wilson RB, Gold B, Flodman P. PMID: 17295057.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    21. Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract. Ophthalmology. 2007 Mar; 114(3):425-32. Bateman JB, von-Bischhoffshaunsen FR, Richter L, Flodman P, Burch D, Spence MA. PMID: 17234267.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    22. A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes. Invest Ophthalmol Vis Sci. 2006 Aug; 47(8):3441-9. Bateman JB, Richter L, Flodman P, Burch D, Brown S, Penrose P, Paul O, Geyer DD, Brooks DG, Spence MA. PMID: 16877414.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    23. Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract. Am J Ophthalmol. 2006 Apr; 141(4):761-3. Geyer DD, Spence MA, Johannes M, Flodman P, Clancy KP, Berry R, Sparkes RS, Jonsen MD, Isenberg SJ, Bateman JB. PMID: 16564824.
      View in: PubMed   Mentions: 37     Fields:    Translation:HumansCells
    24. Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation tests. Genet Med. 2005 May-Jun; 7(5):317-27. Ogino S, Flodman P, Wilson RB, Gold B, Grody WW. PMID: 15915083.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansPHPublic Health
    25. Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): increased prevalence of the 2-repeat allele. . 2005 Feb 05; 133B(1):54-6. Leung PW, Lee CC, Hung SF, Ho TP, Tang CP, Kwong SL, Leung SY, Yuen ST, Lieh-Mak F, Oosterlaan J, Grady D, Harxhi A, Ding YC, Chi HC, Flodman P, Schuck S, Spence MA, Moyzis R, Swanson J. PMID: 15578612.
      View in: PubMed   Mentions:
    26. Risk calculations: still essential in the molecular age. . 2004 Sep 01; 129A(3):215-7. Hodge SE, Flodman PL. PMID: 15326619.
      View in: PubMed   Mentions:
    27. A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R. BMC Med Genet. 2004 Apr 16; 5:10. Ramanathan S, Woodroffe A, Flodman PL, Mays LZ, Hanouni M, Modahl CB, Steinberg-Epstein R, Bocian ME, Spence MA, Smith M. PMID: 15090072.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansCells
    28. Language and other regression: assessment and timing. J Autism Dev Disord. 2003 Dec; 33(6):607-16. Goldberg WA, Osann K, Filipek PA, Laulhere T, Jarvis K, Modahl C, Flodman P, Spence MA. PMID: 14714930.
      View in: PubMed   Mentions: 56     Fields:    Translation:Humans
    29. Sex-specific mutation rates for x-linked disorders: estimation and application. Hum Hered. 2003; 55(1):51-5. Flodman P, Hodge SE. PMID: 12890926.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    30. Identification of quantitative trait loci for prepulse inhibition in rats. Psychopharmacology (Berl). 2003 Jan; 165(3):270-9. Palmer AA, Breen LL, Flodman P, Conti LH, Spence MA, Printz MP. PMID: 12426667.
      View in: PubMed   Mentions: 12     Fields:    Translation:Animals
    31. Presence of large deletions in kindreds with autism. Am J Hum Genet. 2002 Jul; 71(1):100-15. Yu CE, Dawson G, Munson J, D'Souza I, Osterling J, Estes A, Leutenegger AL, Flodman P, Smith M, Raskind WH, Spence MA, McMahon W, Wijsman EM, Schellenberg GD. PMID: 12058345.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    32. Determining Complex Genetic Risks by Computer. J Genet Couns. 2002 Jun; 11(3):213-30. Flodman P, Hodge SE. PMID: 26141858.
      View in: PubMed   Mentions: 1     Fields:    
    33. Heart rate and blood pressure quantitative trait loci for the airpuff startle reaction. Hypertension. 2002 Feb; 39(2 Pt 2):348-52. Jaworski RL, Jirout M, Closson S, Breen L, Flodman PL, Spence MA, Kren V, Krenova D, Pravenec M, Printz MP. PMID: 11882571.
      View in: PubMed   Mentions: 6     Fields:    Translation:Animals
    34. Evidence of positive selection acting at the human dopamine receptor D4 gene locus. Proc Natl Acad Sci U S A. 2002 Jan 08; 99(1):309-14. Ding YC, Chi HC, Grady DL, Morishima A, Kidd JR, Kidd KK, Flodman P, Spence MA, Schuck S, Swanson JM, Zhang YP, Moyzis RK. PMID: 11756666.
      View in: PubMed   Mentions: 123     Fields:    Translation:HumansCells
    35. One or two genetic loci mediate high opiate analgesia in selectively bred mice. Pain. 1995 Feb; 60(2):125-135. Mogil JS, Marek P, Flodman P, Spence AM, Sternberg WF, Kest B, Sadowski B, Liebeskind JC. PMID: 7784097.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
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