Loading...

Pamela L Flodman

Title(s)Adjunct Professor, Pediatrics
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(714) 456-5789, (949) 82
vCardDownload vCard

    Collapse Bibliographic 
    Collapse Publications
    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.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    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. Ethnic disparities in the frequency of cancer reported in family histories. J Genet Couns. 2020 Jun; 29(3):451-459. Maves H, Flodman P, Nathan D, Smith M. PMID: 32222057.
      View in: PubMed   Mentions:    Fields:    
    2. 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:    Fields:    
    3. 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:
    4. 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:
    5. 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: 20     Fields:    Translation:AnimalsCells
    6. 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
    7. 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: 12     Fields:    Translation:Humans
    8. 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
    9. 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: 51     Fields:    Translation:Humans
    10. 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: 13     Fields:    Translation:HumansCellsCTClinical Trials
    11. 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: 42     Fields:    Translation:AnimalsCells
    12. 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. PMID: 19874574.
      View in: PubMed   Mentions: 90     Fields:    Translation:HumansAnimals
    13. 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: 23     Fields:    
    14. 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: 17     Fields:    Translation:HumansCells
    15. 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: 27     Fields:    Translation:Humans
    16. 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: 96     Fields:    Translation:Humans
    17. Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA). Am J Med Genet A. 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: 23     Fields:    Translation:HumansCells
    18. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet. 2007 Mar; 39(3):319-28. 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: 549     Fields:    Translation:Humans
    19. 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
    20. 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: 16     Fields:    Translation:HumansCells
    21. 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
    22. Evidence for multiple loci from a genome scan of autism kindreds. Mol Psychiatry. 2006 Nov; 11(11):1049-60, 979. Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM. PMID: 16880825.
      View in: PubMed   Mentions: 50     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: 34     Fields:    Translation:HumansCells
    24. Sequence variants of the DRD4 gene in autism: further evidence that rare DRD4 7R haplotypes are ADHD specific. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 05; 136B(1):33-5. Grady DL, Harxhi A, Smith M, Flodman P, Spence MA, Swanson JM, Moyzis RK. PMID: 15892149.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    25. 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
    26. Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): increased prevalence of the 2-repeat allele. Am J Med Genet B Neuropsychiatr Genet. 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: 22     Fields:    Translation:HumansCells
    27. Risk calculations: still essential in the molecular age. Am J Med Genet A. 2004 Sep 01; 129A(3):215-7. Hodge SE, Flodman PL. PMID: 15326619.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    28. 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: 20     Fields:    Translation:HumansCells
    29. The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus. Am J Hum Genet. 2004 May; 74(5):931-44. Wang E, Ding YC, Flodman P, Kidd JR, Kidd KK, Grady DL, Ryder OA, Spence MA, Swanson JM, Moyzis RK. PMID: 15077199.
      View in: PubMed   Mentions: 98     Fields:    Translation:HumansCells
    30. 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: 53     Fields:    Translation:Humans
    31. High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder. Mol Psychiatry. 2003 May; 8(5):536-45. Grady DL, Chi HC, Ding YC, Smith M, Wang E, Schuck S, Flodman P, Spence MA, Swanson JM, Moyzis RK. PMID: 12808433.
      View in: PubMed   Mentions: 40     Fields:    Translation:HumansCells
    32. 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
    33. 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
    34. Cleft lip with or without cleft palate and dermatoglyphic asymmetry: evaluation of a Chinese population. Orthod Craniofac Res. 2002 Aug; 5(3):140-6. Neiswanger K, Cooper ME, Weinberg SM, Flodman P, Keglovits AB, Liu Y, Hu DN, Melnick M, Spence MA, Marazita ML. PMID: 12194662.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    35. 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: 17     Fields:    Translation:HumansCells
    36. 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:    
    37. 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: 5     Fields:    Translation:Animals
    38. Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits. Cytogenet Genome Res. 2002; 98(4):233-9. Smith M, Woodroffe A, Smith R, Holguin S, Martinez J, Filipek PA, Modahl C, Moore B, Bocian ME, Mays L, Laulhere T, Flodman P, Spence MA. PMID: 12826745.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    39. 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: 120     Fields:    Translation:HumansCells
    40. A genetic risk calculation surprise. Am J Med Genet. 2001 Apr 22; 100(2):169-71. Flodman P, Hodge SE. PMID: 11298381.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    41. A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22. Proc Natl Acad Sci U S A. 2001 Jan 16; 98(2):585-90. Kelsoe JR, Spence MA, Loetscher E, Foguet M, Sadovnick AD, Remick RA, Flodman P, Khristich J, Mroczkowski-Parker Z, Brown JL, Masser D, Ungerleider S, Rapaport MH, Wishart WL, Luebbert H. PMID: 11149935.
      View in: PubMed   Mentions: 57     Fields:    Translation:HumansCells
    42. Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR. Cytogenet Cell Genet. 2001; 94(1-2):15-22. Smith M, Escamilla JR, Filipek P, Bocian ME, Modahl C, Flodman P, Spence MA. PMID: 11701947.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    43. Preliminary implementation of new data mining techniques for the analysis of simulation data from Genetic Analysis Workshop 12: problem 2. Genet Epidemiol. 2001; 21 Suppl 1:S390-5. Flodman P, Macula AJ, Spence MA, Torney DC. PMID: 11793705.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    44. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract. Invest Ophthalmol Vis Sci. 2000 Oct; 41(11):3278-85. Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA. PMID: 11006214.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansCells
    45. A new locus for autosomal dominant cataract on chromosome 12q13. Invest Ophthalmol Vis Sci. 2000 Aug; 41(9):2665-70. Bateman JB, Johannes M, Flodman P, Geyer DD, Clancy KP, Heinzmann C, Kojis T, Berry R, Sparkes RS, Spence MA. PMID: 10937580.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    46. Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention. Proc Natl Acad Sci U S A. 2000 Apr 25; 97(9):4754-9. Swanson J, Oosterlaan J, Murias M, Schuck S, Flodman P, Spence MA, Wasdell M, Ding Y, Chi HC, Smith M, Mann M, Carlson C, Kennedy JL, Sergeant JA, Leung P, Zhang YP, Sadeh A, Chen C, Whalen CK, Babb KA, Moyzis R, Posner MI. PMID: 10781080.
      View in: PubMed   Mentions: 61     Fields:    Translation:HumansCells
    47. Ultrasonographic detection of orbicularis oris defects in first degree relatives of isolated cleft lip patients. Am J Med Genet. 2000 Jan 17; 90(2):155-61. Martin RA, Hunter V, Neufeld-Kaiser W, Flodman P, Spence MA, Furnas D, Martin KA. PMID: 10607956.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    48. Dopamine genes and ADHD. Neurosci Biobehav Rev. 2000 Jan; 24(1):21-5. Swanson JM, Flodman P, Kennedy J, Spence MA, Moyzis R, Schuck S, Murias M, Moriarity J, Barr C, Smith M, Posner M. PMID: 10654656.
      View in: PubMed   Mentions: 68     Fields:    Translation:HumansCTClinical Trials
    49. Estimating recombination fraction separately for males and females: a counterintuitive result. Hum Hered. 1998 Jan-Feb; 48(1):42-8. Hodge SE, Flodman PL, Duryea MF, Spence MA. PMID: 9463801.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    50. HLA haplotypes, polysomnography, and pedigrees in a case series of patients with narcolepsy. Sleep. 1997 Oct; 20(10):850-7. Hayduk R, Flodman P, Spence MA, Erman MK, Mitler MM. PMID: 9415944.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    51. Bipolar disorder: dominant or recessive on chromosome 5? Genet Epidemiol. 1997; 14(6):647-51. Homer JP, Flodman PL, Spence MA. PMID: 9433557.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    52. Possible locus for bipolar disorder near the dopamine transporter on chromosome 5. Am J Med Genet. 1996 Nov 22; 67(6):533-40. Kelsoe JR, Sadovnick AD, Kristbjarnarson H, Bergesch P, Mroczkowski-Parker Z, Drennan M, Rapaport MH, Flodman P, Spence MA, Remick RA. PMID: 8950410.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
    53. Genetic linkage study of bipolar disorder and the serotonin transporter. Am J Med Genet. 1996 Apr 09; 67(2):215-7. Kelsoe JR, Remick RA, Sadovnick AD, Kristbjarnarson H, Flodman P, Spence MA, Morison M, Mroczkowski-Parker Z, Bergesch P, Rapaport MH, Mirow AL, Blakely RD, Helgason T, Egeland JA. PMID: 8723051.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    54. Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa. Am J Hum Genet. 1996 Feb; 58(2):347-55. Kojis TL, Heinzmann C, Flodman P, Ngo JT, Sparkes RS, Spence MA, Bateman JB, Heckenlively JR. PMID: 8571961.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    55. A genetic linkage map of the rat derived from recombinant inbred strains. Mamm Genome. 1996 Feb; 7(2):117-27. Pravenec M, Gauguier D, Schott JJ, Buard J, Kren V, Bílá V, Szpirer C, Szpirer J, Wang JM, Huang H, St Lezin E, Spence MA, Flodman P, Printz M, Lathrop GM, Vergnaud G, Kurtz TW. PMID: 8835528.
      View in: PubMed   Mentions: 18     Fields:    Translation:AnimalsCells
    56. Bipolar disorder: evidence for a major locus. Am J Med Genet. 1995 Oct 09; 60(5):370-6. Spence MA, Flodman PL, Sadovnick AD, Bailey-Wilson JE, Ameli H, Remick RA. PMID: 8546148.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    57. Oligogenic determination of morphine analgesic magnitude: a genetic analysis of selectively bred mouse lines. Behav Genet. 1995 Jul; 25(4):397-406. Mogil JS, Flodman P, Spence MA, Sternberg WF, Kest B, Sadowski B, Liebeskind JC, Belknap JK. PMID: 7575370.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    58. One or two genetic loci mediate high opiate analgesia in selectively bred mice. Pain. 1995 Feb; 60(2):125-35. Mogil JS, Marek P, Flodman P, Spence MA, Sternberg WF, Kest B, Sadowski B, Liebeskind JC. PMID: 7784097.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
    59. Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees. Hum Genet. 1994 Nov; 94(5):484-90. Munier FL, Arabien L, Flodman P, Spence MA, Pescia G, Rutz HP, Murphree AL. PMID: 7959681.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    60. A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23. Ann N Y Acad Sci. 1991; 615:306-15. Janssen LA, Povey S, Attwood J, Sandkuyl LA, Lindhout D, Flodman P, Smith M, Sampson JR, Haines JL, Merkens EC. PMID: 2039153.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    61. Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset. Ann N Y Acad Sci. 1991; 615:256-64. Haines JL, Amos J, Attwood J, Bech-Hansen NT, Burley M, Conneally PM, Connor JM, Fahsold R, Flodman P, Fryer A. PMID: 1674844.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCellsCTClinical Trials
    62. Genetic heterogeneity in tuberous sclerosis. Map position of the TSC2 locus on chromosome 11q and future prospects. Ann N Y Acad Sci. 1991; 615:274-83. Smith M, Yoshiyama K, Wagner C, Flodman P, Smith B. PMID: 1674845.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    63. An attempt to map two genes for tuberous sclerosis using novel two-point methods. Ann N Y Acad Sci. 1991; 615:298-305. Povey S, Attwood J, Janssen LA, Burley M, Smith M, Flodman P, Morton NE, Edwards JH, Sampson JR, Yates JR. PMID: 1674846.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    64. Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23. Genomics. 1990 Jan; 6(1):105-14. Smith M, Smalley S, Cantor R, Pandolfo M, Gomez MI, Baumann R, Flodman P, Yoshiyama K, Nakamura Y, Julier C. PMID: 2303253.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    Pamela's Networks
    Concepts (281)
    Derived automatically from this person's publications.
    _
    Co-Authors (16)
    People in Profiles who have published with this person.
    _
    Similar People (60)
    People who share similar concepts with this person.
    _
    Same Department
    Search Department
    _