-
Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi Syndrome. J Clin Med. 2022 May 04; 11(9).
Mahmoud R, Swanson HD, Butler MG, Flodman P, Gold JA, Miller JL, Roof E, Osann K, Dykens E, Driscoll DJ, Kimonis V. PMID: 35566699; PMCID: PMC9104315.
View in:
PubMed Mentions:
-
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; PMCID: PMC8568051.
View in:
PubMed Mentions:
5 Fields:
Translation:
Humans
-
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:
1 Fields:
Translation:
Humans
-
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:
6 Fields:
Translation:
HumansCells
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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; PMCID: PMC6591353.
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; PMCID: PMC6277798.
View in:
PubMed Mentions:
9
-
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; PMCID: PMC4573833.
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PubMed Mentions:
36 Fields:
Translation:
AnimalsCells
-
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; PMCID: PMC4142977.
View in:
PubMed Mentions:
9 Fields:
Translation:
Animals
-
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; PMCID: PMC4143991.
View in:
PubMed Mentions:
25 Fields:
Translation:
Humans
-
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; PMCID: PMC4164429.
View in:
PubMed Mentions:
9 Fields:
Translation:
HumansCells
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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:
62 Fields:
Translation:
Humans
-
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; PMCID: PMC3423964.
View in:
PubMed Mentions:
25 Fields:
Translation:
HumansCellsCTClinical Trials
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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; PMCID: PMC2873920.
View in:
PubMed Mentions:
54 Fields:
Translation:
AnimalsCells
-
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; PMCID: PMC2777866.
View in:
PubMed Mentions:
105 Fields:
Translation:
HumansAnimals
-
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; PMCID: PMC2758220.
View in:
PubMed Mentions:
29 Fields:
-
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.
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PubMed Mentions:
28 Fields:
Translation:
HumansCells
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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; PMCID: PMC2630860.
View in:
PubMed Mentions:
37 Fields:
Translation:
Humans
-
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; PMCID: PMC3057666.
View in:
PubMed Mentions:
126 Fields:
Translation:
Humans
-
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:
25 Fields:
Translation:
HumansCells
-
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; PMCID: PMC4867008.
View in:
PubMed Mentions:
631 Fields:
Translation:
Humans
-
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:
3 Fields:
Translation:
Humans
-
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:
20 Fields:
Translation:
HumansCells
-
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
-
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:
59 Fields:
Translation:
HumansCells
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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; PMCID: PMC1463993.
View in:
PubMed Mentions:
36 Fields:
Translation:
HumansCells
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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:
13 Fields:
Translation:
HumansCells
-
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
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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:
25 Fields:
Translation:
HumansCells
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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
-
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; PMCID: PMC411038.
View in:
PubMed Mentions:
31 Fields:
Translation:
HumansCells
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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; PMCID: PMC1181986.
View in:
PubMed Mentions:
113 Fields:
Translation:
HumansCells
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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:
60 Fields:
Translation:
Humans
-
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:
44 Fields:
Translation:
HumansCells
-
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:
2 Fields:
Translation:
HumansCells
-
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:
-
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:
7 Fields:
Translation:
Animals
-
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:
24 Fields:
Translation:
HumansCells
-
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; PMCID: PMC117557.
View in:
PubMed Mentions:
135 Fields:
Translation:
HumansCells
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A genetic risk calculation surprise. Am J Med Genet. 2001 Apr 22; 100(2):169-71.
Flodman P, Hodge SE. PMID: 11298381.
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PubMed Mentions:
3 Fields:
Translation:
HumansCells
-
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; PMCID: PMC14631.
View in:
PubMed Mentions:
60 Fields:
Translation:
HumansCells
-
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:
10 Fields:
Translation:
HumansCells
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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
-
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:
38 Fields:
Translation:
HumansCells
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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:
13 Fields:
Translation:
HumansCells
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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; PMCID: PMC18305.
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PubMed Mentions:
61 Fields:
Translation:
HumansCells
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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:
13 Fields:
Translation:
Humans
-
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:
83 Fields:
Translation:
HumansCTClinical Trials
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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.
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PubMed Mentions: Fields:
Translation:
Animals
-
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; PMCID: PMC2248798.
View in:
PubMed Mentions:
7 Fields:
Translation:
Humans
-
Bipolar disorder: dominant or recessive on chromosome 5? Genet Epidemiol. 1997; 14(6):647-51.
Homer JP, Flodman PL, Spence MA. PMID: 9433557.
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PubMed Mentions:
1 Fields:
Translation:
HumansCells
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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
-
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.
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PubMed Mentions: Fields:
Translation:
HumansCells
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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; PMCID: PMC1914553.
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PubMed Mentions:
3 Fields:
Translation:
HumansCells
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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
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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.
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PubMed Mentions:
14 Fields:
Translation:
Humans
-
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
-
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:
10 Fields:
Translation:
Animals
-
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.
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PubMed Mentions:
4 Fields:
Translation:
Humans
-
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, et al. PMID: 2039153.
View in:
PubMed Mentions:
8 Fields:
Translation:
HumansCells
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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, et al. PMID: 1674844.
View in:
PubMed Mentions:
14 Fields:
Translation:
HumansCellsCTClinical Trials
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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
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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, et al. PMID: 1674846.
View in:
PubMed Mentions:
6 Fields:
Translation:
HumansCells
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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, et al. PMID: 2303253.
View in:
PubMed Mentions:
21 Fields:
Translation:
HumansCells