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Results: 1-25 | 26-36
Results: 1-25/36
Variability in skeletal mass, structure, and biomechanical properties among inbred strains of rats
Authors: Turner, CH Roeder, RK Wieczorek, A Foroud, T Liu, G Peacock, M
Citation: Ch. Turner et al., Variability in skeletal mass, structure, and biomechanical properties among inbred strains of rats, J BONE MIN, 16(8), 2001, pp. 1532-1539
Genome screen for quantitative trait loci underlying normal variation in femoral structure
Authors: Koller, DL Liu, GD Econs, MJ Hui, SL Morin, PA Joslyn, G Rodriguez, LA Conneally, PM Christian, JC Johnston, CC Foroud, T Peacock, M
Citation: Dl. Koller et al., Genome screen for quantitative trait loci underlying normal variation in femoral structure, J BONE MIN, 16(6), 2001, pp. 985-991
Parametric linkage analysis and disequilibrium methods to identify loci for complex disease
Authors: McClintick, J Koller, DL Pankratz, N Kirkwood, SC Naughton, B Foroud, T
Citation: J. Mcclintick et al., Parametric linkage analysis and disequilibrium methods to identify loci for complex disease, GENET EPID, 21, 2001, pp. S528-S533
Use of variable marker density, principal components, and neural networks in the dissection of disease etiology
Authors: Pankratz, N Kirkwood, SC Flury, L Koller, DL Foroud, T
Citation: N. Pankratz et al., Use of variable marker density, principal components, and neural networks in the dissection of disease etiology, GENET EPID, 21, 2001, pp. S732-S737
Stoppage: An issue for segregation analysis
Authors: Slager, SL Foroud, T Haghighi, F Spence, MA Hodge, SE
Citation: Sl. Slager et al., Stoppage: An issue for segregation analysis, GENET EPID, 20(3), 2001, pp. 328-339
Functional relevance of human ADH polymorphism
Authors: Eriksson, CJP Fukunaga, T Sarkola, T Chen, WJ Chen, CC Ju, JM Cheng, ATA Yamamoto, H Kohlenberg-Muller, K Kimura, M Murayama, M Matsushita, S Kashima, H Higuchi, S Carr, L Viljoen, D Brooke, L Stewart, T Foroud, T Su, J Li, TK Whitfield, JB
Citation: Cjp. Eriksson et al., Functional relevance of human ADH polymorphism, ALC CLIN EX, 25(5), 2001, pp. 157S-163S
A genome-wide search for genes that relate to a low level of response to alcohol
Authors: Schuckit, MA Edenberg, HJ Kalmijn, J Flury, L Smith, TL Reich, T Bierut, L Goate, A Foroud, T
Citation: Ma. Schuckit et al., A genome-wide search for genes that relate to a low level of response to alcohol, ALC CLIN EX, 25(3), 2001, pp. 323-329
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
Authors: Levy, GG Nichols, WC Lian, EC Foroud, T McClintick, JN McGee, BM Yang, AY Siemieniak, DR Stark, KR Gruppo, R Sarode, R Shurin, SB Chandrasekaran, V Stabler, SP Sabio, H Bouhassira, EE Upshaw, JD Ginsburg, D Tsai, HM
Citation: Gg. Levy et al., Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura, NATURE, 413(6855), 2001, pp. 488-494
Progression of symptoms in the early and middle stages of Huntington disease
Authors: Kirkwood, SC Su, JL Conneally, PM Foroud, T
Citation: Sc. Kirkwood et al., Progression of symptoms in the early and middle stages of Huntington disease, ARCH NEUROL, 58(2), 2001, pp. 273-278
Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder
Authors: Nurnberger, JI Foroud, T Flury, L Su, J Meyer, ET Hu, KL Crowe, R Edenberg, H Goate, A Bierut, L Reich, T Schuckit, M Reich, W
Citation: Ji. Nurnberger et al., Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder, AM J PSYCHI, 158(5), 2001, pp. 718-724
Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism
Authors: Almasy, L Porjesz, B Blangero, J Goate, A Edenberg, HJ Chorlian, DB Kuperman, S O'Connor, SJ Rohrbaugh, J Bauer, LO Foroud, T Rice, JP Reich, T Begleiter, H
Citation: L. Almasy et al., Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism, AM J HU GEN, 68(1), 2001, pp. 128-135
Sib pair linkage and association studies between bone mineral density and the interleukim-6 gene locus
Authors: Takacs, I Koller, DL Peacock, M Christian, JC Evans, WE Hui, SL Conneally, PM Johnston, CC Foroud, T Econs, MJ
Citation: I. Takacs et al., Sib pair linkage and association studies between bone mineral density and the interleukim-6 gene locus, BONE, 27(1), 2000, pp. 169-173
A genome screen of maximum number of drinks as an alcoholism phenotype
Authors: Saccone, NL Kwon, JM Corbett, J Goate, A Rochberg, N Edenberg, HJ Foroud, T Li, TK Begleiter, H Reich, T Rice, JP
Citation: Nl. Saccone et al., A genome screen of maximum number of drinks as an alcoholism phenotype, AM J MED G, 96(5), 2000, pp. 632-637
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
Authors: 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
Citation: Le. Delisi et al., 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 G, 96(3), 2000, pp. 434-449
Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees
Authors: Foroud, T Castelluccio, PF Koller, DL Edenberg, HJ Miller, M Bowman, E Rau, NL Smiley, C Rice, JP Goate, A Armstrong, C Bierut, LJ Reich, T Detera-Wadleigh, SD Goldin, LR Badner, JA Guroff, JJ Gershon, ES McMahon, FJ Simpson, S MacKinnon, D McInnis, M Stine, OC DePaulo, JR Blehar, MC Nurnberger, JI
Citation: T. Foroud et al., Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees, AM J MED G, 96(1), 2000, pp. 18-23
Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking
Authors: Bierut, LJ Rice, JP Edenberg, HJ Goate, A Foroud, T Cloninger, CR Begleiter, H Conneally, PM Crowe, RR Hesselbrock, V Li, TK Nurnberger, JI Porjesz, B Schuckit, MA Reich, T
Citation: Lj. Bierut et al., Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking, AM J MED G, 90(4), 2000, pp. 299-302
Alcoholism susceptibility loci: Confirmation studies in a replicate sampleand further mapping
Authors: Foroud, T Edenberg, HJ Goate, A Rice, J Flury, L Koller, DL Bierut, LJ Conneally, PM Nurnberger, JI Bucholz, KK Li, TK Hesselbrock, V Crowe, R Schuckit, M Porjesz, B Begleiter, H Reich, T
Citation: T. Foroud et al., Alcoholism susceptibility loci: Confirmation studies in a replicate sampleand further mapping, ALC CLIN EX, 24(7), 2000, pp. 933-945
Subtle changes among presymptomatic carriers of the Huntington's disease gene
Authors: Kirkwood, SC Siemers, E Hodes, ME Conneally, PM Christian, JC Foroud, T
Citation: Sc. Kirkwood et al., Subtle changes among presymptomatic carriers of the Huntington's disease gene, J NE NE PSY, 69(6), 2000, pp. 773-779
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis
Authors: Koller, DL Econs, MJ Morin, PA Christian, JC Hui, SL Parry, P Curran, ME Rodriguez, LA Conneally, PM Joslyn, G Peacock, M Johnston, CC Foroud, T
Citation: Dl. Koller et al., Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis, J CLIN END, 85(9), 2000, pp. 3116-3120
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus (vol 84, pg 4467, 1999)
Authors: Takacs, I Koller, DL Peacock, M Christian, JC Hui, SL Conneally, PM Johnston, CC Foroud, T Econs, MJ
Citation: I. Takacs et al., Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus (vol 84, pg 4467, 1999), J CLIN END, 85(1), 2000, pp. 138-138
Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene
Authors: Kirkwood, SC Siemers, E Bond, C Conneally, PM Christian, JC Foroud, T
Citation: Sc. Kirkwood et al., Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene, ARCH NEUROL, 57(7), 2000, pp. 1040-1044
Identification of quantitative trait loci influencing alcohol consumption in the high alcohol drinking and low alcohol drinkingt rat lines
Authors: Foroud, T Bice, P Castelluccio, P Bo, RH Miller, L Ritchotte, A Lumeng, L Li, TK Carr, LG
Citation: T. Foroud et al., Identification of quantitative trait loci influencing alcohol consumption in the high alcohol drinking and low alcohol drinkingt rat lines, BEHAV GENET, 30(2), 2000, pp. 131-140
Genetics of alcoholism: A review of recent studies in human and animal models
Authors: Foroud, T Li, TK
Citation: T. Foroud et Tk. Li, Genetics of alcoholism: A review of recent studies in human and animal models, AM J ADDICT, 8(4), 1999, pp. 261-278
Nonparametric linkage and family-based association studies of a simulated complex disorder
Authors: Koller, DL Balding, J Foroud, T
Citation: Dl. Koller et al., Nonparametric linkage and family-based association studies of a simulated complex disorder, GENET EPID, 17, 1999, pp. S627-S632
Genome screen for platelet monoamine oxidase (MAO) activity
Authors: Saccone, NL Rice, JP Rochberg, N Goate, A Reich, T Shears, S Wu, W Nurnberger, JI Foroud, T Edenberg, HJ Li, TK
Citation: Nl. Saccone et al., Genome screen for platelet monoamine oxidase (MAO) activity, AM J MED G, 88(5), 1999, pp. 517-521
Risultati: 1-25 | 26-36