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Results: 1-16 |
Results: 16
Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean Hispanics
Authors: Mayeux, R Lee, JH Romas, SN Mayo, D Santana, V Williamson, J Ciappa, A Rondon, HZ Estevez, P Lantigua, R Medrano, M Torres, M Stern, Y Tycko, B Knowles, JA
Citation: R. Mayeux et al., Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean Hispanics, AM J HU GEN, 70(1), 2002, pp. 237-243
No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder
Authors: Hamilton, SP Slager, SL Helleby, L Heiman, GA Klein, DF Hodge, SE Weissman, MM Fyer, AJ Knowles, JA
Citation: Sp. Hamilton et al., No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder, MOL PSYCHI, 6(1), 2001, pp. 59-65
Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner population
Authors: Niehaus, DJH Kinnear, CJ Corfield, VA du Toit, PL van Kradenburg, J Moolman-Smook, JC Weyers, JB Potgieter, A Seedat, S Emsley, RA Knowles, JA Brink, PA Stein, DJ
Citation: Djh. Niehaus et al., Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner population, J AFFECT D, 65(1), 2001, pp. 61-65
Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner population
Authors: Kinnear, CJ Niehaus, DJH Moolman-Smook, JC du Toit, PL van Kradenberg, J Weyers, JB Potgieter, A Marais, V Emsley, RA Knowles, JA Corfield, VA Brink, PA Stein, DJ
Citation: Cj. Kinnear et al., Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner population, IN J NEUROP, 3(4), 2000, pp. 327-331
No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder
Authors: Hamilton, SP Slager, SL Heiman, GA Haghighi, F Klein, DF Hodge, SE Weissman, MM Fyer, AJ Knowles, JA
Citation: Sp. Hamilton et al., No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder, MOL PSYCHI, 5(5), 2000, pp. 465-466
Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33
Authors: Deng, ZM Haghighi, F Helleby, L Vanterpool, K Horn, EM Barst, RJ Hodge, SE Morse, JH Knowles, JA
Citation: Zm. Deng et al., Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33, AM J R CRIT, 161(3), 2000, pp. 1055-1059
The deletion polymorphism and Val1000lle in alpha-2-macroglobulin and Alzheimer disease in Caribbean Hispanics
Authors: Romas, SN Mayeux, R Rabinowitz, D Tang, MX Zadroga, HR Lantigua, R Medrano, M Tycko, B Knowles, JA
Citation: Sn. Romas et al., The deletion polymorphism and Val1000lle in alpha-2-macroglobulin and Alzheimer disease in Caribbean Hispanics, NEUROSCI L, 279(3), 2000, pp. 133-136
Drawbacks of GENEHUNTER for larger pedigrees: Application to panic disorder
Authors: Goedken, R Ludington, E Crowe, R Fyer, AJ Hodge, SE Knowles, JA Vieland, VJ Weissman, MM
Citation: R. Goedken et al., Drawbacks of GENEHUNTER for larger pedigrees: Application to panic disorder, AM J MED G, 96(6), 2000, pp. 781-783
Investigation of dopamine receptor (DRD4) and dopamine transporter (DAT) polymorphisms for genetic linkage or association to panic disorder
Authors: Hamilton, SP Haghighi, F Heiman, GA Klein, DF Hodge, SE Fyer, AJ Weissman, MM Knowles, JA
Citation: Sp. Hamilton et al., Investigation of dopamine receptor (DRD4) and dopamine transporter (DAT) polymorphisms for genetic linkage or association to panic disorder, AM J MED G, 96(3), 2000, pp. 324-330
Potential panic disorder syndrome: Clinical and genetic linkage evidence
Authors: Weissman, MM Fyer, AJ Haghighi, F Heiman, G Deng, ZM Hen, R Hodge, SE Knowles, JA
Citation: Mm. Weissman et al., Potential panic disorder syndrome: Clinical and genetic linkage evidence, AM J MED G, 96(1), 2000, pp. 24-35
Familial primary pulmonary hypertension (gene PPH1) is caused by mutationsin the bone morphogenetic protein receptor-II gene
Authors: Deng, ZM Morse, JH Slager, SL Cuervo, N Moore, KJ Venetos, G Kalachikov, S Cayanis, E Fischer, SG Barst, RJ Hodge, SE Knowles, JA
Citation: Zm. Deng et al., Familial primary pulmonary hypertension (gene PPH1) is caused by mutationsin the bone morphogenetic protein receptor-II gene, AM J HU GEN, 67(3), 2000, pp. 737-744
Women on welfare: A macroeconomic analysis
Authors: Greenwood, J Guner, N Knowles, JA
Citation: J. Greenwood et al., Women on welfare: A macroeconomic analysis, AM ECON REV, 90(2), 2000, pp. 383-388
D8/17 in obsessive-compulsive disorder and trichotillomania
Authors: Niehaus, DJH Knowles, JA van Kradenberg, J du Toit, W Kaminer, D Seedat, S Daniels, W Cotton, M Brink, P Beyers, AD Bouic, P Chapman, F Zabriskie, TB Stein, DJ
Citation: Djh. Niehaus et al., D8/17 in obsessive-compulsive disorder and trichotillomania, S AFR MED J, 89(7), 1999, pp. 755-756
Parent-of-origin effect in panic disorder
Authors: Haghighi, F Fyer, AJ Weissman, MM Knowles, JA Hodge, SE
Citation: F. Haghighi et al., Parent-of-origin effect in panic disorder, AM J MED G, 88(2), 1999, pp. 131-135
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration
Authors: Lewis, CA Batlle, IR Batlle, KGR Banerjee, P Cideciyan, AV Huang, JC Aleman, TS Huang, YJ Ott, J Gilliam, TC Knowles, JA Jacobson, SG
Citation: Ca. Lewis et al., Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration, INV OPHTH V, 40(9), 1999, pp. 2106-2114
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus
Authors: Aita, VM Liu, JJ Knowles, JA Terwilliger, JD Baltazar, R Grunn, A Loth, JE Kanyas, K Lerer, B Endicott, J Wang, ZY Penchaszadeh, G Gilliam, TC Baron, M
Citation: Vm. Aita et al., A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus, AM J HU GEN, 64(1), 1999, pp. 210-217
Risultati: 1-16 |