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Results: 1-24 |
Results: 24
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
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
A common enzyme connects Notch signaling and Alzheimer's disease
Authors: Kopan, R Goate, A
Citation: R. Kopan et A. Goate, A common enzyme connects Notch signaling and Alzheimer's disease, GENE DEV, 14(22), 2000, pp. 2799-2806
Neuropsychological profile of a large kindred with familial Alzheimer's disease caused by the E280A single presenilin-1 mutation
Authors: Ardila, A Lopera, F Rosselli, M Moreno, S Madrigal, L Arango-Lasprilla, JC Arcos, M Murcia, C Arango-Viana, JC Ossa, J Goate, A Kosik, KS
Citation: A. Ardila et al., Neuropsychological profile of a large kindred with familial Alzheimer's disease caused by the E280A single presenilin-1 mutation, ARCH CLIN N, 15(6), 2000, pp. 515-528
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
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
Effect of APOE genotype and promoter polymorphism on risk of Alzheimer's disease
Authors: Wang, JC Kwon, JM Shah, P Morris, JC Goate, A
Citation: Jc. Wang et al., Effect of APOE genotype and promoter polymorphism on risk of Alzheimer's disease, NEUROLOGY, 55(11), 2000, pp. 1644-1649
alpha-2 macroglobulin gene and Alzheimer disease
Authors: Rudrasingham, V Wavrant-De Vrieze, F Lambert, JC Chakraverty, S Kehoe, P Crook, R Amouyel, P Wu, W Rice, F Perez-Tur, J Frigard, B Morris, JC Carty, S Petersen, R Cottel, D Tunstall, N Holmans, P Lovestone, S Chartier-Harlin, MC Goate, A Hardy, J Owen, MJ Williams, J
Citation: V. Rudrasingham et al., alpha-2 macroglobulin gene and Alzheimer disease, NAT GENET, 22(1), 1999, pp. 17-19
A full genome scan for late onset Alzheimer's disease
Authors: Kehoe, P Wavrant-De Vrieze, F Crook, R Wu, WS Holmans, P Fenton, I Spurlock, G Norton, N Williams, H Williams, N Lovestone, S Perez-Tur, J Hutton, M Chartier-Harlin, MC Shears, S Roehl, K Booth, J Van Voorst, W Ramic, D Williams, J Goate, A Hardy, J Owen, MJ
Citation: P. Kehoe et al., A full genome scan for late onset Alzheimer's disease, HUM MOL GEN, 8(2), 1999, pp. 237-245
Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21
Authors: Froelich, S Houlden, H Rizzu, P Chakraverty, S Baker, M Kwon, J Nowotny, P Isaacs, A Nowotny, V Wauters, E van Baren, MJ Oostra, BA Hardy, J Lannfelt, L Goate, A Hutton, M Lendon, CL Heutink, P
Citation: S. Froelich et al., Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21, GENOMICS, 60(2), 1999, pp. 129-136
Sequence-ready contig for the 1.4-cM ductal carcinoma in situ loss of heterozygosity region on chromosome 8p22-p23
Authors: Wang, JC Radford, DM Holt, MS Helms, C Goate, A Brandt, W Parik, M Phillips, NJ DeSchryver, K Schuh, ME Fair, KL Ritter, JH Marshall, P Donis-Keller, H
Citation: Jc. Wang et al., Sequence-ready contig for the 1.4-cM ductal carcinoma in situ loss of heterozygosity region on chromosome 8p22-p23, GENOMICS, 60(1), 1999, pp. 1-11
Description of the Genetic Analysis Workshop 11 Collaborative Study on theGenetics of Alcoholism
Authors: Begleiter, H Reich, T Nurnberger, J Li, TK Conneally, PM Edenberg, H Crowe, R Kuperman, S Schuckit, M Bloom, F Hesselbrock, V Porjesz, B Cloninger, CR Rice, J Goate, A
Citation: H. Begleiter et al., Description of the Genetic Analysis Workshop 11 Collaborative Study on theGenetics of Alcoholism, GENET EPID, 17, 1999, pp. S25-S30
Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease
Authors: Wavrant-De Vrieze, F Crook, R Holmans, P Kehoe, P Owen, MJ Williams, J Roehl, K Laliiri, DK Shears, S Booth, J Wu, W Goate, A Chartier-Harlin, MC Hardy, J Perez-Tur, J
Citation: F. Wavrant-de Vrieze et al., Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease, NEUROSCI L, 269(2), 1999, pp. 67-70
No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease
Authors: Wavrant-DeVrieze, F Rudrasingham, V Lambert, JC Chakraverty, S Kehoe, P Crook, R Amouyel, P Wu, W Holmans, P Rice, F Perez-Tur, J Frigard, B Morris, JC Carty, S Cottel, D Tunstall, N Lovestone, S Petersen, RC Chartier-Harlin, MC Goate, A Owen, MJ Williams, J Hardy, J
Citation: F. Wavrant-devrieze et al., No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease, NEUROSCI L, 262(2), 1999, pp. 137-139
Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations
Authors: Houlden, H Rizzu, P Stevens, M de Knijff, P van Duijn, CM van Swieten, JC Heutink, P Perez-Tur, J Thomas, V Baker, M Morris, H Rossor, M Jannsen, JC Petersen, RC Dodd, P Dark, F Boeve, B Dickson, D Davies, P Pickering-Brown, S Mann, D Adamson, J Lynch, T Payami, H Poorkaj, P Bird, TD Schellenberg, GD Chakraverty, S Norton, J Morris, JC Goate, A Hutton, M Hardy, J
Citation: H. Houlden et al., Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations, NEUROSCI L, 260(3), 1999, pp. 193-195
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
A presenilin-1-dependent gamma-secretase-like protease mediates release ofNotch intracellular domain
Authors: De Strooper, B Annaert, W Cupers, P Saftig, P Craessaerts, K Mumm, JS Schroeter, EH Schrijvers, V Wolfe, MS Ray, WJ Goate, A Kopan, R
Citation: B. De Strooper et al., A presenilin-1-dependent gamma-secretase-like protease mediates release ofNotch intracellular domain, NATURE, 398(6727), 1999, pp. 518-522
Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials
Authors: Williams, JT Begleiter, H Porjesz, B Edenberg, HJ Foroud, T Reich, T Goate, A Van Eerdewegh, P Almasy, L Blangero, J
Citation: Jt. Williams et al., Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials, AM J HU GEN, 65(4), 1999, pp. 1148-1160
Linkage of an alcoholism-related severity phenotype to chromosome 16
Authors: Foroud, T Bucholz, KK Edenberg, HJ Goate, A Neuman, RJ Porjesz, B Koller, DL Rice, J Reich, T Bierut, LJ Cloninger, CR Nurnberger, JI Li, TK Conneally, PM Tischfield, JA Crowe, R Hesselbrock, V Schuckit, M Begleiter, H
Citation: T. Foroud et al., Linkage of an alcoholism-related severity phenotype to chromosome 16, ALC CLIN EX, 22(9), 1998, pp. 2035-2042
Mutation-specific functional impairments in distinct Tau isoforms of hereditary FTDP-17
Authors: Hong, M Zhukareva, V Vogelsberg-Ragaglia, V Wszolek, Z Reed, L Miller, BI Geschwind, DH Bird, TD McKeel, D Goate, A Morris, JC Wilhelmsen, KC Schellenberg, GD Trojanowski, JQ Lee, VMY
Citation: M. Hong et al., Mutation-specific functional impairments in distinct Tau isoforms of hereditary FTDP-17, SCIENCE, 282(5395), 1998, pp. 1914-1917
Mutation, sequence analysis, and association studies of alpha-synuclein inParkinson's disease
Authors: Parsian, A Racette, B Zhang, ZH Chakraverty, S Rundle, M Goate, A Perlmutter, JS
Citation: A. Parsian et al., Mutation, sequence analysis, and association studies of alpha-synuclein inParkinson's disease, NEUROLOGY, 51(6), 1998, pp. 1757-1759
Risultati: 1-24 |