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Results: 1-25 | 26-31
Results: 1-25/31
A meta-analysis of genomic screens in multiple sclerosis
Authors: Pericak-Vance, MA Rimmler, JB Saunders, AM Martin, ER Haines, JL Garcia, ME Oksenberg, JR Barcellos, LF Lincoln, R Goodkin, DE Hauser, SL Compston, DAS Sawcer, SJ Clayton, D Jones, HB Walker, N Goodfellow, PPN Bulman, D Sadovnick, D Ebers, GC Dyment, D Willer, C Risch, N
Citation: Ma. Pericak-vance et al., A meta-analysis of genomic screens in multiple sclerosis, MULT SCLER, 7(1), 2001, pp. 3-11
PTPRC (CD45) is not associated with the development of multiple sclerosis in US patients
Authors: Barcellos, LF Caillier, S Dragone, L Elder, M Vittinghoff, E Bucher, P Lincoln, RR Pericak-Vance, M Haines, JL Weiss, A Hauser, SL Oksenberg, JR
Citation: Lf. Barcellos et al., PTPRC (CD45) is not associated with the development of multiple sclerosis in US patients, NAT GENET, 29(1), 2001, pp. 23-24
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families
Authors: Nurmi, EL Bradford, Y Chen, YH Hall, J Arnone, B Gardiner, MB Hutcheson, HB Gilbert, JR Pericak-Vance, MA Copeland-Yates, SA Michaelis, RC Wassink, TH Santangelo, SL Sheffield, VC Piven, J Folstein, SE Haines, JL Sutcliffe, JS
Citation: El. Nurmi et al., Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families, GENOMICS, 77(1-2), 2001, pp. 105-113
Sequence variation in the transforming growth factor-beta 1 (TGFB1) gene and multiple sclerosis susceptibility
Authors: Green, AJ Barcellos, LF Rimmler, JB Garcia, ME Caillier, S Lincoln, RR Bucher, P Pericak-Vance, MA Haines, JL Hauser, SL Oksenberg, JR
Citation: Aj. Green et al., Sequence variation in the transforming growth factor-beta 1 (TGFB1) gene and multiple sclerosis susceptibility, J NEUROIMM, 116(1), 2001, pp. 116-124
An autosomal genomic screen for autism (vol 88, pg 609, 1999)
Authors: Barrett, S Beck, JC Bernier, R Bisson, E Braun, TA Casavant, TL Childress, D Folstein, SE Garcia, M Gardiner, MB Gilman, S Haines, JL Hopkins, K Landa, R Meyer, NH Mullane, JA Nishimura, DY Palmer, P Piven, J Purdy, J Santangelo, SL Searby, C Sheffield, V Singleton, J Slager, S Struchen, T Svenson, S Vieland, V Wang, K Winklosky, B
Citation: S. Barrett et al., An autosomal genomic screen for autism (vol 88, pg 609, 1999), AM J MED G, 105(8), 2001, pp. 805
Evidence supporting WNT2 as an autism susceptibility gene
Authors: Wassink, TH Piven, J Vieland, VJ Huang, J Swiderski, RE Pietila, J Braun, T Beck, G Folstein, SE Haines, JL Sheffield, VC
Citation: Th. Wassink et al., Evidence supporting WNT2 as an autism susceptibility gene, AM J MED G, 105(5), 2001, pp. 406-413
Complete genomic screen in parkinson disease - Evidence for multiple genes
Authors: Scott, WK Nance, MA Watts, RL Hubble, JP Koller, WC Lyons, K Pahwa, R Stern, MB Colcher, A Hiner, BC Jankovic, J Ondo, WG Allen, FH Goetz, CG Small, GW Masterman, D Mastaglia, F Laing, NG Stajich, JM Slotterbeck, B Booze, MW Ribble, RC Rampersaud, E West, SG Gibson, RA Middleton, LT Roses, AD Haines, JL Scott, BL Vance, JM Pericak-Vance, MA
Citation: Wk. Scott et al., Complete genomic screen in parkinson disease - Evidence for multiple genes, J AM MED A, 286(18), 2001, pp. 2239-2244
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease
Authors: Martin, ER Scott, WK Nance, MA Watts, RL Hubble, JP Koller, WC Lyons, K Pahwa, R Stern, MB Colcher, A Hiner, BC Jankovic, J Ondo, WG Allen, FH Goetz, CG Small, GW Masterman, D Mastaglia, F Laing, NG Stajich, JM Ribble, RC Booze, MW Rogala, A Hauser, MA Zhang, FY Gibson, RA Middleton, LT Roses, AD Haines, JL Scott, BL Pericak-Vance, MA Vance, JM
Citation: Er. Martin et al., Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease, J AM MED A, 286(18), 2001, pp. 2245-2250
Neonatal pulmonary hypertension - Urea-cycle intermediates, nitric oxide production, and carbamoyl-phosphate synthetase function
Authors: Pearson, DL Dawling, S Walsh, WF Haines, JL Christman, BW Bazyk, A Scott, N Summar, ML
Citation: Dl. Pearson et al., Neonatal pulmonary hypertension - Urea-cycle intermediates, nitric oxide production, and carbamoyl-phosphate synthetase function, N ENG J MED, 344(24), 2001, pp. 1832-1838
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda
Authors: Tiller, GE Hannig, VL Dozier, D Carrel, L Trevarthen, KC Wilcox, WR Mundlos, S Haines, JL Gedeon, AK Gecz, J
Citation: Ge. Tiller et al., A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda, AM J HU GEN, 68(6), 2001, pp. 1398-1407
A genomic search for Alzheimer's disease genes
Authors: Haines, JL Bailey, LR Grubber, JM Hedges, D Hall, JL West, S Santoro, L Kemmerer, B Saunders, AM Roses, AD Small, GW Scott, WK Conneally, PM Vance, JM Pericak-Vance, MA
Citation: Jl. Haines et al., A genomic search for Alzheimer's disease genes, ALZHEIMER'S DISEASE, 2001, pp. 33-43
Analysis of chromosome 12 candidate genes in late-onset Alzheimer disease
Authors: Grubber, JM Saunders, AM Yamaoka, LH Scott, WK Martin, ER Hill, DM Standen, CL Conneally, PM Small, GW Lai, EH Gilbert, JR Roses, AD Haines, JL Pericak-Vance, MA
Citation: Jm. Grubber et al., Analysis of chromosome 12 candidate genes in late-onset Alzheimer disease, ALZHEIM REP, 3(4), 2000, pp. 221-226
Association of the Apolipoprotein E gene with age-related macular degeneration: Possible effect modification by family history, age, and gender
Authors: Schmidt, S Saunders, AM De la Paz, M Postel, EA Heinis, RM Agarwal, A Scott, WK Gilbert, JR McDowell, JG Bazyk, A Gass, JDM Haines, JL Pericak-Vance, MA
Citation: S. Schmidt et al., Association of the Apolipoprotein E gene with age-related macular degeneration: Possible effect modification by family history, age, and gender, MOL VIS, 6(35), 2000, pp. 287-293
Genome-wide scan for adult onset primary open angle glaucoma
Authors: Wiggs, JL Allingham, RR Hossain, A Kern, J Auguste, J DelBono, EA Broomer, B Graham, FL Hauser, M Pericak-Vance, M Haines, JL
Citation: Jl. Wiggs et al., Genome-wide scan for adult onset primary open angle glaucoma, HUM MOL GEN, 9(7), 2000, pp. 1109-1117
Identification of novel genes in late-onset Alzheimer's disease
Authors: Pericak-Vance, MA Grubber, J Bailey, LR Hedges, D West, S Santoro, L Kemmerer, B Hall, JL Saunders, AM Roses, AD Small, GW Scott, WK Conneally, PM Vance, JM Haines, JL
Citation: Ma. Pericak-vance et al., Identification of novel genes in late-onset Alzheimer's disease, EXP GERONT, 35(9-10), 2000, pp. 1343-1352
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
Authors: Hosler, BA Siddique, T Sapp, PC Sailor, W Huang, MC Hossain, A Daube, JR Nance, M Fan, CH Kaplan, J Hung, WY McKenna-Yasek, D Haines, JL Pericak-Vance, MA Horvitz, HR Brown, RH
Citation: Ba. Hosler et al., Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22, J AM MED A, 284(13), 2000, pp. 1664-1669
CC-chemokine receptor 5 polymorphism and age of onset in familial multiplesclerosis
Authors: Barcellos, LF Schito, AM Rimmler, JB Vittinghoff, E Shih, A Lincoln, R Callier, S Elkins, MK Goodkin, DE Haines, JL Pericak-Vance, MA Hauser, SL Oksenberg, JR
Citation: Lf. Barcellos et al., CC-chemokine receptor 5 polymorphism and age of onset in familial multiplesclerosis, IMMUNOGENET, 51(4-5), 2000, pp. 281-288
Head injury and the risk of AD in the MIRAGE study
Authors: Guo, Z Cupples, LA Kurz, A Auerbach, SH Volicer, L Chui, H Green, RC Sadovnick, AD Duara, R DeCarli, C Johnson, K Go, RC Growdon, JH Haines, JL Kukull, WA Farrer, LA
Citation: Z. Guo et al., Head injury and the risk of AD in the MIRAGE study, NEUROLOGY, 54(6), 2000, pp. 1316-1323
Human beta(2)-adrenergic receptor polymorphisms: No association with essential hypertension in black or white Americans
Authors: Xie, HG Stein, CM Kim, RB Gainer, JV Sofowora, G Dishy, V Brown, NJ Goree, RE Haines, JL Wood, AJJ
Citation: Hg. Xie et al., Human beta(2)-adrenergic receptor polymorphisms: No association with essential hypertension in black or white Americans, CLIN PHARM, 67(6), 2000, pp. 670-675
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: Potential genetic and phenotypic heterogeneity
Authors: Scott, WK Grubber, JM Conneally, PM Small, GW Hulette, CM Rosenberg, CK Saunders, AM Roses, AD Haines, JL Pericak-Vance, MA
Citation: Wk. Scott et al., Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: Potential genetic and phenotypic heterogeneity, AM J HU GEN, 66(3), 2000, pp. 922-932
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease
Authors: Rogaeva, EA Premkumar, S Grubber, J Serneels, L Scott, WK Kawarai, T Song, YQ Hill, DM Abou-Donia, SM Martin, ER Vance, JJ Yu, G Orlacchio, A Pei, Y Nishimura, M Supala, A Roberge, B Saunders, AM Roses, AD Schmechel, D Crane-Gatherum, A Sorbi, S Bruni, A Small, GW Conneally, PM Haines, JL Van Leuven, F St George-Hyslop, PH Farrer, LA Pericak-Vance, MA
Citation: Ea. Rogaeva et al., An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease, NAT GENET, 22(1), 1999, pp. 19-21
Frequency of functionally important beta-2 adrenoceptor polymorphisms varies markedly among African-American, Caucasian and Chinese individuals
Authors: Xie, HG Stein, CM Kim, RB Xiao, ZS He, N Zhou, HH Gainer, JV Brown, NJ Haines, JL Wood, AJJ
Citation: Hg. Xie et al., Frequency of functionally important beta-2 adrenoceptor polymorphisms varies markedly among African-American, Caucasian and Chinese individuals, PHARMACOGEN, 9(4), 1999, pp. 511-516
Hunting genetic diseases: Exploring a multistage approach to identifying disease loci
Authors: Garcia, ME Haines, JL
Citation: Me. Garcia et Jl. Haines, Hunting genetic diseases: Exploring a multistage approach to identifying disease loci, GENET EPID, 17, 1999, pp. S557-S562
Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K)
Authors: Grubber, JM Saunders, AM Crane-Gatherum, AR Scott, WK Martin, ER Haynes, CS Conneally, PM Small, GW Roses, AD Haines, JL Pericak-Vance, MA
Citation: Jm. Grubber et al., Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K), NEUROSCI L, 269(2), 1999, pp. 115-119
Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration
Authors: De La Paz, MA Guy, VK Abou-Donia, S Heinis, R Bracken, B Vance, JM Gilbert, JR Gass, JDM Haines, JL Pericak-Vance, MA
Citation: Ma. De La Paz et al., Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration, OPHTHALMOL, 106(8), 1999, pp. 1531-1536
Risultati: 1-25 | 26-31