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Results: 1-25 | 26-48
Results: 1-25/48
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
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
Life after the screen: Making sense of many p-values
Authors: Schmidt, S Shao, YJ Hauser, ER Slifer, SH Martin, ER Scott, WK Speer, MC Pericak-Vance, MA
Citation: S. Schmidt et al., Life after the screen: Making sense of many p-values, GENET EPID, 21, 2001, pp. S546-S551
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
De novo partial duplication of chromosome 7p in a male with autistic disorder
Authors: Wolpert, CM Donnelly, SL Cuccaro, ML Hedges, DJ Poole, CP Wright, HH Gilbert, JR Pericak-Vance, MA
Citation: Cm. Wolpert et al., De novo partial duplication of chromosome 7p in a male with autistic disorder, AM J MED G, 105(3), 2001, pp. 222-225
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
Dissecting a complex disease using modern techniques of molecular biology
Authors: Oliveira, SA Scott, WK Pericak-Vance, MA Vance, JM
Citation: Sa. Oliveira et al., Dissecting a complex disease using modern techniques of molecular biology, LAB MED, 32(10), 2001, pp. 594-598
A second leaky splice-site mutation in the spastin gene
Authors: Svenson, IK Ashley-Koch, AE Pericak-Vance, MA Marchuk, DA
Citation: Ik. Svenson et al., A second leaky splice-site mutation in the spastin gene, AM J HU GEN, 69(6), 2001, pp. 1407-1409
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia
Authors: Svenson, IK Ashley-Koch, AE Gaskell, PC Riney, TJ Cumming, WJK Kingston, HM Hogan, EL Boustany, RMN Vance, JM Nance, MA Pericak-Vance, MA Marchuk, DA
Citation: Ik. Svenson et al., Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia, AM J HU GEN, 68(5), 2001, pp. 1077-1085
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis
Authors: Allingham, RR Seo, B Rampersaud, E Bembe, M Challa, P Liu, NP Parrish, T Karolak, L Gilbert, J Pericak-Vance, MA Klintworth, GK Vance, JM
Citation: Rr. Allingham et al., A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis, AM J HU GEN, 68(2), 2001, pp. 491-494
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
Influence of apoE genotype and PET brain imaging on preclinical predictionof Alzheimer's disease
Authors: Small, GW Ercoli, LM Silverman, DHS Huang, SC Bookheimer, SY Lavretsky, H Miller, K Siddarth, P Mazziotta, JC Saunders, AM Pericak-Vance, MA Roses, AD Barrio, JR Phelps, ME
Citation: Gw. Small et al., Influence of apoE genotype and PET brain imaging on preclinical predictionof Alzheimer's disease, ALZHEIMER'S DISEASE, 2001, pp. 193-203
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
Genetic studies in neural tube defects
Authors: Melvin, EC George, TM Worley, G Franklin, A Mackey, J Viles, K Shah, N Drake, CR Enterline, DS McLone, D Nye, J Oakes, WJ McLaughlin, C Walker, ML Peterson, P Brei, T Buran, C Aben, J Ohm, B Bermans, I Qumsiyeh, M Vance, J Pericak-Vance, MA Speer, MC
Citation: Ec. Melvin et al., Genetic studies in neural tube defects, PED NEUROS, 32(1), 2000, pp. 1-9
Myotilin is mutated in limb girdle muscular dystrophy 1A
Authors: Hauser, MA Horrigan, SK Salmikangas, P Torian, UM Viles, KD Dancel, R Tim, RW Taivainen, A Bartoloni, L Gilchrist, JM Stajich, JM Gaskell, PC Gilbert, JR Vance, JM Pericak-Vance, MA Carpen, O Westbrook, CA Speer, MC
Citation: Ma. Hauser et al., Myotilin is mutated in limb girdle muscular dystrophy 1A, HUM MOL GEN, 9(14), 2000, pp. 2141-2147
Analysis of association at single nucleotide polymorphisms in the APOE region
Authors: Martin, ER Gilbert, JR Lai, EH Riley, J Rogala, AR Slotterbeck, BD Sipe, CA Grubber, JM Warren, LL Conneally, PM Saunders, AM Schmechel, DE Purvis, I Pericak-Vance, MA Roses, AD Vance, JM
Citation: Er. Martin et al., Analysis of association at single nucleotide polymorphisms in the APOE region, GENOMICS, 63(1), 2000, pp. 7-12
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
Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome
Authors: Donnelly, SL Wolpert, CM Menold, MM Bass, MP Gilbert, JR Cuccaro, ML DeLong, GR Pericak-Vance, MA
Citation: Sl. Donnelly et al., Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome, AM J MED G, 96(3), 2000, pp. 312-316
Three probands with autistic disorder and isodicentric chromosome 15
Authors: Wolpert, CM Menold, MM Bass, MP Qumsiyeh, MB Donnelly, SL Ravan, SA Vance, JM Gilbert, JR Abramson, RK Wright, HH Cuccaro, ML Pericak-Vance, MA
Citation: Cm. Wolpert et al., Three probands with autistic disorder and isodicentric chromosome 15, AM J MED G, 96(3), 2000, pp. 365-372
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
Authors: Martin, ER Menold, MM Wolpert, CM Bass, MP Donnelly, SL Ravan, SA Zimmerman, A Gilbert, JR Vance, JM Maddox, LO Wright, HH Abramson, RK DeLong, GR Cuccaro, ML Pericak-Vance, MA
Citation: Er. Martin et al., Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder, AM J MED G, 96(1), 2000, pp. 43-48
Autistic symptoms among children and young adults with isodicentric chromosome 15
Authors: Wolpert, C Pericak-Vance, MA Abramson, RK Wright, HH Cuccaro, ML
Citation: C. Wolpert et al., Autistic symptoms among children and young adults with isodicentric chromosome 15, AM J MED G, 96(1), 2000, pp. 128-129
Heterogeneity in Paget disease of the bone
Authors: Nance, MA Nuttall, FQ Econs, MJ Lyles, KW Viles, KD Vance, JM Pericak-Vance, MA Speer, MC
Citation: Ma. Nance et al., Heterogeneity in Paget disease of the bone, AM J MED G, 92(5), 2000, pp. 303-307
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
Risultati: 1-25 | 26-48