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Results: 1-25 | 26-34
Results: 1-25/34
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
High-throughput genotyping with single nucleotide polymorphisms
Authors: Ranade, K Chang, MS Ting, CT Pei, D Hsiao, CF Olivier, M Pesich, R Hebert, J Chen, YDI Dzau, VJ Curb, D Olshen, R Risch, N Cox, DR Botstein, D
Citation: K. Ranade et al., High-throughput genotyping with single nucleotide polymorphisms, GENOME RES, 11(7), 2001, pp. 1262-1268
Bayesian analysis of haplotypes for linkage disequilibrium mapping
Authors: Liu, JS Sabatti, C Teng, J Keats, BJB Risch, N
Citation: Js. Liu et al., Bayesian analysis of haplotypes for linkage disequilibrium mapping, GENOME RES, 11(10), 2001, pp. 1716-1724
Screening a large reference sample to identify very low frequency sequencevariants: comparisons between two genes
Authors: Glatt, CE DeYoung, JA Delgado, S Service, SK Giacomini, KM Edwards, RH Risch, N Freimer, NB
Citation: Ce. Glatt et al., Screening a large reference sample to identify very low frequency sequencevariants: comparisons between two genes, NAT GENET, 27(4), 2001, pp. 435-438
The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches
Authors: Risch, N
Citation: N. Risch, The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches, CANC EPID B, 10(7), 2001, pp. 733-741
Genetic variation in the human urea transporter-2 is associated with variation in blood pressure
Authors: Ranade, K Wu, KD Hwu, CM Ting, CT Pei, D Pesich, R Hebert, J Chen, YDI Pratt, R Olshen, R Masaki, K Risch, N Cox, DR Botstein, D
Citation: K. Ranade et al., Genetic variation in the human urea transporter-2 is associated with variation in blood pressure, HUM MOL GEN, 10(19), 2001, pp. 2157-2164
Tay-sachs screening in the Jewish Ashkenazi population: DNA testing is thepreferred procedure
Authors: Bach, G Tomczak, J Risch, N Ekstein, J
Citation: G. Bach et al., Tay-sachs screening in the Jewish Ashkenazi population: DNA testing is thepreferred procedure, AM J MED G, 99(1), 2001, pp. 70-75
Molecular epidemiology of Tay-Sachs disease
Authors: Risch, N
Citation: N. Risch, Molecular epidemiology of Tay-Sachs disease, ADV GENETIC, 44, 2001, pp. 233-252
Genetic variation in aldosterone synthase predicts plasma glucose levels
Authors: Ranade, K Wu, KD Risch, N Olivier, M Pei, D Hsiao, CF Chuang, LM Ho, LT Jorgenson, E Pesich, R Chen, YDI Dzau, V Lin, A Olshen, RA Curb, D Cox, DR Botstein, D
Citation: K. Ranade et al., Genetic variation in aldosterone synthase predicts plasma glucose levels, P NAS US, 98(23), 2001, pp. 13219-13224
Evidence of linkage with HLA-DR in DRB115-negative families with multiplesclerosis
Authors: Ligers, A Dyment, DA Willer, CJ Sadovnick, AD Ebers, G Risch, N Hillert, J
Citation: A. Ligers et al., Evidence of linkage with HLA-DR in DRB115-negative families with multiplesclerosis, AM J HU GEN, 69(4), 2001, pp. 900-903
Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy inthree ethnic groups
Authors: Mignot, E Lin, L Rogers, W Honda, Y Qiu, XH Lin, XY Okun, M Hohjoh, H Miki, T Hsu, SH Leffell, MS Grumet, FC Fernandez-Vina, M Honda, M Risch, N
Citation: E. Mignot et al., Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy inthree ethnic groups, AM J HU GEN, 68(3), 2001, pp. 686-699
Synthesis of novel functionalized bi- and oligopyridines
Authors: Sielemann, D Keuper, R Risch, N
Citation: D. Sielemann et al., Synthesis of novel functionalized bi- and oligopyridines, EUR J ORG C, (3), 2000, pp. 543-548
A straightforward synthesis of enantiomerically pure trans-2,5-bis(alkyloxymethyl) pyrrolidines by 1,3-dipolar cycloaddition reactions of azomethine ylides
Authors: Wittland, C Risch, N
Citation: C. Wittland et N. Risch, A straightforward synthesis of enantiomerically pure trans-2,5-bis(alkyloxymethyl) pyrrolidines by 1,3-dipolar cycloaddition reactions of azomethine ylides, J PRAK CH C, 342(3), 2000, pp. 311-315
Lack of evidence for an association between alpha-adducin and blood pressure regulation in Asian populations
Authors: Ranade, K Hsuing, AC Wu, KD Chang, MS Chen, YT Hebert, J Chen, YDI Olshen, R Curb, D Dzau, V Botstein, D Cox, D Risch, N
Citation: K. Ranade et al., Lack of evidence for an association between alpha-adducin and blood pressure regulation in Asian populations, AM J HYPERT, 13(6), 2000, pp. 704-709
Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program
Authors: Province, MA Boerwinkle, E Chakravarti, A Cooper, R Fornage, M Leppert, M Risch, N Ranade, K
Citation: Ma. Province et al., Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program, J HYPERTENS, 18(7), 2000, pp. 867-876
Genetic analysis of vitamin D related genes in Canadian multiple sclerosispatients
Authors: Steckley, JL Dyment, DA Sadovnick, AD Risch, N Hayes, C Ebers, GC
Citation: Jl. Steckley et al., Genetic analysis of vitamin D related genes in Canadian multiple sclerosispatients, NEUROLOGY, 54(3), 2000, pp. 729-732
Searching for genes in complex diseases: lessons from systemic lupus erythematosus
Authors: Risch, N
Citation: N. Risch, Searching for genes in complex diseases: lessons from systemic lupus erythematosus, J CLIN INV, 105(11), 2000, pp. 1503-1506
Familial aggregation absolute pitch
Authors: Baharloo, S Service, SK Risch, N Gitschier, J Freimer, NB
Citation: S. Baharloo et al., Familial aggregation absolute pitch, AM J HU GEN, 67(3), 2000, pp. 755-758
Gaucher disease: The origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations
Authors: Diaz, GA Gelb, BD Risch, N Nygaard, TG Frisch, A Cohen, IJ Miranda, CS Amaral, O Maire, I Poenaru, L Caillaud, C Weizberg, M Mistry, P Desnick, RJ
Citation: Ga. Diaz et al., Gaucher disease: The origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations, AM J HU GEN, 66(6), 2000, pp. 1821-1832
The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases. II. Individual genotyping
Authors: Teng, J Risch, N
Citation: J. Teng et N. Risch, The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases. II. Individual genotyping, GENOME RES, 9(3), 1999, pp. 234-241
Preparation, characterization and selective reactions of novel [1,3]diazetidine-2,4-diones (uretdiones) - A new route to generate asymmetric substituted toluylenediisocyanate-derivatives
Authors: Risch, N Westerwelle, U Kiene, J Keuper, R
Citation: N. Risch et al., Preparation, characterization and selective reactions of novel [1,3]diazetidine-2,4-diones (uretdiones) - A new route to generate asymmetric substituted toluylenediisocyanate-derivatives, J PRAK CH C, 341(7), 1999, pp. 616-619
Aminoalkylation of cyclic and acyclic alkyl vinyl ethers
Authors: Merla, B Risch, N
Citation: B. Merla et N. Risch, Aminoalkylation of cyclic and acyclic alkyl vinyl ethers, J PRAK CH C, 341(5), 1999, pp. 472-476
Efficient preparation of substituted 5,6,7,8-tetrahydroquinolines and octahydroacridine derivatives
Authors: Sielemann, D Keuper, R Risch, N
Citation: D. Sielemann et al., Efficient preparation of substituted 5,6,7,8-tetrahydroquinolines and octahydroacridine derivatives, J PRAK CH C, 341(5), 1999, pp. 487-491
Sib-pair analysis of the Collaborative Study on the Genetics of Alcoholismdata set
Authors: Jorgenson, E Hinds, D Risch, N
Citation: E. Jorgenson et al., Sib-pair analysis of the Collaborative Study on the Genetics of Alcoholismdata set, GENET EPID, 17, 1999, pp. S187-S191
Exclusion of linkage to the HLA region in ninety multiplex sibships with autism
Authors: Rogers, T Kalaydjieva, L Hallmayer, J Petersen, PB Nicholas, P Pingree, C McMahon, WM Spiker, D Lotspeich, L Kraemer, H McCague, P Dimiceli, S Nouri, N Peachy, T Yang, J Hinds, D Risch, N Myers, RM
Citation: T. Rogers et al., Exclusion of linkage to the HLA region in ninety multiplex sibships with autism, J AUTISM D, 29(3), 1999, pp. 195-201
Risultati: 1-25 | 26-34