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Results: 1-25 | 26-38
Results: 1-25/38
Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium
Authors: Turecki, G Grof, P Grof, E D'Souza, V Lebuis, L Marineau, C Cavazzoni, P Duffy, A Betard, C Zvolsky, P Robertson, C Brewer, C Hudson, TJ Rouleau, GA Alda, M
Citation: G. Turecki et al., Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium, MOL PSYCHI, 6(5), 2001, pp. 570-578
A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians
Authors: St-Pierre, J Vohl, MC Brisson, D Perron, P Despres, JP Hudson, TJ Gaudet, D
Citation: J. St-pierre et al., A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians, MOL GEN MET, 72(3), 2001, pp. 209-217
Variations in prescribing practices for novel antipsychotic medications among veterans affairs hospitals
Authors: Owen, RR Feng, WW Thrush, CR Hudson, TJ Austen, MA
Citation: Rr. Owen et al., Variations in prescribing practices for novel antipsychotic medications among veterans affairs hospitals, PSYCH SERV, 52(11), 2001, pp. 1523-1525
A radiation hybrid map of mouse genes
Authors: Hudson, TJ Church, DM Greenaway, S Nguyen, H Cook, A Steen, RG Van Etten, WJ Castle, AB Strivens, MA Trickett, P Heuston, C Davison, C Southwell, A Hardisty, R Varela-Carver, A Haynes, AR Rodriguez-Tome, P Doi, H Ko, MSH Pontius, J Schriml, L Wagner, L Maglott, D Brown, SDM Lander, ES Schuler, G Denny, P
Citation: Tj. Hudson et al., A radiation hybrid map of mouse genes, NAT GENET, 29(2), 2001, pp. 201-205
Genetic variation in the 5q31 cytokine gene cluster confers susceptibilityto Crohn disease
Authors: Rioux, JD Daly, MJ Silverberg, MS Lindblad, K Steinhart, H Cohen, Z Delmonte, T Kocher, K Miller, K Guschwan, S Kulbokas, EJ O'Leary, S Winchester, E Dewar, K Green, T Stone, V Chow, C Cohen, A Langelier, D Lapointe, G Gaudet, D Faith, J Branco, N Bull, SB McLeod, RS Griffiths, AM Bitton, A Greenberg, GR Lander, ES Siminovitch, KA Hudson, TJ
Citation: Jd. Rioux et al., Genetic variation in the 5q31 cytokine gene cluster confers susceptibilityto Crohn disease, NAT GENET, 29(2), 2001, pp. 223-228
High-resolution haplotype structure in the human genome
Authors: Daly, MJ Rioux, JD Schaffner, SE Hudson, TJ Lander, ES
Citation: Mj. Daly et al., High-resolution haplotype structure in the human genome, NAT GENET, 29(2), 2001, pp. 229-232
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population
Authors: Laitinen, T Daly, MJ Rioux, JD Kauppi, P Laprise, C Petays, T Green, T Cargill, M Haahtela, T Lander, ES Laitinen, LA Hudson, TJ Kere, J
Citation: T. Laitinen et al., A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population, NAT GENET, 28(1), 2001, pp. 87-91
Microarray analysis of gene expression mirrors the biology of an ovarian cancer model
Authors: Tonin, PN Hudson, TJ Rodier, F Bossolasco, M Lee, PD Novak, J Manderson, EN Provencher, D Mes-Masson, AM
Citation: Pn. Tonin et al., Microarray analysis of gene expression mirrors the biology of an ovarian cancer model, ONCOGENE, 20(45), 2001, pp. 6617-6626
Second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma
Authors: Kauppi, P Lindblad-Toh, K Sevon, P Toivonen, HTT Rioux, JD Villapakkam, A Laitinen, LA Hudson, TJ Kere, J Laitinen, T
Citation: P. Kauppi et al., Second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma, GENOMICS, 77(1-2), 2001, pp. 35-42
A distal upstream enhancer from the myelin basic protein gene regulates expression in myelin-forming schwann cells
Authors: Forghani, R Garofalo, L Foran, DR Farhadi, HF Lepage, P Hudson, TJ Tretjakoff, I Valera, P Peterson, A
Citation: R. Forghani et al., A distal upstream enhancer from the myelin basic protein gene regulates expression in myelin-forming schwann cells, J NEUROSC, 21(11), 2001, pp. 3780-3787
Glycerol: a neglected variable in metabolic processes?
Authors: Brisson, D Vohl, MC St-Pierre, J Hudson, TJ Gaudet, D
Citation: D. Brisson et al., Glycerol: a neglected variable in metabolic processes?, BIOESSAYS, 23(6), 2001, pp. 534-542
Haplotype mapping indicates two independent origins for the Cmv1(s) susceptibility allele to cytomegalovirus infection and refines its localization within the Ly49 cluster
Authors: Lee, SH Gitas, J Zafer, A Lepage, P Hudson, TJ Belouchi, A Vidal, SM
Citation: Sh. Lee et al., Haplotype mapping indicates two independent origins for the Cmv1(s) susceptibility allele to cytomegalovirus infection and refines its localization within the Ly49 cluster, IMMUNOGENET, 53(6), 2001, pp. 501-505
Diagnostic misclassification reduces the ability to detect linkage in inflammatory bowel disease genetic studies
Authors: Silverberg, MS Daly, MJ Moskovitz, DN Rioux, JD McLeod, RS Cohen, Z Greenberg, GR Hudson, TJ Siminovitch, KA Steinhart, AH
Citation: Ms. Silverberg et al., Diagnostic misclassification reduces the ability to detect linkage in inflammatory bowel disease genetic studies, GUT, 49(6), 2001, pp. 773-776
Manganese superoxide dismutase induction by iron is impaired in Friedreichataxia cells
Authors: Jiralerspong, S Ge, B Hudson, TJ Pandolfo, M
Citation: S. Jiralerspong et al., Manganese superoxide dismutase induction by iron is impaired in Friedreichataxia cells, FEBS LETTER, 509(1), 2001, pp. 101-105
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
Authors: Clee, SM Zwinderman, AH Engert, JC Zwarts, KY Molhuizen, HOF Roomp, K Jukema, JW van Wijland, M van Dam, M Hudson, TJ Brooks-Wilson, A Genest, J Kastelein, JJ Hayden, MR
Citation: Sm. Clee et al., Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease, CIRCULATION, 103(9), 2001, pp. 1198-1205
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height
Authors: Hirschhorn, JN Lindgren, CM Daly, MJ Kirby, A Schaffner, SF Burtt, NP Altshuler, D Parker, A Rioux, JD Platko, J Gaudet, D Hudson, TJ Groop, LC Lander, ES
Citation: Jn. Hirschhorn et al., Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height, AM J HU GEN, 69(1), 2001, pp. 106-116
Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7
Authors: Goobie, S Popovic, M Morrison, J Ellis, L Ginzberg, H Boocock, GRB Ehtesham, N Betard, C Brewer, CG Roslin, NM Hudson, TJ Morgan, K Fujiwara, TM Durie, PR Rommens, JM
Citation: S. Goobie et al., Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7, AM J HU GEN, 68(4), 2001, pp. 1048-1054
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22
Authors: Heon, E Paterson, AD Fraser, M Billingsley, G Priston, M Balmer, A Schorderet, DF Verner, A Hudson, TJ Munier, FL
Citation: E. Heon et al., A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22, AM J HU GEN, 68(3), 2001, pp. 772-777
A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13
Authors: Seyda, A Newbold, RF Hudson, TJ Verner, A MacKay, N Winter, S Feigenbaum, A Malaney, S Gonzalez-Halphen, D Cuthbert, AP Robinson, BH
Citation: A. Seyda et al., A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13, AM J HU GEN, 68(2), 2001, pp. 386-396
A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16
Authors: Lee, N Daly, MJ Delmonte, T Lander, ES Xu, FH Hudson, TJ Mitchell, GA Morin, CC Robinson, BH Rioux, JD
Citation: N. Lee et al., A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16, AM J HU GEN, 68(2), 2001, pp. 397-409
Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays
Authors: Lindblad-Toh, K Tanenbaum, DM Daly, MJ Winchester, E Lui, WO Villapakkam, A Stanton, SE Larsson, C Hudson, TJ Johnson, BE Lander, ES Meyerson, M
Citation: K. Lindblad-toh et al., Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays, NAT BIOTECH, 18(9), 2000, pp. 1001-1005
The common PPAR gamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
Authors: Altshuler, D Hirschhorn, JN Klannemark, M Lindgren, CM Vohl, MC Nemesh, J Lane, CR Schaffner, SF Bolk, S Brewer, C Tuomi, T Gaudet, D Hudson, TJ Daly, M Groop, L Lander, ES
Citation: D. Altshuler et al., The common PPAR gamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes, NAT GENET, 26(1), 2000, pp. 76-80
Large-scale discovery and genotyping of single-nucleotide polymorphisms inthe mouse
Authors: Lindblad-Toh, K Winchester, E Daly, MJ Wang, DG Hirschhorn, JN Laviolette, JP Ardlie, K Reich, DE Robinson, E Sklar, P Shah, N Thomas, D Fan, JB Gingeras, T Warrington, J Patil, N Hudson, TJ Lander, ES
Citation: K. Lindblad-toh et al., Large-scale discovery and genotyping of single-nucleotide polymorphisms inthe mouse, NAT GENET, 24(4), 2000, pp. 381-386
ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF
Authors: Engert, JC Berube, P Mercier, J Dore, C Lepage, P Ge, B Bouchard, JP Mathieu, J Melancon, SB Schalling, M Lander, ES Morgan, K Hudson, TJ Richter, A
Citation: Jc. Engert et al., ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF, NAT GENET, 24(2), 2000, pp. 120-125
Complete nucleotide sequence and genomic structure of the human NRAMP1 gene region on Chromosome region 2q35
Authors: Marquet, S Lepage, P Hudson, TJ Musser, JM Schurr, E
Citation: S. Marquet et al., Complete nucleotide sequence and genomic structure of the human NRAMP1 gene region on Chromosome region 2q35, MAMM GENOME, 11(9), 2000, pp. 755-762
Risultati: 1-25 | 26-38