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Results: 1-12 |
Results: 12
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
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
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
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
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
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland
Authors: Pajukanta, P Cargill, M Viitanen, L Nuotio, I Kareinen, A Perola, M Terwilliger, JD Kempas, E Day, M Lilja, H Rioux, JD Brettin, T Viikari, JSA Ronnemaa, T Laakso, M Lander, ES Peltonen, L
Citation: P. Pajukanta et al., Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland, AM J HU GEN, 67(6), 2000, pp. 1481-1493
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci
Authors: Rioux, JD Silverberg, MS Daly, MJ Steinhart, AH McLeod, RS Griffiths, AM Green, T Brettin, TS Stone, V Bull, SB Bitton, A Williams, CN Greenberg, GR Cohen, Z Lander, ES Hudson, TJ Siminovitch, KA
Citation: Jd. Rioux et al., Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci, AM J HU GEN, 66(6), 2000, pp. 1863-1870
Glycerol as a correlate of impaired glucose tolerance: Dissection of a complex system by use of a simple genetic trait
Authors: Gaudet, D Arsenault, S Perusse, L Vohl, MC St-Pierre, J Bergeron, J Despres, JP Dewar, K Daly, MJ Hudson, T Rioux, JD
Citation: D. Gaudet et al., Glycerol as a correlate of impaired glucose tolerance: Dissection of a complex system by use of a simple genetic trait, AM J HU GEN, 66(5), 2000, pp. 1558-1568
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): High-resolution physical and transcript map of the candidate region in chromosomeregion 13q11
Authors: Engert, JC Dore, C Mercier, J Ge, B Betard, C Rioux, JD Owen, C Berube, P Devon, K Birren, B Melancon, SB Morgan, K Hudson, TJ Richter, A
Citation: Jc. Engert et al., Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): High-resolution physical and transcript map of the candidate region in chromosomeregion 13q11, GENOMICS, 62(2), 1999, pp. 156-164
Location score and haplotype analyses of the locus for autosomal recessivespastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11
Authors: Richter, A Rioux, JD Bouchard, JP Mercier, J Mathieu, J Ge, B Poirier, J Julien, D Gyapay, G Weissenbach, J Hudson, TJ Melancon, SB Morgan, K
Citation: A. Richter et al., Location score and haplotype analyses of the locus for autosomal recessivespastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11, AM J HU GEN, 64(3), 1999, pp. 768-775
Risultati: 1-12 |