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Volumn 92, Issue 2, 2016, Pages 333-335

NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk

(84)  Antel, Jack a   Ban, Maria a   Baranzini, Sergio a   Barcellos, Lisa a   Barizzone, Nadia a   Beecham, Ashley a   Berge, Tone a   Bernardinelli, Luisa a   Booth, David a   Bos, Steffan a   Buck, Dorothea a   Butkiewicz, Mariusz a   Celius, Elisabeth G a   Comabella, Manuel a   Compston, Alastair a   Dedham, Katrina a   Cotsapas, Chris a   D’ Alfonso, Sandra a   De Jager, Phil a   Dubois, Benedicte a   more..

a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; GLUTAMINE;

EID: 84992371844     PISSN: 08966273     EISSN: 10974199     Source Type: Journal    
DOI: 10.1016/j.neuron.2016.09.052     Document Type: Article
Times cited : (22)

References (16)
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    • 84982091049 scopus 로고    scopus 로고
    • The Added Value of Family Material in the Discovery of Multiple Sclerosis Genes
    • Hain, H.S., Hakonarson, H., The Added Value of Family Material in the Discovery of Multiple Sclerosis Genes. Neuron 90 (2016), 905–906.
    • (2016) Neuron , vol.90 , pp. 905-906
    • Hain, H.S.1    Hakonarson, H.2
  • 6
    • 84555191729 scopus 로고    scopus 로고
    • Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
    • Hunt, K.A., Smyth, D.J., Balschun, T., Ban, M., Mistry, V., Ahmad, T., Anand, V., Barrett, J.C., Bhaw-Rosun, L., Bockett, N.A., et al. Type 1 Diabetes Genetics Consortium UK Inflammatory Bowel Disease (IBD) Genetics Consortium, Wellcome Trust Case Control Consortium. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nat. Genet. 44 (2011), 3–5.
    • (2011) Nat. Genet. , vol.44 , pp. 3-5
    • Hunt, K.A.1    Smyth, D.J.2    Balschun, T.3    Ban, M.4    Mistry, V.5    Ahmad, T.6    Anand, V.7    Barrett, J.C.8    Bhaw-Rosun, L.9    Bockett, N.A.10
  • 7
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    • Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
    • International Multiple Sclerosis Genetics Consortium, Beecham, A.H., Patsopoulos, N.A., Xifara, D.K., Davis, M.F., Kemppinen, A., Cotsapas, C., Shah, T.S., Spencer, C., Booth, D., Goris, A., et al. Wellcome Trust Case Control Consortium 2 (WTCCC2), International IBD Genetics Consortium (IIBDGC). Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat. Genet. 45 (2013), 1353–1360.
    • (2013) Nat. Genet. , vol.45 , pp. 1353-1360
    • Beecham, A.H.1    Patsopoulos, N.A.2    Xifara, D.K.3    Davis, M.F.4    Kemppinen, A.5    Cotsapas, C.6    Shah, T.S.7    Spencer, C.8    Booth, D.9    Goris, A.10
  • 8
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    • Complete multipoint sib-pair analysis of qualitative and quantitative traits
    • Kruglyak, L., Lander, E.S., Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am. J. Hum. Genet. 57 (1995), 439–454.
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  • 10
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    • Publicly available data provide evidence against NR1H3 R415Q causing multiple sclerosis
    • this issue
    • Minikel, E.V., MacArthur, D.G., Publicly available data provide evidence against NR1H3 R415Q causing multiple sclerosis. Neuron 92 (2016), 336–338 this issue.
    • (2016) Neuron , vol.92 , pp. 336-338
    • Minikel, E.V.1    MacArthur, D.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.