-
1
-
-
58049217860
-
-
Available at: Accessed [22.08.12].
-
Hindorff LA, MacArthur J, Wise A, Junkins HA, Hall PN, Klemm AK, Manolio TA: A Catalog of Published Genome-Wide Association Studies. Available at: Accessed [22.08.12]. http://www.genome.gov/gwastudies.
-
Manolio TA: A Catalog of Published Genome-Wide Association Studies
-
-
Hindorff, L.A.1
MacArthur, J.2
Wise, A.3
Junkins, H.A.4
Hall, P.N.5
Klemm, A.K.6
-
2
-
-
79851468862
-
Synthetic associations are unlikely to account for many common disease genome-wide association signals
-
Anderson C.A., Soranzo N., Zeggini E., Barrett J.C. Synthetic associations are unlikely to account for many common disease genome-wide association signals. PLoS Biol 2011, 9:e1000580.
-
(2011)
PLoS Biol
, vol.9
-
-
Anderson, C.A.1
Soranzo, N.2
Zeggini, E.3
Barrett, J.C.4
-
3
-
-
80455174463
-
Protein characterization of a candidate mechanism SNP for Crohn's disease: the macrophage stimulating protein R689C substitution
-
Gorlatova N., Chao K., Pal L.R., Araj R.H., Galkin A., Turko I., Moult J., Herzberg O. Protein characterization of a candidate mechanism SNP for Crohn's disease: the macrophage stimulating protein R689C substitution. PLoS ONE 2011, 6:e27269.
-
(2011)
PLoS ONE
, vol.6
-
-
Gorlatova, N.1
Chao, K.2
Pal, L.R.3
Araj, R.H.4
Galkin, A.5
Turko, I.6
Moult, J.7
Herzberg, O.8
-
4
-
-
84855764355
-
A functional variant in ERAP1 predisposes to multiple sclerosis
-
Guerini F.R., Cagliani R., Forni D., Agliardi C., Caputo D., Cassinotti A., Galimberti D., Fenoglio C., Biasin M., Asselta R., et al. A functional variant in ERAP1 predisposes to multiple sclerosis. PLoS ONE 2012, 7:e29931.
-
(2012)
PLoS ONE
, vol.7
-
-
Guerini, F.R.1
Cagliani, R.2
Forni, D.3
Agliardi, C.4
Caputo, D.5
Cassinotti, A.6
Galimberti, D.7
Fenoglio, C.8
Biasin, M.9
Asselta, R.10
-
5
-
-
80053991071
-
Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381Q
-
Pidasheva S., Trifari S., Phillips A., Hackney J.A., Ma Y., Smith A., Sohn S.J., Spits H., Little R.D., Behrens T.W., et al. Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381Q. PLoS ONE 2011, 6:e25038.
-
(2011)
PLoS ONE
, vol.6
-
-
Pidasheva, S.1
Trifari, S.2
Phillips, A.3
Hackney, J.A.4
Ma, Y.5
Smith, A.6
Sohn, S.J.7
Spits, H.8
Little, R.D.9
Behrens, T.W.10
-
6
-
-
80054933395
-
The kinase LRRK2 is a regulator of the transcription factor NFAT that modulates the severity of inflammatory bowel disease
-
Liu Z., Lee J., Krummey S., Lu W., Cai H., Lenardo M.J. The kinase LRRK2 is a regulator of the transcription factor NFAT that modulates the severity of inflammatory bowel disease. Nat Immunol 2011, 12:1063-1070.
-
(2011)
Nat Immunol
, vol.12
, pp. 1063-1070
-
-
Liu, Z.1
Lee, J.2
Krummey, S.3
Lu, W.4
Cai, H.5
Lenardo, M.J.6
-
7
-
-
80052111188
-
HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease
-
e861-865
-
Okada Y., Yamazaki K., Umeno J., Takahashi A., Kumasaka N., Ashikawa K., Aoi T., Takazoe M., Matsui T., Hirano A., et al. HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease. Gastroenterology 2011, 141:864-871. e861-865.
-
(2011)
Gastroenterology
, vol.141
, pp. 864-871
-
-
Okada, Y.1
Yamazaki, K.2
Umeno, J.3
Takahashi, A.4
Kumasaka, N.5
Ashikawa, K.6
Aoi, T.7
Takazoe, M.8
Matsui, T.9
Hirano, A.10
-
8
-
-
84862776511
-
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis
-
Raychaudhuri S., Sandor C., Stahl E.A., Freudenberg J., Lee H.S., Jia X., Alfredsson L., Padyukov L., Klareskog L., Worthington J. Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis. Nat Genet 2012, 44:291-296.
-
(2012)
Nat Genet
, vol.44
, pp. 291-296
-
-
Raychaudhuri, S.1
Sandor, C.2
Stahl, E.A.3
Freudenberg, J.4
Lee, H.S.5
Jia, X.6
Alfredsson, L.7
Padyukov, L.8
Klareskog, L.9
Worthington, J.10
-
9
-
-
84860478400
-
The Cannabinoid Receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention
-
Rossi F., Bellini G., Tolone C., Luongo L., Mancusi S., Papparella A., Sturgeon C., Fasano A., Nobili B., Perrone L., et al. The Cannabinoid Receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention. Pharmacol Res 2012, 66:88-94.
-
(2012)
Pharmacol Res
, vol.66
, pp. 88-94
-
-
Rossi, F.1
Bellini, G.2
Tolone, C.3
Luongo, L.4
Mancusi, S.5
Papparella, A.6
Sturgeon, C.7
Fasano, A.8
Nobili, B.9
Perrone, L.10
-
10
-
-
84857037386
-
TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis
-
Tejasvi T., Stuart P.E., Chandran V., Voorhees J.J., Gladman D.D., Rahman P., Elder J.T., Nair R.P. TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis. J Invest Dermatol 2012, 132:593-600.
-
(2012)
J Invest Dermatol
, vol.132
, pp. 593-600
-
-
Tejasvi, T.1
Stuart, P.E.2
Chandran, V.3
Voorhees, J.J.4
Gladman, D.D.5
Rahman, P.6
Elder, J.T.7
Nair, R.P.8
-
11
-
-
84864131309
-
A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus
-
Wang S., Adrianto I., Wiley G.B., Lessard C.J., Kelly J.A., Adler A.J., Glenn S.B., Williams A.H., Ziegler J.T., Comeau M.E., et al. A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus. Genes Immun 2012, 13:380-387.
-
(2012)
Genes Immun
, vol.13
, pp. 380-387
-
-
Wang, S.1
Adrianto, I.2
Wiley, G.B.3
Lessard, C.J.4
Kelly, J.A.5
Adler, A.J.6
Glenn, S.B.7
Williams, A.H.8
Ziegler, J.T.9
Comeau, M.E.10
-
12
-
-
84055191068
-
T cell protein tyrosine phosphatase attenuates T cell signaling to maintain tolerance in mice
-
Wiede F., Shields B.J., Chew S.H., Kyparissoudis K., van Vliet C., Galic S., Tremblay M.L., Russell S.M., Godfrey D.I., Tiganis T. T cell protein tyrosine phosphatase attenuates T cell signaling to maintain tolerance in mice. J Clin Invest 2011, 121:4758-4774.
-
(2011)
J Clin Invest
, vol.121
, pp. 4758-4774
-
-
Wiede, F.1
Shields, B.J.2
Chew, S.H.3
Kyparissoudis, K.4
van Vliet, C.5
Galic, S.6
Tremblay, M.L.7
Russell, S.M.8
Godfrey, D.I.9
Tiganis, T.10
-
13
-
-
81055141569
-
A20-binding inhibitor of NF-kappaB (ABIN1) controls Toll-like receptor-mediated CCAAT/enhancer-binding protein beta activation and protects from inflammatory disease
-
Zhou J., Wu R., High A.A., Slaughter C.A., Finkelstein D., Rehg J.E., Redecke V., Hacker H. A20-binding inhibitor of NF-kappaB (ABIN1) controls Toll-like receptor-mediated CCAAT/enhancer-binding protein beta activation and protects from inflammatory disease. Proc Natl Acad Sci USA 2011, 108:E998-E1006.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
-
-
Zhou, J.1
Wu, R.2
High, A.A.3
Slaughter, C.A.4
Finkelstein, D.5
Rehg, J.E.6
Redecke, V.7
Hacker, H.8
-
14
-
-
0018251171
-
HLA-D and Ia antigens in rheumatoid arthritis and systemic lupus erythematosus
-
Stastny P. HLA-D and Ia antigens in rheumatoid arthritis and systemic lupus erythematosus. Arthritis Rheum 1978, 21:S139-S143.
-
(1978)
Arthritis Rheum
, vol.21
-
-
Stastny, P.1
-
15
-
-
80055031911
-
A new methodology to associate SNPs with human diseases according to their pathway related context
-
Bakir-Gungor B., Sezerman O.U. A new methodology to associate SNPs with human diseases according to their pathway related context. PLoS ONE 2011, 6:e26277.
-
(2011)
PLoS ONE
, vol.6
-
-
Bakir-Gungor, B.1
Sezerman, O.U.2
-
16
-
-
79955573495
-
Incorporating biological pathways via a Markov random field model in genome-wide association studies
-
Chen M., Cho J., Zhao H. Incorporating biological pathways via a Markov random field model in genome-wide association studies. PLoS Genet 2011, 7:e1001353.
-
(2011)
PLoS Genet
, vol.7
-
-
Chen, M.1
Cho, J.2
Zhao, H.3
-
17
-
-
80052519447
-
Genetic evidence supporting the association of protease and protease inhibitor genes with inflammatory bowel disease: a systematic review
-
Cleynen I., Juni P., Bekkering G.E., Nuesch E., Mendes C.T., Schmied S., Wyder S., Kellen E., Villiger P.M., Rutgeerts P., et al. Genetic evidence supporting the association of protease and protease inhibitor genes with inflammatory bowel disease: a systematic review. PLoS ONE 2011, 6:e24106.
-
(2011)
PLoS ONE
, vol.6
-
-
Cleynen, I.1
Juni, P.2
Bekkering, G.E.3
Nuesch, E.4
Mendes, C.T.5
Schmied, S.6
Wyder, S.7
Kellen, E.8
Villiger, P.M.9
Rutgeerts, P.10
-
18
-
-
80053237445
-
A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis
-
Nakaoka H., Cui T., Tajima A., Oka A., Mitsunaga S., Kashiwase K., Homma Y., Sato S., Suzuki Y., Inoko H., et al. A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis. PLoS ONE 2011, 6:e25389.
-
(2011)
PLoS ONE
, vol.6
-
-
Nakaoka, H.1
Cui, T.2
Tajima, A.3
Oka, A.4
Mitsunaga, S.5
Kashiwase, K.6
Homma, Y.7
Sato, S.8
Suzuki, Y.9
Inoko, H.10
-
19
-
-
80053896562
-
Integrating autoimmune risk loci with gene-expression data identifies specific pathogenic immune cell subsets
-
Hu X., Kim H., Stahl E., Plenge R., Daly M., Raychaudhuri S. Integrating autoimmune risk loci with gene-expression data identifies specific pathogenic immune cell subsets. Am J Hum Genet 2011, 89:496-506.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 496-506
-
-
Hu, X.1
Kim, H.2
Stahl, E.3
Plenge, R.4
Daly, M.5
Raychaudhuri, S.6
-
20
-
-
79959898376
-
Prioritizing candidate disease genes by network-based boosting of genome-wide association data
-
Lee I., Blom U.M., Wang P.I., Shim J.E., Marcotte E.M. Prioritizing candidate disease genes by network-based boosting of genome-wide association data. Genome Res 2011, 21:1109-1121.
-
(2011)
Genome Res
, vol.21
, pp. 1109-1121
-
-
Lee, I.1
Blom, U.M.2
Wang, P.I.3
Shim, J.E.4
Marcotte, E.M.5
-
21
-
-
84859526125
-
Identification of novel type 1 diabetes candidate genes by integrating genome-wide association data, protein-protein interactions, and human pancreatic islet gene expression
-
Bergholdt R., Brorsson C., Palleja A., Berchtold L.A., Floyel T., Bang-Berthelsen C.H., Frederiksen K.S., Jensen L.J., Storling J., Pociot F. Identification of novel type 1 diabetes candidate genes by integrating genome-wide association data, protein-protein interactions, and human pancreatic islet gene expression. Diabetes 2012, 61:954-962.
-
(2012)
Diabetes
, vol.61
, pp. 954-962
-
-
Bergholdt, R.1
Brorsson, C.2
Palleja, A.3
Berchtold, L.A.4
Floyel, T.5
Bang-Berthelsen, C.H.6
Frederiksen, K.S.7
Jensen, L.J.8
Storling, J.9
Pociot, F.10
-
22
-
-
80052493684
-
A network-based approach to prioritize results from genome-wide association studies
-
Akula N., Baranova A., Seto D., Solka J., Nalls M.A., Singleton A., Ferrucci L., Tanaka T., Bandinelli S., Cho Y.S., et al. A network-based approach to prioritize results from genome-wide association studies. PLoS ONE 2011, 6:e24220.
-
(2011)
PLoS ONE
, vol.6
-
-
Akula, N.1
Baranova, A.2
Seto, D.3
Solka, J.4
Nalls, M.A.5
Singleton, A.6
Ferrucci, L.7
Tanaka, T.8
Bandinelli, S.9
Cho, Y.S.10
-
23
-
-
79851502150
-
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology
-
Rossin E.J., Lage K., Raychaudhuri S., Xavier R.J., Tatar D., Benita Y., Cotsapas C., Daly M.J. Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology. PLoS Genet 2011, 7:e1001273.
-
(2011)
PLoS Genet
, vol.7
-
-
Rossin, E.J.1
Lage, K.2
Raychaudhuri, S.3
Xavier, R.J.4
Tatar, D.5
Benita, Y.6
Cotsapas, C.7
Daly, M.J.8
-
24
-
-
80052322958
-
Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA
-
Fehrmann R.S., Jansen R.C., Veldink J.H., Westra H.J., Arends D., Bonder M.J., Fu J., Deelen P., Groen H.J., Smolonska A., et al. Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. PLoS Genet 2011, 7:e1002197.
-
(2011)
PLoS Genet
, vol.7
-
-
Fehrmann, R.S.1
Jansen, R.C.2
Veldink, J.H.3
Westra, H.J.4
Arends, D.5
Bonder, M.J.6
Fu, J.7
Deelen, P.8
Groen, H.J.9
Smolonska, A.10
-
25
-
-
77957879688
-
Extreme evolutionary disparities seen in positive selection across seven complex diseases
-
Corona E., Dudley J.T., Butte A.J. Extreme evolutionary disparities seen in positive selection across seven complex diseases. PLoS ONE 2010, 5:e12236.
-
(2010)
PLoS ONE
, vol.5
-
-
Corona, E.1
Dudley, J.T.2
Butte, A.J.3
-
26
-
-
77956645141
-
Overlapping genetic susceptibility variants between three autoimmune disorders: rheumatoid arthritis, type 1 diabetes and coeliac disease
-
Eyre S., Hinks A., Bowes J., Flynn E., Martin P., Wilson A.G., Morgan A.W., Emery P., Steer S., Hocking L.J., et al. Overlapping genetic susceptibility variants between three autoimmune disorders: rheumatoid arthritis, type 1 diabetes and coeliac disease. Arthritis Res Ther 2010, 12:R175.
-
(2010)
Arthritis Res Ther
, vol.12
-
-
Eyre, S.1
Hinks, A.2
Bowes, J.3
Flynn, E.4
Martin, P.5
Wilson, A.G.6
Morgan, A.W.7
Emery, P.8
Steer, S.9
Hocking, L.J.10
-
27
-
-
81755179420
-
Insight from genome-wide association studies in rheumatoid arthritis and multiple sclerosis
-
Suzuki A., Kochi Y., Okada Y., Yamamoto K. Insight from genome-wide association studies in rheumatoid arthritis and multiple sclerosis. FEBS Lett 2011, 585:3627-3632.
-
(2011)
FEBS Lett
, vol.585
, pp. 3627-3632
-
-
Suzuki, A.1
Kochi, Y.2
Okada, Y.3
Yamamoto, K.4
-
28
-
-
84855257058
-
A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap
-
Ramos P.S., Criswell L.A., Moser K.L., Comeau M.E., Williams A.H., Pajewski N.M., Chung S.A., Graham R.R., Zidovetzki R., Kelly J.A., et al. A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap. PLoS Genet 2011, 7:e1002406.
-
(2011)
PLoS Genet
, vol.7
-
-
Ramos, P.S.1
Criswell, L.A.2
Moser, K.L.3
Comeau, M.E.4
Williams, A.H.5
Pajewski, N.M.6
Chung, S.A.7
Graham, R.R.8
Zidovetzki, R.9
Kelly, J.A.10
-
29
-
-
79955453474
-
Shared molecular and functional frameworks among five complex human disorders: a comparative study on interactomes linked to susceptibility genes
-
Menon R., Farina C. Shared molecular and functional frameworks among five complex human disorders: a comparative study on interactomes linked to susceptibility genes. PLoS ONE 2011, 6:e18660.
-
(2011)
PLoS ONE
, vol.6
-
-
Menon, R.1
Farina, C.2
-
30
-
-
80455145185
-
Prediction of disease and phenotype associations from genome-wide association studies
-
Lewis S.N., Nsoesie E., Weeks C., Qiao D., Zhang L. Prediction of disease and phenotype associations from genome-wide association studies. PLoS ONE 2011, 6:e27175.
-
(2011)
PLoS ONE
, vol.6
-
-
Lewis, S.N.1
Nsoesie, E.2
Weeks, C.3
Qiao, D.4
Zhang, L.5
-
31
-
-
80052325959
-
Pervasive sharing of genetic effects in autoimmune disease
-
Cotsapas C., Voight B.F., Rossin E., Lage K., Neale B.M., Wallace C., Abecasis G.R., Barrett J.C., Behrens T., Cho J., et al. Pervasive sharing of genetic effects in autoimmune disease. PLoS Genet 2011, 7:e1002254.
-
(2011)
PLoS Genet
, vol.7
-
-
Cotsapas, C.1
Voight, B.F.2
Rossin, E.3
Lage, K.4
Neale, B.M.5
Wallace, C.6
Abecasis, G.R.7
Barrett, J.C.8
Behrens, T.9
Cho, J.10
-
32
-
-
80051807776
-
Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study
-
So H.C., Li M., Sham P.C. Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study. Genet Epidemiol 2011, 35:447-456.
-
(2011)
Genet Epidemiol
, vol.35
, pp. 447-456
-
-
So, H.C.1
Li, M.2
Sham, P.C.3
-
33
-
-
84862909349
-
Five years of GWAS discovery
-
Visscher P.M., Brown M.A., McCarthy M.I., Yang J. Five years of GWAS discovery. Am J Hum Genet 2012, 90:7-24.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 7-24
-
-
Visscher, P.M.1
Brown, M.A.2
McCarthy, M.I.3
Yang, J.4
-
34
-
-
77954136357
-
Hints of hidden heritability in GWAS
-
Gibson G. Hints of hidden heritability in GWAS. Nat Genet 2010, 42:558-560.
-
(2010)
Nat Genet
, vol.42
, pp. 558-560
-
-
Gibson, G.1
-
35
-
-
79952489475
-
Estimating missing heritability for disease from genome-wide association studies
-
Lee S.H., Wray N.R., Goddard M.E., Visscher P.M. Estimating missing heritability for disease from genome-wide association studies. Am J Hum Genet 2011, 88:294-305.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 294-305
-
-
Lee, S.H.1
Wray, N.R.2
Goddard, M.E.3
Visscher, P.M.4
-
36
-
-
84860333083
-
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
-
Stahl E.A., Wegmann D., Trynka G., Gutierrez-Achury J., Do R., Voight B.F., Kraft P., Chen R., Kallberg H.J., Kurreeman F.A., et al. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nat Genet 2012, 44:483-489.
-
(2012)
Nat Genet
, vol.44
, pp. 483-489
-
-
Stahl, E.A.1
Wegmann, D.2
Trynka, G.3
Gutierrez-Achury, J.4
Do, R.5
Voight, B.F.6
Kraft, P.7
Chen, R.8
Kallberg, H.J.9
Kurreeman, F.A.10
-
37
-
-
77954133026
-
Estimation of effect size distribution from genome-wide association studies and implications for future discoveries
-
Park J.H., Wacholder S., Gail M.H., Peters U., Jacobs K.B., Chanock S.J., Chatterjee N. Estimation of effect size distribution from genome-wide association studies and implications for future discoveries. Nat Genet 2010, 42:570-575.
-
(2010)
Nat Genet
, vol.42
, pp. 570-575
-
-
Park, J.H.1
Wacholder, S.2
Gail, M.H.3
Peters, U.4
Jacobs, K.B.5
Chanock, S.J.6
Chatterjee, N.7
-
38
-
-
77956059154
-
Genome-wide searching of rare genetic variants in WTCCC data
-
Feng T., Zhu X. Genome-wide searching of rare genetic variants in WTCCC data. Hum Genet 2010, 128:269-280.
-
(2010)
Hum Genet
, vol.128
, pp. 269-280
-
-
Feng, T.1
Zhu, X.2
-
39
-
-
79351469297
-
Exome localization of complex disease association signals
-
Lehne B., Lewis C.M., Schlitt T. Exome localization of complex disease association signals. BMC Genomics 2011, 12:92.
-
(2011)
BMC Genomics
, vol.12
, pp. 92
-
-
Lehne, B.1
Lewis, C.M.2
Schlitt, T.3
-
40
-
-
80054975975
-
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
-
Rivas M.A., Beaudoin M., Gardet A., Stevens C., Sharma Y., Zhang C.K., Boucher G., Ripke S., Ellinghaus D., Burtt N., et al. Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease. Nat Genet 2011, 43:1066-1073.
-
(2011)
Nat Genet
, vol.43
, pp. 1066-1073
-
-
Rivas, M.A.1
Beaudoin, M.2
Gardet, A.3
Stevens, C.4
Sharma, Y.5
Zhang, C.K.6
Boucher, G.7
Ripke, S.8
Ellinghaus, D.9
Burtt, N.10
-
41
-
-
65249131713
-
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
-
Nejentsev S., Walker N., Riches D., Egholm M., Todd J.A. Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes. Science 2009, 324:387-389.
-
(2009)
Science
, vol.324
, pp. 387-389
-
-
Nejentsev, S.1
Walker, N.2
Riches, D.3
Egholm, M.4
Todd, J.A.5
-
42
-
-
82255192188
-
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
-
Trynka G., Hunt K.A., Bockett N.A., Romanos J., Mistry V., Szperl A., Bakker S.F., Bardella M.T., Bhaw-Rosun L., Castillejo G., et al. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet 2011, 43:1193-1201.
-
(2011)
Nat Genet
, vol.43
, pp. 1193-1201
-
-
Trynka, G.1
Hunt, K.A.2
Bockett, N.A.3
Romanos, J.4
Mistry, V.5
Szperl, A.6
Bakker, S.F.7
Bardella, M.T.8
Bhaw-Rosun, L.9
Castillejo, G.10
-
43
-
-
84855561973
-
Unraveling the autoimmune translational research process layer by layer
-
Blumberg R.S., Dittel B., Hafler D., von Herrath M., Nestle F.O. Unraveling the autoimmune translational research process layer by layer. Nat Med 2012, 18:35-41.
-
(2012)
Nat Med
, vol.18
, pp. 35-41
-
-
Blumberg, R.S.1
Dittel, B.2
Hafler, D.3
von Herrath, M.4
Nestle, F.O.5
|