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Cited by 355

The DOI matches its Crossref record; 69 of the 69 references it cites were found in a registry or an index.

Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants

Open access
Jin, Ying, Andersen, Genevieve, Yorgov, Daniel, Ferrara, Tracey M, Ben, Songtao, Brownson, Kelly M, Holland, Paulene J, Birlea, Stanca A, Siebert, Janet, Hartmann, Anke, Lienert, Anne, van Geel, Nanja, Lambert, Jo, Luiten, Rosalie M, Wolkerstorfer, Albert, Wietze van der Veen, J P, Bennett, Dorothy C, Taïeb, Alain, Ezzedine, Khaled, Kemp, E Helen, Gawkrodger, David J, Weetman, Anthony P, Kõks, Sulev, Prans, Ele, Kingo, Külli, Karelson, Maire, Wallace, Margaret R, McCormack, Wayne T, Overbeck, Andreas, Moretti, Silvia, Colucci, Roberta, Picardo, Mauro, Silverberg, Nanette B, Olsson, Mats, Valle, Yan, Korobko, Igor, Böhm, Markus, Lim, Henry W, Hamzavi, Iltefat, Zhou, Li, Mi, Qing-Sheng, Fain, Pamela R, Santorico, Stephanie A, Spritz, Richard A·2016·Nature Genetics

Abstract

Vitiligo is an autoimmune disease in which depigmented skin results from the destruction of melanocytes, with epidemiological association with other autoimmune diseases. In previous linkage and genome-wide association studies (GWAS1 and GWAS2), we identified 27 vitiligo susceptibility loci in patients of European ancestry. We carried out a third GWAS (GWAS3) in European-ancestry subjects, with augmented GWAS1 and GWAS2 controls, genome-wide imputation, and meta-analysis of all three GWAS, followed by an independent replication. The combined analyses, with 4,680 cases and 39,586 controls, identified 23 new significantly associated loci and 7 suggestive loci. Most encode immune and apoptotic regulators, with some also associated with other autoimmune diseases, as well as several melanocyte regulators. Bioinformatic analyses indicate a predominance of causal regulatory variation, some of which corresponds to expression quantitative trait loci (eQTLs) at these loci. Together, the identified genes provide a framework for the genetic architecture and pathobiology of vitiligo, highlight relationships with other autoimmune diseases and melanoma, and offer potential targets for treatment.

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Metadata

Authors
Jin, Y., Andersen, G., Yorgov, D., Ferrara, T. M., Ben, S., Brownson, K. M., Holland, P. J., Birlea, S. A., Siebert, J., Hartmann, A., Lienert, A., van Geel, N., Lambert, J., Luiten, R. M., Wolkerstorfer, A., Wietze van der Veen, J. P., Bennett, D. C., Taïeb, A., Ezzedine, K., Kemp, E. H., Gawkrodger, D. J., Weetman, A. P., Kõks, S., Prans, E., Kingo, K., Karelson, M., Wallace, M. R., McCormack, W. T., Overbeck, A., Moretti, S., Colucci, R., Picardo, M., Silverberg, N. B., Olsson, M., Valle, Y., Korobko, I., Böhm, M., Lim, H. W., Hamzavi, I., Zhou, L., Mi, Q.-S., Fain, P. R., Santorico, S. A., & Spritz, R. A.
Venue
Nature Genetics
Published
2016-10-10
Volume
48
Issue
11
Pages
1418-1424
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
OpenAlex
W2531815874
Cited by
355
References
69
FWCI
15.25
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. https://app.cochat.ai/papers/10.1038/ng.3680
The paper
Jin, Y., Andersen, G., Yorgov, D., Ferrara, T. M., Ben, S., Brownson, K. M., Holland, P. J., Birlea, S. A., Siebert, J., Hartmann, A., Lienert, A., van Geel, N., Lambert, J., Luiten, R. M., Wolkerstorfer, A., Wietze van der Veen, J. P., Bennett, D. C., Taïeb, A., Ezzedine, K., . . . Spritz, R. A. (2016). Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. Nature Genetics. https://doi.org/10.1038/ng.3680

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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