Publications:

Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight

Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL

Publication Date: 2020-09-03

Variant appearance in text: rs1427271

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

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A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses in Leprosy.

Plos Neglected Tropical Diseases

Fava, Vinicius M VM; Manry, Jérémy J; Cobat, Aurélie A; Orlova, Marianna M; Van Thuc, Nguyen N; Ba, Nguyen Ngoc NN; Thai, Vu Hong VH; Abel, Laurent L; Alcaïs, Alexandre A; Schurr, Erwin E; ,

Publication Date: 2016-02

Variant appearance in text: rs1427271

PubMed Link: 26844546

Variant Present in the following documents:

• Main text
• pntd.0004412.pdf

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Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

Bmc Medical Genetics

Liu, Xinmin X; Cheng, Rong R; Verbitsky, Miguel M; Kisselev, Sergey S; Browne, Andrew A; Mejia-Sanatana, Helen H; Louis, Elan D ED; Cote, Lucien J LJ; Andrews, Howard H; Waters, Cheryl C; Ford, Blair B; Frucht, Steven S; Fahn, Stanley S; Marder, Karen K; Clark, Lorraine N LN; Lee, Joseph H JH

Publication Date: 2011-08-03

Variant appearance in text: rs1427271

PubMed Link: 21812969

Variant Present in the following documents:

• Main text
• 1471-2350-12-104.pdf

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Parkinson's disease and low frequency alleles found together throughout LRRK2.

Annals Of Human Genetics

Paisán-Ruiz, Coro C; Washecka, Nicole N; Nath, Priti P; Singleton, Andrew B AB; Corder, Elizabeth H EH

Publication Date: 2009-07

Variant appearance in text: rs1427271

PubMed Link: 19489756

Variant Present in the following documents:

• Main text

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