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: rs1907632

PubMed Link: 32879140

Variant Present in the following documents:

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

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Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.

Annals Of Human Genetics

Edwards, Todd L TL; Scott, William K WK; Almonte, Cherylyn C; Burt, Amber A; Powell, Eric H EH; Beecham, Gary W GW; Wang, Liyong L; Züchner, Stephan S; Konidari, Ioanna I; Wang, Gaofeng G; Singer, Carlos C; Nahab, Fatta F; Scott, Burton B; Stajich, Jeffrey M JM; Pericak-Vance, Margaret M; Haines, Jonathan J; Vance, Jeffery M JM; Martin, Eden R ER

Publication Date: 2010-03

Variant appearance in text: rs1907632

PubMed Link: 20070850

Variant Present in the following documents:

• Main text

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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: rs1907632

PubMed Link: 19489756

Variant Present in the following documents:

• Main text

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