Publications:

Convergent lines of evidence support BIN1 as a risk gene of Alzheimer's disease.

Human Genomics

Zhu, Jin J; Liu, Xia X; Yin, Hongtao H; Gao, Yan Y; Yu, Hao H

Publication Date: 2021-01-30

Variant appearance in text: rs17783630

PubMed Link: 33516273

Variant Present in the following documents:

• Main text
• 40246_2021_Article_307.pdf

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Genetic variants in platelet factor 4 modulate inflammatory and platelet activation biomarkers.

Circulation. Cardiovascular Genetics

Bhatnagar, Pallav P; Lu, Xiaochun X; Evans, Michele K MK; Laveist, Thomas A TA; Zonderman, Alan B AB; Carter, Darryl L DL; Arking, Dan E DE; Fletcher, Craig A CA

Publication Date: 2012-08-01

Variant appearance in text: rs17783630

PubMed Link: 22763266

Variant Present in the following documents:

• Main text

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Genetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies.

Current Hypertension Reports

Kraja, Aldi T AT; Hunt, Steven C SC; Rao, D C DC; Dávila-Román, Victor G VG; Arnett, Donna K DK; Province, Michael A MA

Publication Date: 2011-02

Variant appearance in text: rs17783630

PubMed Link: 21128019

Variant Present in the following documents:

• Main text

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Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

American Journal Of Human Genetics

Melquist, Stacey S; Craig, David W DW; Huentelman, Matthew J MJ; Crook, Richard R; Pearson, John V JV; Baker, Matt M; Zismann, Victoria L VL; Gass, Jennifer J; Adamson, Jennifer J; Szelinger, Szabolcs S; Corneveaux, Jason J; Cannon, Ashley A; Coon, Keith D KD; Lincoln, Sarah S; Adler, Charles C; Tuite, Paul P; Calne, Donald B DB; Bigio, Eileen H EH; Uitti, Ryan J RJ; Wszolek, Zbigniew K ZK; Golbe, Lawrence I LI; Caselli, Richard J RJ; Graff-Radford, Neill N; Litvan, Irene I; Farrer, Matthew J MJ; Dickson, Dennis W DW; Hutton, Mike M; Stephan, Dietrich A DA

Publication Date: 2007-04

Variant appearance in text: rs17783630

PubMed Link: 17357082

Variant Present in the following documents:

• Main text

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