Publications:

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Association of triglyceride levels and prostate cancer: a Mendelian randomization study.

Bmc Urology

Zhu, Shusheng S; Hu, Xia X; Fan, Yanpeng Y

Publication Date: 2022-10-31

Variant appearance in text: rs10501321

PubMed Link: 36316671

Variant Present in the following documents:

• Main text
• 12894_2022_Article_1120.pdf

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Genes in human obesity loci are causal obesity genes in C. elegans.

Plos Genetics

Ke, Wenfan W; Reed, Jordan N JN; Yang, Chenyu C; Higgason, Noel N; Rayyan, Leila L; Wählby, Carolina C; Carpenter, Anne E AE; Civelek, Mete M; O'Rourke, Eyleen J EJ

Publication Date: 2021-09

Variant appearance in text: rs10501321

PubMed Link: 34492009

Variant Present in the following documents:

• Main text
• pgen.1009736.pdf

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Genome-wide association study of metabolic syndrome in koreans.

Genomics & Informatics

Jeong, Seok Won SW; Chung, Myungguen M; Park, Soo-Jung SJ; Cho, Seong Beom SB; Hong, Kyung-Won KW

Publication Date: 2014-12

Variant appearance in text: rs10501321

PubMed Link: 25705157

Variant Present in the following documents:

• gni-12-187-s002.pdf

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Liver X receptor α gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study.

Pharmacogenetics And Genomics

Price, Elvin Tyrone ET; Pacanowski, Michael A MA; Martin, Michael A MA; Cooper-DeHoff, Rhonda M RM; Pepine, Carl J CJ; Zineh, Issam I; Johnson, Julie A JA

Publication Date: 2011-06

Variant appearance in text: rs10501321

PubMed Link: 21562465

Variant Present in the following documents:

• Main text

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A genome-wide linkage scan reveals CD53 as an important regulator of innate TNF-alpha levels.

European Journal Of Human Genetics : Ejhg

Bos, Steffan D SD; Lakenberg, Nico N; van der Breggen, Ruud R; Houwing-Duistermaat, Jeanine J JJ; Kloppenburg, Margreet M; de Craen, Anton J M AJ; Beekman, Marian M; Meulenbelt, Ingrid I; Slagboom, P Eline PE

Publication Date: 2010-08

Variant appearance in text: rs10501321

PubMed Link: 20407468

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: rs10501321

PubMed Link: 17357082

Variant Present in the following documents:

• Main text

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