Publications:

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Summary-data-based Mendelian randomization prioritizes potential druggable targets for multiple sclerosis.

Brain Communications

Jacobs, Benjamin M BM; Taylor, Thomas T; Awad, Amine A; Baker, David D; Giovanonni, Gavin G; Noyce, Alastair J AJ; Dobson, Ruth R

Publication Date: 2020

Variant appearance in text: rs2957873

PubMed Link: 33005893

Variant Present in the following documents:

• Main text
• fcaa119.pdf

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Single nucleotide polymorphisms in nucleotide excision repair genes, cancer treatment, and head and neck cancer survival.

Cancer Causes & Control : Ccc

Wyss, Annah B AB; Weissler, Mark C MC; Avery, Christy L CL; Herring, Amy H AH; Bensen, Jeannette T JT; Barnholtz-Sloan, Jill S JS; Funkhouser, William K WK; Olshan, Andrew F AF

Publication Date: 2014-04

Variant appearance in text: rs2957873

PubMed Link: 24487794

Variant Present in the following documents:

• Main text

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Single-nucleotide polymorphisms in nucleotide excision repair genes, cigarette smoking, and the risk of head and neck cancer.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology

Wyss, Annah B AB; Herring, Amy H AH; Avery, Christy L CL; Weissler, Mark C MC; Bensen, Jeannette T JT; Barnholtz-Sloan, Jill S JS; Funkhouser, William K WK; Olshan, Andrew F AF

Publication Date: 2013-08

Variant appearance in text: rs2957873

PubMed Link: 23720401

Variant Present in the following documents:

• Main text

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Comprehensive pathway-based interrogation of genetic variations in the nucleotide excision DNA repair pathway and risk of bladder cancer.

Cancer

Xing, Jinliang J; Dinney, Colin P CP; Shete, Sanjay S; Huang, Maosheng M; Hildebrandt, Michelle A MA; Chen, Zhinan Z; Gu, Jian J

Publication Date: 2012-01-01

Variant appearance in text: rs2957873

PubMed Link: 21692063

Variant Present in the following documents:

• Main text

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Variation within DNA repair pathway genes and risk of multiple sclerosis.

American Journal Of Epidemiology

Briggs, Farren B S FB; Goldstein, Benjamin A BA; McCauley, Jacob L JL; Zuvich, Rebecca L RL; De Jager, Philip L PL; Rioux, John D JD; Ivinson, Adrian J AJ; Compston, Alastair A; Hafler, David A DA; Hauser, Stephen L SL; Oksenberg, Jorge R JR; Sawcer, Stephen J SJ; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; Barcellos, Lisa F LF; ,

Publication Date: 2010-07-15

Variant appearance in text: rs2957873

PubMed Link: 20522537

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: rs2957873

PubMed Link: 17357082

Variant Present in the following documents:

• Main text

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