Publications:

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A Genetic Approach to the Association Between PCSK9 and Sepsis.

Jama Network Open

Feng, QiPing Q; Wei, Wei-Qi WQ; Chaugai, Sandip S; Carranza Leon, Barbara G BG; Kawai, Vivian V; Carranza Leon, Daniel A DA; Jiang, Lan L; Zhong, Xue X; Liu, Ge G; Ihegword, Andrea A; Shaffer, Christian M CM; Linton, MacRae F MF; Chung, Cecilia P CP; Stein, C Michael CM

Publication Date: 2019-09-04

Variant appearance in text: rs682705

PubMed Link: 31509211

Variant Present in the following documents:

• jamanetwopen-2-e1911130-s001.pdf

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Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases

Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ

Publication Date: 2017-05-23

Variant appearance in text: rs682705

PubMed Link: 28535796

Variant Present in the following documents:

• 13023_2017_647_MOESM1_ESM.xlsx, sheet 4

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Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease.

Genetic Epidemiology

Payami, Haydeh H; Kay, Denise M DM; Zabetian, Cyrus P CP; Schellenberg, Gerard D GD; Factor, Stewart A SA; McCulloch, Colin C CC

Publication Date: 2010-01

Variant appearance in text: rs682705

PubMed Link: 19582778

Variant Present in the following documents:

• Main text

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Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.

The Lancet. Neurology

Elbaz, Alexis A; Nelson, Lorene M LM; Payami, Haydeh H; Ioannidis, John P A JP; Fiske, Brian K BK; Annesi, Grazia G; Carmine Belin, Andrea A; Factor, Stewart A SA; Ferrarese, Carlo C; Hadjigeorgiou, Georgios M GM; Higgins, Donald S DS; Kawakami, Hideshi H; Krüger, Rejko R; Marder, Karen S KS; Mayeux, Richard P RP; Mellick, George D GD; Nutt, John G JG; Ritz, Beate B; Samii, Ali A; Tanner, Caroline M CM; Van Broeckhoven, Christine C; Van Den Eeden, Stephen K SK; Wirdefeldt, Karin K; Zabetian, Cyrus P CP; Dehem, Marie M; Montimurro, Jennifer S JS; Southwick, Audrey A; Myers, Richard M RM; Trikalinos, Thomas A TA

Publication Date: 2006-11

Variant appearance in text: rs682705

PubMed Link: 17052658

Variant Present in the following documents:

• Main text

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No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

American Journal Of Human Genetics

Goris, A A; Williams-Gray, C H CH; Foltynie, T T; Compston, D A S DA; Barker, R A RA; Sawcer, S J SJ

Publication Date: 2006-06

Variant appearance in text: rs682705

PubMed Link: 16685662

Variant Present in the following documents:

• Main text

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Genomewide association, Parkinson disease, and PARK10.

American Journal Of Human Genetics

Farrer, Matthew J MJ; Haugarvoll, Kristoffer K; Ross, Owen A OA; Stone, Jeremy T JT; Milkovic, Nicole M NM; Cobb, Stephanie A SA; Whittle, Andrew J AJ; Lincoln, Sarah J SJ; Hulihan, Mary M MM; Heckman, Michael G MG; White, Linda R LR; Aasly, Jan O JO; Gibson, J Mark JM; Gosal, David D; Lynch, Timothy T; Wszolek, Zbigniew K ZK; Uitti, Ryan J RJ; Toft, Mathias M

Publication Date: 2006-06

Variant appearance in text: rs682705

PubMed Link: 16685661

Variant Present in the following documents:

• Main text

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High-resolution whole-genome association study of Parkinson disease.

American Journal Of Human Genetics

Maraganore, Demetrius M DM; de Andrade, Mariza M; Lesnick, Timothy G TG; Strain, Kari J KJ; Farrer, Matthew J MJ; Rocca, Walter A WA; Pant, P V Krishna PV; Frazer, Kelly A KA; Cox, David R DR; Ballinger, Dennis G DG

Publication Date: 2005-11

Variant appearance in text: rs682705

PubMed Link: 16252231

Variant Present in the following documents:

• Main text

View BVdb publication page

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