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Genetic Variation in the Platelet Endothelial Aggregation Receptor 1 Gene Results in Endothelial Dysfunction.
Published in:
PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138795
By:
- Fisch, Adam S.;
- Yerges-Armstrong, Laura M.;
- Backman, Joshua D.;
- Wang, Hong;
- Donnelly, Patrick;
- Ryan, Kathleen A.;
- Parihar, Ankita;
- Pavlovich, Mary A.;
- Mitchell, Braxton D.;
- O’Connell, Jeffrey R.;
- Herzog, William;
- Harman, Christopher R.;
- Wren, Jonathan D.;
- Lewis, Joshua P.
Publication type:
Article
From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.
Published in:
G3: Genes | Genomes | Genetics, 2016, v. 6, n. 9, p. 2909, doi. 10.1534/g3.116.032979
By:
- Tise, Christina G.;
- Perry, James A.;
- Anforth, Leslie E.;
- Pavlovich, Mary A.;
- Backman, Joshua D.;
- Ryan, Kathleen A.;
- Lewis, Joshua P.;
- O'Connell, Jeffrey R.;
- Yerges-Armstrong, Laura M.;
- Shuldiner, Alan R.
Publication type:
Article
The genomics of heart failure: design and rationale of the HERMES consortium.
Published in:
ESC Heart Failure, 2021, v. 8, n. 6, p. 5531, doi. 10.1002/ehf2.13517
By:
- Lumbers, R. Thomas;
- Shah, Sonia;
- Lin, Honghuang;
- Czuba, Tomasz;
- Henry, Albert;
- Swerdlow, Daniel I.;
- Mälarstig, Anders;
- Andersson, Charlotte;
- Verweij, Niek;
- Holmes, Michael V.;
- Ärnlöv, Johan;
- Svensson, Per;
- Hemingway, Harry;
- Sallah, Neneh;
- Almgren, Peter;
- Aragam, Krishna G.;
- Asselin, Geraldine;
- Backman, Joshua D.;
- Biggs, Mary L.;
- Bloom, Heather L.
Publication type:
Article
Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals.
Published in:
Genetic Epidemiology, 2021, v. 45, n. 6, p. 664, doi. 10.1002/gepi.22392
By:
- Gao, Chuan;
- Marcketta, Anthony;
- Backman, Joshua D.;
- O'Dushlaine, Colm;
- Staples, Jeffrey;
- Ferreira, Manuel Allen Revez;
- Lotta, Luca A.;
- Overton, John D.;
- Reid, Jeffrey G.;
- Mirshahi, Tooraj;
- Regeneron Genetics Center;
- Geisinger Regeneron Discovehr Collaboration;
- Baras, Aris;
- Abecasis, Gonçalo;
- Shuldiner, Alan R.;
- Van Hout, Cristopher V.;
- McCarthy, Shane
Publication type:
Article
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Published in:
Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-13690-5
By:
- Shah, Sonia;
- Henry, Albert;
- Roselli, Carolina;
- Lin, Honghuang;
- Sveinbjörnsson, Garðar;
- Fatemifar, Ghazaleh;
- Hedman, Åsa K.;
- Wilk, Jemma B.;
- Morley, Michael P.;
- Chaffin, Mark D.;
- Helgadottir, Anna;
- Verweij, Niek;
- Dehghan, Abbas;
- Almgren, Peter;
- Andersson, Charlotte;
- Aragam, Krishna G.;
- Ärnlöv, Johan;
- Backman, Joshua D.;
- Biggs, Mary L.;
- Bloom, Heather L.
Publication type:
Article

Found: 5

Genetic Variation in the Platelet Endothelial Aggregation Receptor 1 Gene Results in Endothelial Dysfunction.

From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.

The genomics of heart failure: design and rationale of the HERMES consortium.

Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals.

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.