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2016
Mark Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
Peloso, Gina M. ; Lange, Leslie A. ; Varga, Tibor V. ^LU ; Nickerson, Deborah A. ; Smith, Joshua D. ; Griswold, Michael E. ; Musani, Solomon ; Polfus, Linda M. ; Mei, Hao and Gabriel, Stacey , et al. (2016) In Circulation: Cardiovascular Genetics 9(4). p.368-374
- Contribution to journal › Article
Mark A reference panel of 64,976 haplotypes for genotype imputation
McCarthy, Shane ; Das, Sayantan ; Kretzschmar, Warren ; Delaneau, Olivier ; Wood, Andrew R. ; Teumer, Alexander ; Kang, Hyun Min ; Fuchsberger, Christian ; Danecek, Petr and Sharp, Kevin , et al. (2016) In Nature Genetics 48(10). p.1279-1283
- Contribution to journal › Article
2015
Mark Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
Schick, Ursula M ; Auer, Paul L ; Bis, Joshua C ; Lin, Honghuang ; Wei, Peng ; Pankratz, Nathan ; Lange, Leslie A ; Brody, Jennifer ; Stitziel, Nathan O and Kim, Daniel S , et al. (2015) In Human Molecular Genetics 24(2). p.559-571
- Contribution to journal › Article
Mark Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus.
Mahajan, Anubha ; Sim, Xueling ; Ng, Hui Jin ; Manning, Alisa ; Rivas, Manuel A ; Highland, Heather M ; Locke, Adam E ; Grarup, Niels ; Im, Hae Kyung and Cingolani, Pablo , et al. (2015) In PLoS Genetics 11(1).
- Contribution to journal › Article
2014
Mark Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
Majithia, Amit R ; Flannick, Jason ; Shahinian, Peter ; Guo, Michael ; Bray, Mark-Anthony ; Fontanillas, Pierre ; Gabriel, Stacey B ; Rosen, Evan D and Altshuler, David (2014) In Proceedings of the National Academy of Sciences of the United States of America 111(36). p.32-13127
- Contribution to journal › Article
Mark Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes.
Jaiswal, Siddhartha ; Fontanillas, Pierre ; Flannick, Jason ; Manning, Alisa ; Grauman, Peter V ; Mar, Brenton G ; Lindsley, R Coleman ; Mermel, Craig H ; Burtt, Noel and Chavez, Alejandro , et al. (2014) In New England Journal of Medicine 371(26). p.2488-2498
- Contribution to journal › Article
Mark Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
Lim, Elaine T ; Würtz, Peter ; Havulinna, Aki S ; Palta, Priit ; Tukiainen, Taru ; Rehnström, Karola ; Esko, Tõnu ; Mägi, Reedik ; Inouye, Michael and Lappalainen, Tuuli , et al. (2014) In PLoS Genetics 10(7).
- Contribution to journal › Article
Mark Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
Flannick, Jason ; Thorleifsson, Gudmar ; Beer, Nicola L ; Jacobs, Suzanne B R ; Grarup, Niels ; Burtt, Noël P ; Mahajan, Anubha ; Fuchsberger, Christian ; Atzmon, Gil and Benediktsson, Rafn , et al. (2014) In Nature Genetics 46(4). p.357-357
- Contribution to journal › Article
Mark Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
Crosby, Jacy ; Peloso, Gina M. ; Auer, Paul L. ; Crosslin, David R. ; Stitziel, Nathan O. ; Lange, Leslie A. ; Lu, Yingchang ; Tang, Zheng-zheng ; Zhang, He and Hindy, George ^LU , et al. (2014) In New England Journal of Medicine 371(1). p.22-31
- Contribution to journal › Article
Mark Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
Lange, Leslie A ; Hu, Youna ; Zhang, He ; Xue, Chenyi ; Schmidt, Ellen M ; Tang, Zheng-Zheng ; Bizon, Chris ; Lange, Ethan M ; Smith, Joshua D and Turner, Emily H , et al. (2014) In American Journal of Human Genetics 94(2). p.233-245
- Contribution to journal › Article

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