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2018
Mark Multi-ethnic genome-wide association study for atrial fibrillation
Roselli, Carolina ; Chaffin, Mark D. ; Weng, Lu Chen ; Aeschbacher, Stefanie ; Ahlberg, Gustav ; Albert, Christine M. ; Almgren, Peter ^LU ; Alonso, Alvaro ; Anderson, Christopher D. and Aragam, Krishna G. , et al. (2018) In Nature Genetics 50(9). p.1225-1233
- Contribution to journal › Article
2017
Mark Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
Wild, Philipp S. ; Felix, Janine F. ; Schillert, Arne ; Teumer, Alexander ; Chen, Ming-Huei ; Leening, Maarten J.G. ; Völker, Uwe ; Großmann, Vera ; Brody, Jennifer A and Irvin, Marguerite R. , et al. (2017) In Journal of Clinical Investigation 127(5). p.1798-1812
- Contribution to journal › Article
2016
Mark Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
Jakobsdottir, Johanna ; van der Lee, Sven J. ; Bis, Joshua C. ; Chouraki, Vincent ; Li-Kroeger, David ; Yamamoto, Shinya ; Grove, Megan L. ; Naj, Adam ; Vronskaya, Maria and Salazar, Jose L. , et al. (2016) In PLoS Genetics 12(10).
- Contribution to journal › Article
Mark Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits
Chami, Nathalie ; Chen, Ming Huei ; Slater, Andrew J. ; Eicher, John D. ; Evangelou, Evangelos ; Tajuddin, Salman M. ; Love-Gregory, Latisha ; Kacprowski, Tim ; Schick, Ursula M. and Nomura, Akihiro , et al. (2016) In American Journal of Human Genetics 99(1). p.8-21
- Contribution to journal › Article
2015
Mark Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
Wessel, Jennifer ; Chu, Audrey Y ; Willems, Sara M ; Wang, Shuai ; Yaghootkar, Hanieh ; Brody, Jennifer A ; Dauriz, Marco ; Hivert, Marie-France ; Raghavan, Sridharan and Lipovich, Leonard , et al. (2015) In Nature Communications 6.
- Contribution to journal › Article
2014
Mark Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
Peloso, Gina M ; Auer, Paul L ; Bis, Joshua C ; Voorman, Arend ; Morrison, Alanna C ; Stitziel, Nathan O ; Brody, Jennifer A ; Khetarpal, Sumeet A ; Crosby, Jacy R and Fornage, Myriam , et al. (2014) In American Journal of Human Genetics 94(2). p.223-232
- Contribution to journal › Article

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