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Number of items: 12.


Pulit, Sara L, Weng, Lu-Chen, McArdle, Patrick F, Trinquart, Ludovic, Choi, Seung Hoan, Mitchell, Braxton D, Rosand, Jonathan, de Bakker, Paul IW, Benjamin, Emelia J, Ellinor, Patrick T
et al (show 353 more authors) (2018) Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. NEUROLOGY-GENETICS, 4 (6).


Surendran, Praveen, Feofanova, Elena V, Lahrouchi, Najim, Ntalla, Ioanna, Karthikeyan, Savita, Cook, James, Chen, Lingyan, Mifsud, Borbala, Yao, Chen, Kraja, Aldi T
et al (show 271 more authors) (2020) Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. NATURE GENETICS, 52 (12). 1314 - 1332.


van Rooij, Frank JA, Qayyum, Rehan, Smith, Albert V, Zhou, Yi, Trompet, Stella, Tanaka, Toshiko, Keller, Margaux F, Chang, Li-Ching, Schmidt, Helena, Yang, Min-Lee
et al (show 91 more authors) (2017) Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. AMERICAN JOURNAL OF HUMAN GENETICS, 100 (1). 51 - 63.


Sung, Yun J, Winkler, Thomas W, de las Fuentes, Lisa, Bentley, Amy R, Brown, Michael R, Kraja, Aldi T, Schwander, Karen, Ntalla, Ioanna, Guo, Xiuqing, Franceschini, Nora
et al (show 291 more authors) (2018) A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. AMERICAN JOURNAL OF HUMAN GENETICS, 102 (3). 375 - 400.


Wild, Philipp S, Felix, Janine F, Schillert, Arne, Teumer, Alexander, Chen, Ming-Huei, Leening, Maarten JG, Voelker, Uwe, Grossmann, Vera, Brody, Jennifer A, Irvin, Marguerite R
et al (show 116 more authors) (2017) Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. JOURNAL OF CLINICAL INVESTIGATION, 127 (5). 1798 - 1812.


Liu, Chunyu, Kraja, Aldi T, Smith, Jennifer A, Brody, Jennifer A, Franceschini, Nora, Bis, Joshua C, Rice, Kenneth, Morrison, Alanna C, Lu, Yingchang, Weiss, Stefan
et al (show 91 more authors) (2016) Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. NATURE GENETICS, 48 (10). 1162 - 1170.


Jackson, Victoria E ORCID: 0000-0002-9758-9784, Latourelle, Jeanne C, Wain, Louise V ORCID: 0000-0003-4951-1867, Smith, Albert V, Grove, Megan L, Bartz, Traci M, Obeidat, Ma'en ORCID: 0000-0002-5443-2752, Province, Michael A, Gao, Wei, Qaiser, Beenish
et al (show 97 more authors) (2018) Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome Open Research, 3. 4 - 4.


Jackson, Victoria E ORCID: 0000-0002-9758-9784, Latourelle, Jeanne C, Wain, Louise V ORCID: 0000-0003-4951-1867, Smith, Albert V, Grove, Megan L, Bartz, Traci M, Obeidat, Ma'en ORCID: 0000-0002-5443-2752, Province, Michael A, Gao, Wei, Qaiser, Beenish
et al (show 98 more authors) (2018) Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome open research, 3. 4 - ?.


Ntalla, Ioanna, Weng, Lu-Chen, Cartwright, James H, Hall, Amelia Weber, Sveinbjornsson, Gardar, Tucker, Nathan R, Choi, Seung Hoan, Chaffin, Mark D, Roselli, Carolina, Barnes, Michael R
et al (show 177 more authors) (2020) Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nature communications, 11 (1).


Roselli, Carolina, Chaffin, Mark D, Weng, Lu-Chen, Aeschbacher, Stefanie, Ahlberg, Gustav, Albert, Christine M, Almgren, Peter, Alonso, Alvaro, Anderson, Christopher D, Aragam, Krishna G
et al (show 208 more authors) (2018) Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics, 50. 1225 - 1233.


Floyd, James S, Bloch, Katarzyna M, Brody, Jennifer A, Maroteau, Cyrielle, Siddiqui, Moneeza K, Gregory, Richard, Carr, Daniel F ORCID: 0000-0001-8028-4282, Molokhia, Mariam, Liu, Xiaoming, Bis, Joshua C
et al (show 32 more authors) (2019) Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing. PLoS One, 14 (6).


Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N William
et al (show 233 more authors) (2018) Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. NATURE GENETICS, 50 (4). 559 - 571+.

This list was generated on Sat May 1 19:00:45 2021 BST.