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Number of items: 11.


Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer
et al (show 561 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313-+.


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 351 more authors) (2018) Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. NEUROLOGY-GENETICS, 4 (6). e293-.


Ligthart, Symen, Vaez, Ahmad, Vosa, Urmo, Stathopoulou, Maria G, de Vries, Paul S, Prins, Bram P, Van der Most, Peter J, Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M
et al (show 276 more authors) (2018) Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. AMERICAN JOURNAL OF HUMAN GENETICS, 103 (5). pp. 691-706.


Justice, Anne E, Winkler, Thomas W, Feitosa, Mary F, Graff, Misa, Fisher, Virginia A, Young, Kristin, Barata, Llilda, Deng, Xuan, Czajkowski, Jacek, Hadley, David
et al (show 307 more authors) (2017) Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. NATURE COMMUNICATIONS, 8 (1). 14977-.


Wheeler, Eleanor, Leong, Aaron, Liu, Ching-Ti, Hivert, Marie-France, Strawbridge, Rona J, Podmore, Clara, Li, Man, Yao, Jie, Sim, Xueling, Hong, Jaeyoung
et al (show 205 more authors) (2017) Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. PLOS MEDICINE, 14 (9). e1002383-.


Zhao, S ORCID: 0000-0002-3558-7353, Hong, Chuan, Cai, Tianrun, Xu, Chang, Huang, Jie, Ermann, Joerg, Goodson, Nicola ORCID: 0000-0003-0714-3568, Solomon, Daniel, Cai, Tianxi and Liao, Katherine
(2020) Incorporating natural language processing to improve classification of axial spondyloarthritis using electronic health records. Rheumatology, 59 (5). pp. 1059-1065.


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 113 more authors) (2017) Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. JOURNAL OF CLINICAL INVESTIGATION, 127 (5). pp. 1798-1812.


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 (9). pp. 1225-1233.


Loley, Christina, Alver, Maris, Assimes, Themistocles L, Bjonnes, Andrew, Goel, Anuj, Gustafsson, Stefan, Hernesniemi, Jussi, Hopewell, Jemma C, Kanoni, Stavroula, Kleber, Marcus E
et al (show 68 more authors) (2016) No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis. SCIENTIFIC REPORTS, 6 (1). 35278-.


Szenasi, Attila, Sivasudhan, Enakshi, Du, Hong, Zhang, Peizhuo, Huang, Jie, Zhang, Zhijun, Rocha, Sonia and Wang, Mu
(2023) Targeting SOD1 via RNAi with PEGylated graphene oxide nanoparticles in platinum-resistant ovarian cancer. CANCER GENE THERAPY, 30 (11). pp. 1554-1568.


Tachmazidou, Ioanna, Suveges, Daniel, Min, Josine L, Ritchie, Graham RS, Steinberg, Julia, Walter, Klaudia, Iotchkova, Valentina, Schwartzentruber, Jeremy, Huang, Jie, Memari, Yasin
et al (show 93 more authors) (2017) Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. AMERICAN JOURNAL OF HUMAN GENETICS, 100 (6). pp. 865-884.

This list was generated on Sun Mar 3 06:46:43 2024 GMT.