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Number of items: 10.


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-.


Flannick, Jason, Fuchsberger, Christian, Mahajan, Anubha, Teslovich, Tanya M, Agarwala, Vineeta, Gaulton, Kyle J, Caulkins, Lizz, Koesterer, Ryan, Ma, Clement, Moutsianas, Loukas
et al (show 291 more authors) (2017) Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. SCIENTIFIC DATA, 4 (1). 170179-.


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). pp. 1314-1332.


Scott, Robert A, Scott, Laura J, Maegi, Reedik, Marullo, Letizia, Gaulton, Kyle J, Kaakinen, Marika, Pervjakova, Natalia, Pers, Tune H, Johnson, Andrew D, Eicher, John D
et al (show 165 more authors) (2017) An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. DIABETES, 66 (11). pp. 2888-2902.


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.


Manning, Alisa, Highland, Heather M, Gasser, Jessica, Sim, Xueling, Tukiainen, Taru, Fontanillas, Pierre, Grarup, Niels, Rivas, Manuel A, Mahajan, Anubha, Locke, Adam E
et al (show 253 more authors) (2017) A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. DIABETES, 66 (7). pp. 2019-2032.


Forsberg, Lars A, Rasi, Chiara, Malmqvist, Niklas, Davies, Hanna, Pasupulati, Saichand, Pakalapati, Geeta, Sandgren, Johanna, Diaz de Ståhl, Teresita, Zaghlool, Ammar, Giedraitis, Vilmantas
et al (show 10 more authors) (2014) Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer. Nature Genetics, 46 (6). pp. 624-628.


Flannick, Jason, Fuchsberger, Christian, Mahajan, Anubha, Teslovich, Tanya M, Agarwala, Vineeta, Gaulton, Kyle J, Caulkins, Lizz, Koesterer, Ryan, Ma, Clement, Moutsianas, Loukas
et al (show 291 more authors) (2018) Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (vol 4, 170179, 2017). SCIENTIFIC DATA, 5 (1). 180002-.


Surendran, Praveen, Drenos, Fotios, Young, Robin, Warren, Helen, Cook, James P, Manning, Alisa K, Grarup, Niels, Sim, Xueling, Barnes, Daniel R, Witkowska, Kate
et al (show 200 more authors) (2016) Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. NATURE GENETICS, 48 (10). pp. 1151-1161.


Fuchsberger, Christian, Flannick, Jason, Teslovich, Tanya M, Mahajan, Anubha, Agarwala, Vineeta, Gaulton, Kyle J, Ma, Clement, Fontanillas, Pierre, Moutsianas, Loukas, McCarthy, Davis J
et al (show 291 more authors) (2016) The genetic architecture of type 2 diabetes. NATURE, 536 (7614). 41-+.

This list was generated on Mon Apr 8 19:43:54 2024 BST.