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Number of items: 23.


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-.


Arloth, Janine, Eraslan, Gökcen, Andlauer, Till FM, Martins, Jade, Iurato, Stella, Kühnel, Brigitte, Waldenberger, Melanie, Frank, Josef, Gold, Ralf, Hemmer, Bernhard
et al (show 18 more authors) (2020) DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. PLoS computational biology, 16 (2). e1007616-e1007616.


Karasik, David, Zillikens, M Carola, Hsu, Yi-Hsiang, Aghdassi, Ali, Akesson, Kristina, Amin, Najaf, Barroso, Inês, Bennett, David A, Bertram, Lars, Bochud, Murielle
et al (show 147 more authors) (2019) Disentangling the genetics of lean mass. The American journal of clinical nutrition, 109 (2). pp. 276-287.


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.


Mahajan, Anubha, Taliun, Daniel, Thurner, Matthias, Robertson, Neil R, Torres, Jason M, Rayner, N William, Payne, Anthony J, Steinthorsdottir, Valgerdur, Scott, Robert A, Grarup, Niels
et al (show 105 more authors) (2018) Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. NATURE GENETICS, 50 (11). pp. 1505-1513.


Zhao, Huiying, Eising, Else, de Vries, Boukje, Vijfhuizen, Lisanne S, Anttila, Verneri, Winsvold, Bendik S, Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer
et al (show 26 more authors) (2016) Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. CEPHALALGIA, 36 (7). pp. 648-657.


Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tonu, van Mill, Josine G, Mbarek, Hamdi
et al (show 64 more authors) (2016) Genetic variants in <i>RBFOX3</i> are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10). pp. 1488-1495.


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.


Teumer, Alexander, Li, Yong, Ghasemi, Sahar, Prins, Bram P, Wuttke, Matthias, Hermle, Tobias, Giri, Ayush, Sieber, Karsten B, Qiu, Chengxiang, Kirsten, Holger
et al (show 176 more authors) (2019) Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. NATURE COMMUNICATIONS, 10 (1). 4130-.


Rothwell, Simon, Cooper, Robert G ORCID: 0000-0001-8337-9973, Lundberg, Ingrid E, Gregersen, Peter K, Hanna, Michael G, Machado, Pedro M, Herbert, Megan K, Pruijn, Ger JM, Lilleker, James B, Roberts, Mark
et al (show 22 more authors) (2017) Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum. ARTHRITIS & RHEUMATOLOGY, 69 (5). pp. 1090-1099.


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-.


Zillikens, M Carola, Demissie, Serkalem, Hsu, Yi-Hsiang, Yerges-Armstrong, Laura M, Chou, Wen-Chi, Stolk, Lisette, Livshits, Gregory, Broer, Linda, Johnson, Toby, Koller, Daniel L
et al (show 183 more authors) (2017) Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. NATURE COMMUNICATIONS, 8 (1). 80-.


Zillikens, M Carola, Demissie, Serkalem, Hsu, Yi-Hsiang, Yerges-Armstrong, Laura M, Chou, Wen-Chi, Stolk, Lisette, Livshits, Gregory, Broer, Linda, Johnson, Toby, Koller, Daniel L
et al (show 183 more authors) (2017) Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (vol 8, 80, 2017). NATURE COMMUNICATIONS, 8 (1). 1414-.


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 287 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). pp. 375-400.


Flannick, Jason, Thorleifsson, Gudmar, Beer, Nicola L, Jacobs, Suzanne BR, Grarup, Niels, Burtt, Noel P, Mahajan, Anubha, Fuchsberger, Christian, Atzmon, Gil, Benediktsson, Rafn
et al (show 70 more authors) (2014) Loss-of-function mutations in <i>SLC30A8</i> protect against type 2 diabetes. NATURE GENETICS, 46 (4). 357-+.


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.


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). 2542-.


Bentley, Amy R, Sung, Yun J, Brown, Michael R, Winkler, Thomas W, Kraja, Aldi T, Ntalla, Ioanna, Schwander, Karen, Chasman, Daniel I, Lim, Elise, Deng, Xuan
et al (show 291 more authors) (2019) Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. NATURE GENETICS, 51 (4). 636-+.


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+.


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-.


Wuttke, Matthias, Li, Yong, Li, Man, Sieber, Karsten B, Feitosa, Mary F, Gorski, Mathias, Tin, Adrienne, Wang, Lihua, Chu, Audrey Y, Hoppmann, Anselm
et al (show 318 more authors) (2019) A catalog of genetic loci associated with kidney function from analyses of a million individuals. NATURE GENETICS, 51 (6). 957-+.


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-+.


Zeng, Lingyao, Moser, Sylvain, Mirza-Schreiber, Nazanin, Lamina, Claudia, Coassin, Stefan, Nelson, Christopher P, Annilo, Tarmo, Franzen, Oscar, Kleber, Marcus E, Mack, Salome
et al (show 25 more authors) (2022) <i>Cis</i>-epistasis at the <i>LPA</i> locus and risk of cardiovascular diseases. CARDIOVASCULAR RESEARCH, 118 (4). pp. 1088-1102.

This list was generated on Sun Apr 21 10:55:49 2024 BST.