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Number of items: 22.


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.


Jun, Goo, Manning, Alisa, Almeida, Marcio, Zawistowski, Matthew, Wood, Andrew R, Teslovich, Tanya M, Fuchsberger, Christian, Feng, Shuang, Cingolani, Pablo, Gaulton, Kyle J
et al (show 64 more authors) (2018) Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 115 (2). 379 - 384.


Liu, Dajiang J, Peloso, Gina M, Yu, Haojie, Butterworth, Adam S, Wang, Xiao, Mahajan, Anubha, Saleheen, Danish, Emdin, Connor, Alam, Dewan, Alves, Alexessander Couto
et al (show 222 more authors) (2017) Exome-wide association study of plasma lipids in > 300,000 individuals. NATURE GENETICS, 49 (12). 1758 - +.


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.


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.


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 208 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).


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 72 more authors) (2014) Loss-of-function mutations in SLC30A8 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 AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. DIABETES, 66 (7). 2019 - 2032.


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 - ?.


Malik, Rainer, Chauhan, Ganesh, Traylor, Matthew, Sargurupremraj, Muralidharan, Okada, Yukinori, Mishra, Aniket, Rutten-Jacobs, Loes, Giese, Anne-Katrin, van der Laan, Sander W, Gretarsdottir, Solveig
et al (show 176 more authors) (2018) Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. NATURE GENETICS, 50 (4). 524 - 537.


Kraja, Aldi T, Cook, James P, Warren, Helen R, Surendran, Praveen, Liu, Chunyu, Evangelou, Evangelos, Manning, Alisa K, Grarup, Niels, Drenos, Fotios, Sim, Xueling
et al (show 135 more authors) (2017) New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475000 Individuals. CIRCULATION-CARDIOVASCULAR GENETICS, 10 (5).


Kraja, Aldi T, Chasman, Daniel I, North, Kari E, Reiner, Alexander P, Yanek, Lisa R, Kilpeläinen, Tuomas O, Smith, Jennifer A, Dehghan, Abbas, Dupuis, Josée, Johnson, Andrew D
et al (show 58 more authors) (2014) Pleiotropic genes for metabolic syndrome and inflammation. Molecular Genetics and Metabolism, 112 (4). 317 - 338.


Turcot, Valerie, Lu, Yingchang, Highland, Heather M, Schurmann, Claudia, Justice, Anne E, Fine, Rebecca S, Bradfield, Jonathan P, Esko, Tonu, Giri, Ayush, Graff, Mariaelisa
et al (show 401 more authors) (2018) Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. NATURE GENETICS, 50. 26 - 41.


Justice, Anne E, Karaderi, Tugce, Highland, Heather M, Young, Kristin L, Graff, Mariaelisa, Lu, Yingchang, Turcot, Valérie, Auer, Paul L, Fine, Rebecca S, Guo, Xiuqing
et al (show 279 more authors) (2019) Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nature genetics.


Marouli, Eirini, Graff, Mariaelisa, Medina-Gomez, Carolina, Lo, Ken Sin, Wood, Andrew R, Kjaer, Troels R, Fine, Rebecca S, Lu, Yingchang, Schurmann, Claudia, Highland, Heather M
et al (show 372 more authors) (2017) Rare and low-frequency coding variants alter human adult height. NATURE, 542 (7640). 186 - 190.


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.


Liu, Ching-Ti, Raghavan, Sridharan, Maruthur, Nisa, Kabagambe, Edmond Kato, Hong, Jaeyoung, Ng, Maggie CY, Hivert, Marie-France, Lu, Yingchang, An, Ping, Bentley, Amy R
et al (show 111 more authors) (2016) Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin. AMERICAN JOURNAL OF HUMAN GENETICS, 99 (1). 56 - 75.


Horikoshi, Momoko, Pasquali, Lorenzo, Wiltshire, Steven, Huyghe, Jeroen R, Mahajan, Anubha, Asimit, Jennifer L, Ferreira, Teresa, Locke, Adam E, Robertson, Neil R, Wang, Xu
et al (show 49 more authors) (2016) Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. HUMAN MOLECULAR GENETICS, 25 (10). 2070 - 2081.


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 319 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 - +.

This list was generated on Tue Dec 1 19:44:00 2020 GMT.