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Number of items: 102.


Parra, Esteban J, Mazurek, Andrew, Gignoux, Christopher R, Sockell, Alexandra, Agostino, Michael, Morris, Andrew P, Petty, Lauren E, Hanis, Craig L, Cox, Nancy J, Valladares-Salgado, Adan
et al (show 2 more authors) (2017) Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the <i>BUD13</i>/<i>ZNF259</i>/<i>APOA5</i> region and fine mapping points to rs964184 as the main driver of the association signal. PLOS ONE, 12 (2). e0172880-.


Sapkota, Yadav, De Vivo, Immaculata, Steinthorsdottir, Valgerdur, Fassbender, Amelie, Bowdler, Lisa, Buring, Julie E, Edwards, Todd L, Jones, Sarah, Dorien, O, Peterse, Danielle
et al (show 15 more authors) (2017) Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry. SCIENTIFIC REPORTS, 7 (1). 11380-.


Thompson, Andrew ORCID: 0000-0002-7087-9415, King, Katharine, Morris, Andrew P and Pirmohamed, Munir ORCID: 0000-0002-7534-7266
(2021) Assessing the impact of alcohol consumption on the genetic contribution to mean corpuscular volume. HUMAN MOLECULAR GENETICS, 30 (21). pp. 2040-2051.


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-.


Zondervan, Krina T, Rahmioglu, Nilufer, Morris, Andrew P, Nyholt, Dale R, Montgomery, Grant W, Becker, Christian M and Missmer, Stacey A
(2016) Beyond Endometriosis Genome-Wide Association Study: From Genomics to Phenomics to the Patient. SEMINARS IN REPRODUCTIVE MEDICINE, 34 (4). pp. 242-254.


Doerr, Marcus, Hamburg, Naomi M, Mueller, Christian, Smith, Nicholas L, Gustafsson, Stefan, Lehtimaeki, Terho, Teumer, Alexander, Zeller, Tanja, Li, Xiaohui, Lind, Lars
et al (show 21 more authors) (2019) Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation. CIRCULATION-GENOMIC AND PRECISION MEDICINE, 12 (2). e002409-.


Fryett, James J, Inshaw, Jamie, Morris, Andrew P and Cordell, Heather J
(2018) Comparison of methods for transcriptome imputation through application to two common complex diseases. , England.


Fryett, James J ORCID: 0000-0003-3139-5466, Inshaw, Jamie, Morris, Andrew P and Cordell, Heather J
(2018) Comparison of methods for transcriptome imputation through application to two common complex diseases. European Journal of Human Genetics, 26 (11). pp. 1658-1667.


Windholz, Jan, Kovacs, Peter, Schlicke, Marina, Franke, Christin, Mahajan, Anubha, Morris, Andrew P, Lemke, Johannes R, Klammt, Juergen, Kiess, Wieland, Schoeneberg, Torsten
et al (show 2 more authors) (2017) Copy number variations in "classical" obesity candidate genes are not frequently associated with severe early-onset obesity in children. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 30 (5). pp. 507-515.


van der Laan, Sander W, Fall, Tove, Soumare, Aicha, Teumer, Alexander, Sedaghat, Sanaz, Baumert, Jens, Zabaneh, Delilah, van Setten, Jessica, Isgum, Ivana, Galesloot, Tessel E
et al (show 62 more authors) (2016) Cystatin C and Cardiovascular Disease A Mendelian Randomization Study. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 68 (9). pp. 934-945.


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.


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.


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). pp. 379-384.


Syed, Hamzah, Jorgensen, Andrea L ORCID: 0000-0002-6977-9337 and Morris, Andrew P
(2016) Evaluation of methodology for the analysis of 'time-to-event' data in pharmacogenomic genome-wide association studies. PHARMACOGENOMICS, 17 (8). pp. 907-915.


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 217 more authors) (2017) Exome-wide association study of plasma lipids in &gt;300,000 individuals. NATURE GENETICS, 49 (12). 1758-+.


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.


Thompson, Andrew ORCID: 0000-0002-7087-9415, Cook, James, Choquet, Hélène, Jorgenson, Eric, Yin, Jie, Kinnunen, Tarja, Barclay, Jeff, Morris, Andrew P and Pirmohamed, Munir ORCID: 0000-0002-7534-7266
(2020) Functional validity, role, and implications of heavy alcohol consumption genetic loci. Science Advances, 6 (3). eaay5034-eaay5034.


Tyrrell, Jessica, Richmond, Rebecca C, Palmer, Tom M, Feenstra, Bjarke, Rangarajan, Janani, Metrustry, Sarah, Cavadino, Alana, Paternoster, Lavinia, Armstrong, Loren L, De Silva, N Maneka G
et al (show 54 more authors) (2016) Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 315 (11). pp. 1129-1140.


Evangelou, Evangelos, Warren, Helen R, Mosen-Ansorena, David, Mifsu, Borbala, Pazoki, Raha, Gao, He, Ntritsos, Georgios, Dimou, Niki, Cabrer, Claudia P, Karaman, Ibrahim
et al (show 271 more authors) (2018) Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics, 50 (10). pp. 1412-1425.


Lind, Lars, Ng, Esther, Ingelsson, Erik, Lindgren, Cecilia, Salihovic, Samira, van Bavel, Bert, Mahajan, Anubha, Lampa, Erik, Morris, Andrew P and Lind, P Monica
(2017) Genetic and methylation variation in the CYP2B6 gene is related to circulating <i>p</i>,<i>p</i>′-dde levels in a population-based sample. ENVIRONMENT INTERNATIONAL, 98. pp. 212-218.


Lacaze, Paul, Ronaldson, Kathlyn J, Zhang, Eunice J ORCID: 0000-0003-1813-2207, Alfirevic, Ana ORCID: 0000-0002-2801-9817, Shah, Hardik, Newman, Leah, Strahl, Maya, Smith, Melissa, Bousman, Chad, Francis, Ben
et al (show 8 more authors) (2020) Genetic associations with clozapine-induced myocarditis in patients with schizophrenia. TRANSLATIONAL PSYCHIATRY, 10 (1). 37-.


Gusarova, Viktoria, O'Dushlaine, Colm, Teslovich, Tanya M, Benotti, Peter N, Mirshahi, Tooraj, Gottesman, Omri, Van Hout, Cristopher V, Murray, Michael F, Mahajan, Anubha, Nielsen, Jonas B
et al (show 71 more authors) (2018) Genetic inactivation of <i>ANGPTL4</i> improves glucose homeostasis and is associated with reduced risk of diabetes. NATURE COMMUNICATIONS, 9 (1). 2252-.


Sakornsakolpat, Phuwanat, Prokopenko, Dmitry, Lamontagne, Maxime, Reeve, Nicola F, Guyatt, Anna L, Jackson, Victoria E, Shrine, Nick, Qiao, Dandi, Bartz, Traci M, Kim, Deog Kyeom
et al (show 146 more authors) (2019) Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. NATURE GENETICS, 51 (3). 494-+.


Nolte, Ilja M, Munoz, M Loretto, Tragante, Vinicius, Amare, Azmeraw T, Jansen, Rick, Vaez, Ahmad, von der Heyde, Benedikt, Avery, Christy L, Bis, Joshua C, Dierckx, Bram
et al (show 154 more authors) (2017) Genetic loci associated with heart rate variability and their effects on cardiac disease risk. NATURE COMMUNICATIONS, 8 (1). 15805-.


Painter, Jodie N, O'Mara, Tracy A, Morris, Andrew P, Cheng, Timothy HT, Gorman, Maggie, Martin, Lynn, Hodson, Shirley, Jones, Angela, Martin, Nicholas G, Gordon, Scott
et al (show 66 more authors) (2018) Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. CANCER MEDICINE, 7 (5). pp. 1978-1987.


Rahmioglu, Nilufer, Nyholt, Dale R, Morris, Andrew P, Missmer, Stacey A, Montgomery, Grant W and Zondervan, Krina T
(2014) Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. HUMAN REPRODUCTION UPDATE, 20 (5). pp. 702-716.


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.


Marklund, Matti, Morris, Andrew P, Mahajan, Anubha, Ingelsson, Erik, Lindgren, Cecilia M, Lind, Lars and Riserus, Ulf
(2018) Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity. NUTRIENTS, 10 (11). E1791-.


Allen, Richard J, Guillen-Guio, Beatriz, Oldham, Justin M, Ma, Shwu-Fan, Dressen, Amy, Paynton, Megan L, Kraven, Luke M, Obeidat, Ma'en, Li, Xuan, Ng, Michael
et al (show 56 more authors) (2020) Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 201 (5). pp. 564-574.


Walford, Geoffrey A, Gustafsson, Stefan, Rybin, Denis, Stancakova, Alena, Chen, Han, Liu, Ching-Ti, Hong, Jaeyoung, Jensen, Richard A, Rice, Ken, Morris, Andrew P
et al (show 69 more authors) (2016) Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies <i>BCL2</i> and <i>FAM19A2</i> as Novel Insulin Sensitivity Loci. DIABETES, 65 (10). pp. 3200-3211.


Bourgeois, Stephane, Carr, Daniel F, Musumba, Crispin O, Penrose, Alexander, Esume, Celestine, Morris, Andrew P, Jorgensen, Andrea L ORCID: 0000-0002-6977-9337, Zhang, J Eunice ORCID: 0000-0003-1813-2207, Pritchard, D Mark ORCID: 0000-0001-7971-3561, Deloukas, Panos
et al (show 1 more authors) (2021) Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration. EBioMedicine, 74. p. 103728.


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 90 more authors) (2017) Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for <i>RBPMS</i> in Erythropoiesis. AMERICAN JOURNAL OF HUMAN GENETICS, 100 (1). pp. 51-63.


Shah, Sonia, Henry, Albert, Roselli, Carolina, Lin, Honghuang, Sveinbjornsson, Gardar, Fatemifar, Ghazaleh, Hedman, Asa K, Wilk, Jemma B, Morley, Michael P, Chaffin, Mark D
et al (show 194 more authors) (2020) Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nature Communications, 11 (1). 163-.


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-.


Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Brandler, William
et al (show 35 more authors) (2019) Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY, 9 (1). 77-.


Chen, Ji, Sun, Meng, Adeyemo, Adebowale, Pirie, Fraser, Carstensen, Tommy, Pomilla, Cristina, Doumatey, Ayo P, Chen, Guanjie, Young, Elizabeth H, Sandhu, Manjinder
et al (show 7 more authors) (2019) Genome-wide association study of type 2 diabetes in Africa. DIABETOLOGIA, 62 (7). pp. 1204-1211.


Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Honbolygo, Ferenc
et al (show 39 more authors) (2021) Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY, 26 (7). pp. 3004-3017.


Uimari, Outi, Rahmioglu, Nilufer, Nyholt, Dale R, Vincent, Katy, Missmer, Stacey A, Becker, Christian, Morris, Andrew P, Montgomery, Grant W and Zondervan, Krina T
(2017) Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis. HUMAN REPRODUCTION, 32 (4). pp. 780-793.


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-.


Turner, Richard M ORCID: 0000-0002-7315-679X, Fontana, Vanessa ORCID: 0000-0002-0146-9113, Zhang, Jieying E ORCID: 0000-0003-1813-2207, Carr, Daniel, Yin, Peng, FitzGerald, Richard, Morris, Andrew P and Pirmohamed, Munir ORCID: 0000-0002-7534-7266
(2020) A Genome‐wide Association Study of Circulating Levels of Atorvastatin and Its Major Metabolites. Clinical Pharmacology and Therapeutics, 108 (2). pp. 287-297.


Cook, James P, Mahajan, Anubha and Morris, Andrew P
(2017) Guidance for the utility of linear models in meta-analysis of genetic association studies of binary phenotypes. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (2). pp. 240-245.


Strawbridge, Rona J, Silveira, Angela, den Hoed, Marcel, Gustafsson, Stefan, Luan, Jian'an, Rybin, Denis, Dupuis, Josee, Li-Gao, Ruifang, Kavousi, Maryam, Dehghan, Abbas
et al (show 38 more authors) (2017) Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation. ATHEROSCLEROSIS, 266. pp. 196-204.


Loh, Marie, Zhang, Weihua, Ng, Hong Kiat, Schmid, Katharina, Lamri, Amel, Tong, Lin, Ahmad, Meraj, Lee, Jung-Jin, Ng, Maggie CY, Petty, Lauren E
et al (show 37 more authors) (2022) Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. COMMUNICATIONS BIOLOGY, 5 (1). 329-.


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-.


Pervjakova, Natalia, Kasela, Silva, Morris, Andrew P, Kals, Mart, Metspalu, Andres, Lindgren, Cecilia M, Salumets, Andres and Magi, Reedik
(2016) Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues. EPIGENOMICS, 8 (6). pp. 789-799.


Mitt, Mario, Kals, Mart, Parn, Kalle, Gabriel, Stacey B, Lander, Eric S, Palotie, Aarno, Ripatti, Samuli, Morris, Andrew P, Metspalu, Andres, Esko, Tonu
et al (show 2 more authors) (2016) Improved Imputation Accuracy of Rare and Low-Frequency Genetic Variants Using Population-Specific High-Coverage Whole-Genome Sequencing Data Based Imputation Reference Panel. HUMAN HEREDITY, 81 (4). p. 235.


Mitt, Mario, Kals, Mart, Parn, Kalle, Gabriel, Stacey B, Lander, Eric S, Palotie, Aarno, Ripatti, Samuli, Morris, Andrew P, Metspalu, Andres, Esko, Tonu
et al (show 2 more authors) (2017) Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (7). pp. 869-876.


Prins, Bram P, Abbasi, Ali, Wong, Anson, Vaez, Ahmad, Nolte, Ilja, Franceschini, Nora, Stuart, Philip E, Achury, Javier Guterriez, Mistry, Vanisha, Bradfield, Jonathan P
et al (show 37 more authors) (2016) Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study. PLOS MEDICINE, 13 (6). e1001976-.


Turner, Richard M ORCID: 0000-0002-7315-679X, Fontana, Vanessa ORCID: 0000-0002-0146-9113, FitzGerald, Richard, Morris, Andrew P and Pirmohamed, Munir ORCID: 0000-0002-7534-7266
(2020) Investigating the clinical factors and comedications associated with circulating levels of atorvastatin and its major metabolites in secondary prevention. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 86 (1). pp. 62-74.


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.


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.


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.


Kaakinen, Marika, Magi, Reedik, Fischer, Krista, Heikkinen, Jani, Jarvelin, Marjo-Riitta, Morris, Andrew P and Prokopenko, Inga
(2017) MARV: a tool for genome-wide multi-phenotype analysis of rare variants. BMC BIOINFORMATICS, 18 (1). 110-.


Folkersen, Lasse, Fauman, Eric, Sabater-Lleal, Maria, Strawbridge, Rona J, Franberg, Mattias, Sennblad, Bengt, Baldassarre, Damiano, Veglia, Fabrizio, Humphries, Steve E, Rauramaa, Rainer
et al (show 23 more authors) (2017) Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease. PLOS GENETICS, 13 (4). e1006706-.


Warrington, Nicole M, Beaumont, Robin N, Horikoshi, Momoko, Day, Felix R, Helgeland, Oyvind, Laurin, Charles, Bacelis, Jonas, Peng, Shouneng, Hao, Ke, Feenstra, Bjarke
et al (show 198 more authors) (2019) Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. NATURE GENETICS, 51 (5). 804-+.


Jiang, Jiyang, Thalamuthu, Anbupalam, Ho, Jennifer E, Mahajan, Anubha, Ek, Weronica E, Brown, David A, Breit, Samuel N, Wang, Thomas J, Gyllensten, Ulf, Chen, Ming-Huei
et al (show 13 more authors) (2018) A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood. FRONTIERS IN GENETICS, 9 (MAR). 97-.


Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P, Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E, Zhang, Futao, Edwards, Todd L, Jones, Sarah
et al (show 31 more authors) (2017) Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. NATURE COMMUNICATIONS, 8 (1). 15539-.


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. p. 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-.


Pulit, Sara L, Stoneman, Charli, Morris, Andrew P, Wood, AndrewR, Glastonbury, Craig A, Tyrrell, Jessica, Yengo, Loic, Ferreira, Teresa, Marouli, Eirini, Ji, Yingjie
et al (show 12 more authors) (2019) Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. HUMAN MOLECULAR GENETICS, 28 (1). pp. 166-174.


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-+.


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.


Cook, James P and Morris, Andrew P
(2016) Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibility. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (8). pp. 1175-1180.


Shrine, Nick, Guyatt, Anna L, Erzurumluoglu, A Mesut, Jackson, Victoria E, Hobbs, Brian D, Melbourne, Carl A, Batini, Chiara, Fawcett, Katherine A, Song, Kijoung, Sakornsakolpat, Phuwanat
et al (show 99 more authors) (2019) New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. NATURE GENETICS, 51 (3). 481-+.


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-.


Wain, Louise V, Vaez, Ahmad, Jansen, Rick, Joehanes, Roby, van der Most, Peter J, Erzurumluoglu, A Mesut, O'Reilly, Paul F, Cabrera, Claudia P, Warren, Helen R, Rose, Lynda M
et al (show 236 more authors) (2017) Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. HYPERTENSION, 70 (3). E4-+.


Floyd, James S, Bloch, Katarzyna M, Brody, Jennifer A, Maroteau, Cyrielle, Siddiqui, Moneeza K, Gregory, Richard, Carr, Daniel F, 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). e0218115-.


Morris, Andrew P
(2018) Progress in defining the genetic contribution to type 2 diabetes susceptibility. CURRENT OPINION IN GENETICS & DEVELOPMENT, 50. pp. 41-51.


Morris, Andrew P ORCID: 0000-0002-6805-6014
(2018) Progress in defining the genetic contribution to type 2 diabetes susceptibility. Current opinion in genetics & development, 50. pp. 41-51.


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 (1). pp. 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, 51 (3). 452-+.


Shungin, Dmitry, Deng, Wei Q, Varga, Tibor V, Luan, Jian'an, Mihailov, Evelin, Metspalu, Andres, Morris, Andrew P, Forouhi, Nita G, Lindgren, Cecilia, Magnusson, Patrik KE
et al (show 20 more authors) (2017) Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions. PLOS GENETICS, 13 (6). e1006812-.


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 363 more authors) (2017) Rare and low-frequency coding variants alter human adult height. NATURE, 542 (7640). pp. 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+.


Small, Kerrin S, Todorcevic, Marijana, Civelek, Mete, Moustafa, Julia S El-Sayed, Wang, Xiao, Simon, Michelle M, Fernandez-Tajes, Juan, Mahajan, Anubha, Horikoshi, Momoko, Hugill, Alison
et al (show 27 more authors) (2018) Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition. Nature Genetics, 50 (4). pp. 572-580.


Magi, Reedik, Suleimanov, Yury V, Clarke, Geraldine M, Kaakinen, Marika, Fischer, Krista, Prokopenko, Inga and Morris, Andrew P
(2017) SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes. BMC BIOINFORMATICS, 18 (1). 25-.


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-.


Nicoletti, Paola, Barrett, Sarah, McEvoy, Laurence ORCID: 0000-0002-2169-6735, Daly, Ann K, Aithal, Guruprasad, Lucena, M Isabel, Andrade, Raul J, Wadelius, Mia, Hallberg, Pär, Stephens, Camilla
et al (show 21 more authors) (2019) Shared genetic risk factors across carbamazepine-induced hypersensitivity reactions. Clinical pharmacology and therapeutics, 106 (5). pp. 1028-1036.


Syed, Hamzah, Jorgensen, Andrea L ORCID: 0000-0002-6977-9337 and Morris, Andrew P
(2016) SurvivalGWAS_Power: a user friendly tool for power calculations in pharmacogenetic studies with "time to event" outcomes. BMC BIOINFORMATICS, 17 (1). 523-.


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.


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 105 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). pp. 56-75.


Morris, Andrew P, Le, Thu H, Wu, Haojia, Akbarov, Artur, van der Most, Peter J, Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J, Nadkarni, Girish N
et al (show 62 more authors) (2019) Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. Nature communications, 10 (1). p. 29.


Magi, Reedik, Horikoshi, Momoko, Sofer, Tamar, Mahajan, Anubha, Kitajima, Hidetoshi, Franceschini, Nora, McCarthy, Mark I and Morris, Andrew P
(2017) Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution. HUMAN MOLECULAR GENETICS, 26 (18). pp. 3639-3650.


Asimit, Jennifer L, Hatzikotoulas, Konstantinos, McCarthy, Mark, Morris, Andrew P and Zeggini, Eleftheria
(2016) Trans-ethnic study design approaches for fine-mapping. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (9). pp. 1330-1336.


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 48 more authors) (2016) Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. HUMAN MOLECULAR GENETICS, 25 (10). pp. 2070-2081.


Rahmioglu, Nilufer, Drong, Alexander W, Lockstone, Helen, Tapmeier, Thomas, Hellner, Karin, Saare, Merli, Laisk-Podar, Triin, Dew, Christine, Tough, Emily, Nicholson, George
et al (show 5 more authors) (2017) Variability of genome-wide DNA methylation and mRNA expression profiles in reproductive and endocrine disease related tissues. EPIGENETICS, 12 (10). pp. 897-908.


Crawford, Andrew A, Bankier, Sean, Altmaier, Elisabeth, Barnes, Catriona LK, Clark, David W, Ermel, Raili, Friedrich, Nele, van der Harst, Pim, Joshi, Peter K, Karhunen, Ville
et al (show 30 more authors) (2021) Variation in the <i>SERPINA6/SERPINA1</i> locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease. JOURNAL OF HUMAN GENETICS, 66 (6). pp. 625-636.


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.


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-+.


Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Moller, Peter L, Stefansdottir, Lilja, Galarneau, Genevieve, Turman, Constance, Danning, Rebecca, Law, Matthew H, Sapkota, Yadav
et al (show 123 more authors) (2023) The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. NATURE GENETICS, 55 (3). 423-+.


Chen, Xu, Gustafsson, Stefan, Whitington, Thomas, Borne, Yan, Lorentzen, Erik, Sun, Jitong, Almgren, Peter, Su, Jun, Karlsson, Robert, Song, Jie
et al (show 19 more authors) (2018) A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia. HUMAN MOLECULAR GENETICS, 27 (10). pp. 1809-1818.


Scott, Robert A, Freitag, Daniel F, Li, Li, Chu, Audrey Y, Surendran, Praveen, Young, Robin, Grarup, Niels, Stancakova, Alena, Chen, Yuning, Varga, Tibor V
et al (show 129 more authors) (2016) A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease. SCIENCE TRANSLATIONAL MEDICINE, 8 (341). 341ra76-.


Ried, Janina S, Jeff, Janina M, Chu, Audrey Y, Bragg-Gresham, Jennifer L, van Dongen, Jenny, Huffman, Jennifer E, Ahluwalia, Tarunveer S, Cadby, Gemma, Eklund, Niina, Eriksson, Joel
et al (show 266 more authors) (2016) A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. NATURE COMMUNICATIONS, 7 (1). 13357-.


Kaakinen, Marika, Magi, Reedik, Fischer, Krista, Heikkinen, Jani, Jarvelin, Marjo-Riitta, Morris, Andrew P and Prokopenko, Inga
(2017) A rare-variant test for high-dimensional data. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (8). pp. 988-994.


Asimit, Jennifer L, Payne, Felicity, Morris, Andrew P, Cordell, Heather J and Barroso, Ines
(2017) A two-stage inter-rater approach for enrichment testing of variants associated with multiple traits. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (3). pp. 341-349.

This list was generated on Sat Oct 14 03:46:24 2023 BST.