Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Biobanks[original query] |
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Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus.
Nature communications 2023 2 14 (1): 668. Khunsriraksakul Chachrit, Li Qinmengge, Markus Havell, Patrick Matthew T, Sauteraud Renan, McGuire Daniel, Wang Xingyan, Wang Chen, Wang Lida, Chen Siyuan, Shenoy Ganesh, Li Bingshan, Zhong Xue, Olsen Nancy J, Carrel Laura, Tsoi Lam C, Jiang Bibo, Liu Dajiang |
| Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
American journal of human genetics 2011 Oct 89 (4): 529-42. Denny Joshua C, Crawford Dana C, Ritchie Marylyn D, Bielinski Suzette J, Basford Melissa A, Bradford Yuki, Chai High Seng, Bastarache Lisa, Zuvich Rebecca, Peissig Peggy, Carrell David, Ramirez Andrea H, Pathak Jyotishman, Wilke Russell A, Rasmussen Luke, Wang Xiaoming, Pacheco Jennifer A, Kho Abel N, Hayes M Geoffrey, Weston Noah, Matsumoto Martha, Kopp Peter A, Newton Katherine M, Jarvik Gail P, Li Rongling, Manolio Teri A, Kullo Iftikhar J, Chute Christopher G, Chisholm Rex L, Larson Eric B, McCarty Catherine A, Masys Daniel R, Roden Dan M, de Andrade Mari |
| Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Circulation 2013 Apr 127 (13): 1377-85. Ritchie Marylyn D, Denny Joshua C, Zuvich Rebecca L, Crawford Dana C, Schildcrout Jonathan S, Bastarache Lisa, Ramirez Andrea H, Mosley Jonathan D, Pulley Jill M, Basford Melissa A, Bradford Yuki, Rasmussen Luke V, Pathak Jyotishman, Chute Christopher G, Kullo Iftikhar J, McCarty Catherine A, Chisholm Rex L, Kho Abel N, Carlson Christopher S, Larson Eric B, Jarvik Gail P, Sotoodehnia Nona, , Manolio Teri A, Li Rongling, Masys Daniel R, Haines Jonathan L, Roden Dan |
| Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.
PloS one 2014 9 (12): e111301. Malinowski Jennifer R, Denny Joshua C, Bielinski Suzette J, Basford Melissa A, Bradford Yuki, Peissig Peggy L, Carrell David, Crosslin David R, Pathak Jyotishman, Rasmussen Luke, Pacheco Jennifer, Kho Abel, Newton Katherine M, Li Rongling, Kullo Iftikhar J, Chute Christopher G, Chisholm Rex L, Jarvik Gail P, Larson Eric B, McCarty Catherine A, Masys Daniel R, Roden Dan M, de Andrade Mariza, Ritchie Marylyn D, Crawford Dana |
| Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.
Molecular vision 2014 20 1281-95. Ritchie Marylyn D, Verma Shefali S, Hall Molly A, Goodloe Robert J, Berg Richard L, Carrell Dave S, Carlson Christopher S, Chen Lin, Crosslin David R, Denny Joshua C, Jarvik Gail, Li Rongling, Linneman James G, Pathak Jyoti, Peissig Peggy, Rasmussen Luke V, Ramirez Andrea H, Wang Xiaoming, Wilke Russell A, Wolf Wendy A, Torstenson Eric S, Turner Stephen D, McCarty Catherine |
| The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Dec 168 (8): 739-48. Mbarek Hamdi, Milaneschi Yuri, Fedko Iryna O, Hottenga Jouke-Jan, de Moor Marleen H M, Jansen Rick, Gelernter Joel, Sherva Richard, Willemsen Gonneke, Boomsma Dorret I, Penninx Brenda W, Vink Jacqueline |
| Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.
Circulation. Cardiovascular genetics 2017 Apr 10 (2): . Klarin Derek, Emdin Connor A, Natarajan Pradeep, Conrad Mark F, , Kathiresan Sek |
| Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thrombosis and haemostasis 2017 Feb . Heit John A, Armasu Sebastian M, McCauley Bryan M, Kullo Iftikhar J, Sicotte Hugues, Pathak Jyotishman, Chute Christopher G, Gottesman Omri, Bottinger Erwin P, Denny Joshua C, Roden Dan M, Li Rongling, Ritchie Marylyn D, de Andrade Mari |
| Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
Nature genetics 2018 09 50 (9): 1335-1341. Zhou Wei, Nielsen Jonas B, Fritsche Lars G, Dey Rounak, Gabrielsen Maiken E, Wolford Brooke N, LeFaive Jonathon, VandeHaar Peter, Gagliano Sarah A, Gifford Aliya, Bastarache Lisa A, Wei Wei-Qi, Denny Joshua C, Lin Maoxuan, Hveem Kristian, Kang Hyun Min, Abecasis Goncalo R, Willer Cristen J, Lee Seungge |
| Genome-wide association identifies a novel locus for delirium risk.
Neurobiology of aging 2018 Mar . McCoy Thomas H, Hart Kamber, Pellegrini Amelia, Perlis Roy |
| Genetic variants that associate with cirrhosis have pleiotropic effects on human traits.
Liver international : official journal of the International Association for the Study of the Liver 2019 Dec . Chen Vincent L, Chen Yanhua, Du Xiaomeng, Handelman Samuel K, Speliotes Elizabeth |
| Genome-wide Study Identifies Association between HLA-B55:01 and Self-Reported Penicillin Allergy.
American journal of human genetics 2020 Aug . Krebs Kristi, Bovijn Jonas, Zheng Neil, Lepamets Maarja, Censin Jenny C, Jürgenson Tuuli, Särg Dage, Abner Erik, Laisk Triin, Luo Yang, Skotte Line, Geller Frank, Feenstra Bjarke, Wang Wei, Auton Adam, , Raychaudhuri Soumya, Esko Tõnu, Metspalu Andres, Laur Sven, Roden Dan M, Wei Wei-Qi, Holmes Michael V, Lindgren Cecilia M, Phillips Elizabeth J, Mägi Reedik, Milani Lili, Fadista Jo |
| A genome-wide association study of polycystic ovary syndrome identified from electronic health records.
American journal of obstetrics and gynecology 2020 Apr . Zhang Yanfei, Ho Kevin, Keaton Jacob M, Hartzel Dustin N, Day Felix, Justice Anne E, Josyula Navya S, Pendergrass Sarah A, Actkins Ky'Era, Davis Lea K, Velez Edwards Digna R, Holohan Brody, Ramirez Andrea, Stanaway Ian B, Crosslin David R, Jarvik Gail P, Sleiman Patrick, Hakonarson Hakon, Williams Marc S, Lee Ming Ta Micha |
| Reproducible Genetic Risk Loci for Anxiety: Results From ~200,000 Participants in the Million Veteran Program.
The American journal of psychiatry 2020 03 177 (3): 223-232. Levey Daniel F, Gelernter Joel, Polimanti Renato, Zhou Hang, Cheng Zhongshan, Aslan Mihaela, Quaden Rachel, Concato John, Radhakrishnan Krishnan, Bryois Julien, Sullivan Patrick F, , Stein Murray |
| Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.
The pharmacogenomics journal 2020 11 21 (2): 174-189. Wenric Stephane, Jeff Janina M, Joseph Thomas, Yee Muh-Ching, Belbin Gillian M, Owusu Obeng Aniwaa, Ellis Stephen B, Bottinger Erwin P, Gottesman Omri, Levin Matthew A, Kenny Eimear |
| Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations.
Nature communications 2020 3 11 (1): 1467. Cole Joanne B, Florez Jose C, Hirschhorn Joel |
| The influence of rare variants in circulating metabolic biomarkers.
PLoS genetics 2020 3 16 (3): e1008605. Riveros-Mckay Fernando, Oliver-Williams Clare, Karthikeyan Savita, Walter Klaudia, Kundu Kousik, Ouwehand Willem H, Roberts David, Di Angelantonio Emanuele, Soranzo Nicole, Danesh John, , Wheeler Eleanor, Zeggini Eleftheria, Butterworth Adam S, Barroso In |
| Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study.
Cell reports. Medicine 2022 10 3 (10): 100776. Nethander Maria, Coward Eivind, Reimann Ene, Grahnemo Louise, Gabrielsen Maiken E, Wibom Carl, , Mägi Reedik, Funck-Brentano Thomas, Hoff Mari, Langhammer Arnulf, Pettersson-Kymmer Ulrika, Hveem Kristian, Ohlsson Cla |
| Gene-Based Analysis Reveals Sex-Specific Genetic Risk Factors of COPD.
AMIA ... Annual Symposium proceedings. AMIA Symposium 2022 3 2021 601-610. Joo Jaehyun, Himes Blan |
| Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank.
Cell reports. Medicine 2022 12 3 (12): 100855. Park Joseph, MacLean Matthew T, Lucas Anastasia M, Torigian Drew A, Schneider Carolin V, Cherlin Tess, Xiao Brenda, Miller Jason E, Bradford Yuki, Judy Renae L, , Verma Anurag, Damrauer Scott M, Ritchie Marylyn D, Witschey Walter R, Rader Daniel |
| Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity.
Cell genomics 2023 2 2 (12): 100212. Tsuo Kristin, Zhou Wei, Wang Ying, Kanai Masahiro, Namba Shinichi, Gupta Rahul, Majara Lerato, Nkambule Lethukuthula L, Morisaki Takayuki, Okada Yukinori, Neale Benjamin M, , Daly Mark J, Martin Alicia |
| Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics.
Cell genomics 2023 2 2 (10): 100181. Partanen Juulia J, Häppölä Paavo, Zhou Wei, Lehisto Arto A, Ainola Mari, Sutinen Eva, Allen Richard J, Stockwell Amy D, Leavy Olivia C, Oldham Justin M, Guillen-Guio Beatriz, Cox Nancy J, Hirbo Jibril B, Schwartz David A, Fingerlin Tasha E, Flores Carlos, Noth Imre, Yaspan Brian L, Jenkins R Gisli, Wain Louise V, Ripatti Samuli, Pirinen Matti, , , Laitinen Tarja, Kaarteenaho Riitta, Myllärniemi Marjukka, Daly Mark J, Koskela Jukka |
| Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
Nature communications 2023 1 14 (1): 157. Rämö Joel T, Kiiskinen Tuomo, Seist Richard, Krebs Kristi, Kanai Masahiro, Karjalainen Juha, Kurki Mitja, Hämäläinen Eija, Häppölä Paavo, Havulinna Aki S, Hautakangas Heidi, , Mägi Reedik, Palta Priit, Esko Tõnu, Metspalu Andres, Pirinen Matti, Karczewski Konrad J, Ripatti Samuli, Milani Lili, Stankovic Konstantina M, Mäkitie Antti, Daly Mark J, Palotie Aar |
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- Page last updated:Sep 18, 2023
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