Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 4447 Records) |
Query Trace: gwa[original query] |
---|
Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients. Scientific reports 2021 Aug 11 (1): 16013. Qu Jingchun, Qu Hui-Qi, Bradfield Jonathan P, Glessner Joseph T, Chang Xiao, Tian Lifeng, March Michael, Connolly John J, Roizen Jeffrey D, Sleiman Patrick M A, Hakonarson Hak |
Increasing sample diversity in psychiatric genetics - Introducing a new cohort of patients with schizophrenia and controls from Vietnam - Results from a pilot study. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2021 8 23 (3): 219-227. Nguyen V T, Braun A, Kraft J, Ta T M T, Panagiotaropoulou G M, Nguyen V P, Nguyen T H, Trubetskoy V, Le C T, Le T T H, Pham X T, Heuser-Collier I, Lam N H, Böge K, Hahne I M, Bajbouj M, Zierhut M M, Hahn E, Ripke |
Safe Linkage of Cohort and Population-Based Register Data in a Genomewide Association Study on Health Care Expenditure. Twin research and human genetics : the official journal of the International Society for Twin Studies 2021 7 24 (2): 103-109. de Zeeuw Eveline L, Voort Lykle, Schoonhoven Ruurd, Nivard Michel G, Emery Thomas, Hottenga Jouke-Jan, Willemsen Gonneke A H M, Dykstra Pearl A, Zarrabi Narges, Kartopawiro John D, Boomsma Dorret |
A genetic association study of tobacco withdrawal endophenotypes in African Americans. Experimental and clinical psychopharmacology 2021 Jul . Leventhal Adam M, Conti David V, Ray Lara A, Baurley James W, Bello Mariel S, Cho Junhan, Zhang Yi, Pester Mollie S, Lebovitz Lucas, Budiarto Arif, Mahesworo Bharuno, Pardamean Be |
Three genes associated with anterior and posterior cruciate ligament injury : a genome-wide association analysis. Bone & joint open 2021 Jun 2 (6): 414-421. Kim Stuart K, Nguyen Condor, Avins Andrew L, Abrams Geoffrey |
A generalized linear mixed model association tool for biobank-scale data.
![]() Nature genetics 2021 11 53 (11): 1616-1621. Jiang Longda, Zheng Zhili, Fang Hailing, Yang Ji |
Association Between SNPs in 1q32.2 and NSCL?±?P in Han Chinese Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2021 Nov 10556656211052837. Yin Bin, Shi Jia-Yu, Shi Bing, Zheng Qian, Jia Zhong-L |
Generalizability of GWA-Identified Genetic Risk Variants for Metabolic Traits to Populations from the Arabian Peninsula. Genes 2021 10 12 (10): . Hebbar Prashantha, Abu-Farha Mohamed, Abubaker Jehad, Channanath Arshad Mohamed, Al-Mulla Fahd, Thanaraj Thangavel Alphon |
Genome-wide analysis identifies gallstone-susceptibility loci including genes regulating gastrointestinal motility.
![]() Hepatology (Baltimore, Md.) 2021 Oct . Fairfield Cameron J, Drake Thomas M, Pius Riinu, Bretherick Andrew D, Campbell Archie, Clark David W, Fallowfield Jonathan A, Hayward Caroline, Henderson Neil C, Iakovliev Andrii, Joshi Peter K, Mills Nicholas L, Porteous David J, Ramachandran Prakash, Semple Robert K, Shaw Catherine A, Sudlow Cathie L W, Timmers Paul R H J, Wilson James F, Wigmore Stephen J, Spiliopoulou Athina, Harrison Ewen |
The Mediation Effects of Aluminum in Plasma and Dipeptidyl Peptidase Like Protein 6 (DPP6) Polymorphism on Renal Function via Genome-Wide Typing Association.
![]() International journal of environmental research and public health 2021 Oct 18 (19): . Chen Ting-Hao, Yang Chen-Cheng, Luo Kuei-Hau, Dai Chia-Yen, Chuang Yao-Chung, Chuang Hung- |
No evidence that vitamin D is able to prevent or affect the severity of COVID-19 in individuals with European ancestry: a Mendelian randomisation study of open data.
![]() BMJ nutrition, prevention & health 2021 7 4 (1): 42-48. Amin Hasnat A, Drenos Foti |
Role of PAX7 Gene rs766325 and rs4920520 Polymorphisms in the Etiology of Non-syndromic Cleft Lip and Palate: A Genetic Study. Global medical genetics 2022 7 9 (3): 208-211. Khan Mahamad Irfanulla, Cs Prashanth, Srinath Narasimhamur |
Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders.
![]() Translational psychiatry 2022 4 12 (1): 145. Okhuijsen-Pfeifer C, van der Horst M Z, Bousman C A, Lin B, van Eijk K R, Ripke S, Ayhan Y, Babaoglu M O, Bak M, Alink W, van Beek H, Beld E, Bouhuis A, Edlinger M, Erdogan I M, Ertu?rul A, Yoca G, Everall I P, Görlitz T, , Grootens K P, Gutwinski S, Hallikainen T, Jeger-Land E, de Koning M, Lähteenvuo M, Legge S E, Leucht S, Morgenroth C, Müderriso?lu A, Narang A, Pantelis C, Pardiñas A F, Oviedo-Salcedo T, Schneider-Thoma J, Schreiter S, Repo-Tiihonen E, Tuppurainen H, Veereschild M, Veerman S, de Vos M, Wagner E, Cohen D, Bogers J P A M, Walters J T R, Ya?c?o?lu A E Anil, Tiihonen J, Hasan A, Luykx J |
Increased expression of ORMDL3 in allergic asthma: a case control and in vitro study. The Journal of asthma : official journal of the Association for the Care of Asthma 2022 3 1-10. Nowakowska Joanna, Olechnowicz Anna, Langwi?ski Wojciech, Koteluk Oliwia, Lema?ska ?aneta, Jó?wiak Kacper, Kami?ski Kacper, ?osiewski Wojciech, Stegmayr John, Wagner Darcy, Alsafadi Hani N, Lindstedt Sandra, Dziuba Maria, Bielicka Antonina, Graczyk Zuzanna, Szczepankiewicz Aleksand |
Association between host genetics of sheep and the rumen microbial composition. Tropical animal health and production 2022 2 54 (2): 109. Mani Sinalo, Aiyegoro Olayinka Ayobami, Adeleke Matthew Adekun |
Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors.
![]() The Journal of biological chemistry 2022 11 298 (12): 102706. Moore Amy, Busch Michael P, Dziewulska Karolina, Francis Richard O, Hod Eldad A, Zimring James C, D'Alessandro Angelo, Page Grier |
A Genome-Wide Association Study Reveals Two Genetic Markers for Chondromalacia.
![]() Cartilage 0 13 (3): 19476035221121790. Kim Stuart K, Kahn Condor, Abrams Geoffrey |
An extremes of phenotype approach confirms significant genetic heterogeneity in patients with ulcerative colitis. Journal of Crohn's & colitis 2022 Sep . Mortlock Sally, Lord Anton, Montgomery Grant, Zakrzewski Martha, Simms Lisa A, Krishnaprasad Krupa, Hanigan Katherine, Doecke James D, Walsh Alissa, Lawrance Ian C, Bampton Peter A, Andrews Jane M, Mahy Gillian, Connor Susan J, Sparrow Miles P, Bell Sally, Florin Timothy H, Begun Jakob, Gearry Richard B, Radford-Smith Graham |
Nidogen-1 could play a role in diabetic kidney disease development in type 2 diabetes: a genome-wide association meta-analysis.
![]() Human genomics 2022 10 16 (1): 47. Khattab Ahmed, Torkamani A |
Genome-Wide Association Analysis of Over 170,000 Individuals from the UK Biobank Identifies Seven Loci Associated with Dietary Approaches to Stop Hypertension (DASH) Diet.
![]() Nutrients 2022 10 14 (20): . Mompeo Olatz, Freidin Maxim B, Gibson Rachel, Hysi Pirro G, Christofidou Paraskevi, Segal Eran, Valdes Ana M, Spector Tim D, Menni Cristina, Mangino Massi |
Auditory oddball hypoactivation in schizophrenia. Psychiatry research. Neuroimaging 2023 9 335 111710. Soichiro Nakahara, Alie G Male, Jessica A Turner, Vince D Calhoun, Kelvin O Lim, Bryon A Mueller, Juan R Bustillo, Daniel S O'Leary, James Voyvodic, Aysenil Belger, Adrian Preda, Daniel H Mathalon, Judith M Ford, Guia Guffanti, Fabio Macciardi, Steven G Potkin, Theo G M Van E |
Genome-wide study of genetic polymorphisms predictive for outcome from first-line oxaliplatin-based chemotherapy in colorectal cancer patients. International journal of cancer 2023 8 . Hanla A Park, Dominic Edelmann, Federico Canzian, Petra Seibold, Tabitha A Harrison, Xinwei Hua, Qian Shi, Allison Silverman, Axel Benner, Angelica Macauda, Martin Schneider, Richard M Goldberg, Steven R Alberts, Michael Hoffmeister, Hermann Brenner, Andrew T Chan, Ulrike Peters, Polly A Newcomb, Jenny Chang-Clau |
Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study. The Lancet regional health. Southeast Asia 2023 7 14 100190. Esha Bhattacharjee, Ramachandran Thiruvengadam, Ayushi, Chitrarpita Das, , Nitya Wadhwa, Uma Chandra Mouli Natchu, Pallavi Kshetrapal, Shinjini Bhatnagar, Partha Pratim Majumder, Arindam Mait |
A polygenic risk score for predicting racial and genetic susceptibility to prurigo nodularis. The Journal of investigative dermatology 2023 5 . Chirag Vasavda, Guihong Wan, Mindy D Szeto, Melika Marani, Nishadh Sutaria, Ahmad Rajeh, Chenyue Lu, Kevin K Lee, Nga T T Nguyen, Waleed Adawi, Junwen Deng, Varsha Parthasarathy, Zachary A Bordeaux, Matthew T Taylor, Martin P Alphonse, Madan M Kwatra, Sewon Kang, Yevgeniy R Semenov, Alexander Gusev, Shawn G Kwat |
Genetic variants associated with white blood cell count amongst individuals with sickle cell disease. British journal of haematology 2024 9 . Mina Cintho Ozahata, Yuelong Guo, Isabel Gomes, Barbara Malta, André Belisário, Luiz Amorim, Dahra Teles, Miriam Park, Shannon Kelly, Ester C Sabino, Grier P Page, Brian Custer, Carla L Dinardo, |
Association of PHACTR1 with Coronary Artery Calcium Differs by Sex and Cigarette Smoking. Journal of cardiovascular development and disease 2024 7 11 (7): . Kirsten Voorhies, Kendra Young, Fang-Chi Hsu, Nicholette D Palmer, Merry-Lynn N McDonald, Sanghun Lee, Georg Hahn, Julian Hecker, Dmitry Prokopenko, Ann Chen Wu, Elizabeth A Regan, Dawn DeMeo, Greg L Kinney, James D Crapo, Michael H Cho, Edwin K Silverman, Christoph Lange, Matthew J Budoff, John E Hokanson, Sharon M Lu |
Genetic drivers of human plasma metabolites that determine mortality in heart failure patients with reduced ejection fraction. Frontiers in cardiovascular medicine 2024 7 11 1409340. Vandana Revathi Venkateswaran, Ruicong She, Hongsheng Gui, Jasmine A Luzum, Timothy D Bryson, Zack E Malouf, L Keoki Williams, Hani N Sabbah, Stephen J Gardell, David E Lanfe |
Interaction between Risk Single-Nucleotide Polymorphisms of Developmental Dyslexia and Parental Education on Reading Ability: Evidence for Differential Susceptibility Theory. Behavioral sciences (Basel, Switzerland) 2024 6 14 (6): . Qing Yang, Chen Cheng, Zhengjun Wang, Ximiao Zhang, Jingjing Zh |
Identification of genetic loci enriched in obese or lean T2D cases in the Korean population. Genes & genomics 2024 12 . Eun Bi Lim, Yoon Shin C |
Assessment of causal association between differentiated thyroid cancer and disordered serum lipid profile: a Mendelian randomization study. Frontiers in endocrinology 2024 1 14 1291445. Qiang Ma, Yu Li, Lijuan An, Liang Guo, Xiaokang L |
- Page last reviewed:Feb 1, 2024
- Content source: