Human Genome Epidemiology Literature Finder
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Mendelian randomisation identifies priority groups for prophylactic EBV vaccination.
BMC infectious diseases 2023 2 23 (1): 65. Muckian Marisa D, Wilson James F, Taylor Graham S, Stagg Helen R, Pirastu Nico |
Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids.
Biological psychiatry 2023 2 . Davyson Eleanor, Shen Xueyi, Gadd Danni A, Bernabeu Elena, Hillary Robert F, McCartney Daniel L, Adams Mark, Marioni Riccardo, McIntosh Andrew |
Whole-Exome Sequencing Analyses Support a Role of Vitamin D Metabolism in Ischemic Stroke.
Stroke 2023 2 54 (3): 800-809. Xie Yuhan, Acosta Julián N, Ye Yixuan, Demarais Zachariah S, Conlon Carolyn J, Chen Ming, Zhao Hongyu, Falcone Guido |
Genetic basis of STEM occupational choice and regional economic performance: a UK biobank genome-wide association study.
Human genomics 2023 5 17 (1): 40. Zhu Chen, Zhao Qiran, He Jianbo, Böckerman Petri, Luo Siyang, Chen Qih |
Multivariate genetic analysis of personality and cognitive traits reveals abundant pleiotropy.
Nature human behaviour 2023 6 . Hindley Guy, Shadrin Alexey A, van der Meer Dennis, Parker Nadine, Cheng Weiqiu, O'Connell Kevin S, Bahrami Shahram, Lin Aihua, Karadag Naz, Holen Børge, Bjella Thomas, Deary Ian J, Davies Gail, Hill W David, Bressler Jan, Seshadri Sudha, Fan Chun Chieh, Ueland Torill, Djurovic Srdjan, Smeland Olav B, Frei Oleksandr, Dale Anders M, Andreassen Ole |
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure.
Nature communications 2023 7 14 (1): 3826. Rasooly Danielle, Peloso Gina M, Pereira Alexandre C, Dashti Hesam, Giambartolomei Claudia, Wheeler Eleanor, Aung Nay, Ferolito Brian R, Pietzner Maik, Farber-Eger Eric H, Wells Quinn Stanton, Kosik Nicole M, Gaziano Liam, Posner Daniel C, Bento A Patrícia, Hui Qin, Liu Chang, Aragam Krishna, Wang Zeyuan, Charest Brian, Huffman Jennifer E, Wilson Peter W F, Phillips Lawrence S, Whittaker John, Munroe Patricia B, Petersen Steffen E, Cho Kelly, Leach Andrew R, Magariños María Paula, Gaziano John Michael, , Langenberg Claudia, Sun Yan V, Joseph Jacob, Casas Juan |
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration.
Human molecular genetics 2023 6 . Scammell Ben H, Tchio Cynthia, Song Yanwei, Nishiyama Takeshi, Louie Tin L, Dashti Hassan S, Nakatochi Masahiro, Zee Phyllis C, Daghlas Iyas, Momozawa Yukihide, Cai Jianwen, Ollila Hanna M, Redline Susan, Wakai Kenji, Sofer Tamar, Suzuki Sadao, Lane Jacqueline M, Saxena Ric |
Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity.
Science advances 2023 5 9 (17): eadd4984. Schmidt Amand F, Bourfiss Mimount, Alasiri Abdulrahman, Puyol-Anton Esther, Chopade Sandesh, van Vugt Marion, van der Laan Sander W, Gross Christian, Clarkson Chris, Henry Albert, Lumbers Tom R, van der Harst Pim, Franceschini Nora, Bis Joshua C, Velthuis Birgitta K, Te Riele Anneline S J M, Hingorani Aroon D, Ruijsink Bram, Asselbergs Folkert W, van Setten Jessica, Finan Chr |
A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses.
Osteoarthritis and cartilage 2023 3 31 (6): 819-828. Zhang L, Zhang W, Wu X, Cui H, Yan P, Yang C, Zhao X, Xiao J, Xiao C, Tang M, Wang Y, Chen L, Liu Y, Zou Y, Zhang L, Yang Y, Yao Y, Li J, Liu Z, Yang C, Zhang B, Jiang |
Investigation of genetic variants and causal biomarkers associated with brain aging.
Scientific reports 2023 1 13 (1): 1526. Kim Jangho, Lee Junhyeong, Nam Kisung, Lee Seungge |
Genome-wide association study of age at menarche in the Taiwan Biobank suggests NOL4 as a novel associated gene.
Journal of human genetics 2023 1 68 (5): 339-345. Tsai Meng-Che, Hsu Chih-Hui, Chu Shih-Kai, Roy-Gagnon Marie-Hélène, Lin Sheng-Hsia |
Exome-Wide Association Study Reveals Host Genetic Variants Likely Associated with the Severity of COVID-19 in Patients of European Ancestry.
Life (Basel, Switzerland) 2022 Aug 12 (9): . Upadhyai Priyanka, Shenoy Pooja U, Banjan Bhavya, Albeshr Mohammed F, Mahboob Shahid, Manzoor Irfan, Das Ranaj |
The genetic architecture of blood pressure variability: A genome-wide association study of 9370 participants from UK Biobank.
Journal of clinical hypertension (Greenwich, Conn.) 2022 Aug . Jia Pingping, Zhan Na, Bat Baker K K, Feng Qi, Tsoi Kelvin K |
Transcriptome-wide association study of HIV-1 acquisition identifies HERC1 as a susceptibility gene.
iScience 2022 Sep 25 (9): 104854. Duarte Rodrigo R R, Pain Oliver, Furler Robert L, Nixon Douglas F, Powell Timothy |
Prominence of NUDT15 genetic variation associated with 6-mercaptopurine tolerance in a genome-wide association study of Japanese children with acute lymphoblastic leukaemia.
British journal of haematology 2022 Aug . Tanaka Yoichi, Urayama Kevin Y, Mori Makiko, Arakawa Yuki, Hasegawa Daisuke, Noguchi Yasushi, Yanagimachi Masakatsu, Keino Dai, Ota Setsuo, Akahane Koshi, Inukai Takeshi, Hangai Mayumi, Kawaguchi Takahisa, Takagi Masatoshi, Koh Katsuyoshi, Matsuda Fumihiko, Manabe Atsus |
Identification of novel genetic variants, including PIM1 and LINC01491, with ICD-10 based diagnosis of pulmonary arterial hypertension in the UK Biobank cohort.
Frontiers in drug discovery 2023 4 3 . Alex Pu, Gautam Ramani, Yi-Ju Chen, James A Perry, Charles C Ho |
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry.
European urology 2023 3 . Chen Fei, Madduri Ravi K, Rodriguez Alex A, Darst Burcu F, Chou Alisha, Sheng Xin, Wang Anqi, Shen Jiayi, Saunders Edward J, Rhie Suhn K, Bensen Jeannette T, Ingles Sue A, Kittles Rick A, Strom Sara S, Rybicki Benjamin A, Nemesure Barbara, Isaacs William B, Stanford Janet L, Zheng Wei, Sanderson Maureen, John Esther M, Park Jong Y, Xu Jianfeng, Wang Ying, Berndt Sonja I, Huff Chad D, Yeboah Edward D, Tettey Yao, Lachance Joseph, Tang Wei, Rentsch Christopher T, Cho Kelly, Mcmahon Benjamin H, Biritwum Richard B, Adjei Andrew A, Tay Evelyn, Truelove Ann, Niwa Shelley, Sellers Thomas A, Yamoah Kosj, Murphy Adam B, Crawford Dana C, Patel Alpa V, Bush William S, Aldrich Melinda C, Cussenot Olivier, Petrovics Gyorgy, Cullen Jennifer, Neslund-Dudas Christine M, Stern Mariana C, Kote-Jarai Zsofia, Govindasami Koveela, Cook Michael B, Chokkalingam Anand P, Hsing Ann W, Goodman Phyllis J, Hoffmann Thomas J, Drake Bettina F, Hu Jennifer J, Keaton Jacob M, Hellwege Jacklyn N, Clark Peter E, Jalloh Mohamed, Gueye Serigne M, Niang Lamine, Ogunbiyi Olufemi, Idowu Michael O, Popoola Olufemi, Adebiyi Akindele O, Aisuodionoe-Shadrach Oseremen I, Ajibola Hafees O, Jamda Mustapha A, Oluwole Olabode P, Nwegbu Maxwell, Adusei Ben, Mante Sunny, Darkwa-Abrahams Afua, Mensah James E, Diop Halimatou, Van Den Eeden Stephen K, Blanchet Pascal, Fowke Jay H, Casey Graham, Hennis Anselm J, Lubwama Alexander, Thompson Ian M, Leach Robin, Easton Douglas F, Preuss Michael H, Loos Ruth J, Gundell Susan M, Wan Peggy, Mohler James L, Fontham Elizabeth T, Smith Gary J, Taylor Jack A, Srivastava Shiv, Eeles Rosaline A, Carpten John D, Kibel Adam S, Multigner Luc, Parent Marie-Élise, Menegaux Florence, Cancel-Tassin Geraldine, Klein Eric A, Andrews Caroline, Rebbeck Timothy R, Brureau Laurent, Ambs Stefan, Edwards Todd L, Watya Stephen, Chanock Stephen J, Witte John S, Blot William J, Michael Gaziano J, Justice Amy C, Conti David V, Haiman Christopher |
Non-Alcoholic Fatty Liver Disease and Vitamin D in the UK Biobank: A Two-Sample Bidirectional Mendelian Randomisation Study.
Nutrients 2023 3 15 (6): . Zhang Zixuan, Burrows Kimberley, Fuller Harriett, Speliotes Elizabeth K, Abeysekera Kushala W M, Thorne James L, Lewis Sarah J, Zulyniak Michael A, Moore J Bernadet |
Evidence of polygenic regulation of the physiological presence of neurofilament light chain in human serum.
Frontiers in neurology 2023 3 14 1145737. Herrera-Rivero Marisol, Hofer Edith, Maceski Aleksandra, Leppert David, Benkert Pascal, Kuhle Jens, Schmidt Reinhold, Khalil Michael, Wiendl Heinz, Stoll Monika, Berger Kla |
Genome-Wide Analyses Characterize Shared Heritability Among Cancers and Identify Novel Cancer Susceptibility Regions.
Journal of the National Cancer Institute 2023 3 . Lindström Sara, Wang Lu, Feng Helian, Majumdar Arunabha, Huo Sijia, Macdonald James, Harrison Tabitha, Turman Constance, Chen Hongjie, Mancuso Nicholas, Bammler Theo, , Gallinger Steve, Gruber Stephen B, Gunter Marc J, Le Marchand Loic, Moreno Victor, Offit Kenneth, , de Vivo Immaculata, O'Mara Tracy A, Spurdle Amanda B, Tomlinson Ian, , Fitzgerald Rebecca, Gharahkhani Puya, Gockel Ines, Jankowski Janusz, Macgregor Stuart, Schumacher Johannes, Barnholtz-Sloan Jill, Bondy Melissa L, Houlston Richard S, Jenkins Robert B, Melin Beatrice, Wrensch Margaret, Brennan Paul, Christiani David, Johansson Mattias, Mckay James, Aldrich Melinda C, Amos Christopher I, Landi Maria Teresa, Tardon Adonina, , Bishop D Timothy, Demenais Florence, Goldstein Alisa M, Iles Mark M, Kanetsky Peter A, Law Matthew H, , Amundadottir Laufey T, Stolzenberg-Solomon Rachael, Wolpin Brian M, , Klein Alison, Petersen Gloria, Risch Harvey, , , Chanock Stephen J, Purdue Mark P, Scelo Ghislaine, Pharoah Paul, Kar Siddhartha, Hung Rayjean J, Pasaniuc Bogdan, Kraft Pet |
Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Study.
Circulation 2023 2 . Naito Tatsuhiko, Inoue Kosuke, Sonehara Kyuto, Baba Ryuta, Kodama Takaya, Otagaki Yu, Okada Akira, Itcho Kiyotaka, Kobuke Kazuhiro, Kishimoto Shinji, Yamamoto Kenichi, , Morisaki Takayuki, Higashi Yukihito, Hinata Nobuyuki, Arihiro Koji, Hattori Noboru, Okada Yukinori, Oki Ken |
Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents.
Journal of the American Heart Association 2023 1 12 (3): e027993. Pike Mindy M, Schildcrout Jonathan, Baldwin Scott, Edwards Todd, Lipworth Loren, Robinson-Cohen Cassian |
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata.
Nature communications 2023 2 14 (1): 542. Sliz Eeva, Tyrmi Jaakko S, Rahmioglu Nilufer, Zondervan Krina T, Becker Christian M, , Uimari Outi, Kettunen Johann |
Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.
Communications biology 2023 1 6 (1): 71. Helkkula Pyry, Hassan Shabbeer, Saarentaus Elmo, Vartiainen Emilia, Ruotsalainen Sanni, Leinonen Jaakko T, , Palotie Aarno, Karjalainen Juha, Kurki Mitja, Ripatti Samuli, Tukiainen Ta |
A GWAS meta-analysis of alpha angle suggests cam-type morphology may be a specific feature of hip osteoarthritis in older adults.
Arthritis & rheumatology (Hoboken, N.J.) 2023 1 . Faber Benjamin G, Frysz Monika, Hartley April E, Ebsim Raja, Boer Cindy G, Saunders Fiona R, Gregory Jennifer S, Aspden Richard M, Harvey Nicholas C, Southam Lorraine, Giles William, Le Maitre Christine L, Wilkinson J Mark, van Meurs Joyce B J, Zeggini Eleftheria, Cootes Timothy, Lindner Claudia, Kemp John P, Davey Smith George, Tobias Jonathan |
Proteome-Wide Mendelian Randomization Identifies Causal Links Between Blood Proteins and Acute Pancreatitis.
Gastroenterology 2023 2 . Bourgault Jérôme, Abner Erik, Manikpurage Hasanga D, Pujol-Gualdo Natàlia, Laisk Triin, , Gobeil Émilie, Gagnon Eloi, Girard Arnaud, Mitchell Patricia L, Thériault Sébastien, Esko Tõnu, Mathieu Patrick, Arsenault Benoit |
Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study.
Genes 2023 1 14 (1): . Orlova Ekaterina, Dudding Tom, Chernus Jonathan M, Alotaibi Rasha N, Haworth Simon, Crout Richard J, Lee Myoung Keun, Mukhopadhyay Nandita, Feingold Eleanor, Levy Steven M, McNeil Daniel W, Foxman Betsy, Weyant Robert J, Timpson Nicholas J, Marazita Mary L, Shaffer John |
Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation.
PLoS genetics 2023 2 19 (2): e1010587. Currant Hannah, Fitzgerald Tomas W, Patel Praveen J, Khawaja Anthony P, , Webster Andrew R, Mahroo Omar A, Birney Ew |
Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort.
PLoS genetics 2023 1 19 (1): e1010584. Hui Daniel, Mehrabi Shadi, Quimby Alexandra E, Chen Tingfang, Chen Sixing, Park Joseph, Li Binglan, , , Ruckenstein Michael J, Rader Daniel J, Ritchie Marylyn D, Brant Jason A, Epstein Douglas J, Mathieson Ia |
GWAS of depression in 4,520 individuals from the Russian population highlights the role of MAGI2 (S-SCAM) in the gut-brain axis.
Frontiers in genetics 2023 1 13 972196. Pinakhina Daria, Yermakovich Danat, Vergasova Ekaterina, Kasyanov Evgeny, Rukavishnikov Grigory, Rezapova Valeriia, Kolosov Nikita, Sergushichev Alexey, Popov Iaroslav, Kovalenko Elena, Ilinskaya Anna, Kim Anna, Plotnikov Nikolay, Ilinsky Valery, Neznanov Nikholay, Mazo Galina, Kibitov Alexander, Rakitko Alexander, Artomov Myky |
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- Page last updated:May 06, 2024
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