Human Genome Epidemiology Literature Finder
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Query Trace: ALDH1A2[original query] |
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Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2. Birth defects research. Part A, Clinical and molecular teratology 2005 Nov 73 (11): 868-75. Deak Kristen L, Dickerson Margaret E, Linney Elwood, Enterline David S, George Timothy M, Melvin Elizabeth C, Graham Felicia L, Siegel Deborah G, Hammock Preston, Mehltretter Lorraine, Bassuk Alexander G, Kessler John A, Gilbert John R, Speer Marcy C, |
Positive association between ALDH1A2 and schizophrenia in the Chinese population. Progress in neuro-psychopharmacology & biological psychiatry 2009 Nov 33 (8): 1491-5. Wan Chunling, Shi Yongyong, Zhao Xinzhi, Tang Wei, Zhang Ming, Ji Baohu, Zhu Hui, Xu Yifeng, Li Huafang, Feng Guoyin, He L |
ALDH1A2 (RALDH2) genetic variation in human congenital heart disease. BMC medical genetics 2009 10 (1): 113. Pavan Marilene, Ruiz Viviane F, Silva Fábio A, Sobreira Tiago J, Cravo Roberta M, Vasconcelos Michelle, Marques Lívia P, Mesquita Sonia M F, Krieger José E, Lopes Antônio A B, Oliveira Paulo S, Pereira Alexandre C, Xavier-Neto Jo |
A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid. Kidney international 2010 Jul 78 (1): 96-102. El Kares Reyhan, Manolescu Daniel C, Lakhal-Chaieb Lajmi, Montpetit Alexandre, Zhang Zhao, Bhat Pangala V, Goodyer Pa |
Newborn serum retinoic acid level is associated with variants of genes in the retinol metabolism pathway. Pediatric research 2010 Jun 67 (6): 598-602. Manolescu Daniel C, El-Kares Reyhan, Lakhal-Chaieb Lajmi, Montpetit Alexandre, Bhat Pangala V, Goodyer Pa |
Genome-wide association analysis of Sasang constitution in the Korean population. Journal of alternative and complementary medicine (New York, N.Y.) 2012 Mar 18 (3): 262-9. Kim Bu-Yeo, Jin Hee-Jeong, Kim Jong Ye |
Chiari malformation type I: a case-control association study of 58 developmental genes. PloS one 2013 8 (2): e57241. Urbizu Aintzane, Toma Claudio, Poca Maria A, Sahuquillo Juan, Cuenca-León Ester, Cormand Bru, Macaya Alfo |
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.
Nature genetics 2014 May 46 (5): 498-502. Styrkarsdottir Unnur, Thorleifsson Gudmar, Helgadottir Hafdis T, Bomer Nils, Metrustry Sarah, Bierma-Zeinstra S, Strijbosch Annelieke M, Evangelou Evangelos, Hart Deborah, Beekman Marian, Jonasdottir Aslaug, Sigurdsson Asgeir, Eiriksson Finnur F, Thorsteinsdottir Margret, Frigge Michael L, Kong Augustine, Gudjonsson Sigurjon A, Magnusson Olafur T, Masson Gisli, , , Hofman Albert, Arden Nigel K, Ingvarsson Thorvaldur, Lohmander Stefan, Kloppenburg Margreet, Rivadeneira Fernando, Nelissen Rob G H H, Spector Tim, Uitterlinden Andre, Slagboom P Eline, Thorsteinsdottir Unnur, Jonsdottir Ingileif, Valdes Ana M, Meulenbelt Ingrid, van Meurs Joyce, Jonsson Helgi, Stefansson Ka |
Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus. Gastroenterology 2015 Feb 148 (2): 367-78. Palles Claire, Chegwidden Laura, Li Xinzhong, Findlay John M, Farnham Garry, Castro Giner Francesc, Peppelenbosch Maikel P, Kovac Michal, Adams Claire L, Prenen Hans, Briggs Sarah, Harrison Rebecca, Sanders Scott, MacDonald David, Haigh Chris, Tucker Art, Love Sharon, Nanji Manoj, deCaestecker John, Ferry David, Rathbone Barrie, Hapeshi Julie, Barr Hugh, Moayyedi Paul, Watson Peter, Zietek Barbara, Maroo Neera, Gay Laura, Underwood Tim, Boulter Lisa, McMurtry Hugh, Monk David, Patel Praful, Ragunath Krish, Al Dulaimi David, Murray Iain, Koss Konrad, Veitch Andrew, Trudgill Nigel, Nwokolo Chuka, Rembacken Bjorn, Atherfold Paul, Green Elaine, Ang Yeng, Kuipers Ernst J, Chow Wu, Paterson Stuart, Kadri Sudarshan, Beales Ian, Grimley Charles, Mullins Paul, Beckett Conrad, Farrant Mark, Dixon Andrew, Kelly Sean, Johnson Matthew, Wajed Shahjehan, Dhar Anjan, Sawyer Elinor, Roylance Rebecca, Onstad Lynn, Gammon Marilie D, Corley Douglas A, Shaheen Nicholas J, Bird Nigel C, Hardie Laura J, Reid Brian J, Ye Weimin, Liu Geoffrey, Romero Yvonne, Bernstein Leslie, Wu Anna H, Casson Alan G, Fitzgerald Rebecca, Whiteman David C, Risch Harvey A, Levine David M, Vaughan Tom L, Verhaar Auke P, van den Brande Jan, Toxopeus Eelke L, Spaander Manon C, Wijnhoven Bas P L, van der Laan Luc J W, Krishnadath Kausilia, Wijmenga Cisca, Trynka Gosia, McManus Ross, Reynolds John V, O'Sullivan Jacintha, MacMathuna Padraic, McGarrigle Sarah A, Kelleher Dermot, Vermeire Severine, Cleynen Isabelle, Bisschops Raf, Tomlinson Ian, Jankowski Janu |
Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects. BMC medical genetics 2014 15 102. Pangilinan Faith, Molloy Anne M, Mills James L, Troendle James F, Parle-McDermott Anne, Kay Denise M, Browne Marilyn L, McGrath Emily C, Abaan Hatice Ozel, Sutton Marie, Kirke Peadar N, Caggana Michele, Shane Barry, Scott John M, Brody Lawrence |
Alcohol consumption and prostate cancer incidence and progression: A Mendelian randomisation study. International journal of cancer 2017 Jan 140 (1): 75-85. Brunner Clair, Davies Neil M, Martin Richard M, Eeles Rosalind, Easton Doug, Kote-Jarai Zsofia, Al Olama Ali Amin, Benlloch Sara, Muir Kenneth, Giles Graham, Wiklund Fredrik, Gronberg Henrik, Haiman Christopher A, Schleutker Johanna, Nordestgaard Børge G, Travis Ruth C, Neal David, Donovan Jenny, Hamdy Freddie C, Pashayan Nora, Khaw Kay-Tee, Stanford Janet L, Blot William J, Thibodeau Stephen, Maier Christiane, Kibel Adam S, Cybulski Cezary, Cannon-Albright Lisa, Brenner Hermann, Park Jong, Kaneva Radka, Batra Jyotsna, Teixeira Manuel R, Pandha Hardev, , Zuccolo Lui |
Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/?-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials.
Journal of the American Heart Association 2017 Nov 6 (11): . Magvanjav Oyunbileg, Gong Yan, McDonough Caitrin W, Chapman Arlene B, Turner Stephen T, Gums John G, Bailey Kent R, Boerwinkle Eric, Beitelshees Amber L, Tanaka Toshihiro, Kubo Michiaki, Pepine Carl J, Cooper-DeHoff Rhonda M, Johnson Julie |
The rs4238326 polymorphism in ALDH1A2 gene potentially associated with non-post traumatic knee osteoarthritis susceptibility: a two-stage population-based study. Osteoarthritis and cartilage 2017 07 25 (7): 1062-1067. Chu M, Zhu X, Wang C, Rong J, Wang Y, Wang S, Xing B, Tao Y, Zhuang X, Jiang |
Functional Characterization of the Osteoarthritis Genetic Risk Residing at ALDH1A2 Identifies rs12915901 as a Key Target Variant. Arthritis & rheumatology (Hoboken, N.J.) 2018 5 70 (10): 1577-1587. Shepherd Colin, Zhu Dongxing, Skelton Andrew J, Combe Jennifer, Threadgold Harrison, Zhu Linyi, Vincent Tonia L, Stuart Paul, Reynard Louise N, Loughlin Jo |
Genome-wide association study of metabolic syndrome in Korean populations.
PloS one 2020 15 (1): e0227357. Oh Seung-Won, Lee Jong-Eun, Shin Eunsoon, Kwon Hyuktae, Choe Eun Kyung, Choi Su-Yeon, Rhee Hwanseok, Choi Seung |
Associations between ALDH Genetic Variants, Alcohol Consumption, and the Risk of Nasopharyngeal Carcinoma in an East Asian Population. Genes 2021 10 12 (10): . Liao Wen-Ling, Chan Fu-Chun, Chang Kai-Ping, Chang Ya-Wen, Chen Che-Hong, Su Wen-Hui, Chang Hen-Ho |
APOE and KLF14 genetic variants are sex-specific for low high-density lipoprotein cholesterol identified by a genome-wide association study.
Genetics and molecular biology 2022 45 (1): e20210280. Lee Ying-Hui, Chang Ya-Sian, Hsieh Chih-Chang, Wang Rong-Tsorng, Chang Jan-Gowth, Chen Chung-Jen, Chang Shun-J |
An eQTL variant of ALDH1A2 is associated with Kashin-Beck disease in Chinese population. Journal of bone and mineral metabolism 2022 Jan . Zhang Di, Li Qiang, Zhang Dandan, Yang Xiaoli, Wang Chen, Zhang Rongqiang, Yang Xuena, Li Zhaofang, Xiong Yongm |
Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect.
Annals of the rheumatic diseases 2023 3 . Styrkarsdottir Unnur, Stefansdottir Lilja, Thorleifsson Gudmar, Stefansson Olafur A, Saevarsdottir Saedis, Lund Sigrun H, Rafnar Thorunn, Hoshijima Kazuyuki, Novak Kendra, Oreiro Natividad, Rego-Perez Ignacio, Hansen Channing, Kazmers Nikolas, Kiemeney Lambertus A, Blanco Francisco J, Barker Tyler, Kloppenburg Margreet, Jurynec Michael J, Gudbjartsson Daniel F, Jonsson Helgi, Thorsteinsdottir Unnur, Stefansson Ka |
The Genetic Markers of Knee Osteoarthritis in Women from Russia. Biomedicines 2024 4 12 (4): . Anton Tyurin, Karina Akhiiarova, Ildar Minniakhmetov, Natalia Mokrysheva, Rita Khusaino |
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