Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Syndrome and FOXO1[original query] |
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Association of common genetic variation in the FOXO1 gene with beta-cell dysfunction, impaired glucose tolerance, and type 2 diabetes. The Journal of clinical endocrinology and metabolism 2009 Apr 94 (4): 1353-60. Müssig Karsten, Staiger Harald, Machicao Fausto, Stancáková Alena, Kuusisto Johanna, Laakso Markku, Thamer Claus, Machann Jürgen, Schick Fritz, Claussen Claus D, Stefan Norbert, Fritsche Andreas, Häring Hans-Ulri |
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.
PLoS genetics 2010 May 6 (5): e1000947. Lu Yi, Dimasi David P, Hysi Pirro G, Hewitt Alex W, Burdon Kathryn P, Toh Tze'Yo, Ruddle Jonathan B, Li Yi Ju, Mitchell Paul, Healey Paul R, Montgomery Grant W, Hansell Narelle, Spector Timothy D, Martin Nicholas G, Young Terri L, Hammond Christopher J, Macgregor Stuart, Craig Jamie E, Mackey David |
Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182. Journal of molecular medicine (Berlin, Germany) 2014 Sep 92 (9): 961-7. Yu Hongsong, Liu Yunjia, Bai Lin, Kijlstra Aize, Yang Peize |
Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese. PloS one 2014 9 (1): e86252. Zhao Ying, Yu Yanbo, Tian Xiaoli, Yang Xi, Li Xueqi, Jiang Feng, Chen Yundai, Shi Maow |
Germline Cancer Predisposition Variants in?Pediatric Rhabdomyosarcoma: A Report From the Children's Oncology Group. Journal of the National Cancer Institute 2020 12 113 (7): 875-883. Li He, Sisoudiya Saumya D, Martin-Giacalone Bailey A, Khayat Michael M, Dugan-Perez Shannon, Marquez-Do Deborah A, Scheurer Michael E, Muzny Donna, Boerwinkle Eric, Gibbs Richard A, Chi Yueh-Yun, Barkauskas Donald A, Lo Tammy, Hall David, Stewart Douglas R, Schiffman Joshua D, Skapek Stephen X, Hawkins Douglas S, Plon Sharon E, Sabo Aniko, Lupo Philip |
A systematic review of the prevalence of pathogenic or likely pathogenic germline variants in individuals with FOXO1 fusion-positive rhabdomyosarcoma. Pediatric blood & cancer 2023 8 e30651. Claire Freycon, Philip J Lupo, Leora Witkowski, Crystal Budd, William D Foulkes, Catherine Goud |
Association study to evaluate Foxo1 and Foxo3 gene polymorphisms in polycystic ovary syndrome: a preliminary case-control study and in silico analysis. Molecular biology reports 2023 2 . Rakhshani Nejad Arghavan, Sargazi Saman, Ghasemi Marzieh, Samareh Moosavi Saeedeh, Heidari Nia Milad, Saravani Ram |
Molecular Features of HHV8 Monoclonal Microlymphoma Associated with Kaposi Sarcoma and Multicentric Castleman Disease in an HIV-Negative Patient. International journal of molecular sciences 2024 4 25 (7): . Evelina Rogges, Sabrina Pelliccia, Camilla Savio, Gianluca Lopez, Irene Della Starza, Giacinto La Verde, Arianna Di Napo |
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- Page last updated:Apr 22, 2024
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