Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and SLC5A2[original query] |
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Sequence variants associating with urinary biomarkers.
Human molecular genetics 2019 04 28 (7): 1199-1211. Benonisdottir Stefania, Kristjansson Ragnar P, Oddsson Asmundur, Steinthorsdottir Valgerdur, Mikaelsdottir Evgenia, Kehr Birte, Jensson Brynjar O, Arnadottir Gudny A, Sulem Gerald, Sveinbjornsson Gardar, Kristmundsdottir Snaedis, Ivarsdottir Erna V, Tragante Vinicius, Gunnarsson Bjarni, Runolfsdottir Hrafnhildur Linnet, Arthur Joseph G, Deaton Aimee M, Eyjolfsson Gudmundur I, Davidsson Olafur B, Asselbergs Folkert W, Hreidarsson Astradur B, Rafnar Thorunn, Thorleifsson Gudmar, Edvardsson Vidar, Sigurdsson Gunnar, Helgadottir Anna, Halldorsson Bjarni V, Masson Gisli, Holm Hilma, Onundarson Pall T, Indridason Olafur S, Benediktsson Rafn, Palsson Runolfur, Gudbjartsson Daniel F, Olafsson Isleifur, Thorsteinsdottir Unnur, Sulem Patrick, Stefansson Ka |
| Are SGLT2 polymorphisms linked to diabetes mellitus and cardiovascular disease? Prospective study and meta-analysis. Bioscience reports 2019 Apr . Drexel Heinz, Leiherer Andreas, Saely Christoph H, Brandtner Eva Maria, Geiger Kathrin, Vonbank Alexander, Fraunberger Pater, Muendlein Ax |
| Common variation at 16p11.2 is associated with glycosuria in pregnancy: findings from a genome-wide association study in European women.
Human molecular genetics 2020 Jul 29 (12): 2098-2106. Lee Matthew A, McMahon George, Karhunen Ville, Wade Kaitlin H, Corbin Laura J, Hughes David A, Smith George Davey, Lawlor Debbie A, Jarvelin Marjo-Riitta, Timpson Nicholas |
| Genetic Variation in Sodium-glucose Cotransporter 2 and Heart Failure. Clinical pharmacology and therapeutics 2021 Jan . Katzmann Julius L, Mason Amy M, März Winfried, Kleber Marcus E, Niessner Alexander, Blüher Matthias, Speer Thimoteus, Laufs Ulri |
| SGLT2 Inhibition, Choline Metabolites, and Cardiometabolic Diseases: A Mediation Mendelian Randomization Study. Diabetes care 2022 9 45 (11): 2718-2728. Xu Min, Zheng Jie, Hou Tianzhichao, Lin Hong, Wang Tiange, Wang Shuangyuan, Lu Jieli, Zhao Zhiyun, Li Mian, Xu Yu, Ning Guang, Bi Yufang, Wang Weiqi |
| Polymorphisms in glucose homeostasis genes are associated with cardiovascular and renal parameters in patients with diabetic nephropathy. Annals of medicine 2022 10 54 (1): 3039-3051. Mota-Zamorano Sonia, González Luz M, Robles Nicolás R, Valdivielso José M, Arévalo-Lorido José C, López-Gómez Juan, Gervasini Guiller |
| Genetic variation in SLC5A2 mimicking SGLT2-inhibition and risk of cardiovascular disease and all-cause mortality: reduced risk not explained by lower plasma glucose. Cardiovascular research 2023 7 . Louise E Bechmann, Frida Emanuelsson, Børge G Nordestgaard, Marianne Be |
| Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome. medRxiv : the preprint server for health sciences 2023 10 . Hyejeong Hong, Katharina V Schulze, Ian E Copeland, Manasa Atyam, Kendra Kamp, Neil A Hanchard, John Belmont, Tamar Ringel-Kulka, Margaret Heitkemper, Robert J Shulm |
| Role of SLC5A2 polymorphisms and effects of genetic polymorphism on sodium glucose cotransporter 2 inhibitorsinhibitor response. Molecular biology reports 2023 10 . Bo Xu, Shaoqian Li, Bo Kang, Shangzhi Fan, Canyu Chen, Weiyi Li, Jixiang Chen, Zunbo He, Fan Tang, Jiecan Zh |
| Sodium-glucose cotransporter 1/2 inhibition and risk of neurodegenerative disorders: A Mendelian randomization study. Brain and behavior 2024 7 14 (7): e3624. Jinxin Liu, Xinxiu Shi, Yankun Sh |
| SGLT2 inhibition, venous thrombolism, and death due to cardiac causes: a mediation Mendelian randomization study. Frontiers in cardiovascular medicine 2024 5 11 1339094. Lili Shi, Xiupan Wei, Jinlan Luo, Ling |
| Genetic Etiology Investigation in Treatment-Resistant Nocturnal Enuresis Children: A descriptive study. Urology journal 2024 12 . Sevim Yener, Metin Es |
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