Human Genome Epidemiology Literature Finder
|
Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and PDX1[original query] |
|---|
| Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes. Diabetic medicine : a journal of the British Diabetic Association 2011 Jun 28 (6): 681-4. Edghill E L, Khamis A, Weedon M N, Walker M, Hitman G A, McCarthy M I, Owen K R, Ellard S, T Hattersley A, Frayling T |
| Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer. Carcinogenesis 2012 Jul 33 (7): 1384-90. Li Donghui, Duell Eric J, Yu Kai, Risch Harvey A, Olson Sara H, Kooperberg Charles, Wolpin Brian M, Jiao Li, Dong Xiaoqun, Wheeler Bill, Arslan Alan A, Bueno-de-Mesquita H Bas, Fuchs Charles S, Gallinger Steven, Gross Myron, Hartge Patricia, Hoover Robert N, Holly Elizabeth A, Jacobs Eric J, Klein Alison P, LaCroix Andrea, Mandelson Margaret T, Petersen Gloria, Zheng Wei, Agalliu Ilir, Albanes Demetrius, Boutron-Ruault Marie-Christine, Bracci Paige M, Buring Julie E, Canzian Federico, Chang Kenneth, Chanock Stephen J, Cotterchio Michelle, Gaziano J Michael, Giovannucci Edward L, Goggins Michael, Hallmans Göran, Hankinson Susan E, Hoffman Bolton Judith A, Hunter David J, Hutchinson Amy, Jacobs Kevin B, Jenab Mazda, Khaw Kay-Tee, Kraft Peter, Krogh Vittorio, Kurtz Robert C, McWilliams Robert R, Mendelsohn Julie B, Patel Alpa V, Rabe Kari G, Riboli Elio, Shu Xiao-Ou, Tjønneland Anne, Tobias Geoffrey S, Trichopoulos Dimitrios, Virtamo Jarmo, Visvanathan Kala, Watters Joanne, Yu Herbert, Zeleniuch-Jacquotte Anne, Amundadottir Laufey, Stolzenberg-Solomon Rachael |
| Genome-wide associations between genetic and epigenetic variation influence mRNA expression and insulin secretion in human pancreatic islets. PLoS genetics 2014 Nov 10 (11): e1004735. Olsson Anders H, Volkov Petr, Bacos Karl, Dayeh Tasnim, Hall Elin, Nilsson Emma A, Ladenvall Claes, Rönn Tina, Ling Charlot |
| Association of genetic variants with hypertension in a longitudinal population-based genetic epidemiological study. International journal of molecular medicine 2015 May 35 (5): 1189-98. Yamada Yoshiji, Matsui Kota, Takeuchi Ichiro, Oguri Mitsutoshi, Fujimaki Tets |
| Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience. Acta diabetologica 2021 8 58 (12): 1689-1700. Laimon Wafaa, El-Ziny Magdy, El-Hawary Amany, Elsharkawy Ashraf, Salem Nanees Abdel-Badie, Aboelenin Hadil Mohamed, Awad Mohammad Hosny, Flanagan Sarah E, De Franco Eli |
| Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes. Scientific reports 2021 Nov 11 (1): 21565. Deaton Aimee M, Parker Margaret M, Ward Lucas D, Flynn-Carroll Alexander O, BonDurant Lucas, Hinkle Gregory, Akbari Parsa, Lotta Luca A, , , Baras Aris, Nioi Pa |
| PDX1 and MC4R genetic polymorphisms are associated with type 2 diabetes mellitus risk in the Chinese Han population. BMC medical genomics 2021 Oct 14 (1): 249. Wang Ning, Tong Rui, Xu Jing, Tian Yanni, Pan Juan, Cui Jiaqi, Chen Huan, Peng Yanqi, Fei Sijia, Yang Shujun, Wang Lu, Yao Juanchuan, Cui W |
| Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism. EBioMedicine 2024 7 106 105233. Marcus C B Tan, Chelsea A Isom, Yangzi Liu, David-Alexandre Trégouët, , Lang Wu, Dan Zhou, Eric R Gamaz |
| Whole Exome Sequencing in Children With Type 1 Diabetes Before Age 6 Years Reveals Insights Into Disease Heterogeneity. Journal of diabetes research 2024 10 2024 3076895. Andreia Fiúza Ribeiro, Ana Laura Fitas, Marcela Oliveira Pires, Paula Matoso, Dário Ligeiro, Daniel Sobral, Carlos Penha-Gonçalves, Jocelyne Demengeot, Íris Caramalho, Catarina Limbe |
- Page last reviewed:Feb 1, 2024
- Content source: