Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Syndrome and HNF1A[original query] |
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Synergism between mutant HNF1A and the metabolic syndrome in Oji-Cree Type 2 diabetes. Diabetic medicine : a journal of the British Diabetic Association 2005 Nov 22 (11): 1510-5. Pollex R L, Hanley A J G, Zinman B, Harris S B, Khan H M R, Hegele R |
Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
American journal of human genetics 2008 May 82 (5): 1185-92. Ridker Paul M, Pare Guillaume, Parker Alex, Zee Robert Y L, Danik Jacqueline S, Buring Julie E, Kwiatkowski David, Cook Nancy R, Miletich Joseph P, Chasman Daniel |
A-beta-subtype of ketosis-prone diabetes is not predominantly a monogenic diabetic syndrome. Diabetes care 2009 May 32 (5): 873-7. Haaland Wade C, Scaduto Diane I, Maldonado Mario R, Mansouri Dena L, Nalini Ramaswami, Iyer Dinakar, Patel Sanjeet, Guthikonda Anu, Hampe Christiane S, Balasubramanyam Ashok, Metzker Michael |
GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation. Journal of hepatology 2012 Jan 56 (1): 184-91. Nault Jean Charles, Fabre Monique, Couchy Gabrielle, Pilati Camilla, Jeannot Emmanuelle, Tran Van Nhieu Jeanne, Saint-Paul Marie-Christine, De Muret Anne, Redon Marie-José, Buffet Catherine, Salenave Sylvie, Balabaud Charles, Prevot Sophie, Labrune Philippe, Bioulac-Sage Paulette, Scoazec Jean-Yves, Chanson Philippe, Zucman-Rossi Jessi |
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.
Circulation 2011 Feb 123 (7): 731-8. Dehghan Abbas, Dupuis Josée, Barbalic Maja, Bis Joshua C, Eiriksdottir Gudny, Lu Chen, Pellikka Niina, Wallaschofski Henri, Kettunen Johannes, Henneman Peter, Baumert Jens, Strachan David P, Fuchsberger Christian, Vitart Veronique, Wilson James F, Paré Guillaume, Naitza Silvia, Rudock Megan E, Surakka Ida, de Geus Eco J C, Alizadeh Behrooz Z, Guralnik Jack, Shuldiner Alan, Tanaka Toshiko, Zee Robert Y L, Schnabel Renate B, Nambi Vijay, Kavousi Maryam, Ripatti Samuli, Nauck Matthias, Smith Nicholas L, Smith Albert V, Sundvall Jouko, Scheet Paul, Liu Yongmei, Ruokonen Aimo, Rose Lynda M, Larson Martin G, Hoogeveen Ron C, Freimer Nelson B, Teumer Alexander, Tracy Russell P, Launer Lenore J, Buring Julie E, Yamamoto Jennifer F, Folsom Aaron R, Sijbrands Eric J G, Pankow James, Elliott Paul, Keaney John F, Sun Wei, Sarin Antti-Pekka, Fontes João D, Badola Sunita, Astor Brad C, Hofman Albert, Pouta Anneli, Werdan Karl, Greiser Karin H, Kuss Oliver, Meyer zu Schwabedissen Henriette E, Thiery Joachim, Jamshidi Yalda, Nolte Ilja M, Soranzo Nicole, Spector Timothy D, Völzke Henry, Parker Alexander N, Aspelund Thor, Bates David, Young Lauren, Tsui Kim, Siscovick David S, Guo Xiuqing, Rotter Jerome I, Uda Manuela, Schlessinger David, Rudan Igor, Hicks Andrew A, Penninx Brenda W, Thorand Barbara, Gieger Christian, Coresh Joe, Willemsen Gonneke, Harris Tamara B, Uitterlinden Andre G, Järvelin Marjo-Riitta, Rice Kenneth, Radke Dörte, Salomaa Veikko, Willems van Dijk Ko, Boerwinkle Eric, Vasan Ramachandran S, Ferrucci Luigi, Gibson Quince D, Bandinelli Stefania, Snieder Harold, Boomsma Dorret I, Xiao Xiangjun, Campbell Harry, Hayward Caroline, Pramstaller Peter P, van Duijn Cornelia M, Peltonen Leena, Psaty Bruce M, Gudnason Vilmundur, Ridker Paul M, Homuth Georg, Koenig Wolfgang, Ballantyne Christie M, Witteman Jacqueline C M, Benjamin Emelia J, Perola Markus, Chasman Daniel |
Systematic assessment of etiology in adults with a clinical diagnosis of young-onset type 2 diabetes is a successful strategy for identifying maturity-onset diabetes of the young. Diabetes care 2012 Jun 35 (6): 1206-12. Thanabalasingham Gaya, Pal Aparna, Selwood Mary P, Dudley Christina, Fisher Karen, Bingley Polly J, Ellard Sian, Farmer Andrew J, McCarthy Mark I, Owen Katharine |
Variants within HNF1a and ANGPTL4 genes and acute coronary syndrome in Czech population. The GENDEMIP study. Neuro endocrinology letters 2012 Nov 33 (Suppl2): Suppl2. Dlouha D, Pitha J, Adámkova V, Lanska V, Hubacek JA |
Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels.
Nature communications 2015 6 7754. Setoh Kazuya, Terao Chikashi, Muro Shigeo, Kawaguchi Takahisa, Tabara Yasuharu, Takahashi Meiko, Nakayama Takeo, Kosugi Shinji, Sekine Akihiro, Yamada Ryo, Mishima Michiaki, Matsuda Fumihi |
The Pharmacogenetics of Metformin in Women with Polycystic Ovary Syndrome: A Randomized Trial. Basic & clinical pharmacology & toxicology 2017 8 122 (2): 239-244. Pedersen Andreas J T, Stage Tore Bjerregaard, Glintborg Dorte, Andersen Marianne, Christensen Mette Marie Hougaa |
Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population. Diabetes & metabolic syndrome 2017 Jul . Morjane Imane, Kefi Rym, Charoute Hicham, Lakbakbi El Yaagoubi Fouzia, Hechmi Meryem, Saile Rachid, Abdelhak Sonia, Barakat Abdelham |
Association study of HNF1A in women with polycystic ovary syndrome. Journal of assisted reproduction and genetics 2017 Mar . Lv Yue, Sun Changfa, Tian Ye, Zhao Shigang, Bian Yuehong, Cheng Lei, Sun Mei, Liu Hong-Bin, Zhao Han, Ma Jinlo |
Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals. BMC medicine 2017 12 15 (1): 213. Bansal Vikas, Gassenhuber Johann, Phillips Tierney, Oliveira Glenn, Harbaugh Rebecca, Villarasa Nikki, Topol Eric J, Seufferlein Thomas, Boehm Bernhard |
Family-based analysis of GGT1 and HNF1A gene polymorphisms in patients with polycystic ovary syndrome. Reproductive biomedicine online 2017 11 36 (1): 115-119. Xu Xinghua, Qin Lang, Tian Ye, Wang Min, Li Guangyao, Du Yanzhi, Chen Zi-Jiang, Li Weipi |
Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition. PloS one 2018 9 13 (9): e0203885. Martin-Morales Lorena, Rofes Paula, Diaz-Rubio Eduardo, Llovet Patricia, Lorca Victor, Bando Inmaculada, Perez-Segura Pedro, de la Hoya Miguel, Garre Pilar, Garcia-Barberan Vanesa, Caldes Trinid |
High Prevalence of a Monogenic Cause in Han Chinese Diagnosed With Type 1 Diabetes, Partly Driven by Nonsyndromic Recessive WFS1 Mutations. Diabetes 2019 Oct . Li Meihang, Wang Sihua, Xu Kuanfeng, Chen Yang, Fu Qi, Gu Yong, Shi Yun, Zhang Mei, Sun Min, Chen Heng, Han Xiuqun, Li Yangxi, Tang Zhoukai, Cai Lejing, Li Zhiqiang, Shi Yongyong, Yang Tao, Polychronakos Constant |
New clinical screening strategy to distinguish HNF1A variant-induced diabetes from young early-onset type 2 diabetes in a Chinese population. BMJ open diabetes research & care 2020 4 8 (1): . Ma Yumin, Gong Siqian, Wang Xirui, Cai Xiaoling, Xiao Xinhua, Gu Weijun, Yang Jinkui, Zhong Liyong, Xiao Jianzhong, Li Meng, Liu Wei, Zhang Simin, Zhou Xianghai, Li Yufeng, Zhou Lingli, Zhu Yu, Luo Yingying, Ren Qian, Huang Xiuting, Gao Xueying, Zhang Xiuying, Zhang Rui, Chen Ling, Wang Fang, Wang Qiuping, Hu Mengdie, Han Xueyao, Ji Lino |
A Comprehensive Overview of Common Polymorphic Variants in Genes Related to Polycystic Ovary Syndrome. Reproductive sciences (Thousand Oaks, Calif.) 2020 Nov . Castillo-Higuera Tatiana, Alarcón-Granados María Camila, Marin-Suarez Johana, Moreno-Ortiz Harold, Esteban-Pérez Clara Inés, Ferrebuz-Cardozo Atilio Junior, Forero-Castro Maribel, Camargo-Vill Alba Glor |
Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case-control study in the Tunisian population and a meta-analysis. Diabetology & metabolic syndrome 2022 Feb 14 (1): 25. Dallali Hamza, Hechmi Meriem, Morjane Imane, Elouej Sahar, Jmel Haifa, Ben Halima Yosra, Abid Abdelmajid, Bahlous Afef, Barakat Abdelhamid, Jamoussi Henda, Abdelhak Sonia, Kefi R |
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