HuGE Literature Finder
Records 1-30
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Pathogenic variants in actionable MODY genes are associated with type 2 diabetes.
Nature metabolism 2020 Oct 2 (10): 1126-1134. Bonnefond Amélie, Boissel Mathilde, Bolze Alexandre, Durand Emmanuelle, Toussaint Bénédicte, Vaillant Emmanuel, Gaget Stefan, Graeve Franck De, Dechaume Aurélie, Allegaert Frédéric, Guilcher David Le, Yengo Loïc, Dhennin Véronique, Borys Jean-Michel, Lu James T, Cirulli Elizabeth T, Elhanan Gai, Roussel Ronan, Balkau Beverley, Marre Michel, Franc Sylvia, Charpentier Guillaume, Vaxillaire Martine, Canouil Mickaël, Washington Nicole L, Grzymski Joseph J, Froguel Philip |
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Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer.
European urology 2020 Aug . Schaid Daniel J, McDonnell Shannon K, FitzGerald Liesel M, DeRycke Lissa, Fogarty Zachary, Giles Graham G, MacInnis Robert J, Southey Melissa C, Nguyen-Dumont Tu, Cancel-Tassin Geraldine, Cussenot Oliver, Whittemore Alice S, Sieh Weiva, Ioannidis Nilah Monnier, Hsieh Chih-Lin, Stanford Janet L, Schleutker Johanna, Cropp Cheryl D, Carpten John, Hoegel Josef, Eeles Rosalind, Kote-Jarai Zsofia, Ackerman Michael J, Klein Christopher J, Mandal Diptasri, Cooney Kathleen A, Bailey-Wilson Joan E, Helfand Brian, Catalona William J, Wiklund Fredrick, Riska Shaun, Bahetti Saurabh, Larson Melissa C, Cannon Albright Lisa, Teerlink Craig, Xu Jianfeng, Isaacs William, Ostrander Elaine A, Thibodeau Stephen |
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Influence of IGF2BP2, HMG20A, and HNF1B genetic polymorphisms on the susceptibility to type 2 diabetes mellitus in Chinese Han population.
Bioscience reports 2020 Apr . Wang Li, Cui Wei, Bai Mei, Zheng Jianwen, Yuan Dongya, He Yongjun, Wang Yuhe, Jin Tian |
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A diabetes-associated genetic variant is associated with diastolic dysfunction and cardiovascular disease.
ESC heart failure 2019 Dec . Molvin John, Jujic Amra, Nilsson Peter M, Leosdottir Margret, Lindblad Ulf, Daka Bledar, Bennet Louise, Råstam Lennart, Lyssenko Valeriya, Magnusson Mart |
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Clinical relevance of the lnc-HNF1B-3:1 genetic polymorphisms in Western Chinese tuberculosis patients.
Journal of clinical laboratory analysis 2019 Nov e23076. Wu Qian, Zhong Huiyu, Bai Hao, Liu Tangyuheng, Song Jiajia, Wen Yang, Song Xingbo, Ying Bin |
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Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis.
BMC medicine 2019 Jul 17 (1): 132. Donath Xavier, Saint-Martin Cécile, Dubois-Laforgue Danièle, Rajasingham Ramanan, Mifsud François, Ciangura Cécile, Timsit José, Bellanné-Chantelot Christine, |
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HNF1A gene p.I27L is associated with early-onset, maturity-onset diabetes of the young-like diabetes in Turkey.
BMC endocrine disorders 2019 May 19 (1): 51. Beysel Selvihan, Eyerci Nilnur, Pinarli Ferda Alparslan, Kizilgul Muhammed, Ozcelik Ozgur, Caliskan Mustafa, Cakal Erm |
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Identifying Pathogenic Variants of Monogenic Diabetes Using Targeted Panel Sequencing in an East Asian Population.
The Journal of clinical endocrinology and metabolism 2019 Apr . Park Seung Shin, Jang Se Song, Ahn Chang Ho, Kim Jung Hee, Jung Hye Seung, Cho Young Min, Lee Young Ah, Shin Choong Ho, Chae Jong Hee, Kim Jae Hyun, Choi Sung Hee, Jang Hak C, Bae Jee Cheol, Won Jong Cheol, Kim Sung-Hoon, Kim Jong-Il, Kwak Soo Heon, Park Kyong S |
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Survival Following Chemotherapy in Ovarian Clear Cell Carcinoma is Not Associated with Pathological Misclassification of Tumor Histotype.
Clinical cancer research : an official journal of the American Association for Cancer Research 2019 Apr . Takenaka Masataka, Köbel Martin, Garsed Dale W, Fereday Sian, Pandey Ahwan, Etemadmoghadam Dariush, Hendley Joy, Kawabata Ayako, Noguchi Daito, Yanaihara Nozomu, Takahashi Hiroyuki, Kiyokawa Takako, Ikegami Masahiro, Takano Hirokuni, Isonishi Seiji, Ochiai Kazuhiko, Traficante Nadia, Gadipally Sreeja R, Semple Timothy, Vassiliadis Dane, Amarasinghe Kaushalya Christmalee, Li Jason, Mir Arnau Gisela, Okamoto Aikou, Friedlander Michael, Bowtell David D |
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Genetic polymorphisms of diabetes-related genes, their interaction with diabetes status, and breast cancer incidence and mortality: The Long Island Breast Cancer Study Project.
Molecular carcinogenesis 2019 03 58 (3): 436-446. Parada Humberto, Cleveland Rebecca J, North Kari E, Stevens June, Teitelbaum Susan L, Neugut Alfred I, Santella Regina M, Martinez Maria E, Gammon Marilie |
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Cumulative evidence for relationships between multiple variants of HNF1B and the risk of prostate and endometrial cancers.
BMC medical genetics 2018 Jul 19 (1): 128. Tong Yu, Qu Yi, Li Shiping, Zhao Fengyan, Wang Yibin, Mu Dez |
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Genetic factors influencing prostate cancer risk in Norwegian men.
The Prostate 2017 Nov . Chen Haitao, Ewing Charles M, Zheng Sigun, Grindedaal Eli M, Cooney Kathleen A, Wiley Kathleen, Djurovic Srdjan, Andreassen Ole A, Axcrona Karol, Mills Ian G, Xu Jianfeng, Maehle Lovise, Fosså Sophie D, Isaacs William |
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MODY in Ukraine: genes, clinical phenotypes and treatment.
Journal of pediatric endocrinology & metabolism : JPEM 2017 Oct 30 (10): 1095-1103. Globa Evgenia, Zelinska Nataliya, Elblova Lenka, Dusatkova Petra, Cinek Ondrej, Lebl Jan, Colclough Kevin, Ellard Sian, Pruhova Stepan |
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High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus.
Journal of the Endocrine Society 2017 Jun 1 (6): 681-690. Gjesing Anette P, Rui Gao, Lauenborg Jeannet, Have Christian Theil, Hollensted Mette, Andersson Ehm, Grarup Niels, Sun Jihua, Quan Shi, Brandslund Ivan, Damm Peter, Pedersen Oluf, Wang Jun, Hansen Torb |
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Identification of 8 Novel Mutations in Nephrogenesis-Related Genes in Chinese Han Patients with Unilateral Renal Agenesis.
American journal of nephrology 2017 Jun 46 (1): 55-63. Wu Hangdi, Xu Qian, Xie Jingyuan, Ma Jun, Qiao Panpan, Zhang Wen, Yu Haijin, Wang Weiming, Qian Ying, Zhang Qianying, Guo Yiqing, Tang Yonghua, Chen Xiao-Nong, Wang Zhaohui, Chen N |
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Variants in MODY genes associated with maternal lipids profiles in second trimester of pregnancy.
The journal of gene medicine 2017 Jun . Wang Xiaojing, Li Wei, Ma Liangkun, Ping Fan, Liu Juntao, Wu Xueyan, Mao Jiangfeng, Wang Xi, Nie M |
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HNF1B, TSPAN8 and NOTCH2 gene polymorphisms in women with gestational diabetes.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2017 Mar 1-6. Tarnowski Maciej, Malinowski Damian, Safranow Krzysztof, Dziedziejko Violetta, Pawlik Andrz |
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Genetic risk factors for ovarian cancer and their role for endometriosis risk.
Gynecologic oncology 2017 Feb . Burghaus Stefanie, Fasching Peter A, Häberle Lothar, Rübner Matthias, Büchner Kathrin, Blum Simon, Engel Anne, Ekici Arif B, Hartmann Arndt, Hein Alexander, Beckmann Matthias W, Renner Stefan |
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Genetic variants of increased waist circumference in psychosis.
Psychiatric genetics 2017 12 27 (6): 210-218. Hukic Dzana S, Ösby Urban, Olsson Eric, Hilding Agneta, Östenson Claes-Göran, Gu Harvest F, Ehrenborg Ewa, Edman Gunnar, Schalling Martin, Lavebratt Catharina, Frisén Loui |
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HNF1B variants associate with promoter methylation and regulate gene networks activated in prostate and ovarian cancer.
Oncotarget 2016 Oct . Ross-Adams Helen, Ball Stephen, Lawrenson Kate, Halim Silvia, Russell Roslin, Wells Claire, Strand Siri H, Ørntoft Torben F, Larson Melissa, Armasu Sebastian, Massie Charles E, Asim Mohammad, Mortensen Martin M, Borre Michael, Woodfine Kathryn, Warren Anne Y, Lamb Alastair D, Kay Jonathan, Whitaker Hayley, Ramos-Montoya Antonio, Murrell Adele, Sørensen Karina D, Fridley Brooke L, Goode Ellen L, Gayther Simon A, Masters John, Neal David E, Mills Ian |
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Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.
Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep . Bekheirnia Mir Reza, Bekheirnia Nasim, Bainbridge Matthew N, Gu Shen, Coban Akdemir Zeynep Hande, Gambin Tomek, Janzen Nicolette K, Jhangiani Shalini N, Muzny Donna M, Michael Mini, Brewer Eileen D, Elenberg Ewa, Kale Arundhati S, Riley Alyssa A, Swartz Sarah J, Scott Daryl A, Yang Yaping, Srivaths Poyyapakkam R, Wenderfer Scott E, Bodurtha Joann, Applegate Carolyn D, Velinov Milen, Myers Angela, Borovik Lior, Craigen William J, Hanchard Neil A, Rosenfeld Jill A, Lewis Richard Alan, Gonzales Edmond T, Gibbs Richard A, Belmont John W, Roth David R, Eng Christine, Braun Michael C, Lupski James R, Lamb Dolores |
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Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.
Schizophrenia research 2016 Apr . González-Peñas Javier, Amigo Jorge, Santomé Luis, Sobrino Beatriz, Brenlla Julio, Agra Santiago, Paz Eduardo, Páramo Mario, Carracedo Ángel, Arrojo Manuel, Costas Javi |
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Systematic meta-analyses of gene-specific genetic association studies in prostate cancer.
Oncotarget 2016 Mar . Hao Qiang, Wei Dong, Zhang Yaoguang, Chen Xin, Yang Fan, Yang Ze, Zhu Xiaoquan, Wang Jian |
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A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.
Oncotarget 2016 09 7 (37): 59029-59048. Ríos-Tamayo Rafael, Lupiañez Carmen Belén, Campa Daniele, Hielscher Thomas, Weinhold Niels, Martínez-López Joaquin, Jerez Andrés, Landi Stefano, Jamroziak Krzysztof, Dumontet Charles, Watek Marzena, Lesueur Fabienne, Reis Rui Manuel, Marques Herlander, Jurczyszyn Artur, Vogel Ulla, Buda Gabriele, García-Sanz Ramón, Orciuolo Enrico, Petrini Mario, Vangsted Annette J, Gemignani Federica, Försti Asta, Goldschmidt Hartmut, Hemminki Kari, Canzian Federico, Jurado Manuel, Sainz Ju |
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Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing.
Journal of pediatric endocrinology & metabolism : JPEM 2015 Dec . A?lad?o?lu Sebahat Y?lmaz, Aycan Zehra, Çetinkaya Semra, Ba? Veysel Nijat, Önder A?an, Peltek Kendirci Havva Nur, Do?an Haldun, Ceylaner Serd |
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Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT.
Kidney international 2015 Oct . Nicolaou Nayia, Pulit Sara L, Nijman Isaac J, Monroe Glen R, Feitz Wout F J, Schreuder Michiel F, van Eerde Albertien M, de Jong Tom P V M, Giltay Jacques C, van der Zwaag Bert, Havenith Marlies R, Zwakenberg Susan, van der Zanden Loes F M, Poelmans Geert, Cornelissen Elisabeth A M, Lilien Marc R, Franke Barbara, Roeleveld Nel, van Rooij Iris A L M, Cuppen Edwin, Bongers Ernie M H F, Giles Rachel H, Knoers Nine V A M, Renkema Kirsten |
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Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.
Journal of pediatric endocrinology & metabolism : JPEM 2015 Jul . An?k Ahmet, Çatl? Gönül, Abac? Ayhan, Sar? Erkan, Ye?ilkaya Ediz, Korkmaz Hüseyin An?l, Demir Korcan, Alt?nc?k Ayça, Tuhan Hale Ünver, K?z?lda? Sefa, Özkan Behzat, Ceylaner Serdar, Böber E |
Two new loci and gene sets related to sex determination and cancer progression are associated with susceptibility to testicular germ cell tumor.
Human molecular genetics 2015 Jul 24 (14): 4138-46. Kristiansen Wenche, Karlsson Robert, Rounge Trine B, Whitington Thomas, Andreassen Bettina K, Magnusson Patrik K, Fosså Sophie D, Adami Hans-Olov, Turnbull Clare, Haugen Trine B, Grotmol Tom, Wiklund Fredr |
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HNF1B polymorphism influence the prognosis of endometrial cancer patients: a cohort study.
BMC cancer 2015 Apr 15 (1): 229. Mandato Vincenzo Dario, Farnetti Enrico, Torricelli Federica, Abrate Martino, Casali Bruno, Ciarlini Gino, Pirillo Debora, Gelli Maria C, Nicoli Davide, Grassi Mario, LA Sala Giovanni B, Palomba Stefa |
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The Impact of Genetic Variants for Different Physiological Characterization of Type 2 Diabetes Loci on Gestational Insulin Signaling in Nondiabetic Pregnant Chinese Women.
Reproductive sciences (Thousand Oaks, Calif.) 2015 Apr . Liao Shunyao, Liu Yunqiang, Chen Xiaojuan, Tan Yuande, Mei Jie, Song Wenzhong, Gan Lu, Wang Hailian, Yin Shi, Dong Xianjue, Chi Shu, Deng Shaopi |
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Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk.
Human molecular genetics 2015 Mar 24 (5): 1478-92. Painter Jodie N, O'Mara Tracy A, Batra Jyotsna, Cheng Timothy, Lose Felicity A, Dennis Joe, Michailidou Kyriaki, Tyrer Jonathan P, Ahmed Shahana, Ferguson Kaltin, Healey Catherine S, Kaufmann Susanne, Hillman Kristine M, Walpole Carina, Moya Leire, Pollock Pamela, Jones Angela, Howarth Kimberley, Martin Lynn, Gorman Maggie, Hodgson Shirley, , , De Polanco Ma Magdalena Echeverry, Sans Monica, Carracedo Angel, Castellvi-Bel Sergi, Rojas-Martinez Augusto, Santos Erika, Teixeira Manuel R, Carvajal-Carmona Luis, Shu Xiao-Ou, Long Jirong, Zheng Wei, Xiang Yong-Bing, , Montgomery Grant W, Webb Penelope M, Scott Rodney J, McEvoy Mark, Attia John, Holliday Elizabeth, Martin Nicholas G, Nyholt Dale R, Henders Anjali K, Fasching Peter A, Hein Alexander, Beckmann Matthias W, Renner Stefan P, Dörk Thilo, Hillemanns Peter, Dürst Matthias, Runnebaum Ingo, Lambrechts Diether, Coenegrachts Lieve, Schrauwen Stefanie, Amant Frederic, Winterhoff Boris, Dowdy Sean C, Goode Ellen L, Teoman Attila, Salvesen Helga B, Trovik Jone, Njolstad Tormund S, Werner Henrica M J, Ashton Katie, Proietto Tony, Otton Geoffrey, Tzortzatos Gerasimos, Mints Miriam, Tham Emma, , Hall Per, Czene Kamila, Liu Jianjun, Li Jingmei, Hopper John L, Southey Melissa C, , Ekici Arif B, Ruebner Matthias, Johnson Nicola, Peto Julian, Burwinkel Barbara, Marme Frederik, Brenner Hermann, Dieffenbach Aida K, Meindl Alfons, Brauch Hiltrud, , Lindblom Annika, Depreeuw Jeroen, Moisse Matthieu, Chang-Claude Jenny, Rudolph Anja, Couch Fergus J, Olson Janet E, Giles Graham G, Bruinsma Fiona, Cunningham Julie M, Fridley Brooke L, Børresen-Dale Anne-Lise, Kristensen Vessela N, Cox Angela, Swerdlow Anthony J, Orr Nicholas, Bolla Manjeet K, Wang Qin, Weber Rachel Palmieri, Chen Zhihua, Shah Mitul, French Juliet D, Pharoah Paul D P, Dunning Alison M, Tomlinson Ian, Easton Douglas F, Edwards Stacey L, Thompson Deborah J, Spurdle Amanda |
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Meta-analysis of the association between the HNF1B rs4430796 (A>G) polymorphism and risk of prostate cancer based on case-control studies.
Genetics and molecular research : GMR 2015 14 (3): 7426-35. Zhao Y, Liang J, Qi J G, Yang N, Wu G, Lin Y L, Cao J Y, Wang Q, Wang Q |
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Polymorphism in microRNA-binding site in HNF1B influences the susceptibility of type 2 diabetes mellitus: a population based case-control study.
BMC medical genetics 2015 16 (1): 75. Goda Naoki, Murase Haruna, Kasezawa Nobuhiko, Goda Toshinao, Yamakawa-Kobayashi Kimi |
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Shared common variants in prostate cancer and blood lipids.
International journal of epidemiology 2014 Aug 43 (4): 1205-14. Andreassen Ole A, Zuber Verena, Thompson Wesley K, Schork Andrew J, Bettella Francesco, , , Djurovic Srdjan, Desikan Rahul S, Mills Ian G, Dale Anders |
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Cost-effective PKHD1 genetic testing for autosomal recessive polycystic kidney disease.
Pediatric nephrology (Berlin, Germany) 2014 Feb 29 (2): 223-34. Krall Paola, Pineda Cristina, Ruiz Patricia, Ejarque Laia, Vendrell Teresa, Camacho Juan Antonio, Mendizábal Santiago, Oliver Artur, Ballarín José, Torra Roser, Ars Elisab |
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Genome-wide association study of endometrial cancer in E2C2.
Human genetics 2014 Feb 133 (2): 211-24. De Vivo Immaculata, Prescott Jennifer, Setiawan Veronica Wendy, Olson Sara H, Wentzensen Nicolas, , Attia John, Black Amanda, Brinton Louise, Chen Chu, Chen Constance, Cook Linda S, Crous-Bou Marta, Doherty Jennifer, Dunning Alison M, Easton Douglas F, Friedenreich Christine M, Garcia-Closas Montserrat, Gaudet Mia M, Haiman Christopher, Hankinson Susan E, Hartge Patricia, Henderson Brian E, Holliday Elizabeth, Horn-Ross Pamela L, Hunter David J, Le Marchand Loic, Liang Xiaolin, Lissowska Jolanta, Long Jirong, Lu Lingeng, Magliocco Anthony M, McEvoy Mark, O'Mara Tracy A, Orlow Irene, Painter Jodie N, Pooler Loreall, Rastogi Radhai, Rebbeck Timothy R, Risch Harvey, Sacerdote Carlotta, Schumacher Fredrick, Scott Rodney J, Sheng Xin, Shu Xiao-ou, Spurdle Amanda B, Thompson Deborah, Vanden Berg David, Weiss Noel S, Xia Lucy, Xiang Yong-Bing, Yang Hannah P, Yu Herbert, Zheng Wei, Chanock Stephen, Kraft Pet |
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Sleep duration does not mediate or modify association of common genetic variants with type 2 diabetes.
Diabetologia 2014 Feb 57 (2): 339-46. Tare Archana, Lane Jacqueline M, Cade Brian E, Grant Struan F A, Chen Ting-Hsu, Punjabi Naresh M, Lauderdale Diane S, Zee Phyllis C, Gharib Sina A, Gottlieb Daniel J, Scheer Frank A J L, Redline Susan, Saxena Ric |
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Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
Clinical journal of the American Society of Nephrology : CJASN 2013 Jul 8 (7): 1179-87. Madariaga Leire, Morinière Vincent, Jeanpierre Cécile, Bouvier Raymonde, Loget Philippe, Martinovic Jelena, Dechelotte Pierre, Leporrier Nathalie, Thauvin-Robinet Christel, Jensen Uffe Birk, Gaillard Dominique, Mathieu Michele, Turlin Bruno, Attie-Bitach Tania, Salomon Rémi, Gübler Marie-Claire, Antignac Corinne, Heidet Lauren |
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A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.
Diabetes 2013 Jan 62 (1): 291-8. Li Huaixing, Gan Wei, Lu Ling, Dong Xiao, Han Xueyao, Hu Cheng, Yang Zhen, Sun Liang, Bao Wei, Li Pengtao, He Meian, Sun Liangdan, Wang Yiqin, Zhu Jingwen, Ning Qianqian, Tang Yong, Zhang Rong, Wen Jie, Wang Di, Zhu Xilin, Guo Kunquan, Zuo Xianbo, Guo Xiaohui, Yang Handong, Zhou Xianghai, , , Zhang Xuejun, Qi Lu, Loos Ruth J F, Hu Frank B, Wu Tangchun, Liu Ying, Liu Liegang, Yang Ze, Hu Renming, Jia Weiping, Ji Linong, Li Yixue, Lin |
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HNF1B deletions in patients with young-onset diabetes but no known renal disease.
Diabetic medicine : a journal of the British Diabetic Association 2013 Jan 30 (1): 114-7. Edghill E L, Stals K, Oram R A, Shepherd M H, Hattersley A T, Ellard |
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Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer.
Nature communications 2013 4 1628. Shen Hui, Fridley Brooke L, Song Honglin, Lawrenson Kate, Cunningham Julie M, Ramus Susan J, Cicek Mine S, Tyrer Jonathan, Stram Douglas, Larson Melissa C, Köbel Martin, , Ziogas Argyrios, Zheng Wei, Yang Hannah P, Wu Anna H, Wozniak Eva L, Woo Yin Ling, Winterhoff Boris, Wik Elisabeth, Whittemore Alice S, Wentzensen Nicolas, Weber Rachel Palmieri, Vitonis Allison F, Vincent Daniel, Vierkant Robert A, Vergote Ignace, Van Den Berg David, Van Altena Anne M, Tworoger Shelley S, Thompson Pamela J, Tessier Daniel C, Terry Kathryn L, Teo Soo-Hwang, Templeman Claire, Stram Daniel O, Southey Melissa C, Sieh Weiva, Siddiqui Nadeem, Shvetsov Yurii B, Shu Xiao-Ou, Shridhar Viji, Wang-Gohrke Shan, Severi Gianluca, Schwaab Ira, Salvesen Helga B, Rzepecka Iwona K, Runnebaum Ingo B, Rossing Mary Anne, Rodriguez-Rodriguez Lorna, Risch Harvey A, Renner Stefan P, Poole Elizabeth M, Pike Malcolm C, Phelan Catherine M, Pelttari Liisa M, Pejovic Tanja, Paul James, Orlow Irene, Omar Siti Zawiah, Olson Sara H, Odunsi Kunle, Nickels Stefan, Nevanlinna Heli, Ness Roberta B, Narod Steven A, Nakanishi Toru, Moysich Kirsten B, Monteiro Alvaro N A, Moes-Sosnowska Joanna, Modugno Francesmary, Menon Usha, McLaughlin John R, McGuire Valerie, Matsuo Keitaro, Adenan Noor Azmi Mat, Massuger Leon F A G, Lurie Galina, Lundvall Lene, Lubi?ski Jan, Lissowska Jolanta, Levine Douglas A, Leminen Arto, Lee Alice W, Le Nhu D, Lambrechts Sandrina, Lambrechts Diether, Kupryjanczyk Jolanta, Krakstad Camilla, Konecny Gottfried E, Kjaer Susanne Krüger, Kiemeney Lambertus A, Kelemen Linda E, Keeney Gary L, Karlan Beth Y, Karevan Rod, Kalli Kimberly R, Kajiyama Hiroaki, Ji Bu-Tian, Jensen Allan, Jakubowska Anna, Iversen Edwin, Hosono Satoyo, Høgdall Claus K, Høgdall Estrid, Hoatlin Maureen, Hillemanns Peter, Heitz Florian, Hein Rebecca, Harter Philipp, Halle Mari K, Hall Per, Gronwald Jacek, Gore Martin, Goodman Marc T, Giles Graham G, Gentry-Maharaj Aleksandra, Garcia-Closas Montserrat, Flanagan James M, Fasching Peter A, Ekici Arif B, Edwards Robert, Eccles Diana, Easton Douglas F, Dürst Matthias, du Bois Andreas, Dörk Thilo, Doherty Jennifer A, Despierre Evelyn, Dansonka-Mieszkowska Agnieszka, Cybulski Cezary, Cramer Daniel W, Cook Linda S, Chen Xiaoqing, Charbonneau Bridget, Chang-Claude Jenny, Campbell Ian, Butzow Ralf, Bunker Clareann H, Brueggmann Doerthe, Brown Robert, Brooks-Wilson Angela, Brinton Louise A, Bogdanova Natalia, Block Matthew S, Benjamin Elizabeth, Beesley Jonathan, Beckmann Matthias W, Bandera Elisa V, Baglietto Laura, Bacot François, Armasu Sebastian M, Antonenkova Natalia, Anton-Culver Hoda, Aben Katja K, Liang Dong, Wu Xifeng, Lu Karen, Hildebrandt Michelle A T, , , Schildkraut Joellen M, Sellers Thomas A, Huntsman David, Berchuck Andrew, Chenevix-Trench Georgia, Gayther Simon A, Pharoah Paul D P, Laird Peter W, Goode Ellen L, Pearce Celeste Lei |
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Use of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes.
PloS one 2013 8 (12): e83093. Tam Claudia H T, Ho Janice S K, Wang Ying, Lam Vincent K L, Lee Heung Man, Jiang Guozhi, Lau Eric S H, Kong Alice P S, Fan Xiaodan, Woo Jean L F, Tsui Stephen K W, Ng Maggie C Y, So Wing Yee, Chan Juliana C N, Ma Ronald C |
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Association of type 2 diabetes susceptibility variants with advanced prostate cancer risk in the Breast and Prostate Cancer Cohort Consortium.
American journal of epidemiology 2012 Dec 176 (12): 1121-9. Machiela Mitchell J, Lindström Sara, Allen Naomi E, Haiman Christopher A, Albanes Demetrius, Barricarte Aurelio, Berndt Sonja I, Bueno-de-Mesquita H Bas, Chanock Stephen, Gaziano J Michael, Gapstur Susan M, Giovannucci Edward, Henderson Brian E, Jacobs Eric J, Kolonel Laurence N, Krogh Vittorio, Ma Jing, Stampfer Meir J, Stevens Victoria L, Stram Daniel O, Tjønneland Anne, Travis Ruth, Willett Walter C, Hunter David J, Le Marchand Loic, Kraft Pet |
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Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs.
Diabetologia 2012 Feb 55 (2): 349-57. Gupta V, Vinay D G, Rafiq S, Kranthikumar M V, Janipalli C S, Giambartolomei C, Evans D M, Mani K R, Sandeep M N, Taylor A E, Kinra S, Sullivan R M, Bowen L, Timpson N J, Smith G D, Dudbridge F, Prabhakaran D, Ben-Shlomo Y, Reddy K S, Ebrahim S, Chandak G R, |
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Association of six susceptibility Loci with prostate cancer in northern chinese men.
Asian Pacific journal of cancer prevention : APJCP 2012 13 (12): 6273-6. Zhang Yu-Rong, Xu Yong, Yang Kuo, Liu Ming, Wei Dong, Zhang Yao-Guang, Shi Xiao-Hong, Wang Jian-Ye, Yang Fan, Wang Xin, Liang Si-Ying, Zhao Cheng-Xiao, Wang Fei, Chen Xin, Sun Liang, Zhu Xiao-Quan, Zhu Ling, Yang Yi-Ge, Tang Lei, Jiao Hai-Yan, Huo Zheng-Hao, Yang |
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HNF1B and endometrial cancer risk: results from the PAGE study.
PloS one 2012 7 (1): e30390. Setiawan Veronica Wendy, Haessler Jeffrey, Schumacher Fredrick, Cote Michele L, Deelman Ewa, Fesinmeyer Megan D, Henderson Brian E, Jackson Rebecca D, Vöckler Jens-S, Wilkens Lynne R, Yasmeen Shagufta, Haiman Christopher A, Peters Ulrike, Le Marchand Loïc, Kooperberg Charl |
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Association of variants in genes involved in pancreatic ?-cell development and function with type 2 diabetes in North Indians.
Journal of human genetics 2011 Oct 56 (10): 695-700. Chavali Sreenivas, Mahajan Anubha, Tabassum Rubina, Dwivedi Om Prakash, Chauhan Ganesh, Ghosh Saurabh, Tandon Nikhil, Bharadwaj Dwaipay |
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HNF1B polymorphism associated with development of prostate cancer in Korean patients.
Urology 2011 Oct 78 (4): 969.e1-6. Kim Hae Jong, Bae Joon Seol, Lee Jaehyouk, Chang In Ho, Kim Kyung Do, Shin Hyoung Doo, Han June Hyun, Lee Shin Young, Kim Wonyong, Myung Soon Ch |
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Large-scale fine mapping of the HNF1B locus and prostate cancer risk.
Human molecular genetics 2011 Aug 20 (16): 3322-9. Berndt Sonja I, Sampson Joshua, Yeager Meredith, Jacobs Kevin B, Wang Zhaoming, Hutchinson Amy, Chung Charles, Orr Nick, Wacholder Sholom, Chatterjee Nilanjan, Yu Kai, Kraft Peter, Feigelson Heather Spencer, Thun Michael J, Diver W Ryan, Albanes Demetrius, Virtamo Jarmo, Weinstein Stephanie, Schumacher Fredrick R, Cancel-Tassin Geraldine, Cussenot Olivier, Valeri Antoine, Andriole Gerald L, Crawford E David, Haiman Christopher, Henderson Brian, Kolonel Laurence, Le Marchand Loic, Siddiq Afshan, Riboli Elio, Travis Ruth C, Kaaks Rudolf, Isaacs William, Isaacs Sarah, Wiley Kathleen E, Gronberg Henrik, Wiklund Fredrik, Stattin Pär, Xu Jianfeng, Zheng S Lilly, Sun Jielin, Vatten Lars J, Hveem Kristian, Njølstad Inger, Gerhard Daniela S, Tucker Margaret, Hayes Richard B, Hoover Robert N, Fraumeni Joseph F, Hunter David J, Thomas Gilles, Chanock Stephen |
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Effects of 34 risk loci for type 2 diabetes or hyperglycemia on lipoprotein subclasses and their composition in 6,580 nondiabetic Finnish men.
Diabetes 2011 May 60 (5): 1608-16. Stan?áková Alena, Paananen Jussi, Soininen Pasi, Kangas Antti J, Bonnycastle Lori L, Morken Mario A, Collins Francis S, Jackson Anne U, Boehnke Michael L, Kuusisto Johanna, Ala-Korpela Mika, Laakso Mark |
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Genome-wide association study identifies a common variant associated with risk of endometrial cancer.
Nature genetics 2011 May 43 (5): 451-4. Spurdle Amanda B, Thompson Deborah J, Ahmed Shahana, Ferguson Kaltin, Healey Catherine S, O'Mara Tracy, Walker Logan C, Montgomery Stephen B, Dermitzakis Emmanouil T, , Fahey Paul, Montgomery Grant W, Webb Penelope M, Fasching Peter A, Beckmann Matthias W, Ekici Arif B, Hein Alexander, Lambrechts Diether, Coenegrachts Lieve, Vergote Ignace, Amant Frederic, Salvesen Helga B, Trovik Jone, Njolstad Tormund S, Helland Harald, Scott Rodney J, Ashton Katie, Proietto Tony, Otton Geoffrey, , Tomlinson Ian, Gorman Maggie, Howarth Kimberley, Hodgson Shirley, Garcia-Closas Montserrat, Wentzensen Nicolas, Yang Hannah, Chanock Stephen, Hall Per, Czene Kamila, Liu Jianjun, Li Jingmei, Shu Xiao-Ou, Zheng Wei, Long Jirong, Xiang Yong-Bing, Shah Mitul, Morrison Jonathan, Michailidou Kyriaki, Pharoah Paul D, Dunning Alison M, Easton Douglas |
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Association of indices of liver and adipocyte insulin resistance with 19 confirmed susceptibility loci for type 2 diabetes in 6,733 non-diabetic Finnish men.
Diabetologia 2011 Mar 54 (3): 563-71. Vangipurapu J, Stan?áková A, Pihlajamäki J, Kuulasmaa T M, Kuulasmaa T, Paananen J, Kuusisto J, Ferrannini E, Laakso |
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Mutations in the hepatocyte nuclear factor-1? (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations.
American journal of obstetrics and gynecology 2010 Oct 203 (4): 364.e1-5. Oram Richard A, Edghill Emma L, Blackman Jenny, Taylor Miles J O, Kay Tracey, Flanagan Sarah E, Ismail-Pratt Ida, Creighton Sarah M, Ellard Sian, Hattersley Andrew T, Bingham Coral |
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HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.
Pediatric nephrology (Berlin, Germany) 2010 Jun 25 (6): 1073-9. Nakayama Makiko, Nozu Kandai, Goto Yuki, Kamei Koichi, Ito Shuichi, Sato Hidenori, Emi Mitsuru, Nakanishi Koichi, Tsuchiya Shigeru, Iijima Kazumo |
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HNF1B and JAZF1 genes, diabetes, and prostate cancer risk.
The Prostate 2010 May 70 (6): 601-7. Stevens Victoria L, Ahn Jiyoung, Sun Juzhong, Jacobs Eric J, Moore Steven C, Patel Alpa V, Berndt Sonja I, Albanes Demetrius, Hayes Richard |
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Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases.
Clinical journal of the American Society of Nephrology : CJASN 2010 Apr . Heidet L, Decramer S, Pawtowski A, Morinière V, Bandin F, Knebelmann B, Lebre AS, Faguer S, Guigonis V, Antignac C, Salomon R |
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Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function.
Diabetes 2010 Jan 59 (1): 293-301. Simonis-Bik Annemarie M, Nijpels Giel, van Haeften Timon W, Houwing-Duistermaat Jeanine J, Boomsma Dorret I, Reiling Erwin, van Hove Els C, Diamant Michaela, Kramer Mark H H, Heine Robert J, Maassen J Antonie, Slagboom P Eline, Willemsen Gonneke, Dekker Jacqueline M, Eekhoff Elisabeth M, de Geus Eco J, 't Hart Leen |
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Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux.
Journal of the American Society of Nephrology : JASN 2010 Jan 21 (1): 113-23. Cordell Heather J, Darlay Rebecca, Charoen Pimphen, Stewart Aisling, Gullett Ambrose M, Lambert Heather J, Malcolm Sue, Feather Sally A, Goodship Timothy H J, Woolf Adrian S, Kenda Rajko B, Goodship Judith A, |
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Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies.
PloS one 2010 5 (5): e10858. Elliott Katherine S, Zeggini Eleftheria, McCarthy Mark I, Gudmundsson Julius, Sulem Patrick, Stacey Simon N, Thorlacius Steinunn, Amundadottir Laufey, Grönberg Henrik, Xu Jianfeng, Gaborieau Valerie, Eeles Rosalind A, Neal David E, Donovan Jenny L, Hamdy Freddie C, Muir Kenneth, Hwang Shih-Jen, Spitz Margaret R, Zanke Brent, Carvajal-Carmona Luis, Brown Kevin M, , Hayward Nicholas K, Macgregor Stuart, Tomlinson Ian P M, Lemire Mathieu, Amos Christopher I, Murabito Joanne M, Isaacs William B, Easton Douglas F, Brennan Paul, , Barkardottir Rosa B, Gudbjartsson Daniel F, Rafnar Thorunn, Hunter David J, Chanock Stephen J, Stefansson Kari, Ioannidis John P |
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Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk.
Human heredity 2010 69 (3): 193-201. Pierce Brandon L, Ahsan Habib |
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No association of multiple type 2 diabetes loci with type 1 diabetes.
Diabetologia 2009 Oct 52 (10): 2109-16. Raj S M, Howson J M M, Walker N M, Cooper J D, Smyth D J, Field S F, Stevens H E, Todd J |
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Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men.
Diabetes 2009 Sep 58 (9): 2129-36. Stancáková Alena, Kuulasmaa Teemu, Paananen Jussi, Jackson Anne U, Bonnycastle Lori L, Collins Francis S, Boehnke Michael, Kuusisto Johanna, Laakso Mark |
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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 |
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HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.
Journal of the American Society of Nephrology : JASN 2009 May 20 (5): 1123-31. Adalat Shazia, Woolf Adrian S, Johnstone Karen A, Wirsing Andrea, Harries Lorna W, Long David A, Hennekam Raoul C, Ledermann Sarah E, Rees Lesley, van't Hoff William, Marks Stephen D, Trompeter Richard S, Tullus Kjell, Winyard Paul J, Cansick Janette, Mushtaq Imran, Dhillon Harjeeta K, Bingham Coralie, Edghill Emma L, Shroff Rukshana, Stanescu Horia, Ryffel Gerhart U, Ellard Sian, Bockenhauer Detl |
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Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association.
Journal of human genetics 2009 Apr 54 (4): 236-41. Miyake Kazuaki, Yang Woosung, Hara Kazuo, Yasuda Kazuki, Horikawa Yukio, Osawa Haruhiko, Furuta Hiroto, Ng Maggie C Y, Hirota Yushi, Mori Hiroyuki, Ido Keisuke, Yamagata Kazuya, Hinokio Yoshinori, Oka Yoshitomo, Iwasaki Naoko, Iwamoto Yasuhiko, Yamada Yuichiro, Seino Yutaka, Maegawa Hiroshi, Kashiwagi Atsunori, Wang He-Yao, Tanahashi Toshihito, Nakamura Naoto, Takeda Jun, Maeda Eiichi, Yamamoto Ken, Tokunaga Katsushi, Ma Ronald C W, So Wing-Yee, Chan Juliana C N, Kamatani Naoyuki, Makino Hideichi, Nanjo Kishio, Kadowaki Takashi, Kasuga Masa |
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Generalizability of Associations from Prostate Cancer Genome-Wide Association Studies in Multiple Populations.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Mar . Waters KM, Le Marchand L, Kolonel LN, Monroe KR, Stram DO, Henderson BE, Haiman CA |
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Previously associated type 2 diabetes variants may interact with physical activity to modify the risk of impaired glucose regulation and type 2 diabetes: a study of 16,003 Swedish adults.
Diabetes 2009 Mar . Brito EC, Lyssenko V, Renström F, Berglund G, Nilsson PM, Groop L, Franks PW |
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Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT).
Pediatric nephrology (Berlin, Germany) 2009 Jan 24 (1): 55-60. Wolf Matthias T F, Hoskins Bethan E, Beck Bodo B, Hoppe Bernd, Tasic Velibor, Otto Edgar A, Hildebrandt Friedhe |
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Evidence of interaction between type 2 diabetes susceptibility genes and dietary fat intake for adiposity and glucose homeostasis-related phenotypes.
Journal of nutrigenetics and nutrigenomics 2009 2 (4-5): 225-34. Ruchat Stephanie-May, Elks Cathy E, Loos Ruth J F, Vohl Marie-Claude, Weisnagel S John, Rankinen Tuomo, Bouchard Claude, Pérusse Lou |
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Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12.
Nature genetics 2008 Oct 40 (10): 1153-5. Sun Jielin, Zheng Siqun Lilly, Wiklund Fredrik, Isaacs Sarah D, Purcell Lina D, Gao Zhengrong, Hsu Fang-Chi, Kim Seong-Tae, Liu Wennuan, Zhu Yi, Stattin Pär, Adami Hans-Olov, Wiley Kathleen E, Dimitrov Latchezar, Sun Jishan, Li Tao, Turner Aubrey R, Adams Tamara S, Adolfsson Jan, Johansson Jan-Erik, Lowey James, Trock Bruce J, Partin Alan W, Walsh Patrick C, Trent Jeffrey M, Duggan David, Carpten John, Chang Bao-Li, Grönberg Henrik, Isaacs William B, Xu Jianfe |
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Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young.
The Journal of clinical endocrinology and metabolism 2008 Sep 93 (9): 3505-9. Vesterhus Mette, Haldorsen Ingfrid S, Raeder Helge, Molven Anders, Njølstad Pål |
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Association analysis of type 2 diabetes Loci in type 1 diabetes.
Diabetes 2008 Jul 57 (7): 1983-6. Qu Hui-Qi, Grant Struan F A, Bradfield Jonathan P, Kim Cecilia, Frackelton Edward, Hakonarson Hakon, Polychronakos Constant |
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Multiple loci identified in a genome-wide association study of prostate cancer.
Nature genetics 2008 Mar 40 (3): 310-5. Thomas Gilles, Jacobs Kevin B, Yeager Meredith, Kraft Peter, Wacholder Sholom, Orr Nick, Yu Kai, Chatterjee Nilanjan, Welch Robert, Hutchinson Amy, Crenshaw Andrew, Cancel-Tassin Geraldine, Staats Brian J, Wang Zhaoming, Gonzalez-Bosquet Jesus, Fang Jun, Deng Xiang, Berndt Sonja I, Calle Eugenia E, Feigelson Heather Spencer, Thun Michael J, Rodriguez Carmen, Albanes Demetrius, Virtamo Jarmo, Weinstein Stephanie, Schumacher Fredrick R, Giovannucci Edward, Willett Walter C, Cussenot Olivier, Valeri Antoine, Andriole Gerald L, Crawford E David, Tucker Margaret, Gerhard Daniela S, Fraumeni Joseph F, Hoover Robert, Hayes Richard B, Hunter David J, Chanock Stephen |
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Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns.
Diabetes 2006 Sep 55 (9): 2534-40. Bonnycastle Lori L, Willer Cristen J, Conneely Karen N, Jackson Anne U, Burrill Cecily P, Watanabe Richard M, Chines Peter S, Narisu Narisu, Scott Laura J, Enloe Sareena T, Swift Amy J, Duren William L, Stringham Heather M, Erdos Michael R, Riebow Nancy L, Buchanan Thomas A, Valle Timo T, Tuomilehto Jaakko, Bergman Richard N, Mohlke Karen L, Boehnke Michael, Collins Francis |
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