HuGE Literature Finder
Records 1-30
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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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Common Type 2 Diabetes Genetic Risk Variants Improve the Prediction of Gestational Diabetes.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2019 Jul . Dziedziejko Violetta, Safranow Krzysztof, Tarnowski Maciej, Pawlik Andrz |
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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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Serum magnesium, hepatocyte nuclear factor 1ß genotype and post-transplant diabetes mellitus: a prospective study.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2019 Jul . van der Burgh Anna C, Moes Arthur, Kieboom Brenda C T, van Gelder Teun, Zietse Robert, van Schaik Ron H N, Hesselink Dennis A, Hoorn Ewout |
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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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Association between the clinical presentation of congenital anomalies of the kidney and urinary tract (CAKUT) and gene mutations: an analysis of 66 patients at a single institution.
Pediatric nephrology (Berlin, Germany) 2019 Apr . Ishiwa Sho, Sato Mai, Morisada Naoya, Nishi Kentaro, Kanamori Toru, Okutsu Mika, Ogura Masao, Sako Mayumi, Kosuga Motomichi, Kamei Koichi, Ito Shuichi, Nozu Kandai, Iijima Kazumoto, Ishikura Ken |
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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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Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer.
Nature communications 2018 Feb 9 (1): 556. Klein Alison P, Wolpin Brian M, Risch Harvey A, Stolzenberg-Solomon Rachael Z, Mocci Evelina, Zhang Mingfeng, Canzian Federico, Childs Erica J, Hoskins Jason W, Jermusyk Ashley, Zhong Jun, Chen Fei, Albanes Demetrius, Andreotti Gabriella, Arslan Alan A, Babic Ana, Bamlet William R, Beane-Freeman Laura, Berndt Sonja I, Blackford Amanda, Borges Michael, Borgida Ayelet, Bracci Paige M, Brais Lauren, Brennan Paul, Brenner Hermann, Bueno-de-Mesquita Bas, Buring Julie, Campa Daniele, Capurso Gabriele, Cavestro Giulia Martina, Chaffee Kari G, Chung Charles C, Cleary Sean, Cotterchio Michelle, Dijk Frederike, Duell Eric J, Foretova Lenka, Fuchs Charles, Funel Niccola, Gallinger Steven, M Gaziano J Michael, Gazouli Maria, Giles Graham G, Giovannucci Edward, Goggins Michael, Goodman Gary E, Goodman Phyllis J, Hackert Thilo, Haiman Christopher, Hartge Patricia, Hasan Manal, Hegyi Peter, Helzlsouer Kathy J, Herman Joseph, Holcatova Ivana, Holly Elizabeth A, Hoover Robert, Hung Rayjean J, Jacobs Eric J, Jamroziak Krzysztof, Janout Vladimir, Kaaks Rudolf, Khaw Kay-Tee, Klein Eric A, Kogevinas Manolis, Kooperberg Charles, Kulke Matthew H, Kupcinskas Juozas, Kurtz Robert J, Laheru Daniel, Landi Stefano, Lawlor Rita T, Lee I-Min, LeMarchand Loic, Lu Lingeng, Malats Núria, Mambrini Andrea, Mannisto Satu, Milne Roger L, Mohelníková-Ducho?ová Beatrice, Neale Rachel E, Neoptolemos John P, Oberg Ann L, Olson Sara H, Orlow Irene, Pasquali Claudio, Patel Alpa V, Peters Ulrike, Pezzilli Raffaele, Porta Miquel, Real Francisco X, Rothman Nathaniel, Scelo Ghislaine, Sesso Howard D, Severi Gianluca, Shu Xiao-Ou, Silverman Debra, Smith Jill P, Soucek Pavel, Sund Malin, Talar-Wojnarowska Renata, Tavano Francesca, Thornquist Mark D, Tobias Geoffrey S, Van Den Eeden Stephen K, Vashist Yogesh, Visvanathan Kala, Vodicka Pavel, Wactawski-Wende Jean, Wang Zhaoming, Wentzensen Nicolas, White Emily, Yu Herbert, Yu Kai, Zeleniuch-Jacquotte Anne, Zheng Wei, Kraft Peter, Li Donghui, Chanock Stephen, Obazee Ofure, Petersen Gloria M, Amundadottir Laufey |
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Systematic analysis of copy number variation associated with congenital diaphragmatic hernia.
Proceedings of the National Academy of Sciences of the United States of America 2018 05 115 (20): 5247-5252. Zhu Qihui, High Frances A, Zhang Chengsheng, Cerveira Eliza, Russell Meaghan K, Longoni Mauro, Joy Maliackal P, Ryan Mallory, Mil-Homens Adam, Bellfy Lauren, Coletti Caroline M, Bhayani Pooja, Hila Regis, Wilson Jay M, Donahoe Patricia K, Lee Charl |
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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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Network-directed cis-mediator analysis of normal prostate tissue expression profiles reveals downstream regulatory associations of prostate cancer susceptibility loci.
Oncotarget 2017 Oct 8 (49): 85896-85908. Larson Nicholas B, McDonnell Shannon K, Fogarty Zach, Larson Melissa C, Cheville John, Riska Shaun, Baheti Saurabh, Weber Alexandra M, Nair Asha A, Wang Liang, O'Brien Daniel, Davila Jaime, Schaid Daniel J, Thibodeau Stephen |
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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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Genetic variants associated with lean and obese type 2 diabetes in a Han Chinese population: A case-control study.
Medicine 2016 Jun 95 (23): e3841. Kong Xiaomu, Xing Xiaoyan, Hong Jing, Zhang Xuelian, Yang Wenyi |
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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 Single Nucleotide Variant in HNF-1? is Associated with Maturity-Onset Diabetes of the Young in a Large Chinese Family.
Iranian journal of public health 2016 Feb 45 (2): 170-8. Zhou Peng, Wei Ran, Guo Zhenkui, Zhu Haining, Campbell Desmond, Li Qi, Xu Xiaoqun, Wang Junfu, Luan Meng, Chen Xing, Chen Ga |
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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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Atypical Polypoid Adenomyoma of the Uterus: An Immunohistochemical and Molecular Study of 21 Cases.
The American journal of surgical pathology 2015 Aug 39 (8): 1148-55. N?mejcová Kristýna, Kenny Sarah L, Laco Jan, Škapa Petr, Stan?k Libor, Zikán Michal, Kleiblová Petra, McCluggage W Glenn, Dundr Pav |
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Endometrial Carcinomas With Clear Cells: A Study of a Heterogeneous Group of Tumors Including Interobserver Variability, Mutation Analysis, and Immunohistochemistry With HNF-1?.
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2015 Jul 34 (4): 323-33. Han Guangming, Soslow Robert A, Wethington Stephanie, Levine Douglas A, Bogomolniy Faina, Clement Philip B, Köbel Martin, Gilks Blake, DeLair Debor |
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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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The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes.
PloS one 2015 10 (11): e0143607. Kong Xiaomu, Zhang Xuelian, Xing Xiaoyan, Zhang Bo, Hong Jing, Yang Wenyi |
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Assessment of association between common variants at 17q12 and prostate cancer risk-evidence from Serbian population and meta--analysis.
Clinical and translational science 2014 Aug 7 (4): 307-13. Nikoli? Zorana Z, Brankovi? Ana S, Savi?-Pavi?evi? Dušanka L J, Prekovi? Stefan M, Vukoti? Vinka D, Cerovi? Snežana J, Filipovi? Nataša N, Tomovi? Saša M, Romac Stanka P, Brajuškovi? Goran |
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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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Screening of diabetes of youth for hepatocyte nuclear factor 1 mutations: clinical phenotype of HNF1?-related maturity-onset diabetes of the young and HNF1?-related maturity-onset diabetes of the young in Japanese.
Diabetic medicine : a journal of the British Diabetic Association 2014 Jun 31 (6): 721-7. Horikawa Y, Enya M, Fushimi N, Fushimi Y, Takeda |
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Association of a single-nucleotide polymorphism from chromosome 17q12 with the aggressiveness of prostate cancer in a Hispanic population.
Journal of cancer research and clinical oncology 2014 May 140 (5): 783-8. Rojas Pablo A, Torres-Estay Verónica, Cerda-Infante Javier, Montecinos Viviana P, Domínguez Javier, Arenas José, Godoy Alejandro S, San Francisco Ignacio |
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Validation of association of genetic variants at 10q with prostate-specific antigen (PSA) levels in men at high risk for prostate cancer.
BJU international 2014 May 113 (5b): E150-6. Chang Bao-Li, Hughes Lucinda, Chen David Y T, Gross Laura, Ruth Karen, Giri Veda |
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The presence of prostate cancer at biopsy is predicted by a number of genetic variants.
International journal of cancer. Journal international du cancer 2014 Mar 134 (5): 1139-46. Kashyap Aniruddh, Klu?niak Wojciech, Woko?orczyk Dominika, Go??b Adam, Sikorski Andrzej, S?ojewski Marcin, Gliniewicz Bart?omiej, ?wita?a Jerzy, Borkowski Tomasz, Borkowski Andrzej, Antczak Andrzej, Wojnar ?ukasz, Przyby?a Jacek, Sosnowski Marek, Ma?kiewicz Bartosz, Zdrojowy Romuald, Sikorska-Radek Paulina, Matych Józef, Wilkosz Jacek, Ró?a?ski Waldemar, Ki? Jacek, Bar Krzysztof, Bryniarski Piotr, Paradysz Andrzej, Jersak Konrad, Niemirowicz Jerzy, S?upski Piotr, Jarzemski Piotr, Skrzypczyk Micha?, Dobruch Jakub, Domaga?a Pawe?, Piotrowski Krzysztof, Jakubowska Anna, Gronwald Jacek, Huzarski Tomasz, Byrski Tomasz, D?bniak Tadeusz, Górski Bohdan, Masoj? Bart?omiej, van de Wetering Thierry, Menkiszak Janusz, Akbari Mohammad R, Lubi?ski Jan, Narod Steven A, Cybulski Cezary, |
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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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Racial disparities in the association between diabetes mellitus-associated polymorphic locus rs4430796 of the HNF1? gene and prostate cancer: a systematic review and meta-analysis.
Genetics and molecular research : GMR 2014 13 (3): 6582-92. Xiang Y Z, Jiang S B, Zhao J, Xiong H, Cui Z L, Li G B, Jin X |
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A replication study of 19 GWAS-validated type 2 diabetes at-risk variants in the Lebanese population.
Diabetes research and clinical practice 2013 Nov 102 (2): 117-22. Almawi Wassim Y, Nemr Rita, Keleshian Sose H, Echtay Akram, Saldanha Fabiola Lisa, AlDoseri Fatima A, Racoubian Edd |
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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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GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
Nature genetics 2013 Apr 45 (4): 362-70, 370e1-2. Pharoah Paul D P, Tsai Ya-Yu, Ramus Susan J, Phelan Catherine M, Goode Ellen L, Lawrenson Kate, Buckley Melissa, Fridley Brooke L, Tyrer Jonathan P, Shen Howard, Weber Rachel, Karevan Rod, Larson Melissa C, Song Honglin, Tessier Daniel C, Bacot François, Vincent Daniel, Cunningham Julie M, Dennis Joe, Dicks Ed, , , Aben Katja K, Anton-Culver Hoda, Antonenkova Natalia, Armasu Sebastian M, Baglietto Laura, Bandera Elisa V, Beckmann Matthias W, Birrer Michael J, Bloom Greg, Bogdanova Natalia, Brenton James D, Brinton Louise A, Brooks-Wilson Angela, Brown Robert, Butzow Ralf, Campbell Ian, Carney Michael E, Carvalho Renato S, Chang-Claude Jenny, Chen Y Anne, Chen Zhihua, Chow Wong-Ho, Cicek Mine S, Coetzee Gerhard, Cook Linda S, Cramer Daniel W, Cybulski Cezary, Dansonka-Mieszkowska Agnieszka, Despierre Evelyn, Doherty Jennifer A, Dörk Thilo, du Bois Andreas, Dürst Matthias, Eccles Diana, Edwards Robert, Ekici Arif B, Fasching Peter A, Fenstermacher David, Flanagan James, Gao Yu-Tang, Garcia-Closas Montserrat, Gentry-Maharaj Aleksandra, Giles Graham, Gjyshi Anxhela, Gore Martin, Gronwald Jacek, Guo Qi, Halle Mari K, Harter Philipp, Hein Alexander, Heitz Florian, Hillemanns Peter, Hoatlin Maureen, Høgdall Estrid, Høgdall Claus K, Hosono Satoyo, Jakubowska Anna, Jensen Allan, Kalli Kimberly R, Karlan Beth Y, Kelemen Linda E, Kiemeney Lambertus A, Kjaer Susanne Krüger, Konecny Gottfried E, Krakstad Camilla, Kupryjanczyk Jolanta, Lambrechts Diether, Lambrechts Sandrina, Le Nhu D, Lee Nathan, Lee Janet, Leminen Arto, Lim Boon Kiong, Lissowska Jolanta, Lubi?ski Jan, Lundvall Lene, Lurie Galina, Massuger Leon F A G, Matsuo Keitaro, McGuire Valerie, McLaughlin John R, Menon Usha, Modugno Francesmary, Moysich Kirsten B, Nakanishi Toru, Narod Steven A, Ness Roberta B, Nevanlinna Heli, Nickels Stefan, Noushmehr Houtan, Odunsi Kunle, Olson Sara, Orlow Irene, Paul James, Pejovic Tanja, Pelttari Liisa M, Permuth-Wey Jenny, Pike Malcolm C, Poole Elizabeth M, Qu Xiaotao, Risch Harvey A, Rodriguez-Rodriguez Lorna, Rossing Mary Anne, Rudolph Anja, Runnebaum Ingo, Rzepecka Iwona K, Salvesen Helga B, Schwaab Ira, Severi Gianluca, Shen Hui, Shridhar Vijayalakshmi, Shu Xiao-Ou, Sieh Weiva, Southey Melissa C, Spellman Paul, Tajima Kazuo, Teo Soo-Hwang, Terry Kathryn L, Thompson Pamela J, Timorek Agnieszka, Tworoger Shelley S, van Altena Anne M, van den Berg David, Vergote Ignace, Vierkant Robert A, Vitonis Allison F, Wang-Gohrke Shan, Wentzensen Nicolas, Whittemore Alice S, Wik Elisabeth, Winterhoff Boris, Woo Yin Ling, Wu Anna H, Yang Hannah P, Zheng Wei, Ziogas Argyrios, Zulkifli Famida, Goodman Marc T, Hall Per, Easton Douglas F, Pearce Celeste L, Berchuck Andrew, Chenevix-Trench Georgia, Iversen Edwin, Monteiro Alvaro N A, Gayther Simon A, Schildkraut Joellen M, Sellers Thomas |
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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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[Susceptibility to prostate cancer in Han Chinese: single nucleotide polymorphism analysis of 1 667 cases].
Zhonghua nan ke xue = National journal of andrology 2012 Dec 18 (12): 1069-74. Cui Yong, Shi Yi-Chao, Shen Hua, Fan You-Zhang, Cao Wen-Zhou, Xie Jian-Jun, Su Huai-Qing, Shao Qia |
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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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Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012 Jun 27 (6): 2328-37. Bertinetto Francesca Eleonora, Calafell Francesc, Roggero Stefano, Chidichimo Rossella, Garino Elena, Marcuccio Cristina, Coppo Rosanna, Scolari Francesco, Frascá Giovanni Maria, Savoldi Silvana, Schena Francesco Paolo, Amoroso Antonio, |
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A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
Carcinogenesis 2012 Mar 33 (3): 598-603. Tao Sha, Wang Zhong, Feng Junjie, Hsu Fang-Chi, Jin Guangfu, Kim Seong-Tae, Zhang Zheng, Gronberg Henrik, Zheng Lilly S, Isaacs William B, Xu Jianfeng, Sun Jiel |
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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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Significant associations of prostate cancer susceptibility variants with survival in patients treated with androgen-deprivation therapy.
International journal of cancer. Journal international du cancer 2012 Feb 130 (4): 876-84. Bao Bo-Ying, Pao Jiunn-Bey, Huang Chun-Nung, Pu Yeong-Shiau, Chang Ta-Yuan, Lan Yu-Hsuan, Lu Te-Ling, Lee Hong-Zin, Chen Lu-Min, Ting Wen-Chien, Hsieh Chi-Jeng, Huang Shu-P |
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Assessing the clinical role of genetic markers of early-onset prostate cancer among high-risk men enrolled in prostate cancer early detection.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2012 Jan 21 (1): 53-60. Hughes Lucinda, Zhu Fang, Ross Eric, Gross Laura, Uzzo Robert G, Chen David Y T, Viterbo Rosalia, Rebbeck Timothy R, Giri Veda |
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Phenotypic heterogeneity in Chinese patients with hepatocyte nuclear factor-1? mutations.
Diabetes research and clinical practice 2012 Jan 95 (1): 119-24. Wang Congrong, Zhang Rong, Lu Jingyi, Jiang Feng, Hu Cheng, Zhou Jian, Liu Fang, Zhang Feng, Qin Wen, Li Mei, Ma Xiaojing, Yan Jingbin, Bao Yuqian, Xiang Kunsan, Jia Weipi |
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Prostate cancer risk variants are not associated with disease progression.
The Prostate 2012 Jan 72 (1): 30-9. Szulkin Robert, Holmberg Erik, Stattin Pär, Xu Jianfeng, Zheng Sigun, Palmgren Juni, Grönberg Henrik, Wiklund Fredr |
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Association of single nucleotide polymorphisms in TCF2 with type 2 diabetes susceptibility in a Han Chinese population.
PloS one 2012 7 (12): e52938. Zhang Xuelong, Qiao Hong, Zhao Yanling, Wang Xi, Sun Haiming, Liu An, Xu Lidan, Sun Donglin, Jin Yan, Yu Yang, Meng Xiangning, Bai Jing, Chen Feng, Fu Songb |
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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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Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).
Human genetics 2011 Dec . Jin G, Lu L, Cooney KA, Ray AM, Zuhlke KA, Lange EM, Cannon-Albright LA, Camp NJ, Teerlink CC, Fitzgerald LM, Stanford JL, Wiley KE, Isaacs SD, Walsh PC, Foulkes WD, Giles GG, Hopper JL, Severi G, Eeles R, Easton D, Kote-Jarai Z, Guy M, Rinckleb A, Maier C, Vogel W, Cancel-Tassin G, Egrot C, Cussenot O, Thibodeau SN, McDonnell SK, Schaid DJ, Wiklund F, Grönberg H, Emanuelsson M, Whittemore AS, Oakley-Girvan I, Hsieh CL, Wahlfors T, Tammela T, Schleutker J, Catalona WJ, Zheng SL, Ostrander EA, Isaacs WB, Xu J |
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Association between single nucleotide polymorphisms on chromosome 17q and the risk of prostate cancer in a Chinese population.
Chinese journal of cancer 2011 Oct 30 (10): 721-30. Zhou Chang-Hu, Wang Jian-Ye, Cao Su-Yan, Shi Xiao-Hong, Zhang Yao-Guang, Liu Ming, Wang Xin, Huang Jin, Yang Yi-Ge, Wei Dong, Yang |
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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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Systematic confirmation study of reported prostate cancer risk-associated single nucleotide polymorphisms in Chinese men.
Cancer science 2011 Oct 102 (10): 1916-20. Liu Fang, Hsing Ann W, Wang Xiang, Shao Qiang, Qi Jun, Ye Yu, Wang Zhong, Chen Hongyan, Gao Xin, Wang Guozeng, Chu Lisa W, Ding Qiang, OuYang Jun, Gao Xu, Huang Yichen, Chen Yanbo, Gao Yu Tang, Zhang Zuo-Feng, Rao Jianyu, Shi Rong, Wu Qijun, Wang Meilin, Zhang Zhengdong, Zhang Yuanyuan, Jiang Haowen, Zheng Jie, Hu Yanlin, Guo Ling, Lin Xiaoling, Tao Sha, Jin Guangfu, Sun Jielin, Lu Daru, Zheng S Lilly, Sun Yinghao, Mo Zengnan, Xu Jianfe |
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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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A replication study examining three common single-nucleotide polymorphisms and the risk of prostate cancer in a Japanese population.
The Prostate 2011 Jul 71 (10): 1023-32. Liu Miao, Suzuki Motofumi, Arai Tomio, Sawabe Motoji, Enomoto Yutaka, Nishimatsu Hiroaki, Kume Haruki, Homma Yukio, Kitamura Tadaic |
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Polygenic risk score improves prostate cancer risk prediction: results from the Stockholm-1 cohort study.
European urology 2011 Jul 60 (1): 21-8. Aly Markus, Wiklund Fredrik, Xu Jianfeng, Isaacs William B, Eklund Martin, D'Amato Mauro, Adolfsson Jan, Grönberg Henr |
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Association study of type 2 diabetes genetic susceptibility variants and risk of pancreatic cancer: an analysis of PanScan-I data.
Cancer causes & control : CCC 2011 Jun 22 (6): 877-83. Pierce Brandon L, Austin Melissa A, Ahsan Habib |
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Association of prostate cancer risk Loci with disease aggressiveness and prostate cancer-specific mortality.
Cancer prevention research (Philadelphia, Pa.) 2011 May 4 (5): 719-28. Pomerantz Mark M, Werner Lillian, Xie Wanling, Regan Meredith M, Lee Gwo-Shu Mary, Sun Tong, Evan Carolyn, Petrozziello Gillian, Nakabayashi Mari, Oh William K, Kantoff Philip W, Freedman Matthew |
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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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Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program.
Diabetes 2011 Apr 60 (4): 1340-8. Hivert Marie-France, Jablonski Kathleen A, Perreault Leigh, Saxena Richa, McAteer Jarred B, Franks Paul W, Hamman Richard F, Kahn Steven E, Haffner Steven, , Meigs James B, Altshuler David, Knowler William C, Florez Jose C, |
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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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Identification of metabolic modifiers that underlie phenotypic variations in energy-balance regulation.
Diabetes 2011 Mar 60 (3): 726-34. Chang Chia Lin, Cai James J, Cheng Po Jen, Chueh Ho Yen, Hsu Sheau Yu Ted |
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Inherited genetic markers discovered to date are able to identify a significant number of men at considerably elevated risk for prostate cancer.
The Prostate 2011 Mar 71 (4): 421-30. Sun Jielin, Kader A Karim, Hsu Fang-Chi, Kim Seong-Tae, Zhu Yi, Turner Aubrey R, Jin Tao, Zhang Zheng, Adolfsson Jan, Wiklund Fredrik, Zheng S Lilly, Isaacs William B, Grönberg Henrik, Xu Jianfe |
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Prostate cancer predisposition loci and risk of metastatic disease and prostate cancer recurrence.
Clinical cancer research : an official journal of the American Association for Cancer Research 2011 Mar 17 (5): 1075-81. Ahn Jiyoung, Kibel Adam S, Park Jong Y, Rebbeck Timothy R, Rennert Hanna, Stanford Janet L, Ostrander Elaine A, Chanock Stephen, Wang Ming-Hsi, Mittal Rama D, Isaacs William B, Platz Elizabeth A, Hayes Richard |
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Evidence for an association between prostate cancer and chromosome 8q24 and 10q11 genetic variants in African American men: the Flint Men's Health Study.
The Prostate 2011 Feb 71 (3): 225-31. Wang Yunfei, Ray Anna M, Johnson Emilie K, Zuhlke Kimberly A, Cooney Kathleen A, Lange Ethan |
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Meta-analysis of genome-wide and replication association studies on prostate cancer.
The Prostate 2011 Feb 71 (2): 209-24. Liu Hong, Wang Bo, Han Chunshe |
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Genetic risk reclassification for type 2 diabetes by age below or above 50 years using 40 type 2 diabetes risk single nucleotide polymorphisms.
Diabetes care 2011 Jan 34 (1): 121-5. de Miguel-Yanes Jose M, Shrader Peter, Pencina Michael J, Fox Caroline S, Manning Alisa K, Grant Richard W, Dupuis Josèe, Florez Jose C, D'Agostino Ralph B, Cupples L Adrienne, Meigs James B, , |
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Polymorphisms associated with type 2 diabetes in familial longevity: The Leiden Longevity Study.
Aging 2011 Jan 3 (1): 55-62. Mooijaart Simon P, van Heemst Diana, Noordam Raymond, Rozing Maarten P, Wijsman Carolien A, de Craen Anton J M, Westendorp Rudi G J, Beekman Marian, Slagboom P Eli |
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Validation of genome-wide prostate cancer associations in men of African descent.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 Jan 20 (1): 23-32. Chang Bao-Li, Spangler Elaine, Gallagher Stephen, Haiman Christopher A, Henderson Brian, Isaacs William, Benford Marnita L, Kidd LaCreis R, Cooney Kathleen, Strom Sara, Ingles Sue Ann, Stern Mariana C, Corral Roman, Joshi Amit D, Xu Jianfeng, Giri Veda N, Rybicki Benjamin, Neslund-Dudas Christine, Kibel Adam S, Thompson Ian M, Leach Robin J, Ostrander Elaine A, Stanford Janet L, Witte John, Casey Graham, Eeles Rosalind, Hsing Ann W, Chanock Stephen, Hu Jennifer J, John Esther M, Park Jong, Stefflova Klara, Zeigler-Johnson Charnita, Rebbeck Timothy |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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A replication study examining three common single-nucleotide polymorphisms and the risk of prostate cancer in a Japanese population.
The Prostate 2010 Dec . Liu M, Suzuki M, Arai T, Sawabe M, Enomoto Y, Nishimatsu H, Kume H, Homma Y, Kitamura T |
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Number of prostate cancer risk alleles may identify possibly 'insignificant' disease.
BJU international 2010 Dec 106 (11): 1602-6. Helfand Brian T, Loeb Stacy, Kan Donghui, Catalona William |
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Impact of single nucleotide polymorphisms and of clinical risk factors on new?onset diabetes mellitus in HIV?infected individuals.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2010 Nov 51 (9): 1090-8. Rotger Margalida, Gsponer Thomas, Martinez Raquel, Taffé Patrick, Elzi Luigia, Vernazza Pietro, Cavassini Matthias, Bernasconi Enos, Hirschel Bernard, Furrer Hansjakob, Weber Rainer, Ledergerber Bruno, Egger Matthias, Telenti Amalio, Tarr Philip E, |
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Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the diabetes prevention program.
Diabetes 2010 Oct 59 (10): 2672-81. Jablonski Kathleen A, McAteer Jarred B, de Bakker Paul I W, Franks Paul W, Pollin Toni I, Hanson Robert L, Saxena Richa, Fowler Sarah, Shuldiner Alan R, Knowler William C, Altshuler David, Florez Jose C, |
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Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.
Diabetologia 2010 Oct 53 (10): 2155-62. Fontaine-Bisson B, Renström F, Rolandsson O, , Payne F, Hallmans G, Barroso I, Franks P |
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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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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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