Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 53 Records) |
Query Trace: WNT4[original query] |
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A novel functional variant in Wilms' Tumor 1 (WT1) is associated with idiopathic non-obstructive azoospermia. Molecular reproduction and development 2016 Dec . Xu Jin, Jiang Lile, Yu Wenzhu, Guo Haibin, Zhang Helong, Wei Duo, Liang Lingling, Feng Ke, Song Xiaobing, Liu Qi, Song Bingbing, Hao Haoying, Zhang Ying, Zhang Cuili |
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.
The New England journal of medicine 2017 Sep . Zhang Ge, Feenstra Bjarke, Bacelis Jonas, Liu Xueping, Muglia Lisa M, Juodakis Julius, Miller Daniel E, Litterman Nadia, Jiang Pan-Pan, Russell Laura, Hinds David A, Hu Youna, Weirauch Matthew T, Chen Xiaoting, Chavan Arun R, Wagner Günter P, Pavli?ev Mihaela, Nnamani Mauris C, Maziarz Jamie, Karjalainen Minna K, Rämet Mika, Sengpiel Verena, Geller Frank, Boyd Heather A, Palotie Aarno, Momany Allison, Bedell Bruce, Ryckman Kelli K, Huusko Johanna M, Forney Carmy R, Kottyan Leah C, Hallman Mikko, Teramo Kari, Nohr Ellen A, Davey Smith George, Melbye Mads, Jacobsson Bo, Muglia Louis |
The role of gene polymorphisms in endometriosis. Molecular medicine reports 2017 Aug . Matalliotakis Michail, Zervou Maria I, Matalliotaki Charoula, Rahmioglu Nilufer, Koumantakis George, Kalogiannidis Ioannis, Prapas Ioannis, Zondervan Krina, Spandidos Demetrios A, Matalliotakis Ioannis, Goulielmos George |
Genetic association study in a three-generation family with seven members with endometriosis. Molecular medicine reports 2017 Aug . Matalliotakis Michail, Zervou Maria I, Matalliotaki Charoula, Arici Aydin, Spandidos Demetrios A, Matalliotakis Ioannis, Goulielmos George |
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.
Nature communications 2017 Jul 8 (1): 121. Medina-Gomez Carolina, Kemp John P, Dimou Niki L, Kreiner Eskil, Chesi Alessandra, Zemel Babette S, Bønnelykke Klaus, Boer Cindy G, Ahluwalia Tarunveer S, Bisgaard Hans, Evangelou Evangelos, Heppe Denise H M, Bonewald Lynda F, Gorski Jeffrey P, Ghanbari Mohsen, Demissie Serkalem, Duque Gustavo, Maurano Matthew T, Kiel Douglas P, Hsu Yi-Hsiang, C J van der Eerden Bram, Ackert-Bicknell Cheryl, Reppe Sjur, Gautvik Kaare M, Raastad Truls, Karasik David, van de Peppel Jeroen, Jaddoe Vincent W V, Uitterlinden André G, Tobias Jonathan H, Grant Struan F A, Bagos Pantelis G, Evans David M, Rivadeneira Fernan |
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 |
SNP-SNP interactions between WNT4 and WNT5A were associated with obesity related traits in Han Chinese Population. Scientific reports 2017 Mar 7 43939. Dong Shan-Shan, Hu Wei-Xin, Yang Tie-Lin, Chen Xiao-Feng, Yan Han, Chen Xiang-Ding, Tan Li-Jun, Tian Qing, Deng Hong-Wen, Guo Y |
Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. Human molecular genetics 2017 (22): 5046-5058. Powell Joseph E, Fung Jenny N, Shakhbazov Konstantin, Sapkota Yadav, Cloonan Nicole, Hemani Gibran, Hillman Kristine M, Kaufmann Susanne, Luong Hien T, Bowdler Lisa, Painter Jodie N, Holdsworth-Carson Sarah J, Visscher Peter M, Dinger Marcel E, Healey Martin, Nyholt Dale R, French Juliet D, Edwards Stacey L, Rogers Peter A W, Montgomery Grant |
Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development. Reports of biochemistry & molecular biology 2017 11 6 (1): 59-65. Shojaei Azadeh, Ebrahimzadeh-Vesal Reza, Ahani Ali, Razzaghy-Azar Maryam, Khakpour Golnaz, Ghazi Farideh, Tavakkoly-Bazzaz Jav |
Genetic Screening of WNT4 and WNT5B in Two Populations with Deviating Bone Mineral Densities. Calcified tissue international 2017 Jan . Hendrickx Gretl, Boudin Eveline, Steenackers Ellen, Nielsen Torben Leo, Andersen Marianne, Brixen Kim, Van Hul W |
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
Nature communications 2018 Sep 9 (1): 3636. Rafnar Thorunn, Gunnarsson Bjarni, Stefansson Olafur A, Sulem Patrick, Ingason Andres, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Tragante Vinicius, Steinthorsdottir Valgerdur, Styrkarsdottir Unnur, Stacey Simon N, Gudmundsson Julius, Arnadottir Gudny A, Oddsson Asmundur, Zink Florian, Halldorsson Gisli, Sveinbjornsson Gardar, Kristjansson Ragnar P, Davidsson Olafur B, Salvarsdottir Anna, Thoroddsen Asgeir, Helgadottir Elisabet A, Kristjansdottir Katrin, Ingthorsson Orri, Gudmundsson Valur, Geirsson Reynir T, Arnadottir Ragnheidur, Gudbjartsson Daniel F, Masson Gisli, Asselbergs Folkert W, Jonasson Jon G, Olafsson Karl, Thorsteinsdottir Unnur, Halldorsson Bjarni V, Thorleifsson Gudmar, Stefansson Ka |
Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability. eLife 2018 Sep 7 . Välimäki Niko, Kuisma Heli, Pasanen Annukka, Heikinheimo Oskari, Sjöberg Jari, Bützow Ralf, Sarvilinna Nanna, Heinonen Hanna-Riikka, Tolvanen Jaana, Bramante Simona, Tanskanen Tomas, Auvinen Juha, Uimari Outi, Alkodsi Amjad, Lehtonen Rainer, Kaasinen Eevi, Palin Kimmo, Aaltonen Lauri |
The assessment of GWAS - identified polymorphisms associated with infertility risk in Polish women with endometriosis. Ginekologia polska 2018 89 (6): 304-310. Osi?ski Maciej, Mostowska Adrianna, Wirstlein Przemyslaw, Wender-O?egowska Ewa, Jagodzi?ski Pawe? Piotr, Szczepa?ska Ma?gorza |
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes.
Bone 2018 Jun . Gregson Celia L, Newell Felicity, Leo Paul J, Clark Graeme R, Paternoster Lavinia, Marshall Mhairi, Forgetta Vincenzo, Morris John A, Ge Bing, Bao Xiao, Duncan Bassett J H, Williams Graham R, Youlten Scott E, Croucher Peter I, Davey Smith George, Evans David M, Kemp John P, Brown Matthew A, Tobias Jon H, Duncan Emma |
Impact of the Canonical Wnt Pathway Activation on the Pathogenesis and Prognosis of Adamantinomatous Craniopharyngiomas. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2018 Apr . Jucá Carlos Eduardo Barros, Colli Leandro Machado, Martins Clarissa Silva, Campanini Marina Lanciotti, Paixão Beatriz, Jucá Renata Viana, Saggioro Fabiano Pinto, de Oliveira Ricardo Santos, Moreira Ayrton Custódio, Machado Hélio Rubens, Neder Luciano, Antonini Sonir Rauber, de Castro Margar |
Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia. Molecular cytogenetics 2018 2 11 13. Demir Eksi Durkadin, Shen Yiping, Erman Munire, Chorich Lynn P, Sullivan Megan E, Bilekdemir Meric, Y?lmaz Elanur, Luleci Guven, Kim Hyung-Goo, Alper Ozgul M, Layman Lawrence |
[Genetic analysis of a 46,XY female with sex reversal due to duplication of NR0B1 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 12 35 (6): 804-807. Qin Shengfang, Wang Xueyan, Li Yunxi |
Relationship of WNT4 Gene with the Risk of Epithelial Ovarian Cancer: A Han Chinese Population-Based Association Study. Genetic testing and molecular biomarkers 2018 Dec 22 (12): 686-692. Zhang Juanjuan, Zhang Penghua, Shen Yunfeng, Yang Mei, Zou Hongxia, Liu Honglia |
Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease.
The Journal of clinical endocrinology and metabolism 2019 Nov 104 (11): 5008-5023. Pott Janne, Bae Yoon Ju, Horn Katrin, Teren Andrej, Kühnapfel Andreas, Kirsten Holger, Ceglarek Uta, Loeffler Markus, Thiery Joachim, Kratzsch Jürgen, Scholz Mark |
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
Frontiers in genetics 2019 10 511. Edwards Todd L, Giri Ayush, Hellwege Jacklyn N, Hartmann Katherine E, Stewart Elizabeth A, Jeff Janina M, Bray Michael J, Pendergrass Sarah A, Torstenson Eric S, Keaton Jacob M, Jones Sarah H, Gogoi Radhika P, Kuivaniemi Helena, Jackson Kathryn L, Kho Abel N, Kullo Iftikhar J, McCarty Catherine A, Im Hae Kyung, Pacheco Jennifer A, Pathak Jyotishman, Williams Marc S, Tromp Gerard, Kenny Eimear E, Peissig Peggy L, Denny Joshua C, Roden Dan M, Velez Edwards Digna |
Genome-wide association study of right-sided colonic diverticulosis in a Korean population.
Scientific reports 2019 May 9 (1): 7360. Choe Eun Kyung, Lee Jong-Eun, Chung Su Jin, Yang Sun Young, Kim Young Sun, Shin Eun-Soon, Choi Seung Ho, Bae Jung |
Polymorphisms and endometriosis: a systematic review and meta-analyses. Human reproduction update 2019 12 26 (1): 73-102. Méar Loren, Herr Marie, Fauconnier Arnaud, Pineau Charles, Vialard Franço |
LncRNA ZBTB40-IT1 modulated by osteoporosis GWAS risk SNPs suppresses osteogenesis. Human genetics 2019 Jan . Mei Bing, Wang Ya, Ye Weiyuan, Huang Han, Zhou Qian, Chen Yuanyuan, Niu Yajing, Zhang Manling, Huang Qingya |
Genetic Characterization of Endometriosis Patients: Review of the Literature and a Prospective Cohort Study on a Mediterranean Population. International journal of molecular sciences 2020 3 21 (5): . Angioni Stefano, D'Alterio Maurizio Nicola, Coiana Alessandra, Anni Franco, Gessa Stefano, Deiana Dani |
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.
Communications biology 2020 Mar 3 (1): 129. Olafsdottir Thorhildur, Thorleifsson Gudmar, Sulem Patrick, Stefansson Olafur A, Medek Helga, Olafsson Karl, Ingthorsson Orri, Gudmundsson Valur, Jonsdottir Ingileif, Halldorsson Gisli H, Kristjansson Ragnar P, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Oddsson Asmundur, Sigurdsson Asgeir, Eggertsson Hannes P, Melsted Pall, Halldorsson Bjarni V, Lund Sigrun H, Styrkarsdottir Unnur, Steinthorsdottir Valgerdur, Gudmundsson Julius, Holm Hilma, Tragante Vinicius, Asselbergs Folkert W, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Jonsdottir Kristin, Rafnar Thorunn, Stefansson Ka |
WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases. Frontiers in cardiovascular medicine 2021 7 8 675222. Ren Huan, Luo Jian-Quan, Ouyang Fan, Cheng Li, Chen Xiao-Ping, Zhou Hong-Hao, Huang Wei-Hua, Zhang W |
Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies. Orphanet journal of rare diseases 2021 6 16 (1): 258. Zhu Ying, Wang Ruyi, Cheng Yun, Han Yang, Li Tengyan, Cao Yunxia, Wang Binb |
Genome-wide causal mediation analysis identifies genetic loci associated with uterine fibroids mediated by age at menarche. Human reproduction (Oxford, England) 2022 Jun . Tai An-Shun, Lin Ro-Ting, Lin Yi-Chun, Wang Chung-Hsing, Lin Sheng-Hsuan, Imoto Sei |
Insights from genomic studies on the role of sex steroids in the aetiology of endometriosis. Reproduction & fertility 2022 5 3 (2): R51-R65. Saunders Philippa T |
Investigation of biomarkers in Endometriosis-associated infertility: Systematic Review. Anais da Academia Brasileira de Ciencias 2022 94 (suppl 3): e20211572. Egashira Erika M, Trovó-Marqui Alessandra B, Tanaka Sarah C S V, Cintra Mariangela T |
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- Page last updated:Apr 22, 2024
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