Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Endometriosis and GREB1[original query] |
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Genome-wide association meta-analysis identifies new endometriosis risk loci.
Nature genetics 2012 Dec 44 (12): 1355-9. Nyholt Dale R, Low Siew-Kee, Anderson Carl A, Painter Jodie N, Uno Satoko, Morris Andrew P, MacGregor Stuart, Gordon Scott D, Henders Anjali K, Martin Nicholas G, Attia John, Holliday Elizabeth G, McEvoy Mark, Scott Rodney J, Kennedy Stephen H, Treloar Susan A, Missmer Stacey A, Adachi Sosuke, Tanaka Kenichi, Nakamura Yusuke, Zondervan Krina T, Zembutsu Hitoshi, Montgomery Grant |
Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Human reproduction update 0 20 (5): 702-16. Rahmioglu Nilufer, Nyholt Dale R, Morris Andrew P, Missmer Stacey A, Montgomery Grant W, Zondervan Krina |
Independent Replication and Meta-Analysis for Endometriosis Risk Loci. Twin research and human genetics : the official journal of the International Society for Twin Studies 2015 Oct 18 (5): 518-25. Sapkota Yadav, Fassbender Amelie, Bowdler Lisa, Fung Jenny N, Peterse Daniëlle, O Dorien, Montgomery Grant W, Nyholt Dale R, D'Hooghe Thomas |
Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry. Scientific reports 2017 Sep 7 (1): 11380. Sapkota Yadav, Vivo Immaculata De, Steinthorsdottir Valgerdur, Fassbender Amelie, Bowdler Lisa, Buring Julie E, Edwards Todd L, Jones Sarah, O Dorien, Peterse Daniëlle, Rexrode Kathryn M, Ridker Paul M, Schork Andrew J, Thorleifsson Gudmar, Wallace Leanne M, , Kraft Peter, Morris Andrew P, Nyholt Dale R, Edwards Digna R Velez, Nyegaard Mette, D'Hooghe Thomas, Chasman Daniel I, Stefansson Kari, Missmer Stacey A, Montgomery Grant |
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 |
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 |
Role of FN1 and GREB1 gene polymorphisms in endometriosis. Molecular medicine reports 2019 May . Matalliotaki Charoula, Matalliotakis Michail, Rahmioglu Nilufer, Mavromatidis George, Matalliotakis Ioannis, Koumantakis George, Zondervan Krina, Spandidos Demetrios A, Goulielmos George N, Zervou Maria |
Association between Single Nucleotide Polymorphisms and Endometriosis in a Brazilian Population. Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia 2020 4 42 (3): 146-151. Viana Paula Coelho Silva, Mendes Ana Carolina Delgado Malvaccini, Delgado Lucas Farah, Tostes Gustavo, Gonçalves Lidiane, Gonçalves Júnior Homero, Raposo Nádia Rezende Barbosa, Vitral Geraldo Sérgio Farinazzo, Gerheim Pamela Souza Almeida Sil |
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 |
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort. Biomedicines 2023 8 11 (8): . Aurora Santin, Beatrice Spedicati, Anna Morgan, Stefania Lenarduzzi, Paola Tesolin, Giuseppe Giovanni Nardone, Daniela Mazzà, Giovanni Di Lorenzo, Federico Romano, Francesca Buonomo, Alessandro Mangogna, Maria Pina Concas, Gabriella Zito, Giuseppe Ricci, Giorgia Girot |
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- Page last updated:Apr 16, 2024
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