Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality
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Published:2020-09-21
Issue:3
Volume:140
Page:529-552
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ISSN:0340-6717
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Container-title:Human Genetics
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language:en
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Short-container-title:Hum Genet
Author:
Adewuyi Emmanuel O.ORCID, Mehta Divya, Sapkota Yadav, Sapkota Yadav, Yoshihara Kosuke, Nyegaard Mette, Steinthorsdottir Valgerdur, Morris Andrew P., Fassbender Amelie, Rahmioglu Nilufer, De Vivo Immaculata, Buring Julie E., Zhang Futao, Edwards Todd L., Jones Sarah, Dorien , Peterse Daniëlle, Rexrode Kathryn M., Ridker Paul M., Schork Andrew J., MacGregor Stuart, Martin Nicholas G., Becker Christian M., Adachi Sosuke, Enomoto Takayuki, Takahashi Atsushi, Kamatani Yoichiro, Matsuda Koichi, Kubo Michiaki, Thorleifsson Gudmar, Geirsson Reynir T., Thorsteinsdottir Unnur, Wallace Leanne M., Yang Jian, Velez Edwards Digna R., Nyegaard Mette, Low Siew-Kee, Zondervan Krina T., Missmer Stacey A., D’Hooghe Thomas, Stefansson Kari, Tung Joyce Y., Montgomery Grant W., Chasman Daniel I., Nyholt Dale R., Agee Michelle, Alipanahi Babak, Auton Adam, Bell Robert K., Bryc Katarzyna, Elson Sarah L., Fontanillas Pierre, Furlotte Nicholas A., Huber Karen E., Kleinman Aaron, Litterman Nadia K., McIntyre Matthew H., Mountain Joanna L., Noblin Elizabeth S., Northover Carrie A. M., Pitts Steven J., Fah Sathirapongsasuti J., Sazonova Olga V., Shelton Janie F., Shringarpure Suyash, Tian Chao, Vacic Vladimir, Wilson Catherine H., Auta Asa, Yoshihara Kosuke, Nyegaard Mette, Griffiths Lyn R., Montgomery Grant W., Chasman Daniel I., Nyholt Dale R., ,
Funder
Queensland University of Technology National Health and Medical Research Council Cooperative Research Centre for Discovery of Genes for Common Human Diseases Cerylid Biosciences N. Hawkins and S. Hawkins Wellcome Trust The Lundbeck Foundation, Denmark the BioBank Japan project
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference125 articles.
1. Adamson GD, Kennedy S, Hummelshoj L (2010) Creating solutions in endometriosis: global collaboration through the World Endometriosis Research Foundation. J Endometriosis 2:3–6 2. Adewuyi EO et al (2020) Shared molecular genetic mechanisms underlie endometriosis and migraine comorbidity. Genes 11:268. https://doi.org/10.3390/genes11030268 3. Ahn SH, Monsanto SP, Miller C, Singh SS, Thomas R, Tayade C (2015) Pathophysiology and Immune Dysfunction in Endometriosis. Biomed Res Int 2015:795976. https://doi.org/10.1155/2015/795976 4. Al Turki S et al (2014) Rare variants in NR2F2 cause congenital heart defects in humans. Am J Hum Genet 94:574–585. https://doi.org/10.1016/j.ajhg.2014.03.007 5. Altomare A, Guarino MPL, Cocca S, Emerenziani S, Cicala M (2013) Gastroesophageal reflux disease: update on inflammation and symptom perception. World J Gastroenterol WJG 19:6523
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