Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architect...
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
About this item
Full title
Author / Creator
Day, Felix , Karaderi, Tugce , Jones, Michelle R. , Meun, Cindy , He, Chunyan , Drong, Alex , Kraft, Peter , Lin, Nan , Huang, Hongyan , Broer, Linda , Magi, Reedik , Saxena, Richa , Laisk, Triin , Urbanek, Margrit , Hayes, M. Geoffrey , Thorleifsson, Gudmar , Fernandez-Tajes, Juan , Mahajan, Anubha , Mullin, Benjamin H. , Stuckey, Bronwyn G. A. , Spector, Timothy D. , Wilson, Scott G. , Goodarzi, Mark O. , Davis, Lea , Obermayer-Pietsch, Barbara , Uitterlinden, André G. , Anttila, Verneri , Neale, Benjamin M. , Jarvelin, Marjo-Riitta , Fauser, Bart , Kowalska, Irina , Visser, Jenny A. , Andersen, Marianne , Ong, Ken , Stener-Victorin, Elisabet , Ehrmann, David , Legro, Richard S. , Salumets, Andres , McCarthy, Mark I. , Morin-Papunen, Laure , Thorsteinsdottir, Unnur , Stefansson, Kari , Styrkarsdottir, Unnur , Perry, John R. B. , Dunaif, Andrea , Laven, Joop , Franks, Steve , Lindgren, Cecilia M. , Welt, Corrine K. , the 23andMe Research Team and 23andMe Research Team
Publisher
United States: Public Library of Science
Journal title
Language
English
Formats
Publication information
Publisher
United States: Public Library of Science
Subjects
More information
Scope and Contents
Contents
Polycystic ovary syndrome (PCOS) is a disorder characterized by hyperandrogenism, ovulatory dysfunction and polycystic ovarian morphology. Affected women frequently have metabolic disturbances including insulin resistance and dysregulation of glucose homeostasis. PCOS is diagnosed with two different sets of diagnostic criteria, resulting in a pheno...
Alternative Titles
Full title
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Authors, Artists and Contributors
Author / Creator
Karaderi, Tugce
Jones, Michelle R.
Meun, Cindy
He, Chunyan
Drong, Alex
Kraft, Peter
Lin, Nan
Huang, Hongyan
Broer, Linda
Magi, Reedik
Saxena, Richa
Laisk, Triin
Urbanek, Margrit
Hayes, M. Geoffrey
Thorleifsson, Gudmar
Fernandez-Tajes, Juan
Mahajan, Anubha
Mullin, Benjamin H.
Stuckey, Bronwyn G. A.
Spector, Timothy D.
Wilson, Scott G.
Goodarzi, Mark O.
Davis, Lea
Obermayer-Pietsch, Barbara
Uitterlinden, André G.
Anttila, Verneri
Neale, Benjamin M.
Jarvelin, Marjo-Riitta
Fauser, Bart
Kowalska, Irina
Visser, Jenny A.
Andersen, Marianne
Ong, Ken
Stener-Victorin, Elisabet
Ehrmann, David
Legro, Richard S.
Salumets, Andres
McCarthy, Mark I.
Morin-Papunen, Laure
Thorsteinsdottir, Unnur
Stefansson, Kari
Styrkarsdottir, Unnur
Perry, John R. B.
Dunaif, Andrea
Laven, Joop
Franks, Steve
Lindgren, Cecilia M.
Welt, Corrine K.
the 23andMe Research Team
23andMe Research Team
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_plos_journals_2251026494
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2251026494
Other Identifiers
ISSN
1553-7404,1553-7390
E-ISSN
1553-7404
DOI
10.1371/journal.pgen.1007813
