(Q34810858)

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Further investigation in europeans of susceptibility variants for polycystic ovary syndrome discovered in genome-wide association studies of Chinese individuals

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Further investigation in europeans of susceptibility variants for polycystic ovary syndrome discovered in genome-wide association studies of Chinese individuals (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

genome-wide association study

0 references

polycystic ovary syndrome

1 reference

based on heuristic

inferred from title

polycystic ovary

1 reference

based on heuristic

inferred from title

Jerome I Rotter

3

object named as

Jerome I Rotter

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

6

object named as

Ricardo Azziz

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Mark O Goodarzi

7

object named as

Mark O Goodarzi

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Richard S. Legro

object named as

Richard S Legro

5

0 references

author name string

Meredith A Brower

1

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Michelle R Jones

2

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Ronald M Krauss

4

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

language of work or name

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publication date

1 January 2015

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

The Journal of Clinical Endocrinology and Metabolism

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Europe PubMed Central

PubMed publication ID

4 August 2017

100

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

E182-6

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Overexpression of a DENND1A isoform produces a polycystic ovary syndrome theca phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Genetic alterations within the DENND1A gene in patients with polycystic ovary syndrome (PCOS)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Evidence for chromosome 2p16.3 polycystic ovary syndrome susceptibility locus in affected women of European ancestry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Metabolic and cardiovascular genes in polycystic ovary syndrome: a candidate-wide association study (CWAS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Replication of association of a novel insulin receptor gene polymorphism with polycystic ovary syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Polycystic ovary syndrome: etiology, pathogenesis and diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Polycystic ovary syndrome: an ancient disorder?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

FSH directly regulates bone mass

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Explained variation for logistic regression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

A naturally occurring mutation of insulin receptor alanine 1134 impairs tyrosine kinase function and is associated with dominantly inherited insulin resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

8 July 2018

Cross-ethnic meta-analysis of genetic variants for polycystic ovary syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

26 October 2018

Influence of FSHR diplotypes on ovarian response to standard gonadotropin stimulation for IVF/ICSI.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

26 October 2018

Prevalence, phenotype and cardiometabolic risk of polycystic ovary syndrome under different diagnostic criteria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

26 October 2018

Comparison of the phenotype of Chinese versus Dutch Caucasian women presenting with polycystic ovary syndrome and oligo/amenorrhoea.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

26 October 2018

The Pregnancy in Polycystic Ovary Syndrome study: baseline characteristics of the randomized cohort including racial effects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

26 October 2018

Phenotypic predictors of response to simvastatin therapy among African-Americans and Caucasians: the Cholesterol and Pharmacogenetics (CAP) Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283012

26 October 2018

Hypomethylation of the LH/choriogonadotropin receptor promoter region is a potential mechanism underlying susceptibility to polycystic ovary syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25303487

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in a cohort of Caucasian women

1 reference

https://pubmed.ncbi.nlm.nih.gov/25303487

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1210/JC.2014-2689

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

ResearchGate publication ID

0 references

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