(Q35961979)

11 August 2017

Rare coding variants and X-linked loci associated with age at menarche (English)

1 reference

Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

11 August 2017

corrigendum / erratum

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11 August 2017

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11 August 2017

Henry Völzke

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Unnur Þorsteinsdóttir

Unnur Thorsteinsdottir

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David Schlessinger

David Schlessinger

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André Uitterlinden

André G Uitterlinden

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Laura Crisponi

Laura Crisponi

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Alexander Teumer

Alexander Teumer

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Eric Boerwinkle

Eric Boerwinkle

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Igor Rudan

Igor Rudan

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Eleonora Porcu

Eleonora Porcu

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Andres Metspalu

Andres Metspalu

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Caroline Hayward

Caroline Hayward

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Claudia Langenberg

Claudia Langenberg

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Tõnu Esko

Tõnu Esko

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Ailith Pirie

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Carol A Wang

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Ilaria Gandin

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Diego Vozzi

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Felix R Day

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Anna Murray

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Lynne J Hocking

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David Karasik

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Alanna C Morrison

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Kathryn L Lunetta

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Craig E Pennell

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Simin Liu

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David A Hinds

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11 August 2017

Uwe Völker

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Ellen W Demerath

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11 August 2017

Frank B Hu

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11 August 2017

Francesco Cucca

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Douglas F Easton

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11 August 2017

Nicholas J Wareham

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11 August 2017

David Porteous

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11 August 2017

Sheila Ulivi

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11 August 2017

Antonietta Robino

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11 August 2017

Patrick Sulem

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11 August 2017

Albert Hofman

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11 August 2017

Daníel F. Guðbjartsson

Daniel F Gudbjartsson

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11 August 2017

Kari Stefansson

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11 August 2017

Konstantin Strauch

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11 August 2017

Julie E Buring

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11 August 2017

Antonis C Antoniou

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11 August 2017

Paul M Ridker

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11 August 2017

Nora Franceschini

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11 August 2017

Daniel I Chasman

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11 August 2017

Evelin Mihailov

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11 August 2017

Lynda M Rose

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11 August 2017

James G Wilson

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11 August 2017

Laura M Yerges-Armstrong

Laura M Yerges-Armstrong

1 reference

11 August 2017

Elizabeth A Streeten

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11 August 2017

Ken K Ong

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11 August 2017

Jennifer E Huffman

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11 August 2017

Caterina Barbieri

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11 August 2017

Katherine S Ruth

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11 August 2017

Ursula M Schick

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11 August 2017

Andrea D Coviello

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11 August 2017

Robert A Scott

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11 August 2017

Jenny A Visser

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11 August 2017

EPIC InterAct Consortium

EPIC-InterAct Consortium

1 reference

11 August 2017

Joanne M Murabito

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11 August 2017

Generation Scotland

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11 August 2017

Daniela Toniolo

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11 August 2017

Cinzia F Sala

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11 August 2017

Michela Traglia

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11 August 2017

Joyce Y Tung

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11 August 2017

Cathy E Elks

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11 August 2017

Elisabeth Altmaier

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11 August 2017

Lisette Stolk

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11 August 2017

Deborah J Thompson

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11 August 2017

Jinyan Huang

1 reference

11 August 2017

Jennifer Kriebel

1 reference

11 August 2017

Doris Stöckl

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11 August 2017

Rebecca D Jackson

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11 August 2017

Leslie A Lange

1 reference

11 August 2017

Chunyan He

1 reference

11 August 2017

Megan L Grove

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11 August 2017

Ethan M Lange

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11 August 2017

Xin Li

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11 August 2017

Jian'an Luan

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11 August 2017

Alex P Reiner

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11 August 2017

Marek Zygmunt

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11 August 2017

Melissa Wellons

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11 August 2017

John R B Perry

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11 August 2017

language of work or name

English

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publication date

4 August 2015

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11 August 2017

Nature Communications

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11 August 2017

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11 August 2017

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7756

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Defining the role of common variation in the genomic and biological architecture of adult human height

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Epigenetic regulation of female puberty.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Updates in reproduction coming from the endocannabinoid system.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

The IGSF1 deficiency syndrome: characteristics of male and female patients

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

The Genotype-Tissue Expression (GTEx) project

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Over-expressions of AMPK subunits in ovarian carcinomas with significant clinical implications

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Recurrent R-spondin fusions in colon cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Efficient replication of over 180 genetic associations with self-reported medical data

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Web-based, participant-driven studies yield novel genetic associations for common traits

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Transcriptome-wide identification of RNA-binding protein and microRNA target sites by PAR-CLIP

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Regulation of gonadotropin-releasing hormone secretion by cannabinoids

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Alms1-disrupted mice recapitulate human Alström syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

β2 and γ3 laminins are critical cortical basement membrane components: ablation of Lamb2 and Lamc3 genes disrupts cortical lamination and produces dysplasia

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4538850

24 September 2018

Identifiers

DOI

10.1038/NCOMMS8756

1 reference

11 August 2017

0 references

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11 August 2017

PubMed publication ID

26239645

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