Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. (Q50531000)

1 July 2018

meta-analysis

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title

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. (English)

1 reference

1 July 2018

genome-wide association study

main subject

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corrigendum / erratum

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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author

Alexa Beiser

301

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1 July 2018

Claudia L Satizabal

Claudia L Satizabal

371

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Nuria P Torres-Aguila

Nuria P Torres-Aguila

389

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Marcus Dörr

Marcus Dörr

313

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Joanna Pera

Joanna Pera

357

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Unnur Þorsteinsdóttir

114

285

Unnur Thorsteinsdottir

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96

267

Jerome I Rotter

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358

Markus Perola

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101

272

Veikko Salomaa

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Joan Montaner

348

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Paul Elliott

Paul Elliott

Sylvia Wassertheil-Smoller

145

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121

292

Sylvia Wassertheil-Smoller

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44

215

Tamara B Harris

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Christopher R Levi

337

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Erik Ingelsson

53

Erik Ingelsson

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113

284

Gudmar Thorleifsson

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Cornelia M. van Duijn

118

Cornelia M van Duijn

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120

Nicholas J Wareham

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161

Danish Saleheen

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41

Vilmundur Gudnason

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373

Naveed Sattar

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Stella Trompet

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Sudha Seshadri

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Olle Melander

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Anders Hamsten

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Lars Lind

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42

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Stefan Gustafsson

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Lenore J Launer

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346

Koichi Matsuda

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Agnieszka Slowik

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Ralph L Sacco

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Tatjana Rundek

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Marta Ribasés

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Martin Dichgans

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Martin Dichgans

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Martin Dichgans

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Martin Dichgans

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Jonathan Rosand

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Jonathan Rosand

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Vilmundur Gudnason

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Vilmundur Gudnason

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Cornelia M. van Duijn

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Cornelia M van Duijn

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Charles Kooperberg

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Charles Kooperberg

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Kári Stefánsson

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Kari Stefansson

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Konstantin Strauch

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Konstantin Strauch

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Rainer Malik

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Peter M Rothwell

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Erik Ingelsson

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Cecilia Lindgren

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Cecilia M Lindgren

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Linxin Li

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Linxin Li

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Bradford B Worrall

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James F Meschia

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Salim Yusuf

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Salim Yusuf

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Salim Yusuf

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Aki S Havulinna

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Bruce M. Psaty

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Julie E. Buring

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Julie E Buring

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Martin Ingelsson

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Martin Ingelsson

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Susan R Heckbert

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Susan R Heckbert

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Kent D Taylor

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Carl D Langefeld

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Carl D. Langefeld

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Carl D Langefeld

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Alexander Teumer

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Alexander Teumer

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Stella Trompet

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Andreea Ilinca

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Sven J van der Lee

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Daniel L Labovitz

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E Shyong Tai

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Motoki Iwasaki

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International Genomics of Blood Pressure (iGEN-BP) Consortium

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International Stroke Genetics Consortium (ISGC)

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International Stroke Genetics Consortium (ISGC)

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John Attia

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NINDS Stroke Genetics Network (SiGN)

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METASTROKE Consortium

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Neurology Working Group of the CHARGE Consortium

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Neurology Working Group of the CHARGE Consortium

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Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

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Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

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INVENT Consortium

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INVENT Consortium

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BioBank Japan Cooperative Hospital Group

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COMPASS Consortium

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COMPASS Consortium

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UK Young Lacunar DNA Study

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UK Young Lacunar DNA Study

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MEGASTROKE Consortium

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Yukinori Okada

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Wei-Min Chen

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Qing Duan

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Loes Rutten-Jacobs

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Anne-Katrin Giese

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Christopher D Anderson

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Michael Chong

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Hieab H H Adams

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Hakan Ay

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Robert D Brown

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Adam S Butterworth

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Cara L Carty

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Wei-Min Chen

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John W Cole

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Paul I W de Bakker

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Qing Duan

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Stefan T Engelter

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Elizabeth G Holliday

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George Howard

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Fang-Chi Hsu

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Hyacinth I Hyacinth

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Jordi Jiménez-Conde

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Julie A Johnson

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Jin-Moo Lee

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Jane Maguire

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Martin J O'Donnell

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Alexander P Reiner

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1 reference

1 July 2018

Kenneth Rice

262

1 reference

1 July 2018

Stephen S Rich

263

1 reference

1 July 2018

Natalia S Rost

265

1 reference

1 July 2018

Peter M Rothwell

266

1 reference

1 July 2018

Reinhold Schmidt

274

1 reference

1 July 2018

Carsten O Schmidt

275

1 reference

1 July 2018

Pankaj Sharma

277

1 reference

1 July 2018

Cathie L M Sudlow

279

1 reference

1 July 2018

Vincent N S Thijs

283

1 reference

1 July 2018

Matthew Walters

290

1 reference

1 July 2018

Mariana Bustamante

304

1 reference

1 July 2018

Yu-Ching Cheng

306

1 reference

1 July 2018

Natalia Cullell

309

1 reference

1 July 2018

Pilar Delgado

312

1 reference

1 July 2018

Wander S Gurpreet

316

1 reference

1 July 2018

Laura Ibanez

320

1 reference

1 July 2018

Lalit Kalra

328

1 reference

1 July 2018

Masahiro Kamouchi

329

1 reference

1 July 2018

Manja Kloss

332

1 reference

1 July 2018

Jerzy Krupinski

334

1 reference

1 July 2018

Vasileios Lioutas

341

1 reference

1 July 2018

Yong Mei Liu

342

1 reference

1 July 2018

Hirata Makoto

344

1 reference

1 July 2018

Nicolas Martinez-Majander

345

1 reference

1 July 2018

Elena Muiño

350

1 reference

1 July 2018

Bo Norrving

352

1 reference

1 July 2018

Alessandro Pezzini

359

1 reference

1 July 2018

Iolanda Riba-Llena

362

1 reference

1 July 2018

Anthony G Rudd

366

1 reference

1 July 2018

Ralhan Sarju

368

1 reference

1 July 2018

Makoto Sasaki

370

1 reference

1 July 2018

Gerli Sibolt

375

1 reference

1 July 2018

Ásgeir Sigurdsson

376

1 reference

1 July 2018

Carolina Soriano-Tárraga

379

1 reference

1 July 2018

Tara Stanne

380

1 reference

1 July 2018

O Colin Stine

381

1 reference

1 July 2018

Takako Takai

384

1 reference

1 July 2018

Hideo Tanaka

385

1 reference

1 July 2018

Liisa Tomppo

388

1 reference

1 July 2018

Emmanuel Touze

390

1 reference

1 July 2018

Charles D A Wolfe

399

1 reference

1 July 2018

Quenna Wong

400

1 reference

1 July 2018

Huichun Xu

401

1 reference

1 July 2018

Christina Jern

405

1 reference

1 July 2018

Israel Fernandez-Cadenas

407

1 reference

1 July 2018

Arndt Rolfs

409

1 reference

1 July 2018

Guillaume Pare

413

1 reference

1 July 2018

Danish Saleheen

415

1 reference

1 July 2018

Kari Stefansson

416

1 reference

1 July 2018

Joanna M M Howson

422

1 reference

1 July 2018

AFGen Consortium

426

1 reference

1 July 2018

STARNET

430

1 reference

1 July 2018

EPIC-CVD Consortium

433

1 reference

1 July 2018

MEGASTROKE Consortium:

441

1 reference

1 July 2018

language of work or name

English

0 references

publication date

12 March 2018

1 reference

1 July 2018

published in

Nature Genetics

1 reference

1 July 2018

volume

50

1 reference

1 July 2018

page(s)

524-537

1 reference

1 July 2018

issue

4

1 reference

1 July 2018

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

exact match

https://scigraph.springernature.com/pub.10.1038/s41588-018-0058-3

0 references

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Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

3 July 2018

1 reference

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Connecting genetic risk to disease end points through the human blood plasma proteome

3 July 2018

1 reference

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A Novel Approach for Pathway Analysis of GWAS Data Highlights Role of BMP Signaling and Muscle Cell Differentiation in Colorectal Cancer Susceptibility

3 July 2018

1 reference

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Genetic Predisposition to Ischemic Stroke: A Polygenic Risk Score

3 July 2018

1 reference

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Genetic variation at 16q24.2 is associated with small vessel stroke

3 July 2018

1 reference

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Disease variants alter transcription factor levels and methylation of their binding sites

3 July 2018

1 reference

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Global, regional, and national disability-adjusted life-years (DALYs) for 315 diseases and injuries and healthy life expectancy (HALE), 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015.

3 July 2018

1 reference

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Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Cardiometabolic risk loci share downstream cis- and trans-gene regulation across tissues and diseases.

3 July 2018

1 reference

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LNK/SH2B3 Loss of Function Promotes Atherosclerosis and Thrombosis

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseases

3 July 2018

1 reference

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Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Detection and interpretation of shared genetic influences on 42 human traits

3 July 2018

1 reference

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Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Human genetic variation database, a reference database of genetic variations in the Japanese population

3 July 2018

1 reference

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Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Therapeutic target database update 2016: enriched resource for bench to clinical drug target and targeted pathway information

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

A global reference for human genetic variation

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

An atlas of genetic correlations across human diseases and traits

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Prediction of Causal Candidate Genes in Coronary Artery Disease Loci

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

The support of human genetic evidence for approved drug indications

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

The impact of low-frequency and rare variants on lipid levels

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Integrative analysis of 111 reference human epigenomes

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

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

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Biological interpretation of genome-wide association studies using predicted gene functions

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

SNiPA: an interactive, genetic variant-centered annotation browser

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genetic determinants of P wave duration and PR segment

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Quality control and conduct of genome-wide association meta-analyses

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genetics of rheumatoid arthritis contributes to biology and drug discovery

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Identifying multiple causative genes at a single GWAS locus

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Identification of CAD candidate genes in GWAS loci and their expression in vascular cells

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Chromatin marks identify critical cell types for fine mapping complex trait variants

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Bayesian refinement of association signals for 14 loci in 3 common diseases

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

An integrated encyclopedia of DNA elements in the human genome

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Cell-type specific and combinatorial usage of diverse transcription factors revealed by genome-wide binding studies in multiple human cells

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

METAL: fast and efficient meta-analysis of genomewide association scans

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

A versatile gene-based test for genome-wide association studies

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genome-wide association study of PR interval

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

The NCBI BioSystems database

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

A Bayesian measure of the probability of false discovery in genetic epidemiology studies

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Variants conferring risk of atrial fibrillation on chromosome 4q25.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

DrugBank: a comprehensive resource for in silico drug discovery and exploration

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Stroke epidemiology: a review of population-based studies of incidence, prevalence, and case-fatality in the late 20th century

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Human non-synonymous SNPs: server and survey

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Congenital heart disease caused by mutations in the transcription factor NKX2-5

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

VEGAS2: Software for More Flexible Gene-Based Testing

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

BLUEPRINT to decode the epigenetic signature written in blood.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Transethnic meta-analysis of genomewide association studies

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Role of COL4A1 in small-vessel disease and hemorrhagic stroke.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Use of genome-wide association studies for drug repositioning

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases

30 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5968830

The Biological Basis for Cardiac Repair After Myocardial Infarction: From Inflammation to Fibrosis.

30 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FS41588-018-0058-3

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/S41588-018-0058-3

1 reference

1 July 2018

1 reference

1 July 2018

PubMed ID

29531354

1 reference

1 July 2018