ID

44991

Description

Principal Investigator: David Altshuler, MD, PhD, Department of Molecular Biology and Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA MeSH: Myocardial Infarction https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000294 Myocardial infarction (MI) is a common complex disease and the leading cause of death and disability worldwide. The genetic basis of this disease is largely unknown. It has been thought that early-onset MI events would have a substantially greater heritability, thus making DNA collections with younger individuals desirable. More recently, genome-wide association studies have become feasible through the development of whole genome arrays and a large catalogue of common variants reported in the International HapMap database. This study aims to use Affymetrix genotyping platform to do a whole genome scan in 3000 early-onset MI cases and 3000 matched controls from 6 study collection sites.

Lien

https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000294

Mots-clés

  1. 23/06/2022 23/06/2022 - Dr. Christian Niklas
  2. 12/10/2022 12/10/2022 - Adrian Schulz
Détendeur de droits

David Altshuler, MD, PhD, Department of Molecular Biology and Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

Téléchargé le

23 juin 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000294 STAMPEED: Myocardial Infarction Genetics Consortium (MIGen)

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

There were 2,967 cases and 3,075 controls run on Genome-Wide Human SNP Array 6.0 and analyzed for association testing. The age criteria for the cases was men ≤50 y old or women ≤60 y old. The samples were drawn from 6 collection sites: Boston, MA (Masschusetts General Hospital Premature Coronary Artery Disease Study), Seattle, WA (Heart Attack Risk in Puget Sound), Helsinki, Finland (FINRISK), Malmö, Sweden (Malmö Diet and Cancer Study), Barcelona, Spain (REGICOR), and Milan, Italy (Italian Atherosclerosis Thrombosis and Vascular Biology Working Group).
Description

Elig.phs000294.v1.p1.1

Type de données

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C0086287
UMLS CUI [1,3]
C1512693
UMLS CUI [2,1]
C0001779
UMLS CUI [2,2]
C0086582
UMLS CUI [2,3]
C1512693

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
Elig.phs000294.v1.p1.1
Item
There were 2,967 cases and 3,075 controls run on Genome-Wide Human SNP Array 6.0 and analyzed for association testing. The age criteria for the cases was men ≤50 y old or women ≤60 y old. The samples were drawn from 6 collection sites: Boston, MA (Masschusetts General Hospital Premature Coronary Artery Disease Study), Seattle, WA (Heart Attack Risk in Puget Sound), Helsinki, Finland (FINRISK), Malmö, Sweden (Malmö Diet and Cancer Study), Barcelona, Spain (REGICOR), and Milan, Italy (Italian Atherosclerosis Thrombosis and Vascular Biology Working Group).
boolean
C0001779 (UMLS CUI [1,1])
C0086287 (UMLS CUI [1,2])
C1512693 (UMLS CUI [1,3])
C0001779 (UMLS CUI [2,1])
C0086582 (UMLS CUI [2,2])
C1512693 (UMLS CUI [2,3])

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