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
Versions (2)
- 23/06/2022 23/06/2022 - Dr. Christian Niklas
- 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
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Licence
Creative Commons BY 4.0
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dbGaP phs000294 STAMPEED: Myocardial Infarction Genetics Consortium (MIGen)
The data table contains mapping of study subject IDs to sample IDs, and sample IDs to sample IDs of the source repository (MIGen).
- StudyEvent: SEV1
- Eligibility Criteria
- This data table contains a listing of subjects, their consents, and mapping of subject IDs to the subject IDs of the source repository (MIGen). Subjects are early-onset myocardial infarction cases and controls.
- This data table contains pedigree and gender information of study participants.
- The data table contains mapping of study subject IDs to sample IDs, and sample IDs to sample IDs of the source repository (MIGen).
- This is a subject phenotype table of early-onset myocardial infarction (MI) cases and controls. Variables included are sex of subject, MI status and age of MI onset, study center, and principal component clusters 1-7.
Similar models
The data table contains mapping of study subject IDs to sample IDs, and sample IDs to sample IDs of the source repository (MIGen).
- StudyEvent: SEV1
- Eligibility Criteria
- This data table contains a listing of subjects, their consents, and mapping of subject IDs to the subject IDs of the source repository (MIGen). Subjects are early-onset myocardial infarction cases and controls.
- This data table contains pedigree and gender information of study participants.
- The data table contains mapping of study subject IDs to sample IDs, and sample IDs to sample IDs of the source repository (MIGen).
- This is a subject phenotype table of early-onset myocardial infarction (MI) cases and controls. Variables included are sex of subject, MI status and age of MI onset, study center, and principal component clusters 1-7.
C2348585 (UMLS CUI [1,2])
C0370003 (UMLS CUI [1,2])
C1299222 (UMLS CUI [1,2])