ID
44991
Descrição
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.
Link
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000294
Palavras-chave
Versões (2)
- 23/06/2022 23/06/2022 - Dr. Christian Niklas
- 12/10/2022 12/10/2022 - Adrian Schulz
Titular dos direitos
David Altshuler, MD, PhD, Department of Molecular Biology and Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA
Transferido a
23 de junho de 2022
DOI
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Licença
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])