STAMPEED:
SNP Typing for Association with Multiple Phenotypes
from Existing Epidemiologic Data
The purpose of this initiative is to support studies
to identify genetic variants related to heart, lung,
and blood disorders and their risk factors by utilizing
genome-wide association studies in existing human studies.
Multiple GWAS grants were awarded for the study of a
wide variety of cardiovascular, lung and blood disorders.
Data will be available at no cost to all qualified investigators
via an application process involving an NHLBI Data Access
Committee.
The NHLBI Program Officer for STAMPEED is Cashell
Jaquish, Ph.D.
NHLBI
Whole Genome Association at NCBI
Projects
- STAMPEED Studies: A Genome-wide Association Study
for Early-Onset Myocardial Infarction (PI: David Atshuler)
- Genome-Wide Association Studies of Asthma in Populations
of African Descent (PI: Kathleen Barnes)
- Genome-Wide Association of Platelet Phenotypes
(PI: Lewis Becker)
- Genome-Wide Association for Loci Influencing CHD
and Other Heart, Lung and Blood (PI: Eric Boerwinkle)
- A Genome-wide Association Study of Childhood Respiratory
Outcomes (PI: James Gauderman)
- Whole Genome Association Analysis of Hematopoietic
Cell Transplant Outcome (PI: John Hansen)
- Genomic Predictors of Arteriosclerosis in Hypertensives
(PI: Sharon Kardia)
- Genome Wide Association for Asthma and Lung Function
(PI: Deborah Meyers)
- Genetics of Cardiovascular Risk Factors in Large
Founder Population Birth Cohort (PI: Leena Peltonen)
- FHS-SCAN Genome Wide Association Scan for Atherosclerosis
Pathway Genes (PI: Michael Province)
- WGA Study to Identify Genetic Variants Associated
with CV Events in CHS (PI: Bruce Psaty)
- Whole Genome Association for Early Coronary Artery
Disease and Related Phenotypes (PI: Thomas Quertermous)
- Genome-Wide Association Studies in Sickle Cell Anemia
and in Centenarians (PI: Martin Steinberg
Program Start and End Date
April 2006 to August 2009
Genome-Wide
Association Studies to Identify Genetic Components that
Relate to Heart, Lung and Blood Disorders
RFA-HL-06-012 |