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  1. CIDR Whole Exome sequencing of multiplex cleft families dbGaP

    ID: phs000459.v1.p1

    Description: Building upon our previous linkage and association studies, we will use whole exome sequencing studies of second and third degree affected relatives d...

  2. NCI Genome-Wide Association Study of Renal Cell Carcinoma dbGaP

    ID: phs000351.v1.p1

    Description: The National Cancer Institute (NCI) genome-wide association study (GWAS) of renal cell carcinoma (RCC) was conducted to investigate common genetic va...

  3. GWAS of Breast Cancer in the African Diaspora dbGaP

    ID: phs000383.v1.p1

    Description: The paucity of data on the genetic epidemiology of breast cancer for racial/ethnic groups other than those of European ancestry hinders the develo...

    Study Types: Case-Control

  4. Genetic Basis of XMEN Disease dbGaP

    ID: phs000365.v1.p1

    Description: The etiologies of primary immunodeficiencies often yield novel insights about the immune system. Although a genetic etiology has been suspected fo...

    Study Types: Case-Control

  5. Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) dbGaP

    ID: phs000649.v1.p1

    Description: This is a prospective, multicenter, randomized, open-label, parallel-group study to evaluate pharmacogenomic responses to antihypertensives. The prima...

  6. NHLBI TOPMed: Partners HealthCare Biobank dbGaP

    ID: phs001024.v1.p1

    Description: The Atrial Fibrillation Genetics Consortium (AFGen) was organized to identify common and rare genetic variation associated with atrial fibrillation ri...

    Study Types: Case Set

  7. Yale Center for Mendelian Genomics (Y CMG) dbGaP

    ID: phs000744.v2.p1

    Description: Yale University is home to one of three national centers created by the NIH to study the genetics of rare inherited diseases. Researchers at Yale, the...

    Study Types: Mixed

  8. Dental Caries GWAS dbGaP

    ID: phs000095.v2.p1

    Description: Dental caries (also known as tooth decay) remains the most common chronic disease of childhood, five times more common than asthma and seven times mor...

  9. University of Washington Center for Mendelian Genomics (UW CMG) dbGaP

    ID: phs000693.v1.p1

    Description: The Centers for Mendelian Genomics project uses next-generation sequencing and computational approaches to discover the genes and variants that underl...

    Study Types: Multicenter

  10. RAD50 Hypomorphism as Basis for Response to Chemotherapy dbGaP

    ID: phs000706.v1.p1

    Description: Outlier analyses represent a versatile method to identify predictive biomarkers of response to both targeted agents and chemotherapy. We performed who...

    Study Types: Case Set

  11. CCHMC-eMERGE-Phase IIIA dbGaP

    ID: phs001011.v1.p1

    Description: This submission includes genotyping or sequencing data from separate cohorts, each is described in separate paragraphs below. Extreme early onset obes...

  12. HIV-Resistant People with Hemophilia dbGaP

    ID: phs000445.v1.p1

    Description: Rare individuals are highly resistant to infection with human immunodeficiency virus (HIV). Studies of candidate genes resulted in the discovery of a ...

    Study Types: Case-Control

  13. CTLA4 haploinsufficiency and immune dysregulation dbGaP

    ID: phs000797.v1.p1

    Description: We identified germline heterozygous mutations in CTLA4 in members of four families with severe immune dysregulation. Human CTLA4 haploinsufficiency ca...

    Study Types: Case Set

  14. An APOBEC Cytidine Deaminase Mutagenesis in Human Cancers dbGaP

    ID: phs000677.v1.p1

    Description: Reprinted from Roberts et al. "An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers", Nature Genetics, 45:970-976, 2013, wi...

    Study Types: Meta-Analysis

  15. Whole-Genome Sequencing of Acute Myeloid Leukemia dbGaP

    ID: phs000159.v5.p3

    Description: We used massively parallel sequencing technology to sequence the genomic DNA of tumor cells (leukemic bone marrow) and normal cells (skin biopsy) obta...

  16. NHLBI GO-ESP: Early-Onset Myocardial Infarction (Broad EOMI) dbGaP

    ID: phs000279.v1.p1

    Description: The NHLBI "Grand Opportunity" Exome Sequencing Project (GO-ESP), a signature project of the NHLBI Recovery Act investment, was designed to identif...

  17. CATHeterization GENetics (CATHGEN) dbGaP

    ID: phs000703.v1.p1

    Description: The CATHGEN biorepository consists of biological samples collected on 9334 sequential consenting individuals undergoing cardiac catheterization at Duk...

    Study Types: Longitudinal

  18. University of Washington Center for Mendelian Genomics (UW CMG) dbGaP

    ID: phs000693.v2.p1

    Description: The Centers for Mendelian Genomics project uses next-generation sequencing and computational approaches to discover the genes and variants that underl...

    Study Types: Multicenter

  19. Starr County Health Studies' Genetics of Diabetes Study dbGaP

    ID: phs000143.v1.p1

    Description: An initial observation in the 1970s that Starr County, Texas, had the highest diabetes-specific mortality of any of the 254 Texas counties led to the...

    Study Types: Case-Control

  20. Dental Caries GWAS dbGaP

    ID: phs000095.v3.p1

    Description: Dental caries (also known as tooth decay) remains the most common chronic disease of childhood, five times more common than asthma and seven times mor...


Displaying 20 of 79,180 results for " "