DataMed | bioCADDIE Data Discovery Index
Mountain View
biomedical and healthCAre Data Discovery Index Ecosystem
help Advanced Search
Displaying 20 of 79,180 results for " "
i
  1. Trisomy 21 Nondisjunction (T21NDJ) dbGaP

    ID: phs000718.v1.p1

    Description: The overall goal of the project is to identify genetic risk factors associated with chromosome 21 nondisjunction in the oocyte. The dataset derives fr...

  2. eMERGE Network Combined Dataset dbGaP

    ID: phs000360.v3.p1

    Description: The electronic Medical Records and Genomics (eMERGE) Network is a consortium of five participating sites (Group Health Seattle, Marshfield Clinic, May...

    Study Types: Case-Control

  3. Region-specific Transcriptome Analysis of the Human Retina and RPE/Choroid dbGaP

    ID: phs001151.v1.p1

    Description: Proper spatial differentiation of retinal cell types is necessary for normal human vision. Many retinal diseases, such as Best disease and male germ c...

    Study Types: Control Set

  4. Genetic Defects in Familial Renal Disorders dbGaP

    ID: phs000477.v1.p1

    Description: Several different genes cause, when mutated, increased urinary phosphate excretion and hypophosphatemia leading to rickets/osteomalacia; however, the ...

  5. Women's Health Initiative dbGaP

    ID: phs000200.v10.p3

    Description: The Women's Health Initiative (WHI) is a long-term national health study that has focused on strategies for preventing heart disease, breast and c...

  6. Glaucoma Exome Sequencing dbGaP

    ID: phs000558.v1.p1

    Description: This is a study of primary open angle glaucoma (POAG) conducted through exome sequencing of cases and comparison of variant frequencies with general p...

    Study Types: Case Set

  7. The Human Virome and Febrile Illness in Children dbGaP

    ID: phs000264.v2.p1

    Description: Definition of the human microbiome is an important scientific priority. This study will expand the scope of the investigation to include viruses, whic...

    Study Types: Prospective

  8. Genomic Analysis of Pediatric Low Grade Gliomas dbGaP

    ID: phs000614.v1.p1

    Description: Pediatric low-grade gliomas (PLGGs) are among the most common solid tumors in children but, apart from mutations or duplications in the BRAF kinase in...

    Study Types: Case Set

  9. NCI TARGET: Therapeutically Applicable Research to Generate Effective Treatments dbGaP

    ID: phs000218.v17.p6

    Description: The Therapeutically Applicable Research to Generate Effective Treatments (TARGET) Initiative seeks to accelerate research in novel marker and drug dev...

    Study Types: Cohort

  10. NCI TARGET: Therapeutically Applicable Research to Generate Effective Treatments dbGaP

    ID: phs000218.v16.p6

    Description: The Therapeutically Applicable Research to Generate Effective Treatments (TARGET) Initiative seeks to accelerate research in novel marker and drug dev...

    Study Types: Cohort

  11. NCI TARGET: Therapeutically Applicable Research to Generate Effective Treatments dbGaP

    ID: phs000218.v14.p4

    Description: The Therapeutically Applicable Research to Generate Effective Treatments (TARGET) Initiative seeks to accelerate research in novel marker and drug dev...

    Study Types: Cohort

  12. CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) dbGaP

    ID: phs000126.v2.p1

    Description: This proposal brings together the two largest NIH funded genetic studies focused on the identification of novel genes that influence the risk of PD. T...

    Study Types: Case-Control

  13. ADGC Genome Wide Association Study dbGaP

    ID: phs000372.v1.p1

    Description: The National Institute on Aging (NIA) Alzheimer's Disease Centers (ADCs) cohort includes subjects ascertained and evaluated by the clinical an...

    Study Types: Case-Control

  14. Prostate Cancer Genome-Wide Association Study for Uncommon Susceptibility Loci (PEGASUS) dbGaP

    ID: phs000882.v1.p1

    Description: This genome-wide association study was funded by the National Cancer Institute (NCI) to identify uncommon susceptibility loci for prostate cancer. A t...

    Study Types: Case-Control

  15. Health and Retirement Study (HRS) dbGaP

    ID: phs000428.v2.p2

    Description: Introduction to V2: This data release comprises data from the V1 release combined with approximately 3,000 additional samples, collected during the HR...

    Study Types: Longitudinal

  16. Autism Genome Project (AGP) Consortium - GWAS - Stage I and II dbGaP

    ID: phs000267.v2.p2

    Description: Autism spectrum disorders (ASDs) are highly heritable (~90%), yet the underlying genetic determinants are largely unknown. To understand the genetic a...

    Study Types: Parent-Offspring Trios

  17. COGA: African American Family GWAS dbGaP

    ID: phs000976.v1.p1

    Description: COGA is a family study of alcoholism, in which the subjects have been drawn from the Collaborative Study on the Genetics of Alcoholism (COGA), a large...

    Study Types: Family

  18. International Standards for Cytogenomic Arrays dbGaP

    ID: phs000205.v4.p2

    Description: The International Standards for Cytogenomic Arrays (ISCA) Consortium is a rapidly growing group of clinical cytogenetics and molecular genetics labora...

    Study Types: Array Comparative Genomic Hybridization

  19. Whole Exome and Targeted Sequencing in Tourette Syndrome Multiplex Families dbGaP

    ID: phs000415.v1.p1

    Description: This study consists of 771 individuals from 15 extended, multi-generational Tourette Syndrome (TS) pedigrees collected by the Tourette Syndrome Associ...

    Study Types: Extended Pedigrees

  20. Whole Exome Sequencing for Familial Intracranial Aneurysm (FIA I-II) Study dbGaP

    ID: phs000636.v1.p1

    Description: The goal of this study is to identify the genes underlying the risk of intracranial aneurysm (IA). The FIA Study initially recruited families appropri...

    Study Types: Family


Displaying 20 of 79,180 results for " "