-
Genome Wide Association Study of Chronic TMD: Discovery Phase
Study
phs000796
-
Performance Characteristics of Selective Targeted Enrichment in Genetic Diagnostic Testing
Study
phs000798
-
Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
Study
phs000858
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs000799
-
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Study
phs000801
-
Genome Wide Association Study of Serum Creatinine during Vancomycin Therapy and Vancomycin Pharmacokinetics
Study
phs000894
-
Genomic Sequencing of Ewing Sarcoma
Study
phs000804
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Ottawa Heart Study
Study
phs000806
-
PGRN/PAT: The genomic basis for susceptibility to drug-induced long QT syndrome (diLQTS)
Study
phs000808
-
Autosomal Recessive PGM3 Mutations Link Glycosylation Defects to Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment
Study
phs000809
-
The Breast and Prostate Cancer Cohort Consortium (BPC3) GWAS of Aggressive Prostate Cancer and ER- Breast Cancer
Study
phs000812
-
CIDR, NCI, NIDA Sequencing of Targeted Genomic Regions Associated with Smoking
Study
phs000813
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Italian Atherosclerosis Thrombosis and Vascular Biology
Study
phs000814
-
Gene Expression and Regulatory Networks in Human Leukocytes - Immunological Variation Consortium
Study
phs000815
-
Genome-Wide Discovery of Novel Breast Cancer Predisposing Mutations
Study
phs000822
-
Discovery of Novel Melanoma Predisposing Mutations by Exome Sequencing
Study
phs000823
-
Genome-Wide Discovery of Novel Colon Cancer Predisposing Mutations
Study
phs000824
-
Whole Genome Sequencing of Two Family Trios with 22q.11.2 Deletion Syndrome
Study
phs000837
-
North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES)
Study
phs000827
-
Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma
Study
phs000828
-
Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study
Study
phs000830
-
Ghana Prostate Study
Study
phs000838
-
The Genetics of Type 2 Diabetes Consortium (GoT2D): Low-Pass Sequencing and High-Density SNP Genotyping for Type 2 Diabetes
Study
phs000840
-
Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)
Study
phs000842
-
Whole Genome Bisulfite Sequencing of Circulating Cell-Free (CCF) DNA and its Cellular Contributors
Study
phs000846