-
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
-
T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS)
Study
phs000847
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Precocious Coronary Artery Disease Study
Study
phs000883
-
Autosomal recessive
Study
phs000848
-
Resistance studies in Lung Cancer
Study
phs000855
-
Chromothripsis in Patient WHIM-09
Study
phs000856
-
National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans
Study
phs000863
-
Genomic Predictors of Combat Stress Vulnerability and Resilience
Study
phs000864
-
Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
Study
phs000869
-
High-Risk Breast Cancer GWAS
Study
phs000929
-
Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition
Study
phs000873
-
Genetic and Environmental Risk Factors for Hemorrhagic Stroke (GERFHS)
Study
phs000874
-
Transdisciplinary Research Into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing
Study
phs000876
-
Substance Dependence GWAS in European- and African - Americans
Study
phs000952
-
An Omics View of Asthma through Monozygotic Twins
Study
phs000886
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
Genome-Wide Association Study of Endometrial Cancer in the Epidemiology of Endometrial Cancer Consortium (E2C2)
Study
phs000893
-
National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen)
Study
phs000899
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor
Study
phs000902
-
OCD Collaborative Genetic Association Study (OCGAS)
Study
phs000903
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
Next Generation Sequencing of Stage IV Squamous Cell Lung Cancers Reveals an Association of PI3K Aberrations and Evidence of Clonal Heterogeneity in Patients with Brain Metastases
Study
phs000907
-
University of Miami Udall Center of Excellence Identification of Rare Variants in PD through Whole Exome Sequencing
Study
phs000908
-
Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
Study
phs000910
-
Type 1 Diabetes Genetics Consortium (T1DGC): ImmunoChip Study
Study
phs000911
-
San Francisco Bay Area Latina Breast Cancer Study
Study
phs000912
-
Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2
Study
phs000913
-
Genome-wide Association Study of Adiposity in Samoans
Study
phs000914
-
Myocardial Infarction Genetics Exome Sequencing Consortium: German Heart Center in Munich
Study
phs000916
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Pakistan Risk Of Myocardial Infarction Study
Study
phs000917
-
NHLBI TOPMed - NHGRI CCDG: Genes-Environments and Admixture in Latino Asthmatics (GALA II)
Study
phs000920
-
NHLBI TOPMed: Study of African Americans, Asthma, Genes and Environment (SAGE)
Study
phs000921
-
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic
Study
phs000942
-
Genetic Aberrations and Subclonal Structure Impact Chronic Lymphocytic Leukemia
Study
phs000922
-
NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for studying the impact of genetic variation on molecular and physiological phenotypes
Study
phs000924
-
Rare Disease Susceptibility Alleles in Children with Crohn Disease
Study
phs000926
-
CSER: Clinical Implementation of Carrier Testing Using Next Generation Sequencing (NextGen)
Study
phs000927