-
Breast Cancer Family Registry Early-onset Breast Cancer GWAS
Study
phs001589
-
National Epidemiologic Survey on Alcohol and Related Conditions-III (NESARC-III)
Study
phs001590
-
Center for Oral Health Research in Appalachia (COHRA) Genomic Studies of Oral Health and Disease
Study
phs001591
-
NHLBI TOPMed - NHGRI CCDG: The Johns Hopkins University School of Medicine Atrial Fibrillation Genetics Study
Study
phs001598
-
NHLBI TOPMed - NHGRI CCDG: Early-onset Atrial Fibrillation in the CATHeterization GENetics (CATHGEN) Cohort
Study
phs001600
-
NHLBI TOPMed: Children's Health Study (CHS) Integrative Genetic Approaches to Gene-Air Pollution Interactions in Asthma (GAP)
Study
phs001602
-
Comprehensive Epigenetic Landscape of Rheumatoid Arthritis Fibroblast-Like Synoviocytes
Study
phs001615
-
eMERGE Network Phase III Clinical Sequencing: eMERGEseq Panel
Study
phs001616
-
Genetic Causes of Growth Disorders
Study
phs001617
-
NHLBI TOPMed: Outcome Modifying Genes in Sickle Cell Disease (OMG)
Study
phs001608
-
Genetic contributions of lupus nephritis in a multi-ethnic cohort of systemic lupus erythematosus (SLE)
Study
phs001609
-
Genetic analysis of patients with Inherited Retinal Dystrophies (IRDs) using next generation sequencing to identify the causative variants
Study
phs001619
-
Genetic Testing to Understand and Address Renal Disease Disparities
Study
phs001620
-
Genetic Susceptibility and Biomarkers of Platinum-Related Toxicities
Study
phs001621
-
Clinical Resistance to Crenolanib in Acute Myeloid Leukemia Due to Diverse Molecular Mechanisms
Study
phs001628
-
The Immunogenetics of Measles Immunity - Measles (MMR) vaccination (NIAID/NIH)
Study
phs001630
-
Genetics of Mood Disorders: Aging and Emotion Regulation Brain Circuitry in Bipolar
Study
phs001631
-
Prospective Analysis of Genotypes in Adults Undergoing Therapy for Lung Cancer (Paclitaxel Cohort)
Study
phs001660
-
Center for Craniofacial and Dental Genetics: Exome Sequencing of Orofacial Cleft Families
Study
phs001675
-
African American Multiple Myeloma GWAS
Study
phs001632
-
Implementation, Adoption, and Utility of Family History in Diverse Care Settings
Study
phs001641
-
NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai
Study
phs001644
-
Genomic Landscape of Cutaneous Diffuse Large B Cell Lymphoma
Study
phs001645
-
NHLBI TOPMed: Genetic Causes of Complex Pediatric Disorders - Asthma (GCPD-A)
Study
phs001661
-
Varieties of Impulsivity in Opiate and Stimulant Users
Study
phs001647
-
Center for Education and Drug Abuse Research (CEDAR)
Study
phs001649
-
Genetic and Genomic Stability Across Lymphoblastoid Cell Line Expansions
Study
phs001650
-
Whole Exome Characterization of Squamous Cell Lung Cancers (Lung SQCC) from Appalachian Kentucky (APPKY)
Study
phs001651
-
Bayesian-Based Noninvasive Prenatal Diagnosis of Single-Gene Disorders
Study
phs001659
-
Genetic Etiology of Heterotaxy
Study
phs001691
-
NHLBI TOPMed: Lung Tissue Research Consortium (LTRC)
Study
phs001662
-
Parkinson's Disease Cognitive Genetics Consortium (PDCGC) Stage I, NeuroX Dataset
Study
phs001664
-
Genomics of Kidney Transplantation
Study
phs001667
-
Veterans Administration (VA) Million Veteran Program (MVP) Summary Results from Omics Studies
Study
phs001672
-
ADAGESIII: Contribution of genotype to glaucoma phenotype in African Americans
Study
phs001673
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Autism - Simons Simplex Collection (SSC)
Study
phs001676
-
Adolescent Idiopathic Scoliosis (AIS) 1000 Exomes Study
Study
phs001677
-
Defining T cell States Associated with Response to Checkpoint Immunotherapy in Melanoma
Study
phs001680
-
Prediction of DNA Repair Inhibitor Response in Short Term Patient-Derived Ovarian Cancer Organoids
Study
phs001685
-
Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
Study
phs001687
-
National Cancer Institute - Population Structure and Natural Selection in the Epidemiology of Burkitt Lymphoma in East African Children and Minors (EMBLEM) study in Uganda
Study
phs001705
-
Integrative Analysis of Lung Adenocarcinoma in Never Smokers
Study
phs001697
-
CSER: Genomic Sequencing to Aid Diagnosis in Pediatric and Prenatal Practice: Examining Clinical Utility, Ethical Implications, Payer Coverage, and Data Integration in a Diverse Population
Study
phs002324
-
Germline DNA Methylation Associated with Breast Cancer Predisposition
Study
phs001699
-
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing
Study
phs001700
-
INdiana GENomics: Implementing an Opportunity for the Under Served (INGENIOUS)
Study
phs001701
-
Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression
Study
phs001703
-
University of Pennsylvania CAR T Cell Responding and Non-responding Patients
Study
phs001707
-
VCRC Genetic Repository One Time DNA Protocol
Study
phs001712
-
LCCC 1108: Development of a Tumor Molecular Analyses Program and Its Use to Support Treatment Decisions (UNCseqTM)
Study
phs001713