-
Genome-wide Association Study for Non-syndromic Clefts in the African Population: CIDR
Study
phs001090
-
Human Lung Tissue eQTL Study
Study
phs001745
-
Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer
Study
phs003198
-
Precision Medicine for ABCA4 Disease: Modifier Alleles
Study
phs002393
-
NHLBI TOPMed: Children's Health Study (CHS) Integrative Genetic Approaches to Gene-Air Pollution Interactions in Asthma (GAP)
Study
phs001602
-
Population Genetic Testing and SERPINA1 Sequencing Identifies Unidentified Alpha-1 Antitrypsin Deficiency Alleles and Gene-Environment Interaction with Hepatitis C Infection
Study
phs003297
-
Chromothripsis in Patient WHIM-09
Study
phs000856
-
Asian Indian Diabetic Heart Study (AIDHS) /Sikh Diabetes Study (SDS)
Study
phs000583
-
Genetic and Genomic Stability Across Lymphoblastoid Cell Line Expansions
Study
phs001650
-
Genome and Transcriptome Assembly Reveals SVA-Mediated Aberrant Splicing in X-Linked Dystonia Parkinsonism
Study
phs001525
-
Modifier Genes in 21-hydroxylase Deficiency
Study
phs001313
-
Rb and p53-Deficient Myxofibrosarcoma and Undifferentiated Pleomorphic Sarcoma Require Skp2 for Survival
Study
phs001982
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC)
Study
phs000571
-
Metagenomics-Guided Pathogen Discovery in Travelers' Diarrhea
Study
phs001352
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs001088
-
LCCC 1108: Development of a Tumor Molecular Analyses Program and Its Use to Support Treatment Decisions (UNCseqTM)
Study
phs001713
-
NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease
Study
phs001071
-
Genetic Associations in Idiopathic Talipes Equinovarus (Clubfoot) - GAIT
Study
phs000314
-
Myocardial Infarction Genetics Exome Sequencing Consortium: German Heart Center in Munich
Study
phs000916
-
PROstate Cancer Medically Optimized Genome Enhanced ThErapy (PROMOTE) of Castration Resistant Prostate Cancer (CRPC) Patients Treated with Abiraterone Acetate
Study
phs001141
-
The MD Anderson Colorectal Cancer Case Control Study
Study
phs002691
-
Genetic Analysis of Limb Malformation Disorders: Freeman Sheldon Syndrome Exome Sequencing Study (LMD-FSS)
Study
phs000204
-
NHLBI GO-ESP: Family Studies (Familial Atrial Fibrillation)
Study
phs000362
-
Genome-Wide Association Study of Preterm Birth
Study
phs000332
-
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
Study
phs000539
-
The Two Sister Study: A Family-Based Study of Genes and Environment in Young-Onset Breast Cancer
Study
phs000678
-
Gene Expression of Small Cell Carcinoma of the Ovary-Hypercalcemic Type (SCCOHT)
Study
phs001528
-
The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q)
Study
phs000759
-
Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis
Study
phs001288
-
Contribution of Genetic Polymorphisms to the Abuse Liability of Oxycodone
Study
phs001559
-
Genomic Landscape of Cutaneous Diffuse Large B Cell Lymphoma
Study
phs001645
-
E5103 Correlative Studies
Study
phs003201
-
Disorders/Differences of Sex Development (DSD) Study Performed at UCLA in Collaboration with the DSD-Translational Research Network (DSD-TRN), with the Support of the Gabriella Miller Kids First Pediatric Research Program
Study
phs001178
-
CIP: Differential Response to Hydroxyurea and Incidence of Stroke in Sickle Cell Disease
Study
phs000691
-
Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort
Study
phs000448
-
Next Generation Mendelian Genetics: Neonatal Diabetes
Study
phs000542
-
Copy-Number Analysis of Understudied Black Women Ovarian Cancers
Study
phs002313
-
GWAS in African Americans, Latinos and Japanese
Study
phs000517
-
A panel of reference haplotypes for imputing complement component 4 (C4) gene structural variation
Study
phs001992
-
Brigham and Women's Hospital Multiple Sclerosis Genetic Collection
Study
phs000275
-
The Etiological Bases of Giftedness: Epidemiological Study of Cognitive Ability in Children in Saudi Arabia
Study
phs001884
-
Polycystic Ovary Syndrome (PCOS) Genetics
Study
phs000368
-
Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR and PEAR-2)
Study
phs000649
-
Genomic Analysis of Extra-Nodal Natural Killer/T-Cell Lymphoma (ENKTCL)
Study
phs002925
-
Michigan Polybrominated Biphenyl (PBB) Exposure Registry
Study
phs001862
-
Genomic Psychiatry Cohort (GPC) Whole Genome Sequencing and Genotyping Study
Study
phs001020
-
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
Health and Retirement Study (HRS)
Study
phs000428
-
The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma
Study
phs001007
-
Systems genetics in human endothelial cells identifies non-coding variants modifying enhancers, expression, and complex disease traits
Study
phs002057