-
Epigenetic Landscape of Human Parathyroids
Study
phs003302
-
Transcriptomic and Epigenetic Profiling of SCLC Patient Samples
Study
phs003416
-
Postmortem Analysis of the Caudate Nucleus in Schizophrenia
Study
phs003495
-
Genetic Causes of Congenital Anosmia
Study
phs003328
-
BarcUVa-Seq (Biology of Colorectal Cancer Risk Enhancers)
Study
phs003338
-
NHLBI TOPMed - NHGRI CCDG: The GENetics in Atrial Fibrillation (GENAF) Study
Study
phs001547
-
Single Duplex DNA Sequencing with CODEC Detects Mutations with High Sensitivity
Study
phs003255
-
Single Cell Genotypic and Phenotypic Analysis of Measurable Residual Disease in Acute Myeloid Leukemia
Study
phs003233
-
Deterministic Evolution and Stringent Selection During Pre-Neoplasia
Study
phs003249
-
Precision Medicine for Dilated Cardiomyopathy in European and African Ancestry
Study
phs002641
-
Genomic Studies in Charcot-Marie-Tooth Disease
Study
phs003389
-
Sudden Death in the Young Case Registry
Study
phs003221
-
Genetic Markers of Lipids in Indians: A Validation Study of Most Relevant Findings of Genome-Wide Association Studies
Study
phs003469
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
Whole-Exome Sequencing Study of Diabetic Nephropathy
Study
phs003429
-
Genetic Predictors of Ibrutinib-Related Cardiovascular Side Effects in Patients with Chronic Lymphocytic Leukemia
Study
phs003370
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Maternal and Developmental Risks from Environmental and Social Stressors (MADRES) Center for Environmental Health Disparities
Study
phs003194
-
MILK-Omics: Systems Biology of Human Milk and Its Links to Maternal and Infant Health
Study
phs003408
-
A Microwell Platform for High-Throughput Longitudinal Phenotyping and Selective Retrieval of Organoids
Study
phs003315
-
NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for Studying the Impact of Genetic Variation on Molecular and Physiological Phenotypes - Whole Genome Sequence
Study
phs001325
-
Center for Oral Health Research in Appalachia (COHRA) Genomic Studies of Oral Health and Disease
Study
phs001591
-
NHLBI TOPMed: Cleveland Clinic Atrial Fibrillation (CCAF) Study
Study
phs001189
-
NHLBI TOPMed - NHGRI CCDG: AF Biobank LMU in the context of the MED Biobank LMU
Study
phs001543
-
Evolutionary Analysis of Chronic Lymphocytic Leukemia Cells During Relapse After Allogeneic Hematopoietic Stem Cell Transplant
Study
phs001998
-
Genome Studies in Hereditary Spastic Paraplegia
Study
phs001080
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Epilepsy: Epi25 Consortium
Study
phs001489
-
University of Michigan Clinical Sequencing Exploratory Research (CSER)
Study
phs000673
-
Genetic Neuroscience: How Human Genes and Alleles Shape Neuronal Phenotypes
Study
phs002032
-
Gabriella Miller Kids First (GMKF) Pediatric Research Program in Susceptibility to Ewing Sarcoma Based on Germline Risk and Familial History of Cancer
Study
phs001228
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts, Sub-types, and Subclinical Phenotypes - CIDR
Study
phs002815
-
The Institute for Genomic Medicine at Nationwide Children's Hospital Pediatric Cancer and Blood Disorder Project
Study
phs001820
-
Analysis of Epigenomes and Genome Topology in Colorectal Cancer
Study
phs002288
-
WGSPD Project 1: Whole Genome Sequencing for Schizophrenia and Bipolar Disorder
Study
phs002041
-
Unraveling the Genetic Architecture of Diabetic Retinopathy in South India
Study
phs002116
-
The National Myelodysplastic Syndromes (MDS) Study
Study
phs002714
-
Pediatric Preclinical Testing Consortium (PPTC)
Study
phs001437
-
Tourette International Collaborative Genetics (TIC Genetics) Study - NJCTS and NIMH
Study
phs001423
-
Investigating Genetics in Suspected Congenital Syndromes
Study
phs003453
-
Genomics of Kidney Transplantation
Study
phs001667
-
Action to Control Cardiovascular Risk in Diabetes (ACCORD - Imaging)
Study
phs003562
-
Dysregulation of Naive T Cell Quiescence during Aging
Study
phs003400
-
Serrated Colorectal Cancer: An Emerging Disease Subtype
Study
phs002171
-
Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT-BioLINCC)
Study
phs003665
-
Genome-Wide Association Study of Genetic Susceptibility for Graft-vs-Host Disease Cohort 1
Study
phs002185
-
Integrating Genomic and Transcriptomic Data to Identify Breast Cancer Susceptibility Genes
Study
phs003535
-
Using NGS to Sequence Whole Genomes to Identify Genes Underlying ALS
Study
phs003067
-
Association Between Telomere Length and Falciparum Malaria Endemicity in Sub-Saharan Africans
Study
phs003567
-
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Study
phs000206
-
ChiLDReN/BA: Genetic Studies of Biliary Atresia in the Childhood Liver Disease Research Network
Study
phs003356