-
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Study
phs001972
-
NHLBI TOPMed: Genomic Summary Results for the Trans-Omics for Precision Medicine Program
Study
phs001974
-
SNP array analysis of spondylocostal dysostosis patient iPSCs and gene edited isogenic controls
Study
phs001975
-
Natural History, Pathogenesis and Outcome of Melorheostosis
Study
phs001976
-
Genomic Landscape of Human Skin at a Single-Cell Resolution
Study
phs001979
-
National Institute on Alcohol Abuse and Alcoholism (NIAAA) Postmortem Prefrontal Cortex eQTL and mQTL Study
Study
phs001981
-
Rb and p53-Deficient Myxofibrosarcoma and Undifferentiated Pleomorphic Sarcoma Require Skp2 for Survival
Study
phs001982
-
GWAS for Membranous Nephropathy
Study
phs001984
-
A panel of reference haplotypes for imputing complement component 4 (C4) gene structural variation
Study
phs001992
-
Capturing the genetic diversity of the Himba population
Study
phs001995
-
Evolutionary Analysis of Chronic Lymphocytic Leukemia Cells During Relapse After Allogeneic Hematopoietic Stem Cell Transplant
Study
phs001998
-
Advanced Genetic and Molecular Analysis of Solid Tumors
Study
phs001999
-
Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG)
Study
phs002004
-
MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features
Study
phs002005
-
Segmental Overgrowth/Vascular Anomalies/Dermatologic Disorders
Study
phs002006
-
The Research Institute at Nationwide Children's Hospital Genetics of Congenital Heart Disease (CHD)
Study
phs002010
-
National Eye Institute (NEI) Age-Related Eye Disease Study 2 (AREDS2)
Study
phs002015
-
Center Common Disease Genomics [CCDG] - Cardiovascular: Partners Biobank
Study
phs002018
-
Clinical and genetic analysis of retinopathy of prematurity - GWAS
Study
phs002020
-
Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns
Study
phs002022
-
DCCT/EDIC Epigenetics (DNA Methylation) Study
Study
phs002024
-
Early progression to active tuberculosis is a highly heritable trait driven by 3q23 in Peruvians
Study
phs002025
-
Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses
Study
phs002031
-
Genetic Neuroscience: How Human Genes and Alleles Shape Neuronal Phenotypes
Study
phs002032
-
National Heart, Lung and Blood Institute: Regulation of Motile Cilia Assembly in Lung Disease
Study
phs002035
-
WGSPD Project 1: Whole Genome Sequencing for Schizophrenia and Bipolar Disorder
Study
phs002041
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II)
Study
phs002042
-
Drop-BS: High-Throughput Single-Cell Bisulfite Sequencing on a Microfluidic Droplet Platform
Study
phs002123
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Multimodal Developmental Neurogenetics of Females
Study
phs002043
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Victorian Collaborative AuTism Study (CATS): Family and Community Study of the Genetics of Autism Spectrum Disorder
Study
phs002044
-
Grady Trauma Project (GTP)
Study
phs002046
-
Clinical and Genetic Analysis of Retinopathy of Prematurity (ROP)
Study
phs002047
-
OICR: Molecular Pathological Epidemiology of Colorectal Cancer
Study
phs002050
-
Peripheral Blood Transcriptome Analysis of ALS Patients
Study
phs002055
-
Genetic Factors associated with Conversion from Active Surveillance to Treatment for Prostate Cancer
Study
phs002056
-
Systems genetics in human endothelial cells identifies non-coding variants modifying enhancers, expression, and complex disease traits
Study
phs002057
-
Genes for Non-Syndromic Congenital Heart Disease
Study
phs002059
-
Identification and Molecular Characterization of Somatic Mutations in Malformations of Cortical Development
Study
phs002128
-
Pharmacogenomic Analysis of Microtubule Targeting Agent Response and Toxicity
Study
phs002060
-
Temporal Lobe Epilepsy and Retrotransposons
Study
phs002067
-
Sporadic ALS Australia Systems Genomics Consortium (SALSA-SGC)
Study
phs002068
-
Brain Arteriovenous Malformation Genetics Study
Study
phs002069
-
Kids First: Genetics of Kidney and Urinary Tract Malformations
Study
phs002162
-
Role of Tobacco Smoke in Clear Cell Renal Cell Carcinoma
Study
phs002083
-
Bone Microarchitecture
Study
phs002102
-
Gabriella Miller Kids First Pediatric Research Program in Craniofacial Microsomia
Study
phs002130
-
Genomics of Opioid Pharmacogenomics and Acute/Chronic Postsurgical Pain after Major Surgery in Children
Study
phs002105
-
Epigenetic Mechanisms of Inflammation and Fatigue in Head and Neck Cancer
Study
phs002106
-
Unraveling the Genetic Architecture of Diabetic Retinopathy in South India
Study
phs002116
-
Integrated Clinical and Transcriptomic Profiling to Characterize Disease Phenotype
Study
phs002121
-
Environmental Arsenic and Diabetes Mellitus (Chihuahua Cohort)
Study
phs002139
-
Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss
Study
phs002140
-
Molecular Characterization of Hemimegalencephaly
Study
phs002156
-
Genome-Wide Association Study of Patients with Coccidioidomycosis
Study
phs002170
-
Serrated Colorectal Cancer: An Emerging Disease Subtype
Study
phs002171
-
Gabriella Miller Kids First Pediatric Research Project in Microtia in Hispanic Populations
Study
phs002172
-
Gabriella Miller Kids First Pediatric Research Program in Bladder Exstrophy, Epispadias, Complex (BEEC)
Study
phs002173
-
Gabriella Miller Kids First Pediatric Research Project in Cornelia de Lange Syndrome, Related Diagnosis and Structural Birth Defects
Study
phs002174
-
Asthma in the Lives of Families Today (ALOFT)
Study
phs002182
-
Genome-Wide Association Study of Genetic Susceptibility for Graft-vs-Host Disease Cohort 1
Study
phs002185
-
A New High-Throughput Sequencing-Based Technology to Study Heterochromatin Structure
Study
phs002202
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
A Single Cell Atlas of Gene Regulatory Elements in the Human Heart
Study
phs002204
-
Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Study
phs002205
-
Genomic Answers for Kids (GA4K)
Study
phs002206
-
Genetic Determinants of Susceptibility to Severe COVID-19 Infection
Study
phs002245
-
HuBMAP: KULMAP - Human Kidney, Urinary Tract, and Lung Mapping Center
Study
phs002249
-
Genetic Study of Present-Day Populations of Northern Kenya
Study
phs002219
-
Discovering the Genetic Basis of Cleft Palate: CIDR
Study
phs002220
-
Genetic Modifiers of Syndromic Orofacial Clefts
Study
phs002221
-
Multicenter AIDS Cohort Study (MACS)
Study
phs002226
-
Germ Cell Tumor Molecular Heterogeneity Revealed through Analysis of Primary and Metastasis Pairs
Study
phs002229
-
The UCSD / O'Connor "TSP" (Twin/Sibling/Pedigree) Resource in Hypertension
Study
phs002230
-
Germ Cell and Associated Heme Malignancies Evolve from a Common Shared Precursor
Study
phs002231
-
TOPDECC-Trans-omics for Precision Dentistry and Early Childhood Caries: Genome-Wide Genotyping (CIDR) and Microbiome in the ZOE 2.0 Study
Study
phs002232
-
Deletion of FUNDC2 and CMC4 on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in men
Study
phs002234
-
Global Microbiome Conservancy Sequence Data
Study
phs002235
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetic and Phenotypic Determinants of Blood Pressure and Other Cardiovascular Risk Factors
Study
phs002236
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: SWISS-AF/SWISS-AF-PVI/BEAT-AF
Study
phs002242
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: PEGASUS-TIMI 54
Study
phs002243
-
CCG Multicentric Italian Lung Detection (MILD)
Study
phs002253
-
Cystic Fibrosis Nasal Epithelium Gene Expression by RNAseq
Study
phs002254
-
Human CD4 Memory T Cell Activation Time Course
Study
phs002259
-
HuBMAP: A Spatially Resolved Molecular Atlas of Human Endothelium
Study
phs002267
-
Gabriella Miller Kids First Pediatric Research Program in Pediatric T-Cell Acute Lymphoblastic Leukemia
Study
phs002276
-
Selenium Chemoprevention: Benefits and Harms
Study
phs002283
-
Functional Enhancer Elements Drive Subclass-Selective Expression From Mouse to Human Neocortex
Study
phs002292
-
The Immune Microenvironment Shapes Transcriptional and Genetic Heterogeneity in Chronic Lymphocytic Leukemia
Study
phs002297
-
Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs002304
-
CSER: South-Seq: DNA Sequencing for Newborn Nurseries in the South
Study
phs002307
-
International Collaboration of Incident HIV and HCV in Injecting Cohorts (InC3)
Study
phs002310
-
Copy-Number Analysis of Understudied Black Women Ovarian Cancers
Study
phs002313
-
Simultaneous Trimodal Single Cell Measurement of Transcripts, Epitopes, and Chromatin Accessibility Using TEA-Seq
Study
phs002316
-
Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia
Study
phs002317
-
International Verapamil SR/Trandolapril [INVEST] Genes Study
Study
phs002319
-
Kids First: Genetics of Pediatric Germ Cell Tumors
Study
phs002322
-
Center for Common Disease Genomics (CCDG) - Cardiovascular: BioImage Cohort
Study
phs002325
-
International Genetics of Parkinson Disease Progression (IGPP) Consortium: EPIPARK and HBS2 Cohorts
Study
phs002328
-
Kids First and INCLUDE: Down Syndrome, Heart Defects, and Acute Lymphoblastic Leukemia
Study
phs002330
-
Genetic Determinants of EGFR-Driven Lung Cancer Growth and Therapeutic Response In Vivo
Study
phs002334