-
National Institute on Alcohol Abuse and Alcoholism (NIAAA) Postmortem Prefrontal Cortex eQTL and mQTL Study
Study
phs001981
-
University of Illinois at Chicago (UIC) Autism Centers of Excellence (ACE) Exome Sequencing Analysis
Study
phs000712
-
Homozygous Duplication Identified by Whole Genome Sequencing Causes LRBA Deficiency
Study
phs002557
-
Non-coding RNAs Activated by the Wnt/Beta-catenin Signaling Pathway in Hepatoblastoma
Study
phs001433
-
Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss
Study
phs002140
-
The Genetic and Transcriptomic Evolution of Melanoma
Study
phs001550
-
High-Throughput LINE-1 Retrotransposon Discovery in Humans
Study
phs000273
-
Identifying novel DNA damage response genes in radiosensitive individuals
Study
phs001911
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: SPARK Simons Foundation Powering Autism Research for Knowledge
Study
phs002511
-
Genome-Wide Assessment of DNA Methylation in Systemic Lupus Erythematosus-Related Autoantibodies
Study
phs000947
-
Drop-BS: High-Throughput Single-Cell Bisulfite Sequencing on a Microfluidic Droplet Platform
Study
phs002123
-
Genomic and Genetic Characterization of Prostate Tumors Treated with Neoadjuvant Intense Androgen Deprivation Therapy
Study
phs001938
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
A Genome-Wide Association Study of Sporadic ALS in an Irish Population (SIALS) and Sequencing and Analysis of an Irish Human Genome
Study
phs000127
-
Genome-Wide Scan for Genetic Variants Associated with Early-Onset Prostate Cancer
Study
phs001185
-
NIDCD Otitis Media Genetic Susceptibility and Middle Ear Microbial Shifts
Study
phs001941
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - Genome-Wide Association Study Meta-Analysis
Study
phs001263
-
Childhood Cancer Survivor Study (CCSS)
Study
phs001327
-
National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease
Study
phs001172
-
PAK4 inhibition improves PD-1 blockade immunotherapy
Study
phs001919
-
Differential Mutations in Matched Primary and Metastatic Colorectal Cancers
Study
phs001084
-
A New Reference Panel to Boost African American Genotype Imputation
Study
phs001798
-
NCI Expanded Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs001736
-
Genome Wide Association Study of Serum Creatinine during Vancomycin Therapy and Vancomycin Pharmacokinetics
Study
phs000894
-
Integrated Clinical and Transcriptomic Profiling to Characterize Disease Phenotype
Study
phs002121
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetic and Phenotypic Determinants of Blood Pressure and Other Cardiovascular Risk Factors
Study
phs002236
-
Genome Wide Association Study of Chronic TMD: Discovery Phase
Study
phs000796
-
NHLBI GO-ESP: Family Studies (JHMI-Molecular Genetics of Atypical Cystic Fibrosis (CF) Study)
Study
phs000556
-
eMERGE Network Genome-Wide Association Study of Red Cell Indices, White Blood Count (WBC) Differential, Diabetic Retinopathy, Height, Serum Lipid Levels, Specifically Total Cholesterol, HDL (High Density Lipoprotein), LDL (Low Density Lipoprotein), and Triglycerides, and Autoimmune Hypothyroidism.
Study
phs000360
-
GAW16 Framingham and Simulated Data
Study
phs000128
-
DNA Replication Timing Alterations in Genetic Diseases
Study
phs002597
-
Genetic Testing to Understand and Address Renal Disease Disparities
Study
phs001620
-
(Epi)genetic Risk Architectures of Opioid-Dependent Brain
Study
phs002724
-
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics
Study
phs001496
-
A Single Cell Atlas of Gene Regulatory Elements in the Human Heart
Study
phs002204
-
Division of Cancer Epidemiology and Genetics (DCEG) Imputation Reference Dataset
Study
phs000396
-
Multicenter AIDS Cohort Study (MACS)
Study
phs002226
-
Multicenter International Lymphangioleiomyomatosis Efficacy of Sirolimus Trial (The MILES Trial)
Study
phs000605
-
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625
-
NHLBI TOPMed: Australian Familial Atrial Fibrillation Study
Study
phs001435
-
Age related Macular Degeneration (AMD) - Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: Association and Sequencing Studies
Study
phs000684
-
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
-
Lobular Carcinomas In Situ Display Intra-Lesion Genetic Heterogeneity and Clonal Evolution in the Progression to Invasive Disease
Study
phs001006
-
Bone Microarchitecture
Study
phs002102
-
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing
Study
phs001700
-
NHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS
Study
phs000507
-
Genetics of Cutaneous T-Cell Lymphoma
Study
phs001877
-
CIP: Obesity-Diabetes Familial Risk, Viva La Familia Study
Study
phs000616
-
99 Cases of Small Cell Lung Cancer Study
Study
phs001083
-
Whole Exome Sequencing of Uveal Melanoma
Study
phs001370
-
Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study
Study
phs001307
-
Whole Exome Sequencing of Colorectal Cancer Patients from the Nurses' Health Study (NHS) and Health Professionals Follow-up Study (HPFS)
Study
phs000722
-
GUARDIAN: The Insulin Resistance Atherosclerosis Family Study (IRASFS)
Study
phs001008
-
Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)
Study
phs000842
-
New England-Based Case-Control Study of Ovarian Cancer
Study
phs001034
-
Addictions: Genotypes, Polymorphisms, and Function/Human Genetic Correlates of Addictive Diseases
Study
phs001109
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
Genetic Basis of Pulmonary Non-tuberculous Mycobacterial Infections
Study
phs000719
-
Next Generation Mendelian Genetics: Malignant Hyperthermia
Study
phs000405
-
Biological Determinants of Peritoneal Dialysis Outcomes
Study
phs002996
-
Peripheral Blood Transcriptome Analysis of ALS Patients
Study
phs002055
-
Maternal Plasma Folate and DNA Methylation in Epigenome-Wide Meta-Analysis of Newborns
Study
phs001059
-
Population Architecture using Genomics and Epidemiology (PAGE)
Study
phs000356
-
T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS)
Study
phs000847
-
NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai
Study
phs001644
-
Towards a Genomic Understanding of Myeloma
Study
phs000348
-
Intervention with Micronutrients and Long-Term Impact in Brazil-RECODISA
Study
phs003174
-
Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
Study
phs001687
-
Clinical and genetic analysis of retinopathy of prematurity - GWAS
Study
phs002020
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs000799
-
Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study - Maternal Glycemia and Birthweight GEI Study
Study
phs000096
-
Male Infertility: Genetics of Spermatogenic Failure
Study
phs001023
-
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Study
phs000587
-
A Genome-Wide Association Study of Heroin Dependence
Study
phs000277
-
SardiNIA Medical Sequencing Discovery Project
Study
phs000313
-
The Sea Islands Genetic Network (SIGNET): Identifying genetic contributors to diabetes and dyslipidemia in African Americans
Study
phs000433
-
ARRA - NHLBI Lung Cohorts Sequencing Project: Genetic modifiers of
Study
phs000254
-
NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Study
phs001515
-
Genomics of Pediatric Renal Medullary Carcinomas
Study
phs001800
-
Investigating Human Placentation and Pregnancy Using First Trimester Chorionic Villi
Study
phs001320
-
The National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network (SiGN)
Study
phs000615
-
Genetic Association Studies in the Solomon Islanders
Study
phs000493
-
Multiregion Sequencing of Localized Prostate Cancer
Study
phs001465
-
Genomic Variation in Diffuse Large B Cell Lymphomas
Study
phs001444
-
Nature and Contribution of Noncoding, Regulatory Mutations in Neurodevelopmental Disorders
Study
phs001874
-
Next Generation Mendelian Genetics: Muscle Hypertrophy
Study
phs000541
-
Exome Sequencing of Schizophrenia Cases and Controls in the South African Xhosa Population
Study
phs000959
-
Genetic Basis of Isolated Arhinia and Bosma Arhinia Microphthalmia Syndrome
Study
phs001246
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Advanced Genetic and Molecular Analysis of Solid Tumors
Study
phs001999
-
Genomics of Brain Metastases
Study
phs000730
-
Genetic Study of Vascular Anomalies
Study
phs003197
-
NHLBI GO-ESP Family Studies: Idiopathic Bronchiectasis of unknown etiology that is not related to cystic fibrosis or classic primary ciliary dyskinesia or immune deficiency or any other known causes
Study
phs000518
-
Washington University Coronary Artery Disease Study
Study
phs001227
-
Pharmacogenomics of HIV Therapy - Atazanavir Bilirubin-related Side Effects
Study
phs001484
-
Gabriella Miller Kids First Pediatric Research Program in Craniofacial Microsomia
Study
phs002130
-
PGRN-Leducq: Identification of the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
Study
phs000617
-
NHLBI: Genetic modifiers of sickle cell anemia severity and fetal hemoglobin expression in the Cooperative Study of Sickle Cell Disease (CSSCD)
Study
phs000366
-
NHLBI TOPMed: Recipient Epidemiology and Donor Evaluation Study-III Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Study
phs001468