-
NHLBI TOPMed: Pediatric Cardiac Genomics Consortium (PCGC)'s Congenital Heart Disease Biobank
Study
phs001735
-
Genetic Variants Influence on the Placenta Regulatory Landscape
Study
phs001717
-
NIDDK IBD Genetics Consortium Repository Immunochip
Study
phs001721
-
NIDDK IBD Genetics Consortium Repository Exome Chip
Study
phs001723
-
Genomics and Modification of Pain: A peripheral component identified using iPSCs with the S241T mutation
Study
phs001724
-
NHLBI TOPMed - NHGRI CCDG: Groningen Genetics of Atrial Fibrillation (GGAF) Study
Study
phs001725
-
NCI Expanded Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs001736
-
Kids First Pediatric Research Study in Familial Predisposition to Hematopoietic Malignancies (SJFAMILY-HM)
Study
phs001738
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Study of Autism Genetics Exploration (SAGE)
Study
phs001740
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: The Autism Simplex Collection (TASC)
Study
phs001741
-
Genome-Wide Association Study of HCC in Non-Asian USA Population
Study
phs001744
-
Human Lung Tissue eQTL Study
Study
phs001745
-
A Genomic Atlas of Systemic Interindividual Epigenetic Variation in Humans (GTEx)
Study
phs001746
-
Caregiving as a Natural Stressor in Studies of the Role of Genes That Affect Serotonin Function in Regulating Risk Factors for Coronary Heart Disease (CAREGIVER)
Study
phs001747
-
Molecular Genetics of Histiocytic Sarcoma
Study
phs001748
-
Genetics of Congenital Anomalies of the Kidney and Urinary Tract
Study
phs001749
-
Rapid Evolution of a Skin Lightening Allele in Southern African KhoeSan
Study
phs001753
-
Spit for Science
Study
phs001754
-
Identification of Rare Germline Variants in Familial Patients with Non-medullary Thyroid Cancer
Study
phs001758
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Genetic Resource Exchange
Study
phs001766
-
Genomic Diagnosis and Individualized Therapy of Highly Penetrant Genetic Diabetes
Study
phs001771
-
Effect of the Placental Transcriptome on Stunting in a Longitudinal African Cohort
Study
phs001782
-
Center for Inherited Disease Research (CIDR)-National Institute on Aging (NIA) Whole Exome Analysis of Ehlers-Danlos Syndrome
Study
phs001779
-
Genetics of Fuchs Corneal Dystrophy
Study
phs001834
-
Discovery of Colorectal Cancer Susceptibility Genes in High-Risk Families
Study
phs001787
-
Intergenerational Impact of Genetic and Psychological Factors on Blood Pressure (InterGEN Study)
Study
phs001792
-
Genetic Analysis of the Chiari I Malformation
Study
phs001795
-
A New Reference Panel to Boost African American Genotype Imputation
Study
phs001798
-
Kids First: Whole Genome Sequencing of Nonsyndromic Craniosynostosis
Study
phs001806
-
Genomics of Pediatric Renal Medullary Carcinomas
Study
phs001800
-
Genetics of Lymphatic Anomalies from Center of Applied Genomics (CAG) at CHOP
Study
phs001802
-
Identification of Genomic Markers of Cervical Dystonia and Subtypes
Study
phs001803
-
NIDA Genetic Epidemiology of Opioid Dependence in Bulgaria (GEODB)
Study
phs001804
-
InTEAM Consortium - Alcoholic Hepatitis
Study
phs001807
-
Gene-Environment Interactions in COCCaINE Use Disorder: Collaborative Case-Control Initiative in Cocaine Addiction
Study
phs001810
-
Molecular Determinants of Tumor Behavior in Early Lung Adenocarcinoma
Study
phs001811
-
Genetic and Epigenetic Determinants of Pediatric Obesity-Associated Asthma
Study
phs001812
-
Molecular Genetics of Heterotaxy and Related Congenital Heart Defects
Study
phs001814
-
CRISPR-Mediated ASD Gene Knockout Reduces Neuronal Activity
Study
phs001816
-
GeneScreen, a Population Based, Targeted Genomic Screening Study
Study
phs001817
-
The Institute for Genomic Medicine at Nationwide Children's Hospital Pediatric Cancer and Blood Disorder Project
Study
phs001820
-
Mobile Technology to Identify Mechanisms Linking Genetic Variation and Depression in Intern Health Study (IHS)
Study
phs001826
-
Genetic Studies of Chronic Kidney Disease (CKD)
Study
phs001828
-
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Study
phs001831
-
Genetic Model of MS Severity Predicts Future Accumulation of Disability
Study
phs001833
-
Whole-Exome Sequencing and Targeted DNA Sequencing of Matched Ocular Melanocytosis and Uveal Melanoma
Study
phs001835
-
CADD/GADD centers on Antisocial Drug Dependence
Study
phs001841
-
RNAseq of Sjögren's Syndrome and Healthy Volunteers' Salivary Glands
Study
phs001842
-
Genome-Wide Association of Type 2 Diabetes in Africans: The AADM Study
Study
phs001844
-
Transcriptomic Analysis of Human Hematopoietic Progenitors from Healthy Donors and Bone Marrow Failure Patients
Study
phs001845
-
Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects
Study
phs001846
-
Characterization of Structural Variants in Acute Myeloid Leukemia Patients
Study
phs001847
-
RNA sequencing, ATACseq, and TCR-seq of Tfh cells and CXCR5- CD4+ T cells in HIV infected lymph nodes
Study
phs001849
-
A Phenotypic and Genomics Approach in a Multi-Ethnic Cohort to Subtype Systemic Lupus Erythematosus
Study
phs001850
-
Analysis of the Genetic Basis of Height in Large Jewish Nuclear Families
Study
phs001852
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Axiom GWAS
Study
phs001856
-
Genetics of Mammographic Density in Ashkenazi Jews
Study
phs001857
-
Genetics and Pathophysiology of Autoinflammatory Disorders
Study
phs001860
-
Michigan Polybrominated Biphenyl (PBB) Exposure Registry
Study
phs001862
-
Cutaneous Melanoma GWAS Combining Multiple Populations and Risk Phenotypes
Study
phs001868
-
ADHD Genomic Association Study
Study
phs001869
-
Nature and Contribution of Noncoding, Regulatory Mutations in Neurodevelopmental Disorders
Study
phs001874
-
Determinants of Venetoclax Resistance
Study
phs001875
-
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders
Study
phs001876
-
Genetics of Cutaneous T-Cell Lymphoma
Study
phs001877
-
OncoArray: Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)
Study
phs001882
-
CIDR: Molecular Pathological Epidemiology of Colorectal Cancer
Study
phs001905
-
The Etiological Bases of Giftedness: Epidemiological Study of Cognitive Ability in Children in Saudi Arabia
Study
phs001884
-
Genetic Control of Expression and Splicing in Developing Human Brain
Study
phs001900
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA)
Study
phs001894
-
Altered chromosomal topology drives oncogenic programs in gastrointestinal stromal tumors
Study
phs001906
-
NIAID Centralized Sequencing Program
Study
phs001899
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetics of Coronary Heart Disease - Characterizaton of Coronary Prone Pedigrees
Study
phs001901
-
Whole Exome Sequencing Study of TGFΒ Pathway Genes in HCV Liver Fibrosis
Study
phs001902
-
Identifying novel DNA damage response genes in radiosensitive individuals
Study
phs001911
-
Pilot Sequencing Study: DNA Hydroxymethylation and Gene Expression in Peripheral Blood Mononuclear Cells in Healthy Human Aging
Study
phs001916
-
PAK4 inhibition improves PD-1 blockade immunotherapy
Study
phs001919
-
Genomic Characterization of Brain Metastases from Lung Cancer
Study
phs001920
-
NHLBI TOPMed: SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS)
Study
phs001927
-
National Institutes of Health H3Africa African Collaborative Center for Microbiome and Genomics Research (ACCME)
Study
phs001945
-
Neurogenetic Investigations of Obsessive-Compulsive Disorder
Study
phs001929
-
National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer
Study
phs001935
-
DNA Methylomic Profiling of Preeclampsia Across Pregnancy
Study
phs001937
-
Genomic and Genetic Characterization of Prostate Tumors Treated with Neoadjuvant Intense Androgen Deprivation Therapy
Study
phs001938
-
Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer
Study
phs001940
-
NIDCD Otitis Media Genetic Susceptibility and Middle Ear Microbial Shifts
Study
phs001941
-
Molecular Genetics of Secondary Histiocytic/Dendritic Sarcoma
Study
phs001942
-
Hereditary Cancer Predisposition Syndromes and Uveal Melanoma
Study
phs001943
-
Genetic Evaluation of Autoinflammatory Diseases
Study
phs001946
-
Relapsed Acute Lymphoblastic Leukemia (ALL): Mutational Landscape
Study
phs001951
-
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Red Blood Cell Omics (RBC-Omics) Study
Study
phs001955
-
Investigation of Human DNA Replication Timing Variation by Whole Genome Sequencing
Study
phs001957
-
Cell-Type Specific Effects of Genetic Variation on Chromatin Accessibility During Human Neuronal Differentiation
Study
phs001958
-
Genomic Profiling of Peripheral T-cell Lymphoma
Study
phs001962
-
DEMENTIA-SEQ: WGS in Lewy Body Dementia and Frontotemporal Dementia
Study
phs001963
-
MP2PRT: Identification of Genetic Changes Associated with Relapse and/or Adaptive Resistance in Patients Registered as Favorable Histology Wilms Tumor on AREN03B2
Study
phs001965
-
IGNITE: Implementing GeNomics In practice: Genomic Medicine Implementation - The Personalized Medicine Program
Study
phs001978
-
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Study
phs001967
-
Cellular Origins and Genetic Landscape of Cutaneous GD T Cell Lymphoma
Study
phs001969
-
Kidney Two-Hit Mapping
Study
phs001971