-
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