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The Genetic Architecture of Smoking and Smoking Cessation
Study
phs000404
-
eMERGE Network Study of the Genetic Determinants of Resistant Hypertension
Study
phs000297
-
Osteoporotic Fractures in Men (MrOS)
Study
phs000373
-
GA4GH
Documentation
about/projects-and-funders/ga4gh
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CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
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
-
Alzheimer's Disease Sequencing Project (ADSP)
Study
phs000572
-
Framingham Cohort
Study
phs000007
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
California Pacific Medical Center Research Breast Health Cohort
Study
phs000395
-
Federated EGA
Documentation
about/projects-and-funders/federated-ega
-
Multi-Ethnic Study of Atherosclerosis (MESA) Cohort
Study
phs000209
-
FEGA and European GDI: working together to improve human health
Blog
fega-and-gdi
-
Data Use Ontology (DUO)
Documentation
access/data-access-committee/data-use-ontology
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Genome-Wide Association Study of Patients with Coccidioidomycosis
Study
phs002170
-
Detection of Colorectal Cancer Susceptibility Loci Using Genome-Wide Sequencing
Study
phs001554
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
OncoArray: Prostate Cancer
Study
phs001391
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415
-
Identification of Genes Involved in Familial Coronary Artery Disease
Study
phs000514
-
Exome Sequencing Reveals Frequent Inactivating Mutations in BAP1, ARID1A, and PBRM1 in Intrahepatic Cholangiocarcinomas
Study
EGAS00001001108
-
Characterization of Sex Differences in Human Placentas
Study
phs002240
-
Establishment of xenogfafts and cultured cell lines from clinical samples
Study
JGAS000585
-
Screening Cases of Isolated Dystonia for Variants in CIZ1
Study
phs001455
-
RNA-Seq studies of Gene Expression in Cells and Networks in FI and ACC in Autism
Study
phs000609
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (mouse)
Study
EGAS00001004696
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (Human)
Study
EGAS00001004897
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Blood transcriptome profiling links immunity to disease severity in myotonic dystrophy type 1 (DM1).
Study
EGAS00001006926
-
Whole Exome Sequencing Study of TGFΒ Pathway Genes in HCV Liver Fibrosis
Study
phs001902
-
Nasal Polyp RNAsequencing, Skaraborg Sweden
Study
EGAS00001007088
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID‑19
Study
EGAS00001006372
-
Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors
Study
EGAS00001000906
-
Gene Expression between PMD and Control LCLs at Baseline, E2, and E2 Withdrawal
Study
phs003003
-
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
Study
EGAS50000000298
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Rare coding variants in lupus risk genes
Study
EGAS00001003548
-
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
-
An instructive role for IL7RA in the development of human B-cell precursor leukemia
Study
EGAS00001005347
-
Systematic identification of long non-coding RNAs potentially involved in gastrointestinal carncer
Study
JGAS000011
-
ERBB2/HER2 transmembrane and juxtamembrane domain mutations in cancer
Study
EGAS00001003213
-
Efficacy of CDK4/6i in preclinical models of malignant pleural mesothelioma
Study
EGAS00001005352
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Mediators of Atherosclerosis in South Asians Living in America Study (MASALA)
Study
phs002980
-
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Study
phs002816
-
Whole Genome Sequencing to Discover Familial Myeloma Risk Genes
Study
phs001819
-
Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Study
EGAS00001003719
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Study
EGAS00001000714
-
Tumor Mutation Burden, Expressed Neoantigen and Immune Microenvironment in Diffuse Gliomas
Study
phs002653