-
Yale Center for Mendelian Genomics (YCMG)
Study
phs000744
-
Whole Exome and Transcriptome Sequencing in Sporadic ALS
Study
phs000747
-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Study
Study
phs000867
-
Relating Clinical Outcomes in Multiple Myeloma to Personal Assessment of Genetic Profile
Study
phs000748
-
Genomic Origins and Admixture in Latinos (GOAL)
Study
phs000750
-
BrainSpan Atlas of the Human Brain
Study
phs000755
-
Ataxia Gene Identification by Integrated Genomic Analysis
Study
phs000757
-
The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q)
Study
phs000759
-
Orofacial Pain: Prospective Evaluation and Risk Assessment (OPPERA)
Study
phs000761
-
Somatic Mutation Profile by Next Generation Sequencing in HER2+ Breast Cancer
Study
phs000770
-
The Collaborative Study on the Genetics of Alcoholism (COGA)
Study
phs000763
-
GEI Studies - Psoriasis
Study
phs000766
-
The UC San Diego Chronic Lymphocytic Leukemia (CLL) Study
Study
phs000767
-
Genetic Predictors of Adverse Radiotherapy Effects (Gene-PARE)
Study
phs000772
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts and Related Phenotypes
Study
phs000774
-
Transcriptome study of differential expression in schizophrenia
Study
phs000775
-
Consanguinity and rare mutations outside of MCCC genes underlie non-specific phenotypes of MCC Deficiency
Study
phs000776
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Gene Discovery in Autosomal Dominant Focal Segmental Glomerulosclerosis (FSGS)
Study
phs000777
-
Integrated Epigenetic Maps of Human Embryonic, Extraembryonic and Adult Cells
Study
phs000791
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK): Identification of VUR genes by exome sequencing
Study
phs000778
-
Ontario Familial Colon Cancer Registry Single Nucleotide Polymorphisms and CpG Methylation (OFCCR SNP-CpG)
Study
phs000779
-
Whole Exome Sequencing of Congenital Diaphragmatic Hernia Patients and Trios
Study
phs000783
-
Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs000784
-
Collaborative Study of Genes, Nutrients and Metabolites (CSGNM)
Study
phs000789
-
Comparative Sequence Analysis Between Primary and Metastatic Colorectal Cancer Lesions
Study
phs000790
-
Oncogenomics of Malignant Peripheral Nerve Sheath Tumors
Study
phs000792
-
Paired Acute Myeloid Leukemia (AML) Epigenetics Study on Epialleles and Clonality
Study
phs000793
-
Gastric Cancer Genetic Analysis of Metastasis
Study
phs000795
-
Genome Wide Association Study of Chronic TMD: Discovery Phase
Study
phs000796
-
Performance Characteristics of Selective Targeted Enrichment in Genetic Diagnostic Testing
Study
phs000798
-
Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
Study
phs000858
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs000799
-
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Study
phs000801
-
Genome Wide Association Study of Serum Creatinine during Vancomycin Therapy and Vancomycin Pharmacokinetics
Study
phs000894
-
Genomic Sequencing of Ewing Sarcoma
Study
phs000804
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Ottawa Heart Study
Study
phs000806
-
PGRN/PAT: The genomic basis for susceptibility to drug-induced long QT syndrome (diLQTS)
Study
phs000808
-
Autosomal Recessive PGM3 Mutations Link Glycosylation Defects to Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment
Study
phs000809
-
The Breast and Prostate Cancer Cohort Consortium (BPC3) GWAS of Aggressive Prostate Cancer and ER- Breast Cancer
Study
phs000812
-
CIDR, NCI, NIDA Sequencing of Targeted Genomic Regions Associated with Smoking
Study
phs000813
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Italian Atherosclerosis Thrombosis and Vascular Biology
Study
phs000814
-
Gene Expression and Regulatory Networks in Human Leukocytes - Immunological Variation Consortium
Study
phs000815
-
Genome-Wide Discovery of Novel Breast Cancer Predisposing Mutations
Study
phs000822
-
Discovery of Novel Melanoma Predisposing Mutations by Exome Sequencing
Study
phs000823
-
Genome-Wide Discovery of Novel Colon Cancer Predisposing Mutations
Study
phs000824
-
Whole Genome Sequencing of Two Family Trios with 22q.11.2 Deletion Syndrome
Study
phs000837
-
North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES)
Study
phs000827
-
Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma
Study
phs000828
-
Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study
Study
phs000830
-
Ghana Prostate Study
Study
phs000838
-
The Genetics of Type 2 Diabetes Consortium (GoT2D): Low-Pass Sequencing and High-Density SNP Genotyping for Type 2 Diabetes
Study
phs000840
-
Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)
Study
phs000842
-
Whole Genome Bisulfite Sequencing of Circulating Cell-Free (CCF) DNA and its Cellular Contributors
Study
phs000846
-
T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS)
Study
phs000847
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Precocious Coronary Artery Disease Study
Study
phs000883
-
Autosomal recessive
Study
phs000848
-
Resistance studies in Lung Cancer
Study
phs000855
-
Chromothripsis in Patient WHIM-09
Study
phs000856
-
National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans
Study
phs000863
-
Genomic Predictors of Combat Stress Vulnerability and Resilience
Study
phs000864
-
Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
Study
phs000869
-
High-Risk Breast Cancer GWAS
Study
phs000929
-
Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition
Study
phs000873
-
Genetic and Environmental Risk Factors for Hemorrhagic Stroke (GERFHS)
Study
phs000874
-
Transdisciplinary Research Into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing
Study
phs000876
-
Substance Dependence GWAS in European- and African - Americans
Study
phs000952
-
An Omics View of Asthma through Monozygotic Twins
Study
phs000886
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
Genome-Wide Association Study of Endometrial Cancer in the Epidemiology of Endometrial Cancer Consortium (E2C2)
Study
phs000893
-
National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen)
Study
phs000899
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor
Study
phs000902
-
OCD Collaborative Genetic Association Study (OCGAS)
Study
phs000903
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
Next Generation Sequencing of Stage IV Squamous Cell Lung Cancers Reveals an Association of PI3K Aberrations and Evidence of Clonal Heterogeneity in Patients with Brain Metastases
Study
phs000907
-
University of Miami Udall Center of Excellence Identification of Rare Variants in PD through Whole Exome Sequencing
Study
phs000908
-
Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
Study
phs000910
-
Type 1 Diabetes Genetics Consortium (T1DGC): ImmunoChip Study
Study
phs000911
-
San Francisco Bay Area Latina Breast Cancer Study
Study
phs000912
-
Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2
Study
phs000913
-
Genome-wide Association Study of Adiposity in Samoans
Study
phs000914
-
Myocardial Infarction Genetics Exome Sequencing Consortium: German Heart Center in Munich
Study
phs000916
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Pakistan Risk Of Myocardial Infarction Study
Study
phs000917
-
NHLBI TOPMed - NHGRI CCDG: Genes-Environments and Admixture in Latino Asthmatics (GALA II)
Study
phs000920
-
NHLBI TOPMed: Study of African Americans, Asthma, Genes and Environment (SAGE)
Study
phs000921
-
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic
Study
phs000942
-
Genetic Aberrations and Subclonal Structure Impact Chronic Lymphocytic Leukemia
Study
phs000922
-
NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for studying the impact of genetic variation on molecular and physiological phenotypes
Study
phs000924
-
Rare Disease Susceptibility Alleles in Children with Crohn Disease
Study
phs000926
-
CSER: Clinical Implementation of Carrier Testing Using Next Generation Sequencing (NextGen)
Study
phs000927
-
CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology) Consortium Summary Results from Genomic Studies
Study
phs000930
-
DMET Genes, Nicotine Metabolism and Prospective Abstinence
Study
phs000931
-
Genomic Profiling of Melanoma
Study
phs000933
-
The CHOP Pediatric Genetic Sequencing (PediSeq) Project : Applying Genomic Sequencing in Pediatrics
Study
phs000935
-
NHLBI GO-ESP: Early-Onset Myocardial Infarction Exome Chip (Broad EOMI)
Study
phs000936
-
Detection of Enhancer-Associated Rearrangements Reveals Mechanisms of Oncogene Dysregulation in B-cell Lymphoma
Study
phs000939
-
Phylogenetic Analyses of Melanoma Reveal Complex Patterns of Metastatic Dissemination
Study
phs000941
-
NHLBI TOPMed: The Cleveland Family Study (CFS)
Study
phs000954
-
Genome-Wide Assessment of DNA Methylation in Systemic Lupus Erythematosus-Related Autoantibodies
Study
phs000947
-
Genetic Discovery and Application in a Clinical Setting: Continuing a Partnership (eMERGE Phase II)
Study
phs000948
-
Genetic Analysis of Normal Human Facial Variation
Study
phs000949