-
Study of Adaptation to Hypoxia in Ethiopian Highlanders via Whole Genome Sequencing
Study
phs000647
-
Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR and PEAR-2)
Study
phs000649
-
Pediatric Investigation of Genetic Factors Linked with Renal Progression (PediGFR): Chronic Kidney Disease in Children Cohort (CKiD)
Study
phs000650
-
Epi4K: Gene Discovery in 4,000 Epilepsy Genomes
Study
phs000653
-
Genetics of Inherited Muscle Disease
Study
phs000655
-
Genetic measurement of memory B-cell recall using antibody repertoire sequencing
Study
phs000656
-
Chinese Alternating Hemiplegia of Childhood (AHC) Disease Study
Study
phs000660
-
Germline Sequencing for Aggressive Prostate Carcinoma
Study
phs000661
-
National Children's Study Vanguard Study Formative Research Study (NCS)
Study
phs000662
-
The African American Breast Cancer Epidemiology and Risk (AMBER) Consortium Study
Study
phs000669
-
Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomic Study (PGRN-AMPS)
Study
phs000670
-
Somatic Mutations in Variant and IGHV4-34 Expressing Hairy Cell Leukemia
Study
phs000671
-
National Institute of Dental and Craniofacial Research (NIDCR) Sjögren's International Collaborative Clinical Alliance (SICCA): Center for Inherited Disease Research (CIDR) Genome-Wide Genotyping
Study
phs000672
-
University of Michigan Clinical Sequencing Exploratory Research (CSER)
Study
phs000673
-
Resource for Genetic Epidemiology Research on Adult Health and Aging (GERA)
Study
phs000674
-
An APOBEC Cytidine Deaminase Mutagenesis in Human Cancers
Study
phs000677
-
The Two Sister Study: A Family-Based Study of Genes and Environment in Young-Onset Breast Cancer
Study
phs000678
-
Genome-Wide Association Study of Anorexia Nervosa (Price Foundation, Klarman Family Foundation, Center for Applied Genomics at the Children's Hospital of Philadelphia, Scripps Translational Sciences Institute Clinical Translational Science Award)
Study
phs000679
-
Common Variation in Candidate Genes in the Diabetes Prevention Program
Study
phs000681
-
Genetics of Neuropsychiatric and Neurodevelopmental Disorders
Study
phs000682
-
Age related Macular Degeneration (AMD) - Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: Association and Sequencing Studies
Study
phs000684
-
Genomic Analysis of Peripheral T-Cell Lymphomas
Study
phs000689
-
Whole-Genome Sequencing in Multiplex Epilepsy Families
Study
phs000690
-
CIP: Differential Response to Hydroxyurea and Incidence of Stroke in Sickle Cell Disease
Study
phs000691
-
A Pharmcogenetic Study of Bipolar Disorder in a Taiwanese Han Chinese Population (TWBP)
Study
phs000692
-
CATHeterization GENetics (CATHGEN)
Study
phs000703
-
QUANTitative Chest Computed Tomography UnMasking Emphysema Progression in Alpha-1 Antitrypsin Deficiency
Study
phs000698
-
NIH Roadmap Epigenomics Program - Broad Institute
Study
phs000700
-
Efficacy of a Therapeutic Treatment Trial in Angelman Syndrome
Study
phs000701
-
Next Generation Mendelian Genetics: Hereditary Neurological Disorders
Study
phs000707
-
Warfarin Pharmacogenetics: Pharmacogenetic Optimization of Anticoagulant Response (POAT) and Genetic and Environmental Determinants of Warfarin Response (GEDWR)
Study
phs000708
-
University of Illinois at Chicago (UIC) Autism Centers of Excellence (ACE) Exome Sequencing Analysis
Study
phs000712
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
Trisomy21: Risk Factors for Chromosome Nondisjunction (T21NDJ)
Study
phs000718
-
Genetic Basis of Pulmonary Non-tuberculous Mycobacterial Infections
Study
phs000719
-
Whole Exome Sequencing of Colorectal Cancer Patients from the Nurses' Health Study (NHS) and Health Professionals Follow-up Study (HPFS)
Study
phs000722
-
Sequencing of Cervical Cancer
Study
phs000723
-
Genome-wide Association Study of Myasthenia Gravis
Study
phs000726
-
The Genetics of Lung Cancer Susceptibility in Smokers
Study
phs000728
-
Genomics of Brain Metastases
Study
phs000730
-
L1-Seq and Genome-Wide SNP Genotyping in a Multiethnic Asian Population
Study
phs000732
-
The International Consortium for Prostate Cancer Genetics Genome Wide Association Study of Familial Prostate Cancer
Study
phs000733
-
A Genome-wide Association Study (GWAS) of Risk for Osteosarcoma
Study
phs000734
-
The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Genetics of Genetic Epidemiology of Metabolic Syndrome in an Island Population
Study
phs000737
-
Exome Sequencing in Schizophrenia Families
Study
phs000738
-
Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) Lipidomics Study
Study
phs000741
-
Natural History of and Genetic Modifiers in Spinocerebellar Ataxias
Study
phs001332
-
Research Program on Genes, Environment and Health (RPGEH)
Study
phs000788
-
DNA Replication Timing Alterations in Genetic Diseases
Study
phs002597
-
METSIM (METabolic Syndrome In Men) Study
Study
phs000743
-
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