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2025 July 31 Release

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New Datasets and Version Updates

  • phs004080 (BioLINCC_PETAL_CLOVERS): Prevention and Early Treatment of Acute Lung Injury (PETAL) Crystalloid Liberal or Vasopressors Early Resuscitation in Sepsis (CLOVERS) (PETAL CLOVERS-BioLINCC)

  • phs004085 (BioLINCC_IPFNet_STEP_IPF): Idiopathic Pulmonary Fibrosis Network (IPFNet) Sildenafil Trial of Exercise Performance in Idiopathic Pulmonary Fibrosis (IPFNet-STEP-IPF-BioLINCC)

  • phs004077 (BioLINCC_NETT): National Emphysema Treatment Trial (NETT-BioLINCC)

  • phs000285 (dbGaP_CARDIA): Coronary Artery Risk Development in Young Adults (CARDIA) Study - Cohort

  • phs000286 (dbGaP_JHS): Jackson Heart Study (JHS) Cohort

  • phs000280 (dbGaP_ARIC): Atherosclerosis Risk in Communities (ARIC) Cohort

  • phs003045 (COVID19_C4R_CARDIA): Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Coronary Artery Risk Development in Young Adults Study (CARDIA)

  • phs002719 (REGARDS-GWAS): Reasons for Geographic and Racial Differences in Stroke Cardiorenal GWAS

  • phs000886 (HF_Collection_Twins_Asthma): An Omics View of Asthma through Monozygotic Twins

  • phs000902 (HF_Collection_MiGen_EXS_REGICOR): Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor

  • phs000936 (HF_Collection_BroadEOMI_exome): NHLBI GO-ESP: Early-Onset Myocardial Infarction Exome Chip (Broad EOMI)

  • phs000963 (HF_Collection_PGRN_Cardio-Stat): PGRN-RIKEN: Genetic Determinants of Clinical Cardiovascular Events in Patients Receiving Statins

  • phs000998 (HF_Collection_Endothelial_PAH): RNA Sequencing of Pulmonary Arterial Endothelial Cells in Pulmonary Hypertensive Patients and Controls

  • phs001212 (HF_Collection_Globin_iPS): NextGen Consortium: Globin Gene Expression in Sickle Cell Genotype-Specific iPS Cells

  • phs001258 (HF_Collection_exRNA_healthy): Total exRNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects

  • phs000917 (HF_Collection_MiGen_EXS_PROMIS): Myocardial Infarction Genetics Exome Sequencing Consortium: Pakistan Risk Of Myocardial Infarction Study

  • phs001101 (HF_Collection_MiGEN_EXS_MDC): Myocardial Infarction Genetics Exome Sequencing Consortium: Malmo Diet and Cancer Study

  • phs000990 (HF_Collection_MiGen_EX_UL): Myocardial Infarction Genetics Exome Sequencing Consortium: University of Lubeck

  • phs000438 (HF_Collection_PGRN_ACE): A Genome-Wide Association Analysis in Angiotensin-Converting Enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine

  • phs000362 (HF_Collection_Fam_FA): NHLBI GO-ESP: Family Studies (Familial Atrial Fibrillation)

  • phs000481 (HF_Collection_CAP): Cholesterol and Pharmacogenetics (CAP) Study

  • phs000581 (HF_Collection_Fam_DC): NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy)

  • phs000814 (HF_Collection_MiGen_EXS_ItalAmer): Myocardial Infarction Genetics Exome Sequencing Consortium: Italian Atherosclerosis Thrombosis and Vascular Biology

  • phs000758 (HF_Collection_Fam_CHD): Family Genomics of Congenital Heart Defects

  • phs000617 (HF_Collection_KCNE1_TdP): PGRN-Leducq: Identification of the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes

  • phs000354 (HF_Collection_Fam_PAH): NHLBI GO-ESP Family Studies: Pulmonary Arterial Hypertension

  • phs000806 (HF_Collection_MiGen_EXS_Ottawa): Myocardial Infarction Genetics Exome Sequencing Consortium: Ottawa Heart Study

  • phs000808 (HF_Collection_PGRN_diLQTS): PGRN/PAT: The genomic basis for susceptibility to drug-induced long QT syndrome (diLQTS)

  • phs000873 (HF_Collection_Exome_Thrombo-Leuk): Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition

  • phs000507 (HF_Collection_BEN): NHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS

  • phs000335 (HF_Collection_LHS): Genome-Wide associations of Lung Health Study (LHS)

  • phs000442 (HF_Collection_DrugRes_HTN): Drug Resistant Hypertension in African Americans' Exome

  • phs000518 (HF_Collection_Fam_IB): NHLBI GO-ESP Family Studies: Idiopathic Bronchiectasis of unknown etiology that is not related to cystic fibrosis or classic primary ciliary dyskinesia or immune deficiency or any other known causes

  • phs001605 (TOPMed_Freeze10_CHIRAH): NHLBI TOPMed: Chicago Initiative to Raise Asthma Health Equity (CHIRAH)

  • phs001661 (TOPMed_Freeze10_GCPD-A): NHLBI TOPMed: Genetic Causes of Complex Pediatric Disorders - Asthma (GCPD-A)

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