ArticleJournal of thrombosis and haemostasis : JTH2019
Curated disease-causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH.
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Article in Journal of thrombosis and haemostasis : JTH, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.
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47citing papers in PubMed
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Who cites it
47 citing papers in PubMed.
- Risk of venous thromboembolism after SARS-CoV-2 vaccination-Evidence from genome-wide association study and population-based observational study.British journal of clinical pharmacology · 2026Observational
- Inherited Platelet GPIV Deficiency: First Description of a Series of Unrelated Patients with Bleeding Diathesis.Biomolecules · 2026Article
- Genetic and hemostatic characterization of PAI-1 deficiency and isolated hyperfibrinolysis: data from the RBiN study.Research and practice in thrombosis and haemostasis · 2026Article
- How genetic advances are being translated into improved diagnostic outcomes for patients with inherited bleeding disorders.Blood vessels, thrombosis & hemostasis · 2025Review
- Implementation and clinical utility of multigene panels for bleeding, platelet, and thrombotic disorders.Journal of thrombosis and haemostasis : JTH · 2025Review
- Integrating Next-Generation Sequencing Into Routine Molecular Diagnosis of Inherited Coagulation Factor Deficiencies: Real-World Data From Spanish Patients.Haemophilia : the official journal of the World Federation of Hemophilia · 2025Article
- Is genetic testing for heritable thrombocytopenia coming of age?Research and practice in thrombosis and haemostasis · 2025Article
- Diagnosis of Inherited Platelet Disorders: Clinical Evaluation and Functional and Molecular Assays.Biomolecules · 2025Review
- Application of multigene panel testing for bleeding, thrombotic, and platelet disorders in patients and the general population in China.Molecular biomedicine · 2025Article
- Genome-wide association study of direct oral anticoagulants and their relation to bleeding.European journal of clinical pharmacology · 2025Article
- Article
- Screening for gene variants causing inherited platelet disorders: are the cons always cons?Blood vessels, thrombosis & hemostasis · 2025Article
- RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series.Frontiers in medicine · 2025Article
- Low vitamin C status and hypermobility-related disorders in patients with bleeding disorder of unknown cause.Haemophilia : the official journal of the World Federation of Hemophilia · 2024Article
- Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands study.Research and practice in thrombosis and haemostasis · 2024Article
- Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework.Journal of thrombosis and haemostasis : JTH · 2024Article
- Article
- Blood Coagulation and Beyond: Position Paper from the Fourth Maastricht Consensus Conference on Thrombosis.Thrombosis and haemostasis · 2023Article
- Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26.Blood · 2023Article
- Loss of APOLD1: a new vascular bleeding disorder?Haematologica · 2023Article
Corrections and comments
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Authors and funding
15 authors.
Karyn MegyDepartment of Haematology, University of Cambridge, Cambridge, UK.
Kate DownesDepartment of Haematology, University of Cambridge, Cambridge, UK.
Ilenia SimeoniDepartment of Haematology, University of Cambridge, Cambridge, UK.
Loredana BuryDepartment of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Perugia, Italy.
Joannella MoralesEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, UK.
Rutendo MapetaDepartment of Haematology, University of Cambridge, Cambridge, UK.
Daniel B BellissimoClinical Genomics Laboratory, University of Pittsburgh, Pittsburgh, Pennsylvania.
Paul F BrayDivision of Hematology, and Program in Molecular Medicine, University of Utah, Salt Lake City, Utah.
Anne C GoodeveHaemostasis Research Group, Department of Infection, Immunity and Cardiovascular Disease, Faculty of Medicine, Dentistry and Health, Medical School, University of Sheffield, Sheffield, UK.
Paolo GreseleDepartment of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Perugia, Italy.
Michele LambertDepartment of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Pieter ReitsmaEinthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands.
Willem H OuwehandDepartment of Haematology, University of Cambridge, Cambridge, UK.
Kathleen FresonDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.ORCID 0000-0002-4381-2442
Subcommittee on Genomics in Thrombosis and Hemostasis
Funding
Variation in platelet function: the genetics of platelet gene expressionR01HL102482 · NHLBI · UNIVERSITY OF UTAH · PI BRAY, PAUL F. · 2010 to 2018
$4.6MIn vivo studies of megakaryocyte microRNAs regulating platelet number and integrin activationR01HL141424 · NHLBI · UNIVERSITY OF UTAH · PI BRAY, PAUL F. · 2018 to 2021
$2.5MNHLBI NIH HHS R01 HL102482NHLBI NIH HHS R01 HL141424
Abstract
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Indexed as
Genetic VariationBlood Coagulation FactorsBlood Platelet DisordersGenetic Predisposition to DiseaseHemorrhageHemostasisHumansMolecular Diagnostic TechniquesPhenotypePredictive Value of TestsRisk FactorsThrombosisBlood Coagulation Factors
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.