|
| 36928819 | Genetic association analysis of 77,539 genomes reveals rare disease etiologies. | Nat Med | 2023 |
| 37816352 | Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA. | Am J Hum Genet | 2023 |
| 37647652 | A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk. | Blood | 2023 |
| 37647632 | The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140â¿¿214 UK Biobank participants. | Blood | 2023 |
| 37638093 | Pilot of asymptomatic swabbing of humans following exposures to confirmed avian influenza A(H5) in avian species in England, 2021/2022. | Influenza Other Respir Viruses | 2023 |
| 37553192 | Outcome monitoring and risk stratification after cardiac procedure in neonates, infants, children and young adults born with congenital heart disease: protocol for a multicentre prospective cohort study (Children OMACp). | BMJ Open | 2023 |
| 37275180 | Corrigendum to 'The Hemophilia Joint Health Score version 2.1 Validation in Adult Patients Study: A multicenter international study' [Research and Practice in Thrombosis and Haemostasis, 6/2, (2022) e12690]. | Res Pract Thromb Haemost | 2023 |
| 37435838 | Bleeding risk in patients prescribed dual antiplatelet therapy and triple therapy after coronary interventions: the ADAPTT retrospective population-based cohort studies. | Health Technol Assess | 2023 |
| 36928819 | Genetic association analysis of 77,539 genomes reveals rare disease etiologies. | Nat Med | 2023 |
| 36732161 | Corrigendum to Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH [J Thromb Haemost. 2022 Jul;20(7):1735-1743]. | J Thromb Haemost | 2023 |
| 37292802 | Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomisation analysis. | medRxiv | 2023 |
| 36787503 | How I diagnose and treat neonatal thrombocytopenia. | Blood | 2023 |
| 37553192 | Outcome monitoring and risk stratification after cardiac procedure in neonates, infants, children and young adults born with congenital heart disease: protocol for a multicentre prospective cohort study (Children OMACp). | BMJ Open | 2023 |
| 37647652 | A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk. | Blood | 2023 |
| 37647632 | The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140â¿¿214 UK Biobank participants. | Blood | 2023 |
| 37816352 | Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA. | Am J Hum Genet | 2023 |
| 37638093 | Pilot of asymptomatic swabbing of humans following exposures to confirmed avian influenza A(H5) in avian species in England, 2021/2022. | Influenza Other Respir Viruses | 2023 |
| 37292802 | Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomisation analysis. | medRxiv | 2023 |
| 37275180 | Corrigendum to 'The Hemophilia Joint Health Score version 2.1 Validation in Adult Patients Study: A multicenter international study' [Research and Practice in Thrombosis and Haemostasis, 6/2, (2022) e12690]. | Res Pract Thromb Haemost | 2023 |
| 37435838 | Bleeding risk in patients prescribed dual antiplatelet therapy and triple therapy after coronary interventions: the ADAPTT retrospective population-based cohort studies. | Health Technol Assess | 2023 |
| 36787503 | How I diagnose and treat neonatal thrombocytopenia. | Blood | 2023 |
| 36732161 | Corrigendum to Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH [J Thromb Haemost. 2022 Jul;20(7):1735-1743]. | J Thromb Haemost | 2023 |
| 33444767 | Prediction of Bleeding in Pediatric Cardiac Surgery Using Clinical Characteristics and Prospective Coagulation Test Results. | Semin Thorac Cardiovasc Surg | 2022 |
| 35770723 | Expert opinion on the use of platelet secretion assay for the diagnosis of inherited platelet function disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology. | J Thromb Haemost | 2022 |
| 35961692 | Real-world bleeding in patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) and prescribed different combinations of dual antiplatelet therapy (DAPT) in England: a population-based cohort study emulating a 'target trial'. | Open Heart | 2022 |
| 35570324 | Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH. | J Thromb Haemost | 2022 |
| 35852974 | Not Just an Anchor: The Human Filum Terminale Contains Stretch Sensitive and Nociceptive Nerve Endings and Responds to Electrical Stimulation With Paraspinal Muscle Activation. | Neurosurgery | 2022 |
| 36600324 | Surgical-PEARL protocol: a multicentre prospective cohort study exploring aetiology, management and outcomes for patients with congenital anomalies potentially requiring surgical intervention. | BMJ Open | 2022 |
| 33444767 | Prediction of Bleeding in Pediatric Cardiac Surgery Using Clinical Characteristics and Prospective Coagulation Test Results. | Semin Thorac Cardiovasc Surg | 2022 |
| 35012325 | Epigenetic Regulation of <i>F2RL3</i> Associates With Myocardial Infarction and Platelet Function. | Circ Res | 2022 |
| 35068290 | Higher body mass index raises immature platelet count: potential contribution to obesity-related thrombosis. | Platelets | 2022 |
| 35770723 | Expert opinion on the use of platelet secretion assay for the diagnosis of inherited platelet function disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology. | J Thromb Haemost | 2022 |
| 35570324 | Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH. | J Thromb Haemost | 2022 |
| 35852974 | Not Just an Anchor: The Human Filum Terminale Contains Stretch Sensitive and Nociceptive Nerve Endings and Responds to Electrical Stimulation With Paraspinal Muscle Activation. | Neurosurgery | 2022 |
| 36600324 | Surgical-PEARL protocol: a multicentre prospective cohort study exploring aetiology, management and outcomes for patients with congenital anomalies potentially requiring surgical intervention. | BMJ Open | 2022 |
| 35961692 | Real-world bleeding in patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) and prescribed different combinations of dual antiplatelet therapy (DAPT) in England: a population-based cohort study emulating a 'target trial'. | Open Heart | 2022 |
| 35012325 | Epigenetic Regulation of <i>F2RL3</i> Associates With Myocardial Infarction and Platelet Function. | Circ Res | 2022 |
| 35068290 | Higher body mass index raises immature platelet count: potential contribution to obesity-related thrombosis. | Platelets | 2022 |
| 34476343 | The EHA Research Roadmap: Platelet Disorders. | Hemasphere | 2021 |
| 33783834 | Advances in understanding the pathogenesis of hereditary macrothrombocytopenia. | Br J Haematol | 2021 |
| 33662796 | Recombinant ADAMTS13 reduces abnormally up-regulated von Willebrand factor in plasma from patients with severe COVID-19. | Thromb Res | 2021 |
| 34758253 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. | N Engl J Med | 2021 |
| 34476343 | The EHA Research Roadmap: Platelet Disorders. | Hemasphere | 2021 |
| 33783834 | Advances in understanding the pathogenesis of hereditary macrothrombocytopenia. | Br J Haematol | 2021 |
| 33662796 | Recombinant ADAMTS13 reduces abnormally up-regulated von Willebrand factor in plasma from patients with severe COVID-19. | Thromb Res | 2021 |
| 34758253 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. | N Engl J Med | 2021 |
| 31043318 | MicroRNAs as potential biomarkers in congenital heart surgery. | J Thorac Cardiovasc Surg | 2020 |
| 32299270 | <i>FLNA</i> variants associated with disorders of platelet number or function. | Platelets | 2020 |
| 31756037 | Differential effects of direct factor IIa and factor Xa inhibitors in protein C-deficient plasma detected using thrombin generation and viscoelastometry assays. | Int J Lab Hematol | 2020 |
| 32478898 | TEG PlateletMapping assay results may be misleading in the presence of cold stored platelets. | Transfusion | 2020 |