| 36737374 | Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021Â Oct;19(10):2612-2617]. | J Thromb Haemost | 2023 |
| 37596262 | A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. | Nat Commun | 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 |
| 37964899 | Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke. | TH Open | 2023 |
| 37953943 | Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing. | iScience | 2023 |
| 36737374 | Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021Â Oct;19(10):2612-2617]. | J Thromb Haemost | 2023 |
| 37964899 | Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke. | TH Open | 2023 |
| 37596262 | A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. | Nat Commun | 2023 |
| 37953943 | Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing. | iScience | 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 |
| 34581777 | G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. | Blood Adv | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 35764313 | Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency. | Thromb Haemost | 2022 |
| 35568032 | Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites. | Am J Hum Genet | 2022 |
| 36253349 | Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke. | Nat Commun | 2022 |
| 34581777 | G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. | Blood Adv | 2022 |
| 35041713 | Platelet surface receptor glycoprotein VI-dimer is overexpressed in stroke: The Glycoprotein VI in Stroke (GYPSIE) study results. | PLoS One | 2022 |
| 34732567 | Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis. | RNA | 2022 |
| 35218943 | Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency. | J Mol Diagn | 2022 |
| 35072137 | Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease. | Cell Genom | 2022 |
| 35224470 | Coagulation factor V is a T-cell inhibitor expressed by leukocytes in COVID-19. | iScience | 2022 |
| 35764313 | Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency. | Thromb Haemost | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 35568032 | Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites. | Am J Hum Genet | 2022 |
| 36253349 | Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke. | Nat Commun | 2022 |
| 35224470 | Coagulation factor V is a T-cell inhibitor expressed by leukocytes in COVID-19. | iScience | 2022 |
| 35072137 | Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease. | Cell Genom | 2022 |
| 35041713 | Platelet surface receptor glycoprotein VI-dimer is overexpressed in stroke: The Glycoprotein VI in Stroke (GYPSIE) study results. | PLoS One | 2022 |
| 35218943 | Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency. | J Mol Diagn | 2022 |
| 34732567 | Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis. | RNA | 2022 |
| 32703790 | Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas. | Haematologica | 2021 |
| 33587817 | Transcriptional characterization of human megakaryocyte polyploidization and lineage commitment. | J Thromb Haemost | 2021 |
| 34226637 | Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates. | Int J Obes (Lond) | 2021 |
| 33674754 | Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. | Mol Psychiatry | 2021 |
| 34135082 | Plasma Proteomics of Renal Function: A Transethnic Meta-Analysis and Mendelian Randomization Study. | J Am Soc Nephrol | 2021 |
| 34355501 | GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis. | J Thromb Haemost | 2021 |
| 33496751 | Neutrophil specific granule and NETosis defects in gray platelet syndrome. | Blood Adv | 2021 |
| 33496735 | Elevated levels of tissue factor pathway inhibitor in patients with mild to moderate bleeding tendency. | Blood Adv | 2021 |
| 32703790 | Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas. | Haematologica | 2021 |
| 33341984 | Comparison of four methods to measure haemoglobin concentrations in whole blood donors (COMPARE): A diagnostic accuracy study. | Transfus Med | 2021 |
| 34611362 | Polygenic basis and biomedical consequences of telomere length variation. | Nat Genet | 2021 |
| 34426706 | Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases. | Nat Med | 2021 |
| 34758253 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. | N Engl J Med | 2021 |
| 34475573 | Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. | Nat Genet | 2021 |
| 34750571 | Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases. | Nat Metab | 2021 |
| 33674754 | Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. | Mol Psychiatry | 2021 |
| 33587817 | Transcriptional characterization of human megakaryocyte polyploidization and lineage commitment. | J Thromb Haemost | 2021 |
| 33496751 | Neutrophil specific granule and NETosis defects in gray platelet syndrome. | Blood Adv | 2021 |