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| 31822811 | Oral verruciform xanthoma associated with stem cell transplantation and graft versus host disease in a paediatric patient. | Bone Marrow Transplant | 2020 |
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| 28487294 | The effect of variation in donor platelet function on transfusion outcome: a semirandomized controlled trial. | Blood | 2017 |
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| 28064200 | Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia. | Blood | 2017 |
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| 28487294 | The effect of variation in donor platelet function on transfusion outcome: a semirandomized controlled trial. | Blood | 2017 |
| 28612348 | Juvenile myelomonocytic leukemia in an infant with congenital human immunodeficiency virus and cytomegalovirus infection. | Am J Hematol | 2017 |
| 28001309 | Platelet responses to agonists in a cohort of highly characterised platelet donors are consistent over time. | Vox Sang | 2017 |
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| 26912466 | A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss. | Blood | 2016 |
| 27084890 | A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders. | Blood | 2016 |
| 26936507 | A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies. | Sci Transl Med | 2016 |
| 26912466 | A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss. | Blood | 2016 |
| 26936507 | A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies. | Sci Transl Med | 2016 |
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| 25301082 | Neonatal thrombocytopenia and platelet transfusion - a UK perspective. | Neonatology | 2015 |
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| 25949529 | Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders. | Genome Med | 2015 |
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| 24217912 | The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. | Nucleic Acids Res | 2014 |
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| 24509480 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. | Nat Genet | 2014 |
| 25258084 | Transcriptional diversity during lineage commitment of human blood progenitors. | Science | 2014 |
| 24509480 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. | Nat Genet | 2014 |
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