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Mattia Frontini

University of Cambridge
NHS Blood and Transplant
British Heart Foundation

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Assessment of a complete and classified platelet proteome from genome-wide transcripts of human platelets and megakaryocytes covering platelet functions

2021 Scientific Reports
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A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.

2021 PLOS Genetics
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Extreme phenotypes define epigenetic and metabolic signatures in cardiometabolic syndrome.

2020 bioRxiv
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Single cell transcriptional characterization of human megakaryocyte lineage commitment and maturation

2020 bioRxiv
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Extreme phenotypes define epigenetic and metabolic signatures in cardiometabolic syndrome.

2020 bioRxiv
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Two-step penalised logistic regression for multi-omic data with an application to cardiometabolic syndrome

2020 arXiv: Methodology
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Single Cell Transcriptional Characterization of Human Megakaryocyte Lineage Commitment and Maturation

2020 Social Science Research Network
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Paired rRNA-depleted and polyA-selected RNA sequencing data and supporting multi-omics data from human T cells.

2020 Scientific Data
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Activated alphaIIbbeta3 on platelets mediates flow-dependent NETosis via SLC44A2.

2020 eLife
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Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia

2019 Haematologica
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