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Direct activation of the alternative complement pathway by SARS-CoV-2 spike proteins is blocked by factor D inhibition

Blood, 2020-10, Vol.136 (18), p.2080-2089

2020

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Complement dysregulation is associated with severe COVID-19 illness

Haematologica (Roma), 2022-05, Vol.107 (5), p.1095-1105

2022

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SARS-CoV-2 vaccination and immune thrombotic thrombocytopenic purpura

Blood, 2022-04, Vol.139 (16), p.2570-2573

2022

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Aspirin in ET: will twice a day keep thrombosis away?

Blood, 2020-07, Vol.136 (2), p.151-153

2020

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Recurrent germline variant in ATM associated with familial myeloproliferative neoplasms

Leukemia, 2023-03, Vol.37 (3), p.627-635

2023

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Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia

Haematologica (Roma), 2016-06, Vol.101 (6), p.e228-e231

2016

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Chronic myeloid leukemia (CML) evolves from Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs) with unexpected frequency

International journal of hematology, 2023-03, Vol.117 (3), p.456-462

2023

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Antiphospholipid syndrome: Complement activation, complement gene mutations, and therapeutic implications

Journal of thrombosis and haemostasis, 2021-03, Vol.19 (3), p.607-616

2021

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Germline mutations in the alternative pathway of complement predispose to HELLP syndrome

JCI insight, 2018-03, Vol.3 (6)

2018

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A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model

PloS one, 2017-04, Vol.12 (4), p.e0174074

2017

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Complement activity and complement regulatory gene mutations are associated with thrombosis in APS and CAPS

Blood, 2020-01, Vol.135 (4), p.239-251

2020

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Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations

Development (Cambridge), 2006-03, Vol.133 (5), p.977-987

2006

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COVID-19 vaccines induce severe hemolysis in paroxysmal nocturnal hemoglobinuria

Blood, 2021-07, Vol.137 (26), p.3670-3673

2021

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Efficient and Allele-Specific Genome Editing of Disease Loci in Human iPSCs

Molecular therapy, 2015-03, Vol.23 (3), p.570-577

2015

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The roles of sex and genetics in the MPN

International review of cell and molecular biology, 2022, Vol.366, p.1-24

2022

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Reduced ADAMTS13 activity during TTP remission is associated with stroke in TTP survivors

Blood, 2019-09, Vol.134 (13), p.1037-1045

2019

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Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients

Human molecular genetics, 2006-05, Vol.15 (10), p.1629-1639

2006

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Characterization of myeloproliferative neoplasms in the paediatric and young adult population

British journal of haematology, 2023-05, Vol.201 (3), p.449-458

2023

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Silent cerebral infarction during immune TTP remission: prevalence, predictors, and impact on cognition

Blood, 2023-07, Vol.142 (4), p.325-335

2023

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Generation of Glycosylphosphatidylinositol Anchor Protein‐Deficient Blood Cells From Human Induced Pluripotent Stem Cells

Stem cells translational medicine, 2013-11, Vol.2 (11), p.819-829

2013

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Anti-PF4 antibodies associated with disease severity in COVID-19

Proceedings of the National Academy of Sciences - PNAS, 2022-11, Vol.119 (47), p.1-e2213361119

2022

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A prospective quality improvement initiative in adult hemophagocytic lymphohistiocytosis to improve testing and a framework to facilitate trigger identification and mitigate hemorrhage from retrospective analysis

Medicine (Baltimore), 2018-08, Vol.97 (31), p.e11579-e11579

2018

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Ex vivo assays to detect complement activation in complementopathies

Clinical immunology (Orlando, Fla.), 2020-12, Vol.221, p.108616-108616, Article 108616

2020

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Major adverse cardiovascular events in survivors of immune‐mediated thrombotic thrombocytopenic purpura

American journal of hematology, 2021-12, Vol.96 (12), p.1587-1594

2021

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Direct activation of the alternative complement pathway by SARS-CoV-2 spike proteins is blocked by factor D inhibition

Complement dysregulation is associated with severe COVID-19 illness

Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia

SARS-CoV-2 vaccination and immune thrombotic thrombocytopenic purpura

Aspirin in ET: will twice a day keep thrombosis away?

Recurrent germline variant in ATM associated with familial myeloproliferative neoplasms

Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia

Chronic myeloid leukemia (CML) evolves from Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs) with unexpected frequency

Antiphospholipid syndrome: Complement activation, complement gene mutations, and therapeutic implications

Germline mutations in the alternative pathway of complement predispose to HELLP syndrome

A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model

Complement activity and complement regulatory gene mutations are associated with thrombosis in APS and CAPS

Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations

COVID-19 vaccines induce severe hemolysis in paroxysmal nocturnal hemoglobinuria

Efficient and Allele-Specific Genome Editing of Disease Loci in Human iPSCs

The roles of sex and genetics in the MPN

Reduced ADAMTS13 activity during TTP remission is associated with stroke in TTP survivors

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients

Characterization of myeloproliferative neoplasms in the paediatric and young adult population

Silent cerebral infarction during immune TTP remission: prevalence, predictors, and impact on cognition

Generation of Glycosylphosphatidylinositol Anchor Protein‐Deficient Blood Cells From Human Induced Pluripotent Stem Cells

Anti-PF4 antibodies associated with disease severity in COVID-19

A prospective quality improvement initiative in adult hemophagocytic lymphohistiocytosis to improve testing and a framework to facilitate trigger identification and mitigate hemorrhage from retrospective analysis

Ex vivo assays to detect complement activation in complementopathies

Major adverse cardiovascular events in survivors of immune‐mediated thrombotic thrombocytopenic purpura

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