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How I treat autoimmune lymphoproliferative syndrome

Blood, 2011-11, Vol.118 (22), p.5741-5751

2011

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Human PI3Kγ deficiency and its microbiota-dependent mouse model reveal immunodeficiency and tissue immunopathology

Nature communications, 2019-09, Vol.10 (1), p.4364-12, Article 4364

2019

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JMML and RALD (Ras-associated autoimmune leukoproliferative disorder): common genetic etiology yet clinically distinct entities

Blood, 2015-04, Vol.125 (18), p.2753-2758

2015

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Gray platelet syndrome: immunity goes awry

Blood, 2020-10, Vol.136 (17), p.1898-1900

2020

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Multibatch Cytometry Data Integration for Optimal Immunophenotyping

The Journal of immunology (1950), 2021-01, Vol.206 (1), p.206-213

2021

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Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

Blood, 2015-01, Vol.125 (4), p.591-599

2015

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Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop

Blood, 2010-10, Vol.116 (14), p.e35-e40

2010

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Haploinsufficiency of immune checkpoint receptor CTLA4 induces a distinct neuroinflammatory disorder

The Journal of clinical investigation, 2020-10, Vol.130 (10), p.5551-5561

2020

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HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory disease

Science (American Association for the Advancement of Science), 2020-07, Vol.369 (6500), p.202-207

2020

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FAS Inactivation Releases Unconventional Germinal Center B Cells that Escape Antigen Control and Drive IgE and Autoantibody Production

Immunity (Cambridge, Mass.), 2015-05, Vol.42 (5), p.890-902

2015

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When Dumbo meets IKAROS: Fear and hubris

Journal of allergy and clinical immunology, 2024-09, Vol.154 (3), p.552-553

Rao, V. Koneti

2024

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RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency

Blood, 2010-04, Vol.115 (15), p.3128-3135

2010

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Ascending aortic pseudoaneurysm presenting as heart failure in a child - A rare complication associated with coronavirus disease 2019

Annals of pediatric cardiology, 2023-03, Vol.16 (2), p.118-121

2023

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Vaccine utilization and overwhelming post-splenectomy infection risk factors in two asplenia cohorts

Haematologica (Roma), 2024-02, Vol.109 (2), p.622-626

2024

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Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis

Blood, 2011-03, Vol.117 (10), p.2883-2886

2011

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Platelet disorders: the next generation is in

Blood, 2016-06, Vol.127 (23), p.2781-2782

2016

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Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency

Blood, 2010-12, Vol.116 (26), p.6037-6045

2010

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Inherited platelet dysfunction and hematopoietic transcription factor mutations

Platelets (Edinburgh), 2017-01, Vol.28 (1), p.20-26

2017

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Evans syndrome: pathology and genomic hubris

Blood, 2022-01, Vol.139 (3), p.312-313

Rao, V. Koneti

2022

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Editorial: Platelet Genomics and Disorders of Platelet Number and Function

Platelets (Edinburgh), 2017-01, Vol.28 (1), p.2-2

Rao, A. Koneti

2017

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Fas/CD95 prevents autoimmunity independently of lipid raft localization and efficient apoptosis induction

Nature communications, 2016-12, Vol.7 (1), p.13895-13895, Article 13895

2016

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Abnormal B-Cell Maturation in the Bone Marrow of Patients with Germline Mutations in PIK3CD

Journal of allergy and clinical immunology, 2017-03, Vol.139 (3), p.1032-1035.e6

2017

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Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome

Blood, 2010-06, Vol.115 (25), p.5164-5169

2010

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Factor VIIa and tissue factor procoagulant activity in diabetes mellitus after acute ischemic stroke: impact of hyperglycemia

Thrombosis and haemostasis, 2007-11, Vol.98 (5), p.1007-1013

2007

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How I treat autoimmune lymphoproliferative syndrome

Human PI3Kγ deficiency and its microbiota-dependent mouse model reveal immunodeficiency and tissue immunopathology

JMML and RALD (Ras-associated autoimmune leukoproliferative disorder): common genetic etiology yet clinically distinct entities

Gray platelet syndrome: immunity goes awry

Multibatch Cytometry Data Integration for Optimal Immunophenotyping

Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop

Haploinsufficiency of immune checkpoint receptor CTLA4 induces a distinct neuroinflammatory disorder

HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory disease

FAS Inactivation Releases Unconventional Germinal Center B Cells that Escape Antigen Control and Drive IgE and Autoantibody Production

When Dumbo meets IKAROS: Fear and hubris

RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency

Ascending aortic pseudoaneurysm presenting as heart failure in a child - A rare complication associated with coronavirus disease 2019

Vaccine utilization and overwhelming post-splenectomy infection risk factors in two asplenia cohorts

Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis

Platelet disorders: the next generation is in

Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency

Characterization and treatment of chronic active Epstein-Barr virus disease: a 28-year experience in the United States

Inherited platelet dysfunction and hematopoietic transcription factor mutations

Evans syndrome: pathology and genomic hubris

Editorial: Platelet Genomics and Disorders of Platelet Number and Function

Fas/CD95 prevents autoimmunity independently of lipid raft localization and efficient apoptosis induction

Abnormal B-Cell Maturation in the Bone Marrow of Patients with Germline Mutations in PIK3CD

Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome

Factor VIIa and tissue factor procoagulant activity in diabetes mellitus after acute ischemic stroke: impact of hyperglycemia

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