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Multisystem Inflammatory Syndrome Related to COVID-19 in Previously Healthy Children and Adolescents in New York City

JAMA : the journal of the American Medical Association, 2020-07, Vol.324 (3), p.294

2020

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Primary atopic disorders

The Journal of experimental medicine, 2018-04, Vol.215 (4), p.1009-1022

2018

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Potential mechanisms of anaphylaxis to COVID-19 mRNA vaccines

Journal of allergy and clinical immunology, 2021-06, Vol.147 (6), p.2075-2082.e2

2021

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The Ying and Yang of STAT3 in Human Disease

Journal of clinical immunology, 2015-10, Vol.35 (7), p.615-623

2015

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A Critical Role for STAT3 Transcription Factor Signaling in the Development and Maintenance of Human T Cell Memory

Immunity (Cambridge, Mass.), 2011-11, Vol.35 (5), p.806-818

2011

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Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (36), p.10127-10132

2016

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Genetics of allergy and allergic sensitization: common variants, rare mutations

Current opinion in immunology, 2015-10, Vol.36, p.115-126

2015

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TCR Signaling Abnormalities in Human Th2-Associated Atopic Disease

Frontiers in immunology, 2018-04, Vol.9, p.719-719

Milner, Joshua D

2018

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The CBM-opathies-A Rapidly Expanding Spectrum of Human Inborn Errors of Immunity Caused by Mutations in the CARD11-BCL10-MALT1 Complex

Frontiers in immunology, 2018-09, Vol.9, p.2078-2078

2018

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Mechanisms underlying helper T-cell plasticity: Implications for immune-mediated disease

Journal of allergy and clinical immunology, 2013-05, Vol.131 (5), p.1276-1287

2013

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ERBIN and phosphoglucomutase 3 deficiency

Current opinion in immunology, 2023-10, Vol.84, p.102353-102353, Article 102353

Milner, Joshua D

2023

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Opposing roles of STAT1 and STAT3 in IL-21 function in CD4⁺ T cells

Proceedings of the National Academy of Sciences - PNAS, 2015-07, Vol.112 (30), p.9394-9399

2015

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Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrhea

Blood, 2017-02, Vol.129 (5), p.650-653

2017

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Retinoic Acid Receptor Alpha Represses a Th9 Transcriptional and Epigenomic Program to Reduce Allergic Pathology

Immunity (Cambridge, Mass.), 2019-01, Vol.50 (1), p.106-120.e10

2019

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Type I interferon signature predicts response to JAK inhibition in haploinsufficiency of A20

Annals of the rheumatic diseases, 2020-03, Vol.79 (3), p.429

2020

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Diminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxis

Journal of allergy and clinical immunology, 2016-07, Vol.138 (1), p.187-199

2016

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Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects

The Journal of experimental medicine, 2021-03, Vol.218 (3)

2021

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PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients

The Journal of experimental medicine, 2017-09, Vol.214 (9), p.2523-2533

2017

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Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities

Journal of allergy and clinical immunology, 2014-05, Vol.133 (5), p.1471-1474

2014

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PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes

Journal of Clinical Immunology, 2015-08, Vol.35 (6), p.527-530

Milner, Joshua D.

2015

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Mast cell activation syndrome: Importance of consensus criteria and call for research

Journal of allergy and clinical immunology, 2018-09, Vol.142 (3), p.1008-1010

2018

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A mouse model of HIES reveals pro- and anti-inflammatory functions of STAT3

Blood, 2014-05, Vol.123 (19), p.2978-2987

2014

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Gain-of-function STAT1 mutations are associated with PD-L1 overexpression and a defect in B-cell survival

Journal of allergy and clinical immunology, 2013-06, Vol.131 (6), p.1691-1693

2013

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Multisystem Inflammatory Syndrome Related to COVID-19 in Previously Healthy Children and Adolescents in New York City

Primary atopic disorders

Potential mechanisms of anaphylaxis to COVID-19 mRNA vaccines

The Ying and Yang of STAT3 in Human Disease

A Critical Role for STAT3 Transcription Factor Signaling in the Development and Maintenance of Human T Cell Memory

Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

Genetics of allergy and allergic sensitization: common variants, rare mutations

TCR Signaling Abnormalities in Human Th2-Associated Atopic Disease

The CBM-opathies-A Rapidly Expanding Spectrum of Human Inborn Errors of Immunity Caused by Mutations in the CARD11-BCL10-MALT1 Complex

Mechanisms underlying helper T-cell plasticity: Implications for immune-mediated disease

Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation–polyendocrinopathy–enteropathy–X-linked–like syndrome

ERBIN and phosphoglucomutase 3 deficiency

Autosomal recessive phosphoglucomutase 3 ( PGM3 ) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

Opposing roles of STAT1 and STAT3 in IL-21 function in CD4⁺ T cells

Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrhea

Retinoic Acid Receptor Alpha Represses a Th9 Transcriptional and Epigenomic Program to Reduce Allergic Pathology

Type I interferon signature predicts response to JAK inhibition in haploinsufficiency of A20

Diminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxis

Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects

PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients

Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities

PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes

Mast cell activation syndrome: Importance of consensus criteria and call for research

A mouse model of HIES reveals pro- and anti-inflammatory functions of STAT3

Gain-of-function STAT1 mutations are associated with PD-L1 overexpression and a defect in B-cell survival

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