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Author Details

Joshua D Milner
Columbia University
1999
161
53
PMIDPaper TitleJournal TitlePublished Year
36255453Ventricular function and tissue characterization by cardiac magnetic resonance imaging following hospitalization for multisystem inflammatory syndrome in children: a prospective study.Pediatr Radiol2023
37256972Variant <i>STAT4</i> and Response to Ruxolitinib in an Autoinflammatory Syndrome.N Engl J Med2023
37214806Researching COVID to enhance recovery (RECOVER) pediatric study protocol: Rationale, objectives and design.medRxiv2023
37106040Dynamic chromatin accessibility licenses STAT5- and STAT6-dependent innate-like function of T<sub>H</sub>9 cells to promote allergic inflammation.Nat Immunol2023
37369151ERBIN and phosphoglucomutase 3 deficiency.Curr Opin Immunol2023
37133746SARS-CoV-2 infection and recovery in children: Distinct T cell responses in MIS-C compared to COVID-19.J Exp Med2023
36170795Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasms.Blood Adv2023
34634105Assessing the safety of bioactive ingredients in infant formula that affect the immune system: recommendations from an expert panel.Am J Clin Nutr2022
35680527Atopy as Immune Dysregulation: Offender Genes and Targets.J Allergy Clin Immunol Pract2022
35507130Ex vivo effect of JAK inhibition on JAK-STAT1 pathway hyperactivation in patients with dominant-negative STAT3 mutations.J Clin Immunol2022
35753512Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations.J Allergy Clin Immunol2022
36334349Elevated IgE from attenuated CARD11 signaling: lessons from atopic mice and humans.Curr Opin Immunol2022
36306130Risk Variants in the Exomes of Children With Critical Illness.JAMA Netw Open2022
35960817Immunodeficiency, autoimmunity, and increased risk of B cell malignancy in humans with TRAF3 mutations.Sci Immunol2022
35287299Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders.HGG Adv2022
35093604Targeted IL-4Rα blockade ameliorates refractory allergic eosinophilic inflammation in a patient with dysregulated TGF-β signaling due to ERBIN deficiency.J Allergy Clin Immunol Pract2022
35118462Ventricular Function and Tissue Characterization By Cardiac MRI in Children Following Hospitalization for Multisystem Inflammatory Syndrome in Children (MIS-C): A Prospective Study.Res Sq2022
35333544Gain-of-function <i>IKZF1</i> variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation.Sci Immunol2022
32683719Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B.Clin Exp Dermatol2021
33548520Inborn Error of Immunity or Atopic Dermatitis: When to be Concerned and How to Investigate.J Allergy Clin Immunol Pract2021
33645549Epicutaneous Staphylococcus aureus induces IL-36 to enhance IgE production and ensuing allergic disease.J Clin Invest2021
33619160Systematic evaluation of nine monogenic autoinflammatory diseases reveals common and disease-specific correlations with allergy-associated features.Ann Rheum Dis2021
33865872Small intestinal immunopathology and GI-associated antibody formation in hereditary alpha-tryptasemia.J Allergy Clin Immunol2021
33857566Potential mechanisms of anaphylaxis to COVID-19 mRNA vaccines.J Allergy Clin Immunol2021
34887873A Novel Germline Heterozygous <i>BCL11B</i> Variant Causing Severe Atopic Disease and Immune Dysregulation.Front Immunol2021
34400315Clinical relevance of inherited genetic differences in human tryptases: Hereditary alpha-tryptasemia and beyond.Ann Allergy Asthma Immunol2021
34654687STAT3 Gain-of-Function Mutations Underlie Deficiency in Human Nonclassical CD16<sup>+</sup> Monocytes and CD141<sup>+</sup> Dendritic Cells.J Immunol2021
34266903Longitudinal Outcomes for Multisystem Inflammatory Syndrome in Children.Pediatrics2021
33212241Recurrent lymphadenitis in a female XIAP/BIRC4 mutation carrier with normal lyonization.J Allergy Clin Immunol Pract2021
33154590Distinct antibody responses to SARS-CoV-2 in children and adults across the COVID-19 clinical spectrum.Nat Immunol2021
33231617Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects.J Exp Med2021
33065115Discriminating Multisystem Inflammatory Syndrome in Children Requiring Treatment from Common Febrile Conditions in Outpatient Settings.J Pediatr2021
33003176Multisystem Inflammatory Syndrome in Children Associated With Coronavirus Disease 2019 in a Children's Hospital in New York City: Patient Characteristics and an Institutional Protocol for Evaluation, Management, and Follow-Up.Pediatr Crit Care Med2021
31633221PLAID syndrome: Characteristic presentation and a novel therapeutic option.Pediatr Dermatol2020
31981732Usefulness of testing for hereditary alpha tryptasemia in symptomatic patients with elevated tryptase.J Allergy Clin Immunol Pract2020
31767699Type I interferon signature predicts response to JAK inhibition in haploinsufficiency of A20.Ann Rheum Dis2020
31707513Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions.J Clin Immunol2020
33362767Case Report: Secondary Hemophagocytic Lymphohistiocytosis With Disseminated Infection in Chronic Granulomatous Disease-A Serious Cause of Mortality.Front Immunol2020
33202260Multiplexed Functional Assessment of Genetic Variants in CARD11.Am J Hum Genet2020
32830295The Child with Elevated IgE and Infection Susceptibility.Curr Allergy Asthma Rep2020
32771560Asthma among hospitalized patients with COVID-19 and related outcomes.J Allergy Clin Immunol2020
32699861Antibody responses to SARS-CoV2 are distinct in children with MIS-C compared to adults with COVID-19.medRxiv2020
32207811Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.J Exp Med2020
32516385Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.J Exp Med2020
32511676Multisystem Inflammatory Syndrome Related to COVID-19 in Previously Healthy Children and Adolescents in New York City.JAMA2020
32369445Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndrome.J Clin Invest2020
32126183Primary Atopic Disorders.Annu Rev Immunol2020
31605754Clinical response to omalizumab in patients with hereditary α-tryptasemia.Ann Allergy Asthma Immunol2020
30639434IgE testing can predict food allergy status in patients with moderate to severe atopic dermatitis.Ann Allergy Asthma Immunol2019
31666125Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers-Danlos contiguous gene deletion syndrome CAH-X.BMC Res Notes2019
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Collaborators

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Co-authored papers 32
National Institute of Allergy and Infectious Diseases
Co-authored papers 14
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National Institute of Arthritis, National Institutes of Health
Co-authored papers 5
National Cancer Institute, National Institutes of Health
Co-authored papers 5
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National Institute of Arthritis and Musculoskeletal and Skin Diseases
Co-authored papers 4
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National Institutes of Health
Co-authored papers 4
National Institute of Allergy and Infectious Diseases, National Institutes of Health
Co-authored papers 3
National Institute of Allergy and Infectious Diseases, National Institutes of Health
Co-authored papers 3
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
National Institute of Allergy and Infectious Diseases, National Institutes of Health
Co-authored papers 3
Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research
Co-authored papers 3
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Co-authored papers 3
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Co-authored papers 3
National Human Genome Research Institute, National Institutes of Health
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Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 3
National Institute of Diabetes and Digestive and Kidney Diseases
Co-authored papers 3
Kinderklinik und Kinderpoliklinik der Ludwig-Maximilians-Universitat Munchen
Co-authored papers 3
University of California Los Angeles
Co-authored papers 3
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National Human Genome Research Institute, National Institutes of Health (NIH)
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Columbia University Irving Medical Center
Co-authored papers 2