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Systemic Evaluation of the Immune System in Infants to Predict the Development of Pediatric Asthma

Clinical chemistry (Baltimore, Md.), 2020-12, Vol.66 (12), p.1477-1479

Kumanovics, Attila

2020

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Human Leukocyte Antigen Typing by Next-Generation Sequencing

Clinics in laboratory medicine, 2018-12, Vol.38 (4), p.565-578

2018

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Anti-cytokine autoantibodies and inborn errors of immunity

Journal of immunological methods, 2022-09, Vol.508, p.113313-113313, Article 113313

2022

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Identification of FRA1 and FRA2 as Genes Involved in Regulating the Yeast Iron Regulon in Response to Decreased Mitochondrial Iron-Sulfur Cluster Synthesis

The Journal of biological chemistry, 2008-04, Vol.283 (16), p.10276-10286

2008

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Frontline Science: Cxxc5 expression alters cell cycle and myeloid differentiation of mouse hematopoietic stem and progenitor cells

Journal of leukocyte biology, 2020-08, Vol.108 (2), p.469-484

2020

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CXXC5 variant in an immunodeficient patient with a progressive loss of hematopoietic cells

Journal of allergy and clinical immunology, 2021-04, Vol.147 (4), p.1504-1507.e8

2021

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Evolving Approach to Clinical Cytometry for Immunodeficiencies and Other Immune Disorders

Clinics in laboratory medicine, 2023-09, Vol.43 (3), p.467-483

2023

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Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders

Journal of clinical immunology, 2015-02, Vol.35 (2), p.119-124

2015

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Estimated disease incidence of RAG1/2 mutations: A case report and querying the Exome Aggregation Consortium

Journal of allergy and clinical immunology, 2017-02, Vol.139 (2), p.690-692.e3

2017

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Next-generation sequencing of custom amplicons to improve coverage of HaloPlex multigene panels

BioTechniques, 2014-10, Vol.57 (4), p.204-207

2014

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Familial Immune Thrombocytopenia Associated With a Novel Variant in IKZF1

Frontiers in pediatrics, 2019-04, Vol.7, p.139

2019

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Normal hematologic parameters and fetal hemoglobin silencing with heterozygous IKZF1 mutations

Blood, 2016-10, Vol.128 (16), p.2100-2103

2016

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GENOMIC ORGANIZATION OF THE MAMMALIAN MHC

Annual review of immunology, 2003-01, Vol.21 (1), p.629-657

2003

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YKE4 (YIL023C) Encodes a Bidirectional Zinc Transporter in the Endoplasmic Reticulum of Saccharomyces cerevisiae

The Journal of biological chemistry, 2006-08, Vol.281 (32), p.22566-22574

2006

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Severely depressed interleukin-17 production by human neonatal mononuclear cells

Pediatric research, 2014-12, Vol.76 (6), p.522-527

2014

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Expression of the mouse MHC class Ib H2-T11 gene product, a paralog of H2-T23 (Qa-1) with shared peptide-binding specificity

The Journal of immunology (1950), 2014-08, Vol.193 (3), p.1427-1439

2014

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Evaluation of Mass Cytometry in the Clinical Laboratory

Cytometry. Part B, Clinical cytometry, 2019-07, Vol.96 (4), p.266-274

2019

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A Toolkit and Framework for Optimal Laboratory Evaluation of Individuals with Suspected Primary Immunodeficiency

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2021-09, Vol.9 (9), p.3293-3307.e6

2021

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Family ties of gated pores: evolution of the sensor module

The FASEB journal, 2002-10, Vol.16 (12), p.1623-1629

2002

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Diffuse Large B Cell Lymphoma in Hyper-IgE Syndrome Due To STAT3 Mutation

Journal of clinical immunology, 2010-11, Vol.30 (6), p.886-893

2010

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TACI mutation p.Lys154Ter identified in Good Syndrome

Clinical immunology (Orlando, Fla.), 2013-01, Vol.146 (1), p.10-12

2013

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Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency

American journal of human genetics, 2013-11, Vol.93 (5), p.812-824

2013

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Coccidioides immitis meningitis in a patient with hyperimmunoglobulin E syndrome due to a novel mutation in signal transducer and activator of transcription

The Pediatric infectious disease journal, 2009-07, Vol.28 (7), p.664-666

2009

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Flow cytometry for B-cell subset analysis in immunodeficiencies

Journal of immunological methods, 2022-10, Vol.509, p.113327-113327, Article 113327

2022

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A Single Amino Acid Change in the Yeast Vacuolar Metal Transporters Zrc1 and Cot1 Alters Their Substrate Specificity

The Journal of biological chemistry, 2008-12, Vol.283 (49), p.33865-33873

2008

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Systemic Evaluation of the Immune System in Infants to Predict the Development of Pediatric Asthma

Human Leukocyte Antigen Typing by Next-Generation Sequencing

Anti-cytokine autoantibodies and inborn errors of immunity

Identification of FRA1 and FRA2 as Genes Involved in Regulating the Yeast Iron Regulon in Response to Decreased Mitochondrial Iron-Sulfur Cluster Synthesis

Frontline Science: Cxxc5 expression alters cell cycle and myeloid differentiation of mouse hematopoietic stem and progenitor cells

CXXC5 variant in an immunodeficient patient with a progressive loss of hematopoietic cells

Evolving Approach to Clinical Cytometry for Immunodeficiencies and Other Immune Disorders

Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders

Estimated disease incidence of RAG1/2 mutations: A case report and querying the Exome Aggregation Consortium

Next-generation sequencing of custom amplicons to improve coverage of HaloPlex multigene panels

Familial Immune Thrombocytopenia Associated With a Novel Variant in IKZF1

Normal hematologic parameters and fetal hemoglobin silencing with heterozygous IKZF1 mutations

GENOMIC ORGANIZATION OF THE MAMMALIAN MHC

YKE4 (YIL023C) Encodes a Bidirectional Zinc Transporter in the Endoplasmic Reticulum of Saccharomyces cerevisiae

Severely depressed interleukin-17 production by human neonatal mononuclear cells

Expression of the mouse MHC class Ib H2-T11 gene product, a paralog of H2-T23 (Qa-1) with shared peptide-binding specificity

Evaluation of Mass Cytometry in the Clinical Laboratory

A Toolkit and Framework for Optimal Laboratory Evaluation of Individuals with Suspected Primary Immunodeficiency

Family ties of gated pores: evolution of the sensor module

Diffuse Large B Cell Lymphoma in Hyper-IgE Syndrome Due To STAT3 Mutation

TACI mutation p.Lys154Ter identified in Good Syndrome

Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency

Coccidioides immitis meningitis in a patient with hyperimmunoglobulin E syndrome due to a novel mutation in signal transducer and activator of transcription

Flow cytometry for B-cell subset analysis in immunodeficiencies

A Single Amino Acid Change in the Yeast Vacuolar Metal Transporters Zrc1 and Cot1 Alters Their Substrate Specificity

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