Publications by authors named "Jordan Abbott"

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Talimogene laherparepvec induced bullous pemphigoid.
Sahar Davoudi, Fade Mahmoud, Jordan Abbott

JAAD Case Rep· June 2025

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Two unique cases of eosinophilic granulomatosis with polyangiitis in childhood treated with anti-interleukin-5 therapy: infantile-onset and submandibular salivary gland involvement.
Evangelia Constantine, Adam M Bartholomeo, Inna Powers, Jerimiah L Lysinger, Pia J Hauk, Jordan Abbott

Pediatr Rheumatol Online J· June 2025

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Longitudinal monitoring of class-switched memory-B cell proportions identifies plausible germinal center failure in patients with suspected immune disorders.
Vijaya Knight, Olivia Starich, Cullen M Dutmer, Jordan K Abbott

Cytometry B Clin Cytom· May 2025

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Successful treatment of PD1-inhibitor induced psoriasiform dermatitis using IL-17 blockade without compromising immunotherapy efficacy.
Adina Greene, Scott Penner, Amanda Edmond, Monica Camou, Jiaxin Niu, Jordan Abbott

J Oncol Pharm Pract· December 2024

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Meeting Report: 2023 Muscular Dystrophy Association Summit on 'Safety and Challenges in Gene Therapy of Neuromuscular Diseases'.
Angela Lek, Evrim Atas, Brian Lin, Sharon E Hesterlee, Jordan K Abbott

J Neuromuscul Dis· September 2024

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Clinical and functional spectrum of RAC2-related immunodeficiency.
Ágnes Donkó, Svetlana O Sharapova, Juraj Kabat, Sundar Ganesan, Fabian H Hauck, Jordan Abbott

Blood· April 2024

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Composition of the CD27+ Memory-B-Cell Compartment Delineates Immunoglobulin Deficiency Endotypes.
Oliva Starich, Jared M Rieck, Wyatt J Tarter, Camille J Hochheimer, Vijaya Knight, Jordan K Abbott

Res Sq· January 2024

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The Immune Status of Patients with 16p11.2 Deletion Syndrome.
Laura A Wang, Austin Larson, Jordan K Abbott

J Clin Immunol· November 2023

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The pulmonary effects of STAT3 deficiency.
Elizabeth A Gilje, Jordan K Abbott

J Allergy Clin Immunol· August 2023

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Autophagy-associated immune dysregulation and hyperplasia in a patient with compound heterozygous mutations in .
Guowu Hu, Pia J Hauk, Nannan Zhang, Waleed Elsegeiny, Carlos M Guardia, Jordan K Abbott

Autophagy· February 2023

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"Common variable immunodeficiency: Challenges for diagnosis".
Laura A Wang, Jordan K Abbott

J Immunol Methods· October 2022

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Registries are shaping how we think about primary immunodeficiency diseases.
Jordan K Abbott, Erwin W Gelfand

J Allergy Clin Immunol· June 2022

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Fluctuations in quality of life and immune responses during intravenous immunoglobulin infusion cycles.
Jordan K Abbott, Sanny K Chan, Morgan MacBeth, James L Crooks, Cathy Hancock

PLoS One· May 2022

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Cytotoxic T-Lymphocyte-Associated Antigen 4 Haploinsufficiency Mimics Difficult-to-Treat Inflammatory Bowel Disease.
Brad D Constant, Cullen M Dutmer, Michael A Arnold, Caroline Hall, Jordan K Abbott

Clin Gastroenterol Hepatol· April 2022

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Heterozygous IKKβ activation loop mutation results in a complex immunodeficiency syndrome.
Jordan Abbott, Angelica C Ehler, Divya Jayaraman, Paul R Reynolds, Kanao Otsu

J Allergy Clin Immunol· February 2021

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Expression and activation of the steroidogenic enzyme CYP11A1 is associated with IL-13 production in T cells from peanut allergic children.
Meiqin Wang, Matthew J Strand, Bruce J Lanser, Carah Santos, Kreso Bendelja, Jordan K Abbott

PLoS One· August 2020

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Use of Bortezomib in the Treatment of C3 Glomerulonephritis Refractory to Eculizumab and Rituximab.
Jessica W Hui, Mindy Banks, Tibor Nadasdy, Brad H Rovin, Jordan K Abbott

Kidney Int Rep· June 2020

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Vasculitis in a Child With the Hyper-IgM Variant of Ataxia-Telangiectasia.
Anna K Meyer, Mindy Banks, Tibor Nadasdy, Jennifer J Clark, Rui Zheng, Jordan K Abbott

Front Pediatr· October 2019

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Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.
Marita Bosticardo, Yasuhiro Yamazaki, Jennifer Cowan, Giuliana Giardino, Cristina Corsino, Jordan K Abbott

Am J Hum Genet· September 2019

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Biallelic mutations in DNA ligase 1 underlie a spectrum of immune deficiencies.
Patrick Maffucci, Jose Chavez, Thomas J Jurkiw, Patrick J O'Brien, Jordan K Abbott

J Clin Invest· December 2018

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Dominant-negative loss of function arises from a second, more frequent variant within the SAND domain of autoimmune regulator (AIRE).
Jordan K Abbott, Yu-San Huoh, Paul R Reynolds, Liping Yu, Marian Rewers

J Autoimmun· March 2018

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Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease.
Chi A Ma, Jeffrey R Stinson, Yuan Zhang, Jordan K Abbott, Michael A Weinreich

Nat Genet· October 2017

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Germline hypomorphic CARD11 mutations in severe atopic disease.
Chi A Ma, Jeffrey R Stinson, Yuan Zhang, Jordan K Abbott, Michael A Weinreich

Nat Genet· August 2017

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Recurrent rhinovirus infections in a child with inherited MDA5 deficiency.
Ian T Lamborn, Huie Jing, Yu Zhang, Scott B Drutman, Jordan K Abbott

J Exp Med· July 2017

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