MichaelDanielKellerMD

PubMed

• 26 citations
  Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.
  Tom Le Voyer, Audrey V Parent, Xian Liu, Axel Cederholm, Adrian Gervais
  Nature. 2023-11-01
• 45 citations
  Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.
  Michael D. Keller, Rahul Pandey, Dong Li, Joseph T. Glessner, Lifeng Tian
  The Journal of Allergy and Clinical Immunology. 2016-08-01
• 67 citations
  Excellent outcomes following hematopoietic cell transplantation for Wiskott-Aldrich syndrome: a PIDTC report
  Lauri Burroughs, Aleksandra Petrovic, Ruta Brazauskas, Xuerong Liu, Linda M. Griffith
  Blood. 2020-06-04

Journal Articles

• Adoptive Immunotherapy for Primary Immunodeficiency Disorders with Virus-Specific T-lymphocytes  
  Naik S, Nicholas SK, Martinez CA, Leen AM, Hanley PJ, Gottschalk SM, Rooney CM, Hanson IC, Krance RA, Shpall EJ, Cruz CR, Amrolia P, Lucchini G, Bunin N, Heimall J, Kl..., J Allergy Clin Immunol
• Major histocompatibility complex class II deficiency due to a novel mutation in RFXANK in a child of Mexican descent  
  Clarridge K, Leitenberg D, Loechelt B, Picard C, Keller MD, Journal of Clinical Immunology, 1/2016
• Mutation in IRF2BP2 is responsible for a Familial Form of Common Variable Immunodeficiency Disorder  
  Keller MD, Pandey R, Li D, Glessner J, Tian L, Henrickson S, Chinn IK, Monaco-Shawver L, Heimall J, Hou C, Otieno FG, Jyonouchi S, Calabrese L, van Montfrans J, Orange..., J Allergy Clin Immunol, 2016
• Incidence of Immunodeficiency in 49, XXXXY chromosomal variation.  
  Keller MD, Sadeghin T, Samango-Sprouse C, and Orange JS, Am J Med Genet C
• Chipping away at a mountain: Genomic studies in Common Variable Immunodeficiency.  
  Keller MD, Jyonouchi S, Autoimmun Rev, 12: S1568
• Diagnosis of 22q11.2 Deletion syndrome and Artemis deficiency in two children with T-B-NK+ Immunodeficiency.  
  Heimall J, Keller M, Saltzman R, Bunin N, McDonald-McGinn D, Zakai E, de Villartay JP, Moshous D, Ariue B, McCarthy EA, Devlin BH, Parikh S, Buckley RH, and Markert ML, J Clin Immunol. 32: 1141-1144
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Abstracts/Posters

• IRF2BP2 mutation in familial Common Variable Immunodeficiency identified by Support Vector Algorithm and Whole Exome Sequencing.
  Keller MD, Tian L, Glessner J, Orange JS, Hakonarson H, Oral presentation, European Society of Immunodeficiency
• Severe Combined Immunodeficiency resulting from mutations in MTHFD1.
  Keller MD, Ganesh J, Heltzer M, Paessler M, Bergqvist AG, Baluarte HJ, Watkins D, Rosenblatt D, and Orange JS, Oral abstract, Clinical Immunology Society
• Incidence of Immunodeficiency in Patients with 49-XXXXY Chromosomal Variation.
  Keller MD, Sadeghin T, Samango-Sprouse C, and Orange JS, Poster presentation, AAAAI annual meeting
• A three generational kindred demonstrating Ectodermal Dysplasia and Immunodeficiency (ED-ID) with both NEMO and EDA mutations.
  Keller MD, Orange, JS, Ann. Allergy. 105: A98
• Co-localization of Splenic NK and Dendritic Cells in Perforin-deficient Hemophagocytic Syndrome: Insight into Mechanism of HLH.
  Keller MD, Paessler ME, and Orange JS, JACI, AB90
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