| Wintrobe's clinical hematology JP Greer, DA Arber, BE Glader, AF List, RM Means, GM Rodgers Lippincott Williams & Wilkins, 2018 | 1441* | 2018 |
| Inhibition of Nuclear Translocation of Transcription Factor NF-κB by a Synthetic Peptide Containing a Cell Membrane-permeable Motif and Nuclear Localization Sequence∗ YZ Lin, SY Yao, RA Veach, TR Torgerson, J Hawiger Journal of Biological Chemistry 270 (24), 14255-14258, 1995 | 1234 | 1995 |
| Human inborn errors of immunity: 2019 update on the classification from the International Union of Immunological Societies Expert Committee SG Tangye, W Al-Herz, A Bousfiha, T Chatila, C Cunningham-Rundles, ... Journal of clinical immunology 40 (1), 24-64, 2020 | 1228 | 2020 |
| Single-cell analysis of normal and FOXP3-mutant human T cells: FOXP3 expression without regulatory T cell development MA Gavin, TR Torgerson, E Houston, P DeRoos, WY Ho, ... Proceedings of the National Academy of Sciences 103 (17), 6659-6664, 2006 | 991 | 2006 |
| International union of immunological societies: 2017 primary immunodeficiency diseases committee report on inborn errors of immunity C Picard, H Bobby Gaspar, W Al-Herz, A Bousfiha, JL Casanova, ... Journal of clinical immunology 38 (1), 96-128, 2018 | 936 | 2018 |
| Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator … E Gambineri, TR Torgerson, HD Ochs Current opinion in rheumatology 15 (4), 430-435, 2003 | 843 | 2003 |
| Early-onset stroke and vasculopathy associated with mutations in ADA2 Q Zhou, D Yang, AK Ombrello, AV Zavialov, C Toro, AV Zavialov, ... New England Journal of Medicine 370 (10), 911-920, 2014 | 817 | 2014 |
| Human inborn errors of immunity: 2019 update of the IUIS phenotypical classification A Bousfiha, L Jeddane, C Picard, W Al-Herz, F Ailal, T Chatila, ... Journal of clinical immunology 40 (1), 66-81, 2020 | 747 | 2020 |
| Human inborn errors of immunity: 2022 update on the classification from the international union of immunological societies expert committee SG Tangye, W Al-Herz, A Bousfiha, C Cunningham-Rundles, JL Franco, ... Journal of clinical immunology, 1-35, 2022 | 673 | 2022 |
| The 2017 IUIS phenotypic classification for primary immunodeficiencies A Bousfiha, L Jeddane, C Picard, F Ailal, H Bobby Gaspar, W Al-Herz, ... Journal of clinical immunology 38 (1), 129-143, 2018 | 631 | 2018 |
| Astrovirus encephalitis in boy with X-linked agammaglobulinemia PL Quan, TA Wagner, T Briese, TR Torgerson, M Hornig, ... Emerging infectious diseases 16 (6), 918, 2010 | 355 | 2010 |
| Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced TH17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome ED Renner, S Rylaarsdam, S Aňover-Sombke, AL Rack, J Reichenbach, ... Journal of Allergy and Clinical Immunology 122 (1), 181-187, 2008 | 353 | 2008 |
| Analysis of FOXP3 reveals multiple domains required for its function as a transcriptional repressor JE Lopes, TR Torgerson, LA Schubert, SD Anover, EL Ocheltree, ... The Journal of Immunology 177 (5), 3133-3142, 2006 | 346 | 2006 |
| Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation–polyendocrinopathy–enteropathy–X-linked–like syndrome G Uzel, EP Sampaio, MG Lawrence, AP Hsu, M Hackett, MJ Dorsey, ... Journal of allergy and clinical immunology 131 (6), 1611-1623. e3, 2013 | 332 | 2013 |
| Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an … D Moratto, S Giliani, C Bonfim, E Mazzolari, A Fischer, HD Ochs, AJ Cant, ... Blood, The Journal of the American Society of Hematology 118 (6), 1675-1684, 2011 | 331 | 2011 |
| Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells TR Torgerson, HD Ochs Journal of Allergy and Clinical Immunology 120 (4), 744-750, 2007 | 331 | 2007 |
| Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene TR Torgerson, A Linane, N Moes, S Anover, V Mateo, F Rieux–Laucat, ... Gastroenterology 132 (5), 1705-1717, 2007 | 289 | 2007 |
| FOXP3 acts as a rheostat of the immune response HD Ochs, SF Ziegler, TR Torgerson Immunological reviews 203 (1), 156-164, 2005 | 289 | 2005 |
| Regulation of NF-κB, AP-1, NFAT, and STAT1 nuclear import in T lymphocytes by noninvasive delivery of peptide carrying the nuclear localization sequence of NF-κB p50 TR Torgerson, AD Colosia, JP Donahue, YZ Lin, J Hawiger The Journal of Immunology 161 (11), 6084-6092, 1998 | 270 | 1998 |
| The 2022 update of IUIS phenotypical classification for human inborn errors of immunity A Bousfiha, A Moundir, SG Tangye, C Picard, L Jeddane, W Al-Herz, ... Journal of Clinical Immunology 42 (7), 1508-1520, 2022 | 259 | 2022 |
