Standout Papers

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syn... 1993 2026 2004 2015 2.5k
  1. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 (2001)
    Craig L. Bennett, Fred Ramsdell et al. Nature Genetics
  2. Chronic Granulomatous Disease: Report on a National Registry of 368 Patients (2000)
    Jerry A. Winkelstein, Richard B. Johnston et al. Medicine
  3. Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee (2020)
    Stuart G. Tangye, Waleed Al–Herz et al. Journal of Clinical Immunology
  4. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome (1993)
    Alejandro Aruffo, Mary Farrington et al. Cell
  5. Single-cell analysis of normal and FOXP3-mutant human T cells: FOXP3 expression without regulatory T cell development (2006)
    Marc A. Gavin, Troy R. Torgerson et al. Proceedings of the National Academy of Sciences
  6. Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015 (2015)
    Capucine Pïcard, Waleed Al–Herz et al. Journal of Clinical Immunology
  7. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity (2017)
    Capucine Pïcard, H. Bobby Gaspar et al. Journal of Clinical Immunology
  8. Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification (2020)
    Aziz Bousfiha, Leïla Jeddane et al. Journal of Clinical Immunology
  9. Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency (2014)
    Waleed Al–Herz, Aziz Bousfiha et al. Frontiers in Immunology

Immediate Impact

20 by Nobel laureates 27 from Science/Nature 72 standout
Sub-graph 1 of 17

Citing Papers

Targeting a CAR to the TRAC locus with CRISPR/Cas9 enhances tumour rejection
2017 StandoutNature
30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology
2017 StandoutNobel
10 intermediate papers

Works of Hans D. Ochs being referenced

A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy
2013
Partial V(D)J Recombination Activity Leads to Omenn Syndrome
1998
and 10 more

Author Peers

Author Last Decade Papers Cites
Hans D. Ochs 19446 6553 4171 4847 393 28.8k
Max D. Cooper 23194 3598 3092 6914 442 33.1k
Fred S. Rosen 12213 3306 4579 5136 424 25.6k
Raif S. Geha 19161 3167 2372 5185 495 31.3k
Luigi D. Notarangelo 11325 4371 2064 4030 365 17.8k
Frank J. Dixon 12314 2420 1955 5173 328 25.7k
Leonard D. Shultz 13818 5287 4784 10384 449 31.6k
Herman Waldmann 22115 3517 5734 6761 537 36.1k
Jordan S. Orange 13869 2833 2032 3140 319 19.4k
Andreas Radbruch 18832 1930 2264 6712 437 30.3k
Emil R. Unanue 24387 4478 1109 10161 429 39.4k

All Works

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2026