Jennifer M. Puck

Research.com Recognitions

• 2025 - Research.com Best Female Scientists Award

Overview

Best Publications

• Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

  Galen H Fisher;Fredric J Rosenberg;Stephen E Straus;Janet K Dale

  2194
  Citations

• Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee

  Unknown

  1423
  Citations

• STAT3 Mutations in the Hyper-IgE Syndrome

  Steven M. Holland;Frank R. DeLeo;Houda Z. Elloumi;Amy P. Hsu

  1417
  Citations

• Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

  Stuart G. Tangye;Waleed Al-Herz;Aziz Bousfiha;Talal Chatila

  1232
  Citations

• Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

  Unknown

  1120
  Citations

• A prudent path forward for genomic engineering and germline gene modification

  David Baltimore;Paul Berg;Michael Botchan;Dana Carroll

  954
  Citations

• Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder

  Bodo Grimbacher;Steven M. Holland;John I. Gallin;Frank Greenberg

  945
  Citations

• International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity

  Capucine Picard;H. Bobby Gaspar;Waleed Al-Herz;Aziz Bousfiha

  889
  Citations

• Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

  Hyung J. Chun;Lixin Zheng;Manzoor Ahmad;Jin Wang;Jin Wang

  863
  Citations

• Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015

  Capucine Picard;Waleed Al-Herz;Aziz Bousfiha;Jean Laurent Casanova

  857
  Citations

• Transplantation Outcomes for Severe Combined Immunodeficiency, 2000–2009

  Sung Yun Pai;Brent R. Logan;Linda M. Griffith;Rebecca H. Buckley

  802
  Citations

• Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II

  Jin Wang;Lixin Zheng;Adrian Lobito;Francis Ka Ming Chan

  751
  Citations

• Newborn Screening for Severe Combined Immunodeficiency in 11 Screening Programs in the United States

  Antonia Kwan;Roshini S. Abraham;Robert Currier;Amy Brower

  746
  Citations

• Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants.

  Rebecca H. Buckley;Richard I. Schiff;Sherrie E. Schiff;M.Louise Markert

  742
  Citations

• Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

  Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel

  694
  Citations

• Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.

  Aziz Bousfiha;Leila Jeddane;Capucine Picard;Waleed Al-Herz

  665
  Citations

• Primary immunodeficiencies: 2009 update

  Luigi D. Notarangelo;Alain Fischer;Raif S. Geha;Jean-Laurent Casanova

  630
  Citations

• The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity

  Unknown

  611
  Citations

• Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

  Raif S. Geha;Luigi D. Notarangelo;Jean Laurent Casanova;Helen Chapel

  610
  Citations

• The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis.

  Stephen E. Straus;Elaine S. Jaffe;Jennifer M. Puck;Janet K. Dale

  603
  Citations

• Newborn Screening: Toward a Uniform Screening Panel and System—Executive Summary

  Michael S. Watson;Marie Y. Mann;Michele A. Lloyd-Puryear;Piero Rinaldo

  597
  Citations

• Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

  Karin R. Engelhardt;Sean McGhee;Sabine Winkler;Atfa Sassi

  590
  Citations

• The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.

  Aziz Bousfiha;Leïla Jeddane;Capucine Picard;Fatima Ailal

  582
  Citations