Jennifer M. Puck

38.4k total citations · 11 hit papers
245 papers, 19.3k citations indexed

About

Jennifer M. Puck is a scholar working on Immunology, Genetics and Epidemiology. According to data from OpenAlex, Jennifer M. Puck has authored 245 papers receiving a total of 19.3k indexed citations (citations by other indexed papers that have themselves been cited), including 190 papers in Immunology, 76 papers in Genetics and 56 papers in Epidemiology. Recurrent topics in Jennifer M. Puck's work include Immunodeficiency and Autoimmune Disorders (154 papers), Immune Cell Function and Interaction (61 papers) and T-cell and B-cell Immunology (34 papers). Jennifer M. Puck is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (154 papers), Immune Cell Function and Interaction (61 papers) and T-cell and B-cell Immunology (34 papers). Jennifer M. Puck collaborates with scholars based in United States, France and Germany. Jennifer M. Puck's co-authors include Steven M. Holland, Janet K. Dale, Stephen E. Straus, Michael J. Lenardo, Mary Ellen Conley, Jean‐Laurent Casanova, Charlotte Cunningham‐Rundles, Kathleen E. Sullivan, Hans D. Ochs and Christoph Klein and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Jennifer M. Puck

240 papers receiving 18.8k citations

Hit Papers

Dominant interfering fas ... 1995 2026 2005 2015 1995 2020 2015 2022 2002 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Dominant interfering fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome
    1995 1.1k citations Stephen E. Straus, Janet K. Dale et al. profile →
  2. Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
    2020 726 citations Stuart G. Tangye, Waleed Al–Herz et al. Journal of Clinical Immunology profile →
  3. Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015
    2015 645 citations Capucine Pïcard, Waleed Al–Herz et al. Journal of Clinical Immunology profile →
  4. Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
    2022 569 citations Stuart G. Tangye, Waleed Al–Herz et al. Journal of Clinical Immunology profile →
  5. Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency
    2002 544 citations Lixin Zheng, Janet K. Dale et al. profile →
  6. Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder
    1999 504 citations Bodo Grimbacher, Steven M. Holland et al. profile →
  7. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
    2017 479 citations Capucine Pïcard, Waleed Al–Herz et al. Journal of Clinical Immunology profile →
  8. Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification
    2020 414 citations Aziz Bousfiha, Capucine Pïcard et al. Journal of Clinical Immunology profile →
  9. Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
    2014 402 citations Waleed Al–Herz, Aziz Bousfiha et al. Frontiers in Immunology profile →
  10. A prudent path forward for genomic engineering and germline gene modification
    2015 400 citations Jennifer M. Puck et al. profile →
  11. The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity
    2022 244 citations Aziz Bousfiha, Stuart G. Tangye et al. Journal of Clinical Immunology profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jennifer M. Puck United States 73 13.4k 5.8k 4.8k 3.2k 2.3k 245 19.3k
Luigi D. Notarangelo United States 70 11.6k 0.9× 4.5k 0.8× 4.1k 0.9× 2.3k 0.7× 3.2k 1.4× 371 18.2k
Jordan S. Orange United States 74 14.1k 1.1× 2.9k 0.5× 3.2k 0.7× 3.3k 1.0× 3.2k 1.4× 322 19.8k
David Klatzmann France 74 12.0k 0.9× 3.7k 0.6× 4.2k 0.9× 3.8k 1.2× 3.0k 1.3× 358 22.3k
Rebecca H. Buckley United States 58 9.5k 0.7× 3.4k 0.6× 1.9k 0.4× 3.0k 0.9× 1.6k 0.7× 223 14.0k
Charlotte Cunningham‐Rundles United States 70 16.0k 1.2× 5.9k 1.0× 1.6k 0.3× 3.5k 1.1× 1.1k 0.5× 354 20.1k
Françoise Le Deist France 73 10.6k 0.8× 4.0k 0.7× 5.9k 1.2× 2.9k 0.9× 3.4k 1.5× 226 19.4k
Smith Rjh Sweden 68 9.3k 0.7× 3.2k 0.5× 8.5k 1.8× 1.8k 0.6× 1.5k 0.6× 723 20.5k
Robert Winchester United States 68 14.6k 1.1× 1.9k 0.3× 3.3k 0.7× 2.4k 0.7× 2.0k 0.9× 209 28.3k
Herbert C. Morse United States 81 12.1k 0.9× 2.5k 0.4× 8.0k 1.7× 2.8k 0.9× 3.6k 1.6× 437 22.8k
Arne Svejgaard Denmark 71 13.5k 1.0× 3.9k 0.7× 2.7k 0.6× 2.0k 0.6× 1.5k 0.7× 391 21.4k

Countries citing papers authored by Jennifer M. Puck

Since Specialization
Citations

This map shows the geographic impact of Jennifer M. Puck's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jennifer M. Puck with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jennifer M. Puck more than expected).

Fields of papers citing papers by Jennifer M. Puck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer M. Puck. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jennifer M. Puck. The network helps show where Jennifer M. Puck may publish in the future.

Co-authorship network of co-authors of Jennifer M. Puck

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer M. Puck. A scholar is included among the top collaborators of Jennifer M. Puck based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jennifer M. Puck. Jennifer M. Puck is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Gober, Laura, Elizabeth Garabedian, Ramsay Fuleihan, et al.. (2022). Eosinophilic gastrointestinal disorders in patients with inborn errors of immunity: Data from the USIDNET registry. Frontiers in Immunology. 13. 987895–987895. 5 indexed citations
2.
Dvorak, Christopher C., Élie Haddad, Jennifer Heimall, et al.. (2022). The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions. Journal of Allergy and Clinical Immunology. 151(2). 539–546. 53 indexed citations
3.
Buchbinder, David, Jolán E. Walter, Manish J. Butte, et al.. (2021). When Screening for Severe Combined Immunodeficiency (SCID) with T Cell Receptor Excision Circles Is Not SCID: a Case-Based Review. Journal of Clinical Immunology. 41(2). 294–302. 12 indexed citations
4.
Tangye, Stuart G., Waleed Al–Herz, Aziz Bousfiha, et al.. (2020). Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee. Journal of Clinical Immunology. 40(1). 24–64. 726 indexed citations breakdown →
5.
Chan, Alice, Divya Punwani, Theresa A. Kadlecek, et al.. (2016). A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70. The Journal of Experimental Medicine. 213(2). 155–165. 54 indexed citations
6.
Patel, Jay, Jennifer M. Puck, Kunal Kundu, et al.. (2015). Nijmegen Breakage Syndrome Detected By Newborn Screening for T Cell Receptor Excision Circles (TRECs). Journal of Allergy and Clinical Immunology. 135(2). AB14–AB14. 6 indexed citations
7.
Dvorak, Christopher C., Biljana Horn, Jennifer M. Puck, et al.. (2014). A trial of alemtuzumab adjunctive therapy in allogeneic hematopoietic cell transplantation with minimal conditioning for severe combined immunodeficiency. Pediatric Transplantation. 18(6). 609–616. 13 indexed citations
8.
Price, Susan, Pamela A. Shaw, Amy E. Seitz, et al.. (2014). Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations. Blood. 123(13). 1989–1999. 134 indexed citations
9.
Dvorak, Christopher C., Biljana Horn, Jennifer M. Puck, et al.. (2014). A trial of plerixafor adjunctive therapy in allogeneic hematopoietic cell transplantation with minimal conditioning for severe combined immunodeficiency. Pediatric Transplantation. 18(6). 602–608. 12 indexed citations
10.
Ochs, Hans D., Smith Rjh, & Jennifer M. Puck. (2014). Primary immunodeficiency diseases : a molecular and cellular approach. Oxford University Press eBooks. 7 indexed citations
11.
Kwan, Antonia, Joseph A. Church, Morton J. Cowan, et al.. (2013). Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: Results of the first 2 years. Journal of Allergy and Clinical Immunology. 132(1). 140–150.e7. 143 indexed citations
12.
Punwani, Divya, Diana González‐Espinosa, Anne Marie Comeau, et al.. (2012). Cellular calibrators to quantitate T-cell receptor excision circles (TRECs) in clinical samples. Molecular Genetics and Metabolism. 107(3). 586–591. 8 indexed citations
13.
Hsu, Amy P., Kennichi Dowdell, Joie Davis, et al.. (2012). Autoimmune lymphoproliferative syndrome due to FAS mutations outside the signal-transducing death domain: molecular mechanisms and clinical penetrance. Genetics in Medicine. 14(1). 81–89. 25 indexed citations
14.
Oliveira, João Bosco, Nicolas Bidère, Julie E. Niemela, et al.. (2007). NRAS mutation causes a human autoimmune lymphoproliferative syndrome. Proceedings of the National Academy of Sciences. 104(21). 8953–8958. 166 indexed citations
15.
Puck, Jennifer M.. (2007). Population-based newborn screening for severe combined immunodeficiency: Steps toward implementation. Journal of Allergy and Clinical Immunology. 120(4). 760–768. 87 indexed citations
16.
Notarangelo, L. D., Jean‐Laurent Casanova, Mary Ellen Conley, et al.. (2006). Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005. Journal of Allergy and Clinical Immunology. 117(4). 883–896. 144 indexed citations
17.
Chinen, Javier & Jennifer M. Puck. (2004). Perspectives of gene therapy for primary immunodeficiencies. Current Opinion in Allergy and Clinical Immunology. 4(6). 523–527. 8 indexed citations
18.
O’Connell, Anne C., Jennifer M. Puck, Bodo Grimbacher, et al.. (2000). Delayed eruption of permanent teeth in hyperimmunoglobulinemia E recurrent infection syndrome. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 89(2). 177–185. 61 indexed citations
19.
Mignot, Emmanuel, et al.. (1996). Gene localization and syntenic mapping by FISH in the dog. Cytogenetic and Genome Research. 74(1-2). 113–117. 44 indexed citations
20.
Nussbaum, Robert L. & Jennifer M. Puck. (1976). Recurrence Risks for Retinoblastoma: A Model for Autosomal Dominant Disorders With Complex Inheritance. Journal of Pediatric Ophthalmology & Strabismus. 13(2). 89–98. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Luigi D. Notarangelo Breakdown of academic impact, for papers by Jordan S. Orange Breakdown of academic impact, for papers by David Klatzmann Breakdown of academic impact, for papers by Rebecca H. Buckley Breakdown of academic impact, for papers by Charlotte Cunningham‐Rundles Breakdown of academic impact, for papers by Françoise Le Deist Breakdown of academic impact, for papers by Smith Rjh Breakdown of academic impact, for papers by Robert Winchester Breakdown of academic impact, for papers by Herbert C. Morse Breakdown of academic impact, for papers by Arne Svejgaard
Rankless by CCL
2026