Luigi D. Notarangelo

62.1k total citations · 5 hit papers
371 papers, 18.2k citations indexed

About

Luigi D. Notarangelo is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Luigi D. Notarangelo has authored 371 papers receiving a total of 18.2k indexed citations (citations by other indexed papers that have themselves been cited), including 271 papers in Immunology, 79 papers in Genetics and 58 papers in Molecular Biology. Recurrent topics in Luigi D. Notarangelo's work include Immunodeficiency and Autoimmune Disorders (212 papers), Immune Cell Function and Interaction (128 papers) and T-cell and B-cell Immunology (87 papers). Luigi D. Notarangelo is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (212 papers), Immune Cell Function and Interaction (128 papers) and T-cell and B-cell Immunology (87 papers). Luigi D. Notarangelo collaborates with scholars based in United States, Italy and United Kingdom. Luigi D. Notarangelo's co-authors include Anna Villa, Silvia Giliani, Hans D. Ochs, Jean‐Laurent Casanova, Alberto G. Ugazio, Raif S. Geha, Paolo Vezzoni, Chaim M. Roifman, Fabio Candotti and Evelina Mazzolari and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Luigi D. Notarangelo

363 papers receiving 17.8k citations

Hit Papers

The X-linked lymphoproliferative-disease gene product SAP... 1995 2026 2005 2015 1998 1995 1995 2000 2017 200 400 600
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. The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM
    1998 746 citations Luigi D. Notarangelo et al. profile →
  2. Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)
    1995 674 citations Anna Villa, Silvia Giliani et al. profile →
  3. Gene Therapy in Peripheral Blood Lymphocytes and Bone Marrow for ADA − Immunodeficient Patients
    1995 632 citations Luigi D. Notarangelo, Evelina Mazzolari et al. profile →
  4. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis
    2000 503 citations Silvia Giliani, Luigi D. Notarangelo et al. profile →
  5. A three-dimensional model of human lung development and disease from pluripotent stem cells
    2017 441 citations Stefano Volpi, Luigi D. Notarangelo et al. profile →

Peers

Luigi D. Notarangelo
Jordan S. Orange United States
Jennifer M. Puck United States
René E. M. Toes Netherlands
Maria Grazia Roncarolo Italy
Françoise Le Deist France
Robert Winchester United States
Rebecca H. Buckley United States
Robert P. Kimberly United States
Takehiko Sasazuki Japan
Stuart G. Tangye Australia
Jordan S. Orange United States
Luigi D. Notarangelo
Citations per year, relative to Luigi D. Notarangelo Luigi D. Notarangelo (= 1×) peers Jordan S. Orange

Countries citing papers authored by Luigi D. Notarangelo

Since Specialization
Citations

This map shows the geographic impact of Luigi D. Notarangelo'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 Luigi D. Notarangelo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Luigi D. Notarangelo more than expected).

Fields of papers citing papers by Luigi D. Notarangelo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luigi D. Notarangelo. 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 Luigi D. Notarangelo. The network helps show where Luigi D. Notarangelo may publish in the future.

Co-authorship network of co-authors of Luigi D. Notarangelo

This figure shows the co-authorship network connecting the top 25 collaborators of Luigi D. Notarangelo. A scholar is included among the top collaborators of Luigi D. Notarangelo 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 Luigi D. Notarangelo. Luigi D. Notarangelo 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.
Pala, Francesca, Luigi D. Notarangelo, & Marita Bosticardo. (2024). Rediscovering the human thymus through cutting-edge technologies. The Journal of Experimental Medicine. 221(10). 5 indexed citations
2.
Saldaña, Blachy J. Dávila, Catherine M. Bollard, Stanislav V. Sosnovtsev, et al.. (2024). 73 Reconstitution of norovirus-specific T cell responses following hematopoetic stem cell transplantation in patients with inborn errors of immunity and chronic norovirus infection. Clinical Immunology. 262. 110015–110015.
3.
Pala, Francesca, Enrica Calzoni, Anna Villa, et al.. (2023). Transplantation after CD45-ADC corrects Rag1 immunodeficiency in congenic and haploidentical settings. Journal of Allergy and Clinical Immunology. 153(1). 341–348.e3. 3 indexed citations
4.
Kuehn, Hye Sun, Inga Sakovich, Julie E. Niemela, et al.. (2023). Disease-associated AIOLOS variants lead to immune deficiency/dysregulation by haploinsufficiency and redefine AIOLOS functional domains. Journal of Clinical Investigation. 134(3). 8 indexed citations
5.
Pala, Francesca, Luigi D. Notarangelo, & Marita Bosticardo. (2022). Inborn errors of immunity associated with defects of thymic development. Pediatric Allergy and Immunology. 33(8). e13832–e13832. 10 indexed citations
6.
Zimmer, Bastian, Oliver Harschnitz, Yoon Seung Lee, et al.. (2018). Human iPSC-derived trigeminal neurons lack constitutive TLR3-dependent immunity that protects cortical neurons from HSV-1 infection. Proceedings of the National Academy of Sciences. 115(37). E8775–E8782. 56 indexed citations
7.
Rowe, Jared H., Ottavia M. Delmonte, Sevgi Keleş, et al.. (2018). Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function. Blood. 131(21). 2335–2344. 42 indexed citations
8.
Rawat, Amit, Ankur Kumar Jindal, Madhubala Sharma, et al.. (2018). Clinical and molecular features of X-linked hyper IgM syndrome – An experience from North India. Clinical Immunology. 195. 59–66. 11 indexed citations
9.
Bruin, Lisa M. Ott de, Marita Bosticardo, Alessandro Barbieri, et al.. (2018). Hypomorphic Rag1 mutations alter the preimmune repertoire at early stages of lymphoid development. Blood. 132(3). 281–292. 25 indexed citations
10.
Lees, Joshua A., Yixiao Zhang, Michael S. Oh, et al.. (2017). Architecture of the human PI4KIIIα lipid kinase complex. Proceedings of the National Academy of Sciences. 114(52). 13720–13725. 47 indexed citations
11.
Volpi, Stefano, Masayuki Mizui, Carin Dahlberg, et al.. (2015). N-WASP is required for B-cell–mediated autoimmunity in Wiskott-Aldrich syndrome. Blood. 127(2). 216–220. 21 indexed citations
12.
Meazza, Raffaella, Valentina Cetica, Michela Falco, et al.. (2014). Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis. Journal of Allergy and Clinical Immunology. 134(6). 1381–1387.e7. 17 indexed citations
13.
Rogler, Leslie E., David M. Moskowitz, Katrina M. Kutchko, et al.. (2013). Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage–hair hypoplasia. Human Molecular Genetics. 23(2). 368–382. 69 indexed citations
14.
Wesemann, Duane R., Jennifer M. Magee, Cristian Boboilă, et al.. (2011). Immature B cells preferentially switch to IgE with increased direct Sμ to Sε recombination. The Journal of Experimental Medicine. 208(13). 2733–2746. 84 indexed citations
15.
Lanzi, Gaetana, Simona Ferrari, Mauno Vihinen, et al.. (2010). Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. Blood. 116(26). 5867–5874. 23 indexed citations
16.
Notarangelo, Luigi D., Eleonora Gambineri, & Raffaele Badolato. (2006). Immunodeficiencies with Autoimmune Consequences. Advances in immunology. 89. 321–370. 45 indexed citations
17.
Cavadini, Patrizia, William Vermi, Fabio Facchetti, et al.. (2005). AIRE deficiency in thymus of 2 patients with Omenn syndrome. Journal of Clinical Investigation. 115(3). 728–732. 116 indexed citations
18.
Notarangelo, Luigi D., Cinzia Mazza, Concetta Forino, Evelina Mazzolari, & Fabio Buzi. (2004). AIRE and immunological tolerance: insights from the study of autoimmune polyendocrinopathy candidiasis and ectodermal dystrophy. Current Opinion in Allergy and Clinical Immunology. 4(6). 491–496. 10 indexed citations
19.
Schumacher, Richard Fabian & Luigi D. Notarangelo. (2002). Severe combined immunodeficiencies of the common gamma-chain/JAK3 signaling pathway.. PubMed. 4(2). 131–5. 4 indexed citations
20.
Chen, Min, Alan Cheng, Fabio Candotti, et al.. (2000). Complex Effects of Naturally Occurring Mutations in the JAK3 Pseudokinase Domain: Evidence for Interactions between the Kinase and Pseudokinase Domains. Molecular and Cellular Biology. 20(3). 947–956. 100 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.

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