L. D. Notarangelo

1.3k total citations
21 papers, 853 citations indexed

About

L. D. Notarangelo is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, L. D. Notarangelo has authored 21 papers receiving a total of 853 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Immunology, 7 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in L. D. Notarangelo's work include Immunodeficiency and Autoimmune Disorders (9 papers), Immune Cell Function and Interaction (6 papers) and Pneumocystis jirovecii pneumonia detection and treatment (3 papers). L. D. Notarangelo is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (9 papers), Immune Cell Function and Interaction (6 papers) and Pneumocystis jirovecii pneumonia detection and treatment (3 papers). L. D. Notarangelo collaborates with scholars based in Italy, United States and United Kingdom. L. D. Notarangelo's co-authors include Lucia Salvi, Raffaele Badolato, Fabio Facchetti, Helen Chapel, Jean‐Laurent Casanova, Jennifer M. Puck, Chaim M. Roifman, Albert Fischer, Mary Ellen Conley and Reinhard Seger and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Immunity.

In The Last Decade

L. D. Notarangelo

21 papers receiving 827 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L. D. Notarangelo Italy	14	550	200	143	122	90	21	853
H.-P. Brezinschek Austria	11	630 1.1×	93 0.5×	186 1.3×	100 0.8×	65 0.7×	16	1.1k
G Tonietti Italy	19	530 1.0×	94 0.5×	126 0.9×	97 0.8×	133 1.5×	52	1.0k
KI Welsh United Kingdom	16	465 0.8×	191 1.0×	104 0.7×	37 0.3×	206 2.3×	29	895
M.N. Cauchi Australia	18	269 0.5×	161 0.8×	171 1.2×	74 0.6×	74 0.8×	78	1.0k
Martie C. M. Verschuren Netherlands	15	1.1k 2.0×	111 0.6×	204 1.4×	238 2.0×	176 2.0×	21	1.5k
H E Broxmeyer United States	14	392 0.7×	123 0.6×	278 1.9×	346 2.8×	46 0.5×	15	817
Małgorzata Pac Poland	16	445 0.8×	192 1.0×	178 1.2×	49 0.4×	102 1.1×	48	750
Cecilia Oderup United States	10	866 1.6×	113 0.6×	148 1.0×	183 1.5×	53 0.6×	13	1.0k
Shannon O’Neill United States	12	564 1.0×	122 0.6×	132 0.9×	110 0.9×	36 0.4×	18	855
Kira Rubtsova United States	18	1.7k 3.2×	198 1.0×	209 1.5×	183 1.5×	196 2.2×	24	2.2k

Countries citing papers authored by L. D. Notarangelo

Since Specialization

Citations

This map shows the geographic impact of L. 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 L. 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 L. D. Notarangelo more than expected).

Fields of papers citing papers by L. D. Notarangelo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of L. D. Notarangelo. A scholar is included among the top collaborators of L. 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 L. D. Notarangelo. L. D. Notarangelo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Bacchetta, Rosa & L. D. Notarangelo. (2013). Immunodeficiency with Autoimmunity: Beyond the Paradox. Frontiers in Immunology. 4. 77–77. 7 indexed citations

Carvalho, Anna Cristina Calçada, Richard Fabian Schumacher, Elena Soncini, et al.. (2013). Contact investigation based on serial interferon-gamma release assays (IGRA) in children from the hematology-oncology ward after exposure to a patient with pulmonary tuberculosis. Infection. 41(4). 827–831. 10 indexed citations

Sabelli, Cristiano, Paola Melotti, Cecília Garlanda, et al.. (2010). PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients. Genes and Immunity. 11(8). 665–670. 71 indexed citations

Santoro, Alessandra, Sonia Cannella, Antonino Trizzino, et al.. (2008). Mutations affecting mRNA splicing are the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3. Haematologica. 93(7). 1086–1090. 27 indexed citations

Porta, Fulvio, Concetta Forino, Elena Soncini, et al.. (2008). Stem cell transplantation for primary immunodeficiencies. Bone Marrow Transplantation. 41(S2). S83–S86. 11 indexed citations

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

Pilotta, Alba, Patrizia Mella, Barbara Felappi, et al.. (2006). Common Polymorphisms of the Growth Hormone (GH) Receptor Do Not Correlate with the Growth Response to Exogenous Recombinant Human GH in GH-Deficient Children. The Journal of Clinical Endocrinology & Metabolism. 91(3). 1178–1180. 64 indexed citations

Tommasini, Alberto, Sérgio Ferrari, Daniele Moratto, et al.. (2002). X-chromosome inactivation analysis in a female carrier of FOXP3 mutation. Clinical & Experimental Immunology. 130(1). 127–130. 76 indexed citations

Gil, Juana, Fulvio Porta, Joaquín Bartolomé, et al.. (1999). Immune reconstitution after in utero bone marrow transplantation in a fetus with severe combined immunodeficiency with natural killer cells. Transplantation Proceedings. 31(6). 2581–2581. 22 indexed citations

10.

Giliani, Silvia, Maurilia Fiorini, Patrizia Mella, et al.. (1999). Prenatal molecular diagnosis of Wiskott–Aldrich syndrome by direct mutation analysis. Prenatal Diagnosis. 19(1). 36–40. 1 indexed citations

11.

Mallone, Roberto, M. Morra, Elena Zocchi, et al.. (1998). Characterization of a CD38-like 78-kilodalton soluble protein released from B cell lines derived from patients with X-linked agammaglobulinemia.. Journal of Clinical Investigation. 101(12). 2821–2830. 32 indexed citations

12.

Bozzi, Fabio, Marie‐Paule Lefranc, Raffaele Badolato, et al.. (1998). Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment. British Journal of Haematology. 102(5). 1363–1366. 12 indexed citations

13.

Iafusco, Dario, Ethel Felice, L. D. Notarangelo, et al.. (1997). A Girl with Diabetes and Severe Combined Immunodeficiency from Adenosine Deaminase Deficiency. Journal of Pediatric Endocrinology and Metabolism. 10(4). 425–8. 3 indexed citations

14.

Oakes, Scott A., Fabio Candotti, Yiqing Chen, et al.. (1996). Signaling via IL-2 and IL-4 in JAK3-Deficient Severe Combined Immunodeficiency Lymphocytes: JAK3-Dependent and Independent Pathways. Immunity. 5(6). 605–615. 117 indexed citations

15.

Duse, Marzia, et al.. (1996). Intravenous immune globulin in the treatment of intractable childhood epilepsy. Clinical & Experimental Immunology. 104(Supplement_1). 71–76. 33 indexed citations

16.

Facchetti, Fabio, et al.. (1995). Immunohistologic analysis of ineffective CD40-CD40 ligand interaction in lymphoid tissues from patients with X-linked immunodeficiency with hyper-IgM. Abortive germinal center cell reaction and severe depletion of follicular dendritic cells.. The Journal of Immunology. 154(12). 6624–6633. 85 indexed citations

17.

Vihinen, Mauno, David Vetrie, Hina S. Maniar, et al.. (1994). Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease.. Proceedings of the National Academy of Sciences. 91(26). 12803–12807. 70 indexed citations

18.

Notarangelo, L. D., Fabio Candotti, Ornella Parolini, et al.. (1993). Application of Molecular Analysis to Genetic Counseling in the Wiskott–Aldrich Syndrome (WAS). DNA and Cell Biology. 12(7). 645–649. 3 indexed citations

19.

Notarangelo, L. D., Evelina Mazzolari, Adriana M. Coletta, et al.. (1992). Insulin-dependent diabetes mellitus and severe atopic dermatitis in a child with adenosine deaminase deficiency. European Journal of Pediatrics. 151(11). 811–814. 24 indexed citations

20.

Maestrini, Elena, Stefano Rivella, Carla Tribioli, et al.. (1992). Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.. PubMed. 50(1). 156–63. 21 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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