Angelo Notarangelo

1.1k total citations
29 papers, 806 citations indexed

About

Angelo Notarangelo is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Angelo Notarangelo has authored 29 papers receiving a total of 806 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Genetics. Recurrent topics in Angelo Notarangelo's work include Glioma Diagnosis and Treatment (6 papers), MicroRNA in disease regulation (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Angelo Notarangelo is often cited by papers focused on Glioma Diagnosis and Treatment (6 papers), MicroRNA in disease regulation (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Angelo Notarangelo collaborates with scholars based in Italy, New Zealand and Spain. Angelo Notarangelo's co-authors include Leopoldo Zelante, Paolo Gasparini, Luigi Bisceglia, Massimo Carella, Bruno Dallapiccola, Enzo Di Iorio, Tama Sobe, Fabian Glaser, Nadav Ahituv and María L. Arbonés and has published in prestigious journals such as Science, The Journal of Clinical Endocrinology & Metabolism and Cancer Research.

In The Last Decade

Angelo Notarangelo

29 papers receiving 780 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Angelo Notarangelo Italy 13 449 151 148 113 71 29 806
Hassan Chaı̈b United States 16 638 1.4× 66 0.4× 110 0.7× 295 2.6× 137 1.9× 26 1.1k
Elisabetta Flex Italy 21 941 2.1× 159 1.1× 239 1.6× 27 0.2× 158 2.2× 39 1.3k
Alison J. Coffey United Kingdom 17 699 1.6× 41 0.3× 242 1.6× 29 0.3× 147 2.1× 27 1.0k
P. Jaya Kausalya Singapore 14 680 1.5× 210 1.4× 62 0.4× 18 0.2× 101 1.4× 18 1.1k
JT den Dunnen Netherlands 3 402 0.9× 48 0.3× 244 1.6× 18 0.2× 75 1.1× 6 825
Sébastien L’Hoste France 18 818 1.8× 260 1.7× 68 0.5× 22 0.2× 171 2.4× 23 1.0k
Cindy Degerny France 14 697 1.6× 194 1.3× 72 0.5× 50 0.4× 137 1.9× 27 910
Michelle Hussain United Kingdom 4 565 1.3× 66 0.4× 356 2.4× 28 0.2× 42 0.6× 6 966
Vemparala Subbarayan United States 11 996 2.2× 108 0.7× 334 2.3× 25 0.2× 61 0.9× 12 1.3k
Hrvoje Banfíƈ Croatia 20 1.4k 3.1× 562 3.7× 80 0.5× 24 0.2× 110 1.5× 57 1.8k

Countries citing papers authored by Angelo Notarangelo

Since Specialization
Citations

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

Fields of papers citing papers by Angelo Notarangelo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angelo Notarangelo

This figure shows the co-authorship network connecting the top 25 collaborators of Angelo Notarangelo. A scholar is included among the top collaborators of Angelo 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 Angelo Notarangelo. Angelo 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.
Tesolin, Paola, Anna Morgan, Michela Notarangelo, et al.. (2021). Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene. Genes. 12(7). 1043–1043. 4 indexed citations
2.
Micale, Lucia, Elena Manara, Andrea Esposito, et al.. (2021). A novel complex genomic rearrangement affecting the KCNJ2 regulatory region causes a variant of Cooks syndrome. Human Genetics. 141(2). 217–227. 3 indexed citations
3.
Fusco, Carmela, Bartolomeo Augello, Francesca Boccafoschi, et al.. (2020). Pro-Fibrotic Phenotype in a Patient with Segmental Stiff Skin Syndrome via TGF-β Signaling Overactivation. International Journal of Molecular Sciences. 21(14). 5141–5141. 12 indexed citations
4.
Micale, Lucia, Silvia Morlino, Tommaso Biagini, et al.. (2020). Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A > G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(6). 165742–165742. 4 indexed citations
5.
Micale, Lucia, Samantha Cialfi, Carmela Fusco, et al.. (2020). Novel TONSL variants cause SPONASTRIME dysplasia and associate with spontaneous chromosome breaks, defective cell proliferation and apoptosis. Human Molecular Genetics. 29(18). 3122–3131. 4 indexed citations
6.
Morlino, Silvia, Annalucia Carbone, Marco Ritelli, et al.. (2019). TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis. Human Mutation. 40(10). 1886–1898. 4 indexed citations
7.
Loffredo, Rosa, Marina Cardano, Luciano Conti, et al.. (2018). Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutation. Stem Cell Research. 33. 146–150. 2 indexed citations
8.
Maltese, Paolo Enrico, et al.. (2018). Genetic testing for cystic hygroma. The EuroBiotech Journal. 2(s1). 22–25. 1 indexed citations
9.
Sestito, Simona, Giulia Nesi, Simona Daniele, et al.. (2015). Design and synthesis of 2-oxindole based multi-targeted inhibitors of PDK1/Akt signaling pathway for the treatment of glioblastoma multiforme. European Journal of Medicinal Chemistry. 105. 274–288. 41 indexed citations
10.
Ruggieri, Simona, Roberto Tamma, Andrea Marzullo, et al.. (2014). Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme. Cancer Letters. 353(1). 41–51. 12 indexed citations
11.
Notarangelo, Angelo, Domenico Trombetta, Vincenzo D’Angelo, et al.. (2013). Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiforme. International Journal of Oncology. 44(3). 717–724. 7 indexed citations
12.
Venditti, Rossella, Tiziana Scanu, Michele Santoro, et al.. (2012). Sedlin Controls the ER Export of Procollagen by Regulating the Sar1 Cycle. Science. 337(6102). 1668–1672. 133 indexed citations
13.
Parrella, Paola, Massimiliano Copetti, Vanna Maria Valori, et al.. (2009). High Specificity of Quantitative Methylation‐Specific PCR Analysis for MGMT Promoter Hypermethylation Detection in Gliomas. BioMed Research International. 2009(1). 531692–531692. 26 indexed citations
14.
Zelante, L., et al.. (2003). Interstitial “de novo” tandem duplication of 7(q31.1-q35): first reported case. Annales de Génétique. 46(1). 49–52. 5 indexed citations
15.
Perla, Gianni, et al.. (2002). A complex mosaicism 45,X/46,X,del(Xq)/46,X,idic(Xq) in a patient with secondary amenorrhea. Annales de Génétique. 45(3). 137–140. 3 indexed citations
16.
Melchionda, Salvatore, Nadav Ahituv, Luigi Bisceglia, et al.. (2001). MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss. The American Journal of Human Genetics. 69(3). 635–640. 180 indexed citations
17.
Centra, Marta, Maria D’Apolito, Michelangelo Savino, et al.. (1998). Fine Exon–Intron Structure of the Fanconi Anemia Group A (FAA) Gene and Characterization of Two Genomic Deletions. Genomics. 51(3). 463–467. 37 indexed citations
18.
Gasparini, Paolo, Marı́a Julia Calonge, Luigi Bisceglia, et al.. (1995). Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.. PubMed. 57(4). 781–8. 72 indexed citations
19.
Trabetti, Elisabetta, Roberta Galavotti, Elisabetta Zardini, et al.. (1993). The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphisms. Molecular and Cellular Probes. 7(4). 325–329. 10 indexed citations
20.
Martini, G. A., et al.. (1993). On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome. Prenatal Diagnosis. 13(8). 763–766. 14 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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