Angelo Selicorni

1.4k total citations
14 papers, 584 citations indexed

About

Angelo Selicorni is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Angelo Selicorni has authored 14 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in Angelo Selicorni's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Angelo Selicorni is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Angelo Selicorni collaborates with scholars based in Italy, United States and Germany. Angelo Selicorni's co-authors include Marcella Zollino, Giovanni Neri, Rosetta Lecce, Marina Murdolo, Luigi Memo, Giuseppe Capovilla, Rita Fischetto, Francesca Faravelli, Silvana Guerneri and Orsetta Zuffardi and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Angelo Selicorni

14 papers receiving 559 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Angelo Selicorni Italy	10	474	322	221	161	41	14	584
Marina Murdolo Italy	13	491 1.0×	383 1.2×	171 0.8×	146 0.9×	29 0.7×	20	663
Kathrin S. Precht United States	5	501 1.1×	296 0.9×	247 1.1×	146 0.9×	38 0.9×	6	606
Sophie Brisset France	16	378 0.8×	194 0.6×	133 0.6×	183 1.1×	52 1.3×	39	585
N. M. Lawrie United Kingdom	6	451 1.0×	281 0.9×	244 1.1×	128 0.8×	23 0.6×	7	565
Roberta Santos Guilherme Brazil	14	426 0.9×	213 0.7×	194 0.9×	146 0.9×	16 0.4×	26	512
Emily A. Rorem United States	8	698 1.5×	260 0.8×	232 1.0×	409 2.5×	20 0.5×	9	774
Hiba Risheg United States	10	403 0.9×	374 1.2×	53 0.2×	164 1.0×	28 0.7×	13	640
Viv Maloney United Kingdom	14	453 1.0×	256 0.8×	135 0.6×	119 0.7×	57 1.4×	18	587
T. Lukusa Belgium	10	287 0.6×	214 0.7×	89 0.4×	70 0.4×	29 0.7×	32	397
M. S. NEWTON United Kingdom	14	536 1.1×	363 1.1×	310 1.4×	209 1.3×	20 0.5×	23	793

Countries citing papers authored by Angelo Selicorni

Since Specialization

Citations

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

Fields of papers citing papers by Angelo Selicorni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angelo Selicorni

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

All Works

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14 of 14 papers shown

Pasquali, Daniela, Annalaura Torella, Anna Grandone, et al.. (2022). Patients with DeSanto–Shinawi syndrome: Further extension of phenotype from Italy. American Journal of Medical Genetics Part A. 191(3). 823–830. 1 indexed citations

Verrottı, Alberto, Salvatore Savasta, Marco Carotenuto, et al.. (2018). Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications. Acta Neurologica Scandinavica. 138(6). 523–530. 9 indexed citations

Kaur, Maninder, Alessandro Rocca, G Cocchi, et al.. (2018). Prenatal profile of Pallister‐Killian syndrome: Retrospective analysis of 114 pregnancies, literature review and approach to prenatal diagnosis. American Journal of Medical Genetics Part A. 176(12). 2575–2586. 17 indexed citations

Nacinovich, Renata, Nicoletta Villa, Serena Redaelli, et al.. (2014). Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review. BMC Research Notes. 7(1). 248–248. 9 indexed citations

Righini, Andrea, Angelo Selicorni, Elena Bianchini, et al.. (2007). Brain Magnetic Resonance Imaging in Wolf-Hirschhorn Syndrome. Neuropediatrics. 38(1). 25–28. 13 indexed citations

Zollino, Marcella, Rosetta Lecce, Angelo Selicorni, et al.. (2004). A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf–Hirschhorn syndrome. European Journal of Human Genetics. 12(10). 797–804. 25 indexed citations

Zollino, Marcella, Rosetta Lecce, Rita Fischetto, et al.. (2003). Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2. The American Journal of Human Genetics. 72(3). 590–597. 156 indexed citations

Giglio, Sabrina, Vladimiro Calvari, Giuliana Gregato, et al.. (2002). Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation. The American Journal of Human Genetics. 71(2). 276–285. 160 indexed citations

Selicorni, Angelo, Silvana Guerneri, Antonia Ratti, & Antonio Pizzuti. (2001). Cytogenetic mapping of a novel locus for type II Waardenburg syndrome. Human Genetics. 110(1). 64–67. 16 indexed citations

10.

Zollino, Marcella, Cristina Di Stefano, Giuseppe Zampino, et al.. (2000). Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome. American Journal of Medical Genetics. 94(3). 254–261. 125 indexed citations

11.

Selicorni, Angelo, et al.. (2000). Malpuech Syndrome: A Possible Relationship With the Wolf‐Hirschhorn/Pitt‐Roger‐Danks Phenotype. American Journal of Medical Genetics. 95(3). 291–291. 1 indexed citations

12.

Turco, Alberto, Bernard Peissel, Sandro Rossetti, et al.. (1993). Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disese and autosomal recessive junctional epidermolysis bullosa with pyloric atresia. American Journal of Medical Genetics. 47(8). 1225–1230. 4 indexed citations

13.

Dallapiccola, Bruno, Paola Mandich, Emilia Bellone, et al.. (1993). Parental origin of chromosome 4p deletion in Wolf‐Hirschhorn syndrome. American Journal of Medical Genetics. 47(6). 921–924. 37 indexed citations

14.

Floridia, Giovanna, et al.. (1993). Trisomy 10qter confirmed by in situ hybridisation.. Journal of Medical Genetics. 30(7). 601–603. 11 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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