Edoardo Errichiello

923 total citations
37 papers, 319 citations indexed

About

Edoardo Errichiello is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Edoardo Errichiello has authored 37 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 19 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Edoardo Errichiello's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Edoardo Errichiello is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Edoardo Errichiello collaborates with scholars based in Italy, United States and Switzerland. Edoardo Errichiello's co-authors include Orsetta Zuffardi, Tiziana Venesio, Annalisa Vetro, Antonella Balsamo, Sabrina Giglio, Patrizia Morbini, Hugo de Jonge, Berardo Rinaldi, Teresa Mattina and Lucia Dora Notarangelo and has published in prestigious journals such as PLoS ONE, Frontiers in Immunology and The Journal of Pathology.

In The Last Decade

Edoardo Errichiello

36 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Edoardo Errichiello Italy	11	177	93	44	37	36	37	319
Yuri Uchiyama Japan	11	155 0.9×	84 0.9×	43 1.0×	38 1.0×	44 1.2×	52	400
Donatella Conconi Italy	11	178 1.0×	107 1.2×	62 1.4×	19 0.5×	21 0.6×	34	373
Maria Blazo United States	8	140 0.8×	91 1.0×	44 1.0×	20 0.5×	24 0.7×	13	386
Mamoru Ozaki Japan	12	152 0.9×	142 1.5×	59 1.3×	56 1.5×	23 0.6×	38	389
Yu Gyoung Tak United States	6	378 2.1×	151 1.6×	25 0.6×	32 0.9×	34 0.9×	6	509
Bin-Song Qiu China	7	243 1.4×	32 0.3×	57 1.3×	28 0.8×	60 1.7×	15	403
Jianzhi Zhao China	10	195 1.1×	38 0.4×	19 0.4×	37 1.0×	35 1.0×	13	332
Dmitry Penkov Russia	13	407 2.3×	79 0.8×	53 1.2×	13 0.4×	44 1.2×	27	556
Mio Kabata Japan	11	384 2.2×	50 0.5×	49 1.1×	15 0.4×	36 1.0×	16	491
Karl Vandepoele Belgium	12	256 1.4×	122 1.3×	12 0.3×	35 0.9×	35 1.0×	23	428

Countries citing papers authored by Edoardo Errichiello

Since Specialization

Citations

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

Fields of papers citing papers by Edoardo Errichiello

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edoardo Errichiello

This figure shows the co-authorship network connecting the top 25 collaborators of Edoardo Errichiello. A scholar is included among the top collaborators of Edoardo Errichiello 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 Edoardo Errichiello. Edoardo Errichiello 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

Ciccocioppo, Rachele, et al.. (2025). CTLA4 Alteration and Neurologic Manifestations: A New Family with Large Phenotypic Variability and Literature Review. Genes. 16(3). 306–306. 1 indexed citations

Luca, Antonina, Loretta Giuliano, Giuseppina Vitiello, et al.. (2024). Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements. Journal of Clinical Medicine. 13(4). 1109–1109.

Mauri, Lucia, Simone Gana, Alessandra Longo, et al.. (2024). Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract. Clinical Genetics. 106(4). 403–412. 2 indexed citations

Bedeschi, Maria Francesca, Claudia Izzi, Chiara Dordoni, et al.. (2023). Identification of bi‐allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3. Clinical Genetics. 104(2). 230–237. 1 indexed citations

Errichiello, Edoardo, Alessia Arossa, Angela Iasci, et al.. (2020). An additional piece in the TBX6 gene dosage model: A novel nonsense variant in a fetus with severe spondylocostal dysostosis. Clinical Genetics. 98(6). 628–629. 2 indexed citations

Errichiello, Edoardo, Roberto Giorda, Antonella Gambale, et al.. (2020). RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism. Molecular Genetics & Genomic Medicine. 9(1). e1561–e1561. 3 indexed citations

Todisco, Massimiliano, Simone Gana, Giuseppe Cosentino, et al.. (2020). KCTD17-related myoclonus-dystonia syndrome: clinical and electrophysiological findings of a patient with atypical late onset. Parkinsonism & Related Disorders. 78. 129–133. 5 indexed citations

Errichiello, Edoardo, Guido Zagnoli-Vieira, Romana Rizzi, et al.. (2020). Characterization of a novel loss-of-function variant in TDP2 in two adult patients with spinocerebellar ataxia autosomal recessive 23 (SCAR23). Journal of Human Genetics. 65(12). 1135–1141. 9 indexed citations

Errichiello, Edoardo, et al.. (2020). FANCA, TP53, and del(5q)/RPS14 alterations in a patient with T-cell non-Hodgkin lymphoma and concomitant Fanconi anemia and Li-Fraumeni syndrome. Cancer Genetics. 256-257. 179–183. 2 indexed citations

10.

Bossi, Grazia, Edoardo Errichiello, Orsetta Zuffardi, et al.. (2019). Disseminated Mycobacterium Avium Infection in a Child with Complete Interferon-γ Receptor 1 Deficiency due to Compound Heterozygosis of IFNGR1 for a Subpolymorphic Copy Number Variation and a Novel Splice-Site Variant. Journal of Pediatric Genetics. 9(3). 186–192. 6 indexed citations

11.

Andolfo, Immacolata, Gianluca De Rosa, Edoardo Errichiello, et al.. (2019). PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells. Frontiers in Physiology. 10. 258–258. 30 indexed citations

12.

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Maria Elisabeth Street, et al.. (2018). Prominent and elongated coccyx, a new manifestation of KBG syndrome associated with novel mutation in ANKRD11. American Journal of Medical Genetics Part A. 176(9). 1991–1995. 4 indexed citations

13.

Ivanovski, Ivan, Olivera Djurić, Stefano Giuseppe Caraffi, et al.. (2018). Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 34–34. 4 indexed citations

14.

Xumerle, Luciano, Ursula Giussani, Veronica Bertini, et al.. (2018). Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?. Molecular Genetics & Genomic Medicine. 7(2). e00496–e00496. 8 indexed citations

15.

Errichiello, Edoardo, Annalisa Vetro, Anita Wischmeijer, et al.. (2017). Whole exome sequencing in the differential diagnosis of Diamond-Blackfan anemia: Clinical and molecular study of three patients with novel RPL5 and mosaic RPS19 mutations. Blood Cells Molecules and Diseases. 64. 38–44. 9 indexed citations

16.

Cattaneo, Monica, Lucia La Sala, Maurizio Rondinelli, et al.. (2017). A donor splice site mutation in CISD2 generates multiple truncated, non-functional isoforms in Wolfram syndrome type 2 patients. BMC Medical Genetics. 18(1). 147–147. 11 indexed citations

17.

Errichiello, Edoardo, Francesca Novara, Annapia Verri, et al.. (2016). Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature. Molecular Cytogenetics. 9(1). 21–21. 18 indexed citations

18.

Marini, Simone, Ivan Limongelli, Ettore Rizzo, et al.. (2016). A Data Fusion Approach to Enhance Association Study in Epilepsy. PLoS ONE. 11(12). e0164940–e0164940. 3 indexed citations

19.

Gunetti, Monica, Simone Tomasi, Alessandro Giammò, et al.. (2012). Myogenic Potential of Whole Bone Marrow Mesenchymal Stem Cells In Vitro and In Vivo for Usage in Urinary Incontinence. PLoS ONE. 7(9). e45538–e45538. 37 indexed citations

20.

Gunetti, Monica, Alessio Noghero, Fabiola Molla, et al.. (2011). Ex vivo-expanded bone marrow CD34+ for acute myocardial infarction treatment: in vitro and in vivo studies. Cytotherapy. 13(9). 1140–1152. 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.

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