Giuseppina Vitiello

811 total citations
16 papers, 260 citations indexed

About

Giuseppina Vitiello is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Giuseppina Vitiello has authored 16 papers receiving a total of 260 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Giuseppina Vitiello's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Neonatal and fetal brain pathology (2 papers). Giuseppina Vitiello is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Neonatal and fetal brain pathology (2 papers). Giuseppina Vitiello collaborates with scholars based in Italy, United States and Saudi Arabia. Giuseppina Vitiello's co-authors include Achille Iolascon, Boris E. Shmukler, Carlo Brugnara, L. Michael Snyder, Francesco Manna, Seth L. Alper, Immacolata Andolfo, Roberta Russo, Gianluca De Rosa and Antonella Gambale and has published in prestigious journals such as The American Journal of Human Genetics, Digestive Diseases and Sciences and European Journal of Human Genetics.

In The Last Decade

Giuseppina Vitiello

15 papers receiving 259 citations

Peers

Countries citing papers authored by Giuseppina Vitiello

Since Specialization

Citations

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

Fields of papers citing papers by Giuseppina Vitiello

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuseppina Vitiello

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements 2024 ·Journal of Clinical Medicine ·(unknown), (unknown), (unknown), Antonina Luca, Loretta Giuliano, Giuseppina Vitiello, Edoardo Errichiello, Enza Maria Valente, Ennio Del Giudice, Giovanni Mostile, Renata Rizzo, Rita Barone	0
2	Inherited Unbalanced Reciprocal Translocation with 18p11.32p11.21 Tetrasomy and 9q34.3 Trisomy in a Fetus Revealed by Cell-Free Fetal DNA (cffDNA) Testing: Cytogenetic and Cytogenomic Characterization in Prenatal Diagnosis 2024 ·Genes ·(unknown), Luigia De Falco, Giovanni Savarese, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), M. Barbato, Giuseppina Vitiello, (unknown)	1
3	A Case Report of a Feto-Placental Mosaicism Involving a Segmental Aneuploidy: A Challenge for Genome Wide Screening by Non-Invasive Prenatal Testing of Cell-Free DNA in Maternal Plasma 2023 ·Genes ·Luigia De Falco, Giuseppina Vitiello, Giovanni Savarese, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Attilio Di Spiezio Sardo, (unknown)	2
4	Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum 2022 ·Genes ·(unknown), Laura Pignata, Giuseppina Vitiello, Viola Alesi, Gemma D’Elia, (unknown), Fabio Acquaviva, Daniele De Brasi, Antonio Novelli, Andrea Riccio, Achille Iolascon, Flavia Cerrato	2
5	Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 2022 ·European Journal of Paediatric Neurology ·(unknown), Maria Margherita Mancardi, Alfonso Romano, Margherita Santucci, Maria Cristina Scaduto, Maria Stella Vari, Pasquale Striano, Francesca Felicia Operto, Maurizio Elia, Giuseppina Vitiello, Ennio Del Giudice, Gaetano Terrone	3
6	De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity 2020 ·The American Journal of Human Genetics ·Francesca Cristofoli, (unknown), (unknown), Koenraad Devriendt, Heather Flanagan‐Steet, Melanie May, Julie R. Jones, Filip Roelens, Carmen Fons, (unknown), Loreto Martorell, Angelo Selicorni, Silvia Maitz, Giuseppina Vitiello, (unknown), Steven A. Skinner, Mathieu Bollen, Joris Vermeesch, Richard Steet, Hilde Van Esch	24
7	Multi-Gene Next-Generation Sequencing for Molecular Diagnosis of Autosomal Recessive Congenital Ichthyosis: A Genotype-Phenotype Study of Four Italian Patients 2020 ·Diagnostics ·(unknown), (unknown), Angelo Piccirillo, Giuseppina Vitiello, (unknown), Fabio Cattaneo, Rosario Ammendola, Gabriella Esposito	12
8	Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females 2019 ·European Journal of Human Genetics ·Marcello Scala, Annalaura Torella, Mariasavina Severino, Giovanni Morana, Raffaele Castello, Andrea Accogli, Antonio Verrico, Maria Stella Vari, Gerarda Cappuccio, Michele Pinelli, Giuseppina Vitiello, Gaetano Terrone, Alessandra D’Amico, Vincenzo Nigro, Valeria Capra	36
9	A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects 2017 ·European Journal of Paediatric Neurology ·Gaetano Terrone, Giuseppina Vitiello, Rita Genesio, Alessandra D’Amico, (unknown), Lorenzo Ugga, Teresa Giugliano, Giulio Piluso, Lucio Nitsch, Nicola Brunetti‐Pierri, Ennio Del Giudice	3
10	De novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia 2016 ·European Journal of Human Genetics ·Gaetano Terrone, Norine Voisin, Ali Abdullah Alfaiz, Gerarda Cappuccio, Giuseppina Vitiello, Nicolas Guex, Alessandra D’Amico, A. James Barkovich, Nicola Brunetti‐Pierri, Ennio Del Giudice, Alexandre Reymond	17
11	Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis) 2015 ·American Journal of Hematology ·Immacolata Andolfo, Roberta Russo, Francesco Manna, Boris E. Shmukler, Antonella Gambale, Giuseppina Vitiello, Gianluca De Rosa, Carlo Brugnara, Seth L. Alper, L. Michael Snyder, Achille Iolascon	71
12	De Novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver 2014 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·Novella Rapini, (unknown), (unknown), Giuseppina Vitiello, Chiara Grimaldi, Diana Postorivo, Anna Maria Nardone, Francesca Del Bufalo, Francesco Brancati, Maria Luisa Manca Bitti	3
13	Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype 2012 ·Neurogenetics ·Carlo Cosimo Quattrocchi, Ginevra Zanni, Antonio Napolitano, Daniela Longo, Duccio Maria Cordelli, Sabina Barresi, (unknown), Enza Maria Valente, Tommaso Verdolotti, Elisabetta Genovese, Nicola Specchio, Giuseppina Vitiello, Ronen Spiegel, Enrico Bertini, Bruno Bernardi	21
14	Epilepsy in inherited metabolic disorders: a pediatric series. 2012 ·PubMed ·Giuseppina Vitiello, (unknown), Roberto Della Casa, (unknown), (unknown), Antonia Pascarella, (unknown), Giancarlo Parenti, Ennio Del Giudice	6
15	Puzzle of protein complexesin vivo: a present and future challenge for functional proteomics 2009 ·Expert Review of Proteomics ·Maria Monti, (unknown), Flora Cozzolino, Giuseppina Vitiello, (unknown), Angela Flagiello, Piero Pucci	14
16	Abnormalities of gastrointestinal motility in children with nonulcer dyspepsia and in children with gastroesophageal reflux disease 1991 ·Digestive Diseases and Sciences ·Salvatore Cucchiara, M. Bortolotti, Carla Colombo, (unknown), Manuela De Stefano, Giuseppina Vitiello, Antonio Pagano, Andrea Ronchi, Salvatore Auricchio	45

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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