Rita Fischetto

2.5k total citations
33 papers, 837 citations indexed

About

Rita Fischetto is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rita Fischetto has authored 33 papers receiving a total of 837 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 17 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rita Fischetto's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Lysosomal Storage Disorders Research (4 papers) and Prenatal Screening and Diagnostics (4 papers). Rita Fischetto is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Lysosomal Storage Disorders Research (4 papers) and Prenatal Screening and Diagnostics (4 papers). Rita Fischetto collaborates with scholars based in Italy, Germany and United Kingdom. Rita Fischetto's co-authors include F Causio, Rosetta Lecce, Marcella Zollino, Angelo Selicorni, Luigi Memo, Giuseppe Capovilla, Giovanni Neri, Marina Murdolo, Francesca Faravelli and Maria Felicia Faienza and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Rita Fischetto

33 papers receiving 817 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rita Fischetto Italy 15 538 486 219 80 61 33 837
Cathy M. Tuck‐Müller United States 17 428 0.8× 515 1.1× 157 0.7× 167 2.1× 98 1.6× 37 855
Carolina Sismani Cyprus 19 735 1.4× 515 1.1× 266 1.2× 184 2.3× 38 0.6× 75 984
Zhenjuan Wang United States 7 474 0.9× 1.1k 2.3× 95 0.4× 103 1.3× 71 1.2× 9 1.3k
Jean‐Pierre Siffroi France 24 1.2k 2.2× 1.1k 2.2× 620 2.8× 173 2.2× 78 1.3× 70 2.0k
Rhonda E. Schnur United States 20 333 0.6× 505 1.0× 74 0.3× 37 0.5× 72 1.2× 52 919
Sandra Chantot‐Bastaraud France 24 939 1.7× 759 1.6× 404 1.8× 152 1.9× 40 0.7× 67 1.4k
Simon Quenneville Switzerland 14 416 0.8× 1.0k 2.1× 130 0.6× 191 2.4× 110 1.8× 17 1.1k
Anita S. Kulharya United States 14 452 0.8× 509 1.0× 147 0.7× 106 1.3× 64 1.0× 31 843
Fortunato Lonardo Italy 16 350 0.7× 258 0.5× 99 0.5× 53 0.7× 73 1.2× 52 645
Nicolas Gruchy France 15 328 0.6× 285 0.6× 137 0.6× 58 0.7× 69 1.1× 31 572

Countries citing papers authored by Rita Fischetto

Since Specialization
Citations

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

Fields of papers citing papers by Rita Fischetto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Fischetto

This figure shows the co-authorship network connecting the top 25 collaborators of Rita Fischetto. A scholar is included among the top collaborators of Rita Fischetto 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 Rita Fischetto. Rita Fischetto 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.
Toscano, António, Olimpia Musumeci, Michele Sacchini, et al.. (2023). Safety outcomes and patients’ preferences for home-based intravenous enzyme replacement therapy (ERT) in pompe disease and mucopolysaccharidosis type I (MPS I) disorder: COVID-19 and beyond. Orphanet Journal of Rare Diseases. 18(1). 338–338. 2 indexed citations
2.
Rollo, Valentina, Albina Tummolo, Patrizia Suppressa, et al.. (2022). Novel approach to idursulfase and laronidase desensitization in type 2 and type 1 S mucopolysaccharidosis (MPS). Orphanet Journal of Rare Diseases. 17(1). 402–402. 5 indexed citations
3.
4.
Fischetto, Rita, Maria Margherita Mancardi, Thea Giacomini, et al.. (2020). Substrate reduction therapy with Miglustat in pediatric patients with GM1 type 2 gangliosidosis delays neurological involvement: A multicenter experience. Molecular Genetics & Genomic Medicine. 8(10). e1371–e1371. 20 indexed citations
5.
Caciotti, Anna, Elena Procopio, Rita Fischetto, et al.. (2019). Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content. Scientific Reports. 9(1). 17684–17684. 9 indexed citations
6.
Carraro, Andrea, Elisa Benetti, Franz Schaefer, et al.. (2018). Could the interaction between LMX1B and PAX2 influence the severity of renal symptoms?. European Journal of Human Genetics. 26(11). 1708–1712. 6 indexed citations
7.
Palumbo, Orazio, Rita Fischetto, Pietro Palumbo, et al.. (2015). De novo microduplication of CHL1 in a patient with non-syndromic developmental phenotypes. Molecular Cytogenetics. 8(1). 66–66. 19 indexed citations
8.
Guerriero, Silvana, et al.. (2011). Autosomal Recessive Bestrophinopathy: New Observations on the Retinal Phenotype – Clinical and Molecular Report of an Italian Family. Ophthalmologica. 225(4). 228–235. 13 indexed citations
9.
Bertelloni, Silvano, Antonio Balsamo, Lucia Giordani, et al.. (2009). 17β-Hydroxysteroid dehydrogenase-3 deficiency: From pregnancy to adolescence. Journal of Endocrinological Investigation. 32(8). 666–670. 32 indexed citations
10.
Bliek, Jet, Gaetano Verde, Jonathan L A Callaway, et al.. (2008). Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome. European Journal of Human Genetics. 17(5). 611–619. 151 indexed citations
11.
Katzaki, Eleni, Chiara Pescucci, Vera Uliana, et al.. (2007). Clinical and molecular characterization of Italian patients affected by Cohen syndrome. Journal of Human Genetics. 52(12). 1011–1017. 19 indexed citations
12.
Gatta, Valentina, Ivana Antonucci, Elisena Morizio, et al.. (2006). Identification and characterization of different SHOX gene deletions in patients with Leri–Weill dyschondrosteosys by MLPA assay. Journal of Human Genetics. 52(1). 21–27. 27 indexed citations
13.
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
14.
Causio, F, et al.. (2002). 47,XX + mar karyotype containing genes from the azoospermia factor region. A case report.. PubMed. 47(7). 575–80. 1 indexed citations
15.
Causio, F, et al.. (2002). Chromosome analysis of spontaneous abortions after in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). European Journal of Obstetrics & Gynecology and Reproductive Biology. 105(1). 44–48. 40 indexed citations
16.
Sangiorgi, Eugenio, et al.. (2001). Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21. Clinical Genetics. 59(1). 28–36. 36 indexed citations
17.
Palka, Giandomenico, Liborio Stuppia, Paolo Guanciali Franchi, et al.. (2000). Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri–Weill dyschondrosteosis. Clinical Genetics. 57(6). 449–453. 11 indexed citations
18.
Calabrese, G, et al.. (1999). X/Y translocation in a family with Leri-Weill dyschondrosteosis. Human Genetics. 105(4). 367–368. 16 indexed citations
19.
Calabrese, G, et al.. (1999). X/Y translocation in a family with Leri-Weill dyschondrosteosis. Human Genetics. 105(4). 367–368. 2 indexed citations
20.
Fischetto, Rita, et al.. (1997). Pseudodiastrophic dysplasia type Burgio in a newborn. American Journal of Medical Genetics. 71(2). 222–225. 4 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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