Rita Grasso

993 total citations
9 papers, 319 citations indexed

About

Rita Grasso is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rita Grasso has authored 9 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Rita Grasso's work include Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (3 papers) and Genomics and Rare Diseases (2 papers). Rita Grasso is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (3 papers) and Genomics and Rare Diseases (2 papers). Rita Grasso collaborates with scholars based in Italy, Netherlands and United Kingdom. Rita Grasso's co-authors include Renato Borgatti, María Clara Bonaglia, Maria Teresa Bassi, Nereo Bresolin, Maria Francesca Bedeschi, Umberto Balottin, Maja Di Rocco, Orsetta Zuffardi, Roberto Giorda and Susan Marelli and has published in prestigious journals such as European Journal of Human Genetics, American Journal of Medical Genetics and Research in Developmental Disabilities.

In The Last Decade

Rita Grasso

9 papers receiving 301 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rita Grasso Italy	8	139	133	102	34	26	9	319
Magdalena Budișteanu Romania	8	147 1.1×	40 0.3×	129 1.3×	35 1.0×	41 1.6×	46	299
Marianna Zazhytska Ukraine	4	107 0.8×	18 0.1×	134 1.3×	12 0.4×	41 1.6×	8	365
Lina Dom Belgium	6	65 0.5×	84 0.6×	94 0.9×	64 1.9×	12 0.5×	13	241
Lucia Pucci Italy	11	210 1.5×	54 0.4×	143 1.4×	18 0.5×	10 0.4×	21	286
Babett Heye Germany	7	206 1.5×	21 0.2×	147 1.4×	8 0.2×	48 1.8×	7	365
Valérie Nalesso France	9	253 1.8×	68 0.5×	368 3.6×	26 0.8×	45 1.7×	13	612
Sudheer Giddaluru Norway	9	73 0.5×	28 0.2×	73 0.7×	56 1.6×	26 1.0×	13	202
Ahm M. Huq United States	10	89 0.6×	27 0.2×	132 1.3×	39 1.1×	82 3.2×	16	319
Jin Szatkiewicz United States	11	220 1.6×	22 0.2×	125 1.2×	20 0.6×	40 1.5×	30	321
Stanley D. Handmaker United States	8	63 0.5×	188 1.4×	121 1.2×	23 0.7×	50 1.9×	11	429

Countries citing papers authored by Rita Grasso

Since Specialization

Citations

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

Fields of papers citing papers by Rita Grasso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Grasso

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

All Works

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9 of 9 papers shown

Bianchini, Rio, et al.. (2013). Prevalence of ADHD in a sample of Italian students: A population-based study. Research in Developmental Disabilities. 34(9). 2543–2550. 38 indexed citations

Giordano, Lucio, Maurizio Viri, Renato Borgatti, et al.. (2012). Seizures and EEG patterns in Pallister–Killian syndrome: 13 New Italian patients. European Journal of Paediatric Neurology. 16(6). 636–641. 9 indexed citations

Tonelli, A., Romina Romaniello, Rita Grasso, et al.. (2010). Novel splice‐site mutations and a large intragenic deletion in PLA2G6 associated with a severe and rapidly progressive form of infantile neuroaxonal dystrophy. Clinical Genetics. 78(5). 432–440. 28 indexed citations

Bonaglia, María Clara, Roberto Ciccone, Giorgio Gimelli, et al.. (2008). Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype. European Journal of Human Genetics. 16(12). 1443–1449. 75 indexed citations

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

Bedeschi, Maria Francesca, María Clara Bonaglia, Rita Grasso, et al.. (2006). Agenesis of the Corpus Callosum: Clinical and Genetic Study in 63 Young Patients. Pediatric Neurology. 34(3). 186–193. 114 indexed citations

Bonaglia, María Clara, Susan Marelli, Claudio Zucca, et al.. (2006). Subtelomeric trisomy 21q: A new benign chromosomal variant. European Journal of Medical Genetics. 50(1). 54–59. 8 indexed citations

Borgatti, Renato, Antonino Romeo, Maurizio Viri, et al.. (2003). Peripheral Markers of the γ-Aminobutyric Acid (GABA)ergic System in Angelman's Syndrome. Journal of Child Neurology. 18(1). 21–25. 7 indexed citations

Bonaglia, María Clara, Roberto Giorda, Romeo Carrozzo, et al.. (2002). 20‐Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: Narrowing of the 9p duplication critical region to 6 Mb. American Journal of Medical Genetics. 112(2). 154–159. 21 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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