Marina Grasso

1.4k total citations
40 papers, 739 citations indexed

About

Marina Grasso is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marina Grasso has authored 40 papers receiving a total of 739 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 19 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marina Grasso's work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Prenatal Screening and Diagnostics (8 papers). Marina Grasso is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Prenatal Screening and Diagnostics (8 papers). Marina Grasso collaborates with scholars based in Italy, United States and Netherlands. Marina Grasso's co-authors include Cristiana Lo Nigro, A. Morelli, L Perroni, Andrea Menegon, Anurag Tandon, Ági K. Gedeon, Daniela Toniolo, T. Bienvenu, Massimo Gulisano and Filippo Tamanini and has published in prestigious journals such as Nature Genetics, Blood and PLoS ONE.

In The Last Decade

Marina Grasso

39 papers receiving 705 citations

Peers

Marina Grasso

GENET

PPCH

Alexandra Afenjar France

Anneke T. Vulto-van Silfhout Netherlands

Amy Yang United States

Ute Grasshoff Germany

Karen Buysse Belgium

Daniela Orteschi Italy

Lysanne Patry Canada

Thessa Kroes Netherlands

Monika Cohen Germany

Isabelle Maystadt Belgium

Alexandra Afenjar France

Marina Grasso

621 ×1.4

GENET

521 ×1.4

96 ×0.6

69 ×0.6

113 ×1.4

PPCH

Citations per year, relative to Marina Grasso Marina Grasso (= 1×) peers Alexandra Afenjar

Countries citing papers authored by Marina Grasso

Since Specialization

Citations

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

Fields of papers citing papers by Marina Grasso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Grasso

This figure shows the co-authorship network connecting the top 25 collaborators of Marina Grasso. A scholar is included among the top collaborators of Marina 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 Marina Grasso. Marina 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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20 of 20 papers shown

Conteduca, Giuseppina, Marina Grasso, Maurizio Cecconi, et al.. (2023). Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome. Genes. 14(2). 295–295. 9 indexed citations

Pezzani, Lidia, Lucia Mauri, Angelo Selicorni, et al.. (2020). Aortic dilation in Sotos syndrome: An underestimated feature?. American Journal of Medical Genetics Part A. 182(7). 1819–1823. 6 indexed citations

Fontana, Paolo, Marina Grasso, Fabio Acquaviva, et al.. (2017). SNORD116 deletions cause Prader‐Willi syndrome with a mild phenotype and macrocephaly. Clinical Genetics. 92(4). 440–443. 34 indexed citations

Gatta, Valentina, Elena Di Gennaro, Sara Franchi, et al.. (2013). MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting. BMC Medical Genetics. 14(1). 79–79. 9 indexed citations

Piccione, Maria, Gregorio Serra, Simona Cavani, et al.. (2012). 14q13.1‐21.1 deletion encompassing the HPE8 locus in an adolescent with intellectual disability and bilateral microphthalmia, but without holoprosencephaly. American Journal of Medical Genetics Part A. 158A(6). 1427–1433. 28 indexed citations

Piccione, Maria, et al.. (2011). Deletion of NSD1 exon 14 in Sotos syndrome: first description. Journal of Genetics. 90(1). 119–123. 5 indexed citations

Piccione, Maria, Vincenzo Antona, Michela Malacarne, et al.. (2010). Array CGH defined interstitial deletion on chromosome 14: a new case. European Journal of Pediatrics. 169(7). 845–851. 8 indexed citations

Falbo, Vincenzo, Giovanna Floridia, Federica Censi, et al.. (2008). The Italian External Quality Assessment Scheme for Fragile X Syndrome: The Results of a 5-Year Survey. Genetic Testing. 12(2). 279–288. 10 indexed citations

Cecconi, Maurizio, Francesca Forzano, Rosanna Rinaldi, et al.. (2008). A Single Nucleotide Variant in the FMR1 CGG Repeat Results in a “Pseudodeletion” and Is Not Associated with the Fragile X Syndrome Phenotype. Journal of Molecular Diagnostics. 10(3). 272–275. 4 indexed citations

10.

Cecconi, Maurizio, Francesca Forzano, Livia Garavelli, et al.. (2008). Recurrence of Mowat–Wilson syndrome in siblings with a novel mutation in the ZEB2 gene. American Journal of Medical Genetics Part A. 146A(23). 3095–3099. 18 indexed citations

11.

Viassolo, Valeria, Stefano C. Previtali, Giuseppe Magnani, et al.. (2008). Inclusion body myopathy, Paget’s disease of the bone and frontotemporal dementia: recurrence of the VCP R155H mutation in an Italian family and implications for genetic counselling. Clinical Genetics. 74(1). 54–60. 31 indexed citations

12.

Bricarelli, F. Dagna, M. Pierluigi, Marina Grasso, Paolo Strigini, & L Perroni. (2005). Origin of extra chromosome 21 in 343 families: Cytogenetic and molecular approaches. American Journal of Medical Genetics. 37(S7). 129–132. 3 indexed citations

13.

Perroni, L, F. Dagna Bricarelli, Marina Grasso, et al.. (2005). Crossing over and chromosome 21 nondisjunction: A study of 60 families. American Journal of Medical Genetics. 37(S7). 141–147.

14.

Nigro, Cristiana Lo, Francesca Faravelli, Simona Cavani, et al.. (2000). FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother. European Journal of Human Genetics. 8(3). 157–162. 6 indexed citations

15.

D’Adamo, Patrizia, Andrea Menegon, Cristiana Lo Nigro, et al.. (1998). Mutations in GDI1 are responsible for X-linked non-specific mental retardation. Nature Genetics. 19(2). 134–139. 264 indexed citations

16.

Grasso, Marina, L Perroni, Stefano Colella, et al.. (1996). Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome. American Journal of Medical Genetics. 64(1). 187–190. 3 indexed citations

17.

Chiurazzi, Pietro, Maurizio Genuardi, Libor Kozák, et al.. (1996). Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity. American Journal of Medical Genetics. 64(1). 209–215. 36 indexed citations

18.

Grasso, Marina, L Perroni, Franca Dagna‐Bricarelli, et al.. (1996). Premutation for the Martin-Bell syndrome analyzed in a large Sardinian family: III. Molecular analysis with the StB12.3 probe. American Journal of Medical Genetics. 64(2). 283–286. 1 indexed citations

19.

Grasso, Marina, et al.. (1989). Isochromosome not translocation in trisomy 21q21q. Human Genetics. 84(1). 63–65. 32 indexed citations

20.

Bricarelli, F. Dagna, et al.. (1988). High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms. Human Genetics. 79(2). 124–127. 17 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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