Paola Grammatico

8.0k total citations
204 papers, 4.4k citations indexed

About

Paola Grammatico is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Paola Grammatico has authored 204 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Molecular Biology, 91 papers in Genetics and 30 papers in Oncology. Recurrent topics in Paola Grammatico's work include Connective tissue disorders research (31 papers), Genomic variations and chromosomal abnormalities (23 papers) and Cancer Genomics and Diagnostics (15 papers). Paola Grammatico is often cited by papers focused on Connective tissue disorders research (31 papers), Genomic variations and chromosomal abnormalities (23 papers) and Cancer Genomics and Diagnostics (15 papers). Paola Grammatico collaborates with scholars based in Italy, Lebanon and United States. Paola Grammatico's co-authors include Marco Castori, Claudia Celletti, Filippo Camerota, Silvia Morlino, Silvia Majore, F. Roccella, Marina Colombi, Mauro Picardo, Carmelilia De Bernardo and Giuseppe Del Porto and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Neurology.

In The Last Decade

Paola Grammatico

198 papers receiving 4.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Paola Grammatico Italy	34	1.9k	1.8k	696	584	448	204	4.4k
Marco Seri Italy	38	1.4k 0.7×	2.3k 1.3×	1.1k 1.5×	510 0.9×	323 0.7×	193	5.3k
Dirk Schnabel Germany	36	1.4k 0.7×	2.0k 1.1×	408 0.6×	509 0.9×	426 1.0×	120	4.8k
Yasuteru Muragaki Japan	43	1.1k 0.6×	3.4k 1.9×	750 1.1×	650 1.1×	550 1.2×	145	7.0k
Anna Spada Italy	46	1.4k 0.7×	2.6k 1.5×	1.2k 1.7×	600 1.0×	265 0.6×	172	7.0k
Rong Mao United States	35	1.0k 0.5×	1.8k 1.0×	538 0.8×	469 0.8×	238 0.5×	135	4.8k
Youngman Oh United States	46	1.1k 0.6×	3.9k 2.2×	472 0.7×	722 1.2×	346 0.8×	101	7.4k
Ralph S. Lachman United States	39	3.0k 1.6×	2.6k 1.5×	815 1.2×	722 1.2×	374 0.8×	181	5.5k
Riitta Herva Finland	39	1.3k 0.7×	3.4k 1.9×	872 1.3×	377 0.6×	289 0.6×	124	6.6k
Neil V. Morgan United Kingdom	42	1.0k 0.5×	3.0k 1.7×	407 0.6×	505 0.9×	469 1.0×	109	5.7k
Marina Colombi Italy	31	1.8k 1.0×	1.1k 0.6×	477 0.7×	478 0.8×	524 1.2×	181	3.7k

Countries citing papers authored by Paola Grammatico

Since Specialization

Citations

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

Fields of papers citing papers by Paola Grammatico

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paola Grammatico

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

Bottillo, Irene, Alessandro Sciarra, Giulio Bevilacqua, et al.. (2025). Early Detection of the Pathogenetic Variants of Homologous Recombination Repair Genes in Prostate Cancer: Critical Analysis and Experimental Design. Biology. 14(2). 117–117. 1 indexed citations

Bottillo, Irene, Luigi Laino, Alessia Azzarà, et al.. (2024). A pathogenic variant in the FLCN gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?. Frontiers in Neuroscience. 17. 1304080–1304080.

Colombo, Elisa Adele, Alessandro Orro, Silvia Majore, et al.. (2023). Germline NUP98 Variants in Two Siblings with a Rothmund–Thomson-Like Spectrum: Protein Functional Changes Predicted by Molecular Modeling. International Journal of Molecular Sciences. 24(4). 4028–4028. 3 indexed citations

Pascolini, Giulia, Emanuele Agolini, Antonio Novelli, Silvia Majore, & Paola Grammatico. (2020). The p.Arg377Trp variant in ACTL6A underlines a recognizable BAF‐opathy phenotype. Clinical Genetics. 97(4). 672–674. 3 indexed citations

Majore, Silvia, Emanuele Agolini, Lucia Micale, et al.. (2020). Clinical presentation and molecular characterization of a novel patient with variant POC1A ‐ related syndrome. Clinical Genetics. 99(4). 540–546. 9 indexed citations

Micale, Lucia, Silvia Morlino, Emanuele Agolini, et al.. (2020). Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia. Genes. 11(12). 1513–1513. 9 indexed citations

Lancioni, Hovirag, Roberta La Starza, Irene Cardinali, et al.. (2020). Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study. PLoS ONE. 15(10). e0240632–e0240632. 3 indexed citations

Morlino, Silvia, Annalucia Carbone, Marco Ritelli, et al.. (2019). TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis. Human Mutation. 40(10). 1886–1898. 4 indexed citations

D’Andrea, Elvira, Tyra Lagerberg, Corrado De Vito, et al.. (2018). Patient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia. European Journal of Human Genetics. 26(4). 518–526. 10 indexed citations

10.

Morlino, Silvia, Viola Alesi, Francesca Romana Lepri, et al.. (2018). LTBP2‐related “Marfan‐like” phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant. American Journal of Medical Genetics Part A. 179(1). 104–112. 15 indexed citations

11.

Majore, Silvia, Maria Carmela Bonaccorsi di Patti, Fabio Polticelli, et al.. (2017). Characterization of three novel pathogenic SLC40A1 mutations and genotype/phenotype correlations in 7 Italian families with type 4 hereditary hemochromatosis. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(2). 464–470. 7 indexed citations

12.

Castori, Marco, Chiara Dordoni, Silvia Morlino, et al.. (2015). Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers‐Danlos syndrome, hypermobility type. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 43–53. 29 indexed citations

13.

Castori, Marco, Silvia Morlino, Marco Ritelli, et al.. (2013). Late diagnosis of lateral meningocele syndrome in a 55‐year‐old woman with symptoms of joint instability and chronic musculoskeletal pain. American Journal of Medical Genetics Part A. 164(2). 528–534. 15 indexed citations

14.

Castori, Marco, et al.. (2009). Juvenile macular dystrophy and forearm pronation‐supination restriction presenting with features of distal arthrogryposis type 5. American Journal of Medical Genetics Part A. 149A(3). 482–486. 4 indexed citations

15.

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

16.

Tomaselli, Sara, Francesca Megiorni, Carmelilia De Bernardo, et al.. (2007). Syndromic true hermaphroditism due to an R-spondin1 ( RSPO1 ) homozygous mutation. Human Mutation. 29(2). 220–226. 117 indexed citations

17.

Cappellacci, Sandra, et al.. (2006). De novo pure 12q22q24.33 duplication: First report of a case with mental retardation, ADHD, and Dandy‐Walker malformation. American Journal of Medical Genetics Part A. 140A(11). 1203–1207. 12 indexed citations

18.

Parano, Enrico, Piero Pavone, R. R. Trifiletti, et al.. (2004). Fetal Cells in Maternal Blood: A Six-Fold Increase in Women who have Undergone Amniocentesis and Carry a Fetus with Down Syndrome: A Multicenter Study. Neuropediatrics. 35(6). 321–324. 7 indexed citations

19.

Tedde, Andrea, Francesca Vitelli, Franco Ammannati, et al.. (1996). Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin. Human Genetics. 97(5). 638–641. 19 indexed citations

20.

Grammatico, Paola, Susanna Scarpa, Katharina Steindl, et al.. (1991). Effect of azelaic acid on viability, ultrastructure and karyotype of melanoma cells in long-term culture. 4(1). 39–44. 2 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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