Rossella Caselli

1.2k total citations
20 papers, 796 citations indexed

About

Rossella Caselli is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Rossella Caselli has authored 20 papers receiving a total of 796 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Cognitive Neuroscience. Recurrent topics in Rossella Caselli's work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (4 papers). Rossella Caselli is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (4 papers). Rossella Caselli collaborates with scholars based in Italy, Israel and Germany. Rossella Caselli's co-authors include Francesca Mari, Alessandra Renieri, Chiara Pescucci, Ilaria Longo, Francesca Ariani, Joussef Hayek, Paolo Balestri, Salvatore Grosso, Maria Antonietta Mencarelli and Michele Zappella and has published in prestigious journals such as Kidney International, Human Molecular Genetics and Gene.

In The Last Decade

Rossella Caselli

20 papers receiving 775 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rossella Caselli Italy 15 607 401 139 99 68 20 796
Chiara Pescucci Italy 19 745 1.2× 692 1.7× 224 1.6× 119 1.2× 65 1.0× 37 1.3k
G.R. Sutherland Australia 16 355 0.6× 396 1.0× 110 0.8× 46 0.5× 28 0.4× 22 703
Tiina Alitalo Finland 20 332 0.5× 604 1.5× 47 0.3× 11 0.1× 48 0.7× 30 964
Martine Doco‐Fenzy France 15 302 0.5× 349 0.9× 44 0.3× 16 0.2× 80 1.2× 29 690
Pamela Magini Italy 16 349 0.6× 347 0.9× 35 0.3× 23 0.2× 53 0.8× 38 717
Roberto Ciccone Italy 23 956 1.6× 681 1.7× 82 0.6× 10 0.1× 283 4.2× 51 1.4k
Nienke Wieskamp Netherlands 7 531 0.9× 477 1.2× 38 0.3× 25 0.3× 41 0.6× 7 858
Donna M. Muzny United States 15 456 0.8× 551 1.4× 103 0.7× 6 0.1× 25 0.4× 20 854
Fabiola Quintero‐Rivera United States 16 907 1.5× 634 1.6× 83 0.6× 8 0.1× 357 5.3× 54 1.4k
Connie Schrander‐Stumpel Netherlands 18 472 0.8× 382 1.0× 108 0.8× 32 0.3× 132 1.9× 32 828

Countries citing papers authored by Rossella Caselli

Since Specialization
Citations

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

Fields of papers citing papers by Rossella Caselli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rossella Caselli

This figure shows the co-authorship network connecting the top 25 collaborators of Rossella Caselli. A scholar is included among the top collaborators of Rossella Caselli 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 Rossella Caselli. Rossella Caselli 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.
Santis, Maria De, Francesca Motta, Gabriele Todisco, et al.. (2024). Approaches for the diagnosis and treatment of VEXAS syndrome: the importance of clinical suspicion and the use of methotrexate. Annals of Hematology. 103(11). 4789–4791. 1 indexed citations
2.
Caselli, Rossella, Lucia Ballarati, Aglaia Vignoli, et al.. (2015). 7p22.1 microduplication syndrome: Clinical and molecular characterization of an adult case and review of the literature. European Journal of Medical Genetics. 58(11). 578–583. 7 indexed citations
3.
Recalcati, Maria Paola, Melissa Bellini, Lorenzo Norsa, et al.. (2012). Complex rearrangement involving 9p deletion and duplication in a syndromic patient: Genotype/phenotype correlation and review of the literature. Gene. 502(1). 40–45. 10 indexed citations
4.
Vignoli, Aglaia, Renato Borgatti, Angela Peron, et al.. (2012). Electroclinical pattern in MECP2 duplication syndrome: Eight new reported cases and review of literature. Epilepsia. 53(7). 1146–1155. 29 indexed citations
5.
Ballarati, Lucia, Anna Cereda, Rossella Caselli, et al.. (2011). Deletion of the AP1S2 gene in a child with psychomotor delay and hypotonia. European Journal of Medical Genetics. 55(2). 124–127. 8 indexed citations
6.
Ballarati, Lucia, Anna Cereda, Rossella Caselli, et al.. (2010). Genotype–phenotype correlations in a new case of 8p23.1 deletion and review of the literature. European Journal of Medical Genetics. 54(1). 55–59. 38 indexed citations
7.
Caselli, Rossella, Maria Antonietta Mencarelli, Filomena Tiziana Papa, et al.. (2008). Delineation of the phenotype associated with 7q36.1q36.2 deletion: Long QT syndrome, renal hypoplasia and mental retardation. American Journal of Medical Genetics Part A. 146A(9). 1195–1199. 19 indexed citations
8.
Uliana, Vera, N. Giordano, Rossella Caselli, et al.. (2008). Expanding the phenotype of 22q11 deletion syndrome: the MURCS association. Clinical Dysmorphology. 17(1). 13–17. 15 indexed citations
9.
Mencarelli, Maria Antonietta, Eleni Katzaki, Filomena Tiziana Papa, et al.. (2008). Private inherited microdeletion/microduplications: Implications in clinical practice. European Journal of Medical Genetics. 51(5). 409–416. 53 indexed citations
10.
Papa, Filomena Tiziana, Maria Antonietta Mencarelli, Rossella Caselli, et al.. (2008). A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett‐like features. American Journal of Medical Genetics Part A. 146A(15). 1994–1998. 47 indexed citations
11.
Caselli, Rossella, Maria Antonietta Mencarelli, Filomena Tiziana Papa, et al.. (2007). A 2.6 Mb deletion of 6q24.3–25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears. European Journal of Medical Genetics. 50(4). 315–321. 16 indexed citations
12.
Caselli, Rossella, Chiara Pescucci, Vera Uliana, et al.. (2007). Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH. Journal of Human Genetics. 52(6). 535–542. 19 indexed citations
13.
Mencarelli, Maria Antonietta, Rossella Caselli, Chiara Pescucci, et al.. (2007). Clinical and molecular characterization of a patient with a 2q31.2‐32.3 deletion identified by array‐CGH. American Journal of Medical Genetics Part A. 143A(8). 858–865. 34 indexed citations
14.
Pescucci, Chiara, Rossella Caselli, Salvatore Grosso, et al.. (2006). 2q24–q31 Deletion: Report of a case and review of the literature. European Journal of Medical Genetics. 50(1). 21–32. 61 indexed citations
15.
Pescucci, Chiara, Rossella Caselli, Francesca Mari, et al.. (2006). The Italian XLMR bank: a clinical and molecular database. Human Mutation. 28(1). 13–18. 1 indexed citations
16.
Sampieri, Katia, Ilaria Meloni, Francesca Ariani, et al.. (2006). Italian Rett database and biobank. Human Mutation. 28(4). 329–335. 25 indexed citations
17.
Mari, Francesca, Rossella Caselli, Silvia Russo, et al.. (2005). Germline mosaicism in Rett syndrome identified by prenatal diagnosis. Clinical Genetics. 67(3). 258–260. 21 indexed citations
18.
Longo, Ilaria, Francesca Mari, Rossella Caselli, et al.. (2005). Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families. Nephrology Dialysis Transplantation. 21(3). 665–671. 38 indexed citations
19.
Mari, Francesca, Ilaria Bertani, Fabrizio Bolognese, et al.. (2005). CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome. Human Molecular Genetics. 14(14). 1935–1946. 253 indexed citations
20.
Pescucci, Chiara, Francesca Mari, Ilaria Longo, et al.. (2004). Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene. Kidney International. 65(5). 1598–1603. 101 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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