Francesca Crosti

1.5k total citations
40 papers, 884 citations indexed

About

Francesca Crosti is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Francesca Crosti has authored 40 papers receiving a total of 884 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 13 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Francesca Crosti's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Francesca Crosti is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Francesca Crosti collaborates with scholars based in Italy, United States and Canada. Francesca Crosti's co-authors include Giuseppe Leone, Ida Martinelli, Elena M. Faioni, Valerio De Stefano, Emanuela Taioli, Katia Paciaroni, Pier Mannuccio Mannucci, Valentina Rossi, Leda Dalprà and Elena Sala and has published in prestigious journals such as JAMA, Blood and PLoS ONE.

In The Last Decade

Francesca Crosti

39 papers receiving 832 citations

Peers

Francesca Crosti

HEMAT

GENET

PPCH

Christine Wittevrongel Belgium

Xiaohe Cai United States

Jacqueline M. Cale United States

Carly Selan Australia

Christelle Lecut Belgium

Nora Butta Spain

Nadja Bogdanova Germany

Susan L. Dagenais United States

Marie-Luise von Brühl Germany

Lev Khitin United States

Christine Wittevrongel Belgium

Francesca Crosti

241 ×0.9

397 ×1.5

HEMAT

13 ×0.1

175 ×0.9

GENET

38 ×0.3

PPCH

Citations per year, relative to Francesca Crosti Francesca Crosti (= 1×) peers Christine Wittevrongel

Countries citing papers authored by Francesca Crosti

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Crosti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Crosti

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

Villa, Nicoletta, Serena Redaelli, Stefania Farina, et al.. (2023). Genomic Complexity and Complex Chromosomal Rearrangements in Genetic Diagnosis: Two Illustrative Cases on Chromosome 7. Genes. 14(9). 1700–1700.

Milani, Donatella, Federica Alberti, Claudia Cesaretti, et al.. (2023). CATSHL syndrome, a new family and phenotypic expansion. Clinical Genetics. 105(3). 313–316. 1 indexed citations

Redaelli, Serena, Donatella Conconi, Elena Sala, et al.. (2022). Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region. International Journal of Molecular Sciences. 23(6). 3347–3347. 4 indexed citations

Redaelli, Serena, Donatella Conconi, Nicoletta Villa, et al.. (2020). Instability of Short Arm of Acrocentric Chromosomes: Lesson from Non-Acrocentric Satellited Chromosomes. Report of 24 Unrelated Cases. International Journal of Molecular Sciences. 21(10). 3431–3431. 2 indexed citations

Redaelli, Serena, Silvia Maitz, Francesca Crosti, et al.. (2019). Refining the Phenotype of Recurrent Rearrangements of Chromosome 16. International Journal of Molecular Sciences. 20(5). 1095–1095. 28 indexed citations

Conconi, Donatella, Nicoletta Villa, Serena Redaelli, et al.. (2018). Familiar unbalanced complex rearrangements involving 13 p-arm: description of two cases. Molecular Cytogenetics. 11(1). 52–52. 1 indexed citations

Paccagnini, S., Elena Pozzi, Luigina Spaccini, et al.. (2018). Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 59–59. 1 indexed citations

Villa, Nicoletta, Donatella Conconi, Gianluca Tornese, et al.. (2017). A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning. Molecular Cytogenetics. 10(1). 22–22. 2 indexed citations

Baronchelli, Simona, Donatella Conconi, Elena Panzeri, et al.. (2011). Cytogenetics of Premature Ovarian Failure: An Investigation on 269 Affected Women. BioMed Research International. 2011(1). 370195–370195. 44 indexed citations

10.

Marinari, Barbara, Costanza Ballarò, Maranke I. Koster, et al.. (2008). IKKα Is a p63 Transcriptional Target Involved in the Pathogenesis of Ectodermal Dysplasias. Journal of Investigative Dermatology. 129(1). 60–69. 32 indexed citations

11.

Combi, Romina, Elena Sala, Nicoletta Villa, et al.. (2008). Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver–Russell syndrome. Clinical Dysmorphology. 17(1). 35–39. 4 indexed citations

12.

Villa, Nicoletta, Serena Redaelli, Angela Bentivegna, et al.. (2007). X;Y translocations and POF. Chromosome Research. 15. 67–67. 2 indexed citations

13.

Redaelli, Serena, Elena Sala, Nadia Roncaglia, et al.. (2005). Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature. Prenatal Diagnosis. 25(2). 140–147. 26 indexed citations

14.

Riva, Paola, Francesca Crosti, Francesca Orzan, et al.. (2003). Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis. International Journal of Cancer. 107(3). 493–497. 46 indexed citations

15.

Villa, Nicoletta, Paola Riva, Desirée Colombo, et al.. (2001). Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis. Prenatal Diagnosis. 21(10). 801–805. 9 indexed citations

16.

Ferrarese, Carlo, Lucio Tremolizzo, Miriam Rigoldi, et al.. (2001). Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease. Neurological Sciences. 22(1). 65–66. 28 indexed citations

17.

Scarı̀, Giorgio, Francesca Crosti, & Maurizio Francesco Brivio. (1995). The Role of the Cytotoxic Haemocytes (LGC) of Musca domestica. Journal of Experimental & Clinical Cancer Research. 14(1). 49–52. 3 indexed citations

18.

Morandi, Lucía, Pia Bernasconi, Marinella Gebbia, et al.. (1995). Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transfer. Neuromuscular Disorders. 5(4). 291–295. 49 indexed citations

19.

Zocchi, Maria Raffaella, et al.. (1992). Signalling in human tumour infiltrating lymphocytes: The CD28 molecule is functional and is physically associated with the CD45R0 molecule. European Journal of Cancer. 28(4-5). 749–754. 7 indexed citations

20.

Secchi, Antonio, et al.. (1989). Impairment of lymphocyte suppressive system in recent onset insulin-dependent diabetes mellitus. correlation with blood glucose and serum insulin levels. Acta Diabetologica. 26(3). 257–263. 1 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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