Francesca Dulcetti

617 total citations
12 papers, 387 citations indexed

About

Francesca Dulcetti is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Plant Science. According to data from OpenAlex, Francesca Dulcetti has authored 12 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 3 papers in Plant Science. Recurrent topics in Francesca Dulcetti's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (3 papers). Francesca Dulcetti is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (3 papers). Francesca Dulcetti collaborates with scholars based in Italy, United States and Netherlands. Francesca Dulcetti's co-authors include Francesca Romana Grati, Giuseppe Simoni, Beatrice Grimi, Federico Maggi, Anna Ruggeri, Simona De Toffol, Cristina Agrati, Francesca Malvestiti, Elisa Gaetani and Komal Bajaj and has published in prestigious journals such as Genetics in Medicine, European Journal of Human Genetics and Prenatal Diagnosis.

In The Last Decade

Francesca Dulcetti

12 papers receiving 355 citations

Peers

Francesca Dulcetti

PPCH

GENET

PHEOH

Anna Ruggeri Italy

Cristina Agrati Italy

Pascale Kleinfinger France

Simona De Toffol Italy

Ana Bustamante‐Aragonés Spain

Celia Donaghue United Kingdom

Dan Diego‐Álvarez Spain

G. Heleen Schuring‐Blom Netherlands

Pamela Renwick United Kingdom

Cathy Sullivan United States

Anna Ruggeri Italy

Francesca Dulcetti

255 ×0.8

PPCH

197 ×1.0

GENET

76 ×0.9

122 ×1.5

27 ×0.9

PHEOH

Citations per year, relative to Francesca Dulcetti Francesca Dulcetti (= 1×) peers Anna Ruggeri

Countries citing papers authored by Francesca Dulcetti

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Dulcetti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Dulcetti

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

All Works

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12 of 12 papers shown

Grati, Francesca Romana, Francesca Malvestiti, José Carlos Ferreira, et al.. (2014). Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results. Genetics in Medicine. 16(8). 620–624. 144 indexed citations

Malvestiti, Francesca, Simona De Toffol, Beatrice Grimi, et al.. (2014). De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches. Prenatal Diagnosis. 34(5). 460–468. 17 indexed citations

Grati, Francesca Romana, Francesca Malvestiti, Beatrice Grimi, et al.. (2013). QF‐PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first‐trimester prenatal diagnoses. Prenatal Diagnosis. 33(5). 502–508. 14 indexed citations

Toffol, Simona De, Emilia Bellone, Francesca Dulcetti, et al.. (2010). Quantitative Fluorescence-Polymerase Chain Reaction Assay for the Detection of the Duplication of the Charcot Marie Tooth Disease Type 1A Critical Region. Genetic Testing and Molecular Biomarkers. 14(2). 225–231. 1 indexed citations

Grati, Francesca Romana, Beatrice Grimi, Silvia Milani, et al.. (2010). Chromosome abnormalities investigated by non‐invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes. American Journal of Medical Genetics Part A. 152A(6). 1434–1442. 41 indexed citations

Grati, Francesca Romana, Marci M. Lesperance, Simona De Toffol, et al.. (2009). Pure monosomy and pure trisomy of 13q21.2–31.1 consequent to a familial insertional translocation: Exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1). American Journal of Medical Genetics Part A. 149A(5). 906–913. 10 indexed citations

Grati, Francesca Romana, Beatrice Grimi, Simona De Toffol, et al.. (2008). Prenatal detection by subtelomeric FISH and MLPA of unbalanced meiotic recombinants resulting from parental pericentric inversions. Molecular and Cellular Probes. 22(5-6). 316–319. 3 indexed citations

Grati, Francesca Romana, Beatrice Grimi, Silvia Milani, et al.. (2006). Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi. European Journal of Human Genetics. 14(3). 282–288. 61 indexed citations

Grati, Francesca Romana, Faustina Lalatta, Licia Turolla, et al.. (2005). Three cases with de novo 6q imbalance and variable prenatal phenotype. American Journal of Medical Genetics Part A. 136A(3). 254–258. 18 indexed citations

10.

Ruggeri, Anna, Francesca Dulcetti, Monica Miozzo, et al.. (2004). Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations. Prenatal Diagnosis. 24(12). 997–1000. 33 indexed citations

11.

Grati, Francesca Romana, Silvia Maria Sirchia, Isabella Garagiola, et al.. (2000). Losses of Heterozygosity in Oral and Oropharyngeal Epithelial Carcinomas. Cancer Genetics and Cytogenetics. 118(1). 57–61. 24 indexed citations

12.

Sirchia, Silvia Maria, Elena Sironi, Francesca Romana Grati, et al.. (2000). Losses of Heterozygosity in Endometrial Adenocarcinomas. Cancer Genetics and Cytogenetics. 121(2). 156–162. 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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