Fabiola Ceroni

818 total citations
14 papers, 242 citations indexed

About

Fabiola Ceroni is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Fabiola Ceroni has authored 14 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Fabiola Ceroni's work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Fabiola Ceroni is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Fabiola Ceroni collaborates with scholars based in United Kingdom, Italy and United States. Fabiola Ceroni's co-authors include Nicola Ragge, Richard Holt, Elena Maestrini, Nicolas Chassaing, Julie Plaisancié, Patrick Calvas, Celia Zazo Seco, Dianne F. Newbury, Dalila Pinto and Nuala H. Simpson and has published in prestigious journals such as Nature Communications, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Fabiola Ceroni

14 papers receiving 241 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fabiola Ceroni United Kingdom	9	145	125	39	28	25	14	242
Amber Boys Australia	7	154 1.1×	143 1.1×	41 1.1×	35 1.3×	14 0.6×	10	281
Stefanie Beck‐Wödl Germany	13	102 0.7×	178 1.4×	11 0.3×	16 0.6×	55 2.2×	27	401
Haruka Shinohara Japan	7	69 0.5×	224 1.8×	31 0.8×	5 0.2×	13 0.5×	10	310
Ren-Hua Chung United States	6	173 1.2×	100 0.8×	111 2.8×	5 0.2×	20 0.8×	9	292
Sarah M. Guadiana United States	6	240 1.7×	203 1.6×	22 0.6×	24 0.9×	61 2.4×	7	347
Lars R. Jensen Germany	12	102 0.7×	253 2.0×	42 1.1×	4 0.1×	16 0.6×	32	395
Ivana Ricca Italy	10	123 0.8×	156 1.2×	55 1.4×	17 0.6×	26 1.0×	20	303
Nir Oksenberg United States	9	160 1.1×	334 2.7×	78 2.0×	9 0.3×	22 0.9×	12	462
Paramita Chatterjee United States	9	108 0.7×	183 1.5×	14 0.4×	8 0.3×	7 0.3×	16	294

Countries citing papers authored by Fabiola Ceroni

Since Specialization

Citations

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

Fields of papers citing papers by Fabiola Ceroni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabiola Ceroni

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

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

Ceroni, Fabiola, Richard Holt, Елена А. Сорокина, et al.. (2024). Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development. Nature Communications. 15(1). 9245–9245. 2 indexed citations

Ceroni, Fabiola, Paola Visconti, Annio Posar, et al.. (2024). Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. npj Genomic Medicine. 9(1). 21–21. 10 indexed citations

Kesim, Yeşim, Fabiola Ceroni, Fiona Blanco‐Kelly, et al.. (2023). Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia. European Journal of Human Genetics. 31(10). 1175–1180. 2 indexed citations

Ceroni, Fabiola, Samuel Clokie, Dorine A. Bax, et al.. (2022). Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia. European Journal of Human Genetics. 31(3). 353–359. 5 indexed citations

Posar, Annio, Paola Visconti, Maria Cristina Scaduto, et al.. (2022). Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility. Frontiers in Psychiatry. 13. 858238–858238. 9 indexed citations

Rochat, Magali Jane, Alessandra Maresca, Leonardo Caporali, et al.. (2021). An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder. Journal of Cellular and Molecular Medicine. 25(5). 2459–2470. 3 indexed citations

Farah, Carole A., Richard Holt, Fabiola Ceroni, et al.. (2020). Biallelic variants in the small optic lobe calpain CAPN15 are associated with congenital eye anomalies, deafness and other neurodevelopmental deficits. Human Molecular Genetics. 29(18). 3054–3063. 17 indexed citations

Plaisancié, Julie, Fabiola Ceroni, Richard Holt, et al.. (2019). Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia. Human Genetics. 138(8-9). 799–830. 55 indexed citations

Holt, Richard, Fabiola Ceroni, Dorine A. Bax, et al.. (2017). New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders. Scientific Reports. 7(1). 7975–7975. 11 indexed citations

10.

Preković, Stefan, Dušica Filipović Đurđević, Gábor Csifcsák, et al.. (2016). Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation. Scientific Reports. 6(1). 20369–20369. 7 indexed citations

11.

Simpson, Nuala H., Fabiola Ceroni, Laura Covill, et al.. (2015). Genome-wide analysis identifies a role for common copy number variants in specific language impairment. European Journal of Human Genetics. 23(10). 1370–1377. 35 indexed citations

12.

Ceroni, Fabiola, Nuala H. Simpson, Clyde Francks, et al.. (2014). Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. European Journal of Human Genetics. 22(10). 1165–1171. 18 indexed citations

13.

Bacchelli, Elena, Fabiola Ceroni, Dalila Pinto, et al.. (2014). A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. Journal of Neurodevelopmental Disorders. 6(1). 17–17. 37 indexed citations

14.

Ceroni, Fabiola, Nuala H. Simpson, Dianne F. Newbury, et al.. (2014). A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma. Autism Research. 7(2). 254–263. 31 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.

Explore authors with similar magnitude of impact