Elena Bacchelli

9.9k total citations
28 papers, 791 citations indexed

About

Elena Bacchelli is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Elena Bacchelli has authored 28 papers receiving a total of 791 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 21 papers in Cognitive Neuroscience and 10 papers in Molecular Biology. Recurrent topics in Elena Bacchelli's work include Autism Spectrum Disorder Research (21 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Genomic variations and chromosomal abnormalities (12 papers). Elena Bacchelli is often cited by papers focused on Autism Spectrum Disorder Research (21 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Genomic variations and chromosomal abnormalities (12 papers). Elena Bacchelli collaborates with scholars based in Italy, United Kingdom and United States. Elena Bacchelli's co-authors include Elena Maestrini, Anthony Bailey, Francesca Blasi, Anthony P. Monaco, Sabine M. Klauck, Simona Carone, Kim S. Beyer, Annemarie Poustka, Elena Bonora and Agatino Battaglia and has published in prestigious journals such as Scientific Reports, Molecular Psychiatry and Oncotarget.

In The Last Decade

Elena Bacchelli

28 papers receiving 759 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elena Bacchelli Italy 16 512 383 343 96 72 28 791
SakkuBai Naidu United States 15 643 1.3× 354 0.9× 483 1.4× 87 0.9× 92 1.3× 18 991
Claudio Toma Spain 21 527 1.0× 359 0.9× 359 1.0× 153 1.6× 151 2.1× 41 1.0k
Seth Dobrin United States 8 441 0.9× 239 0.6× 372 1.1× 89 0.9× 80 1.1× 15 789
Virpi Leppä United States 9 542 1.1× 421 1.1× 645 1.9× 88 0.9× 66 0.9× 11 1.1k
Ralph Roeth Germany 11 573 1.1× 253 0.7× 545 1.6× 102 1.1× 34 0.5× 19 1.2k
Seda S. Tolu United States 9 421 0.8× 473 1.2× 349 1.0× 212 2.2× 30 0.4× 34 992
Vijayendran Chandran United States 11 542 1.1× 379 1.0× 709 2.1× 169 1.8× 26 0.4× 16 1.1k
Kirstine Ravn Denmark 19 541 1.1× 267 0.7× 606 1.8× 70 0.7× 52 0.7× 37 971
Holly N. Cukier United States 16 518 1.0× 403 1.1× 525 1.5× 147 1.5× 84 1.2× 26 1.0k
Barbara Manzi Italy 13 516 1.0× 633 1.7× 284 0.8× 57 0.6× 197 2.7× 17 979

Countries citing papers authored by Elena Bacchelli

Since Specialization
Citations

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

Fields of papers citing papers by Elena Bacchelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Bacchelli

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Bacchelli. A scholar is included among the top collaborators of Elena Bacchelli 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 Elena Bacchelli. Elena Bacchelli 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.
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
2.
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
3.
Bacchelli, Elena, et al.. (2020). An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Scientific Reports. 10(1). 3198–3198. 37 indexed citations
4.
Loi, Eleonora, Loredana Moi, Sylvain Blois, et al.. (2019). ELMOD3‐SH2D6 gene fusion as a possible co‐star actor in autism spectrum disorder scenario. Journal of Cellular and Molecular Medicine. 24(2). 2064–2069. 12 indexed citations
5.
Pippucci, Tommaso, Laura Licchetta, Sara Baldassari, et al.. (2019). Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies. Annals of Clinical and Translational Neurology. 6(3). 475–485. 10 indexed citations
6.
Bacchelli, Elena, Maria De Paola, Giuliano Giucastro, et al.. (2018). Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment. European Journal of Human Genetics. 26(12). 1824–1831. 15 indexed citations
7.
Bacchelli, Elena, Maria Michela Cainazzo, Simona Guérzoni, et al.. (2016). A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants. The Journal of Headache and Pain. 17(1). 114–114. 36 indexed citations
8.
Magini, Pamela, Monica Poscente, Simona Ferrari, et al.. (2015). Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration. Molecular Cytogenetics. 8(1). 58–58. 15 indexed citations
9.
Toma, Claudio, Bàrbara Torrico, Amaia Hervás, et al.. (2015). Common and rare variants of microRNA genes in autism spectrum disorders. The World Journal of Biological Psychiatry. 16(6). 376–386. 30 indexed citations
10.
Bacchelli, Elena, Agatino Battaglia, Raffaella Tancredi, et al.. (2015). Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility. American Journal of Medical Genetics Part A. 167(4). 715–723. 47 indexed citations
11.
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
12.
Holt, Richard, Gabrielle Barnby, Elena Maestrini, et al.. (2010). Linkage and candidate gene studies of autism spectrum disorders in European populations. European Journal of Human Genetics. 18(9). 1013–1019. 64 indexed citations
13.
Newbury, Dianne F., Elena Bacchelli, Simona Carone, et al.. (2009). Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment. American Journal of Medical Genetics Part A. 149A(4). 588–597. 19 indexed citations
14.
Bacchelli, Elena, Francesco Blasi, Simona Carone, et al.. (2006). A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus. American Journal of Medical Genetics Part A. 767–768. 1 indexed citations
15.
Blasi, Francesca, et al.. (2006). Absence of coding mutations in the X‐linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(3). 220–221. 70 indexed citations
16.
Bacchelli, Elena & Elena Maestrini. (2006). Autism spectrum disorders: Molecular genetic advances. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 142C(1). 13–23. 51 indexed citations
17.
Blasi, Francesca, Elena Bacchelli, Simona Carone, et al.. (2005). SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. European Journal of Human Genetics. 14(1). 123–126. 38 indexed citations
18.
Bacchelli, Elena, Francesco Blasi, Janine A. Lamb, et al.. (2003). Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. Molecular Psychiatry. 8(11). 916–924. 97 indexed citations
19.
Bonora, Elena, Elena Bacchelli, Elaine R. Levy, et al.. (2002). Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. Molecular Psychiatry. 7(3). 289–301. 32 indexed citations
20.
Beyer, Kim S., Francesca Blasi, Elena Bacchelli, et al.. (2002). Mutation analysis of the coding sequence of the MECP2 gene in infantile autism. Human Genetics. 111(4-5). 305–309. 67 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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