Federica Consoli

1.3k total citations
21 papers, 497 citations indexed

About

Federica Consoli is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Federica Consoli has authored 21 papers receiving a total of 497 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Federica Consoli's work include Genetic Neurodegenerative Diseases (8 papers), Genetic Syndromes and Imprinting (4 papers) and Congenital heart defects research (4 papers). Federica Consoli is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Genetic Syndromes and Imprinting (4 papers) and Congenital heart defects research (4 papers). Federica Consoli collaborates with scholars based in Italy, United Kingdom and Argentina. Federica Consoli's co-authors include Alessandro De Luca, Bruno Dallapiccola, Bruno Marino, Rosangela Ferese, M. Cristina Digilio, Valentina Guida, Simona Petrucci, Laura Bernardini, Enza Maria Valente and Anna Sárközy and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Lancet Neurology and International Journal of Molecular Sciences.

In The Last Decade

Federica Consoli

21 papers receiving 482 citations

Peers

Federica Consoli

EPIDE

GENET

CMN

NEURO

Gemma García‐Fructuoso Spain

Dominique J. Verlaan Canada

H. Grehl Germany

Tara Newcomb United States

Vicki Fabian Australia

Hai Jin China

Kenneth G. Kupke United States

Kate Sinclair Australia

Priya Shanmugarajah United Kingdom

Claudia Castiglioni Chile

Gemma García‐Fructuoso Spain

Federica Consoli

104 ×0.3

70 ×0.4

EPIDE

120 ×0.8

GENET

98 ×0.8

CMN

64 ×0.6

NEURO

Citations per year, relative to Federica Consoli Federica Consoli (= 1×) peers Gemma García‐Fructuoso

Countries citing papers authored by Federica Consoli

Since Specialization

Citations

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

Fields of papers citing papers by Federica Consoli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Federica Consoli

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

Esposito, Marcello, et al.. (2023). A novel ANO3 variant in two siblings with different phenotypes. Parkinsonism & Related Disorders. 111. 105413–105413. 1 indexed citations

Luca, Alessandro De, et al.. (2021). A Novel Triplet-Primed PCR Assay to Detect the Full Range of Trinucleotide CAG Repeats in the Huntingtin Gene (HTT). International Journal of Molecular Sciences. 22(4). 1689–1689. 11 indexed citations

Ferrari, Daniela, Marina Goldoni, Laura Bernardini, et al.. (2019). Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA). Stem Cell Research. 40. 101551–101551. 8 indexed citations

Ferrari, Daniela, Laura Bernardini, Federica Consoli, et al.. (2018). Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's Disease. Stem Cell Research. 29. 174–178. 1 indexed citations

Ferrari, Daniela, Laura Bernardini, Federica Consoli, et al.. (2018). Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage. Stem Cell Research. 28. 145–148. 6 indexed citations

Rosati, Jessica, Daniela Ferrari, Bárbara Torres, et al.. (2018). Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease. Stem Cell Research. 27. 86–89. 3 indexed citations

Fusilli, Caterina, Simone Migliore, Tommaso Mazza, et al.. (2018). Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis. The Lancet Neurology. 17(11). 986–993. 96 indexed citations

Ferese, Rosangela, Monica Bonetti, Federica Consoli, et al.. (2018). Heterozygous missense mutations inNFATC1are associated with atrioventricular septal defect. Human Mutation. 39(10). 1428–1441. 14 indexed citations

Marano, Massimo, Francesco Motolese, Federica Consoli, Alessandro De Luca, & Vincenzo Di Lazzaro. (2018). Paroxysmal Dyskinesias in a <i>PRRT2</i> Mutation Carrier. Tremor and Other Hyperkinetic Movements. 8(0). 616–616. 2 indexed citations

10.

Margiotti, Katia, Giulia Pascolini, Federica Consoli, et al.. (2017). Lack of pathogenic mutations in SOS1 gene in phenytoin-induced gingival overgrowth patients. Archives of Oral Biology. 80. 160–163. 2 indexed citations

11.

Niceta, Marcello, Katia Margiotti, M. Cristina Digilio, et al.. (2017). Biallelic mutations in DYNC2LI1 are a rare cause of Ellis‐van Creveld syndrome. Clinical Genetics. 93(3). 632–639. 19 indexed citations

12.

Nicita, Francesco, Giacomo Garone, Laura Papetti, et al.. (2015). Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy. Journal of Neurogenetics. 29(4). 178–182. 1 indexed citations

13.

Petrucci, Simona, Federica Consoli, & Enza Maria Valente. (2014). Parkinson Disease Genetics: A “Continuum” from Mendelian to Multifactorial Inheritance. Current Molecular Medicine. 14(8). 1079–1088. 26 indexed citations

14.

Elia, Antonio Emanuele, Simona Petrucci, Alfonso Fasano, et al.. (2013). Alpha‐synuclein gene duplication: Marked intrafamilial variability in two novel pedigrees. Movement Disorders. 28(6). 813–817. 29 indexed citations

15.

Torrente, Isabella, Federica Consoli, Rosangela Ferese, et al.. (2012). Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis. European Journal of Medical Genetics. 56(2). 80–87. 49 indexed citations

16.

Digilio, M. Cristina, Laura Bernardini, Federica Consoli, et al.. (2012). Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: Rare association with pulmonary valve stenosis. European Journal of Medical Genetics. 56(3). 144–149. 47 indexed citations

17.

Ludwig, Kathrin, Marco Pizzi, Matteo Fassan, et al.. (2012). “Double Trouble” or an Amplification of the Triploidy Phenotype?. Fetal and Pediatric Pathology. 32(1). 60–65. 2 indexed citations

18.

Consoli, Federica, Victoria Villegas, Valeria Maddaloni, et al.. (2011). Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects. European Journal of Medical Genetics. 54(3). 306–309. 34 indexed citations

19.

Luca, Alessandro De, Anna Sárközy, Rosangela Ferese, et al.. (2010). New mutations inZFPM2/FOG2gene in tetralogy of Fallot and double outlet right ventricle. Clinical Genetics. 80(2). 184–190. 59 indexed citations

20.

Luca, Alessandro De, Anna Sárközy, Federica Consoli, et al.. (2009). Familial transposition of the great arteries caused by multiple mutations in laterality genes. Heart. 96(9). 673–677. 85 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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