Andrea Accogli

2.4k total citations
65 papers, 771 citations indexed

About

Andrea Accogli is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andrea Accogli has authored 65 papers receiving a total of 771 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 28 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andrea Accogli's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genomics and Rare Diseases (9 papers). Andrea Accogli is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genomics and Rare Diseases (9 papers). Andrea Accogli collaborates with scholars based in Italy, Canada and United States. Andrea Accogli's co-authors include Valeria Capra, Myriam Srour, Marco Pavanello, Mariasavina Severino, Marcello Scala, Armando Cama, Gianluca Piatelli, Alberto Martini, Antonella Buoncompagni and Sabrina Chiesa and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

Andrea Accogli

62 papers receiving 749 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrea Accogli Italy 17 322 217 116 115 85 65 771
Isabella Torrente Italy 19 414 1.3× 228 1.1× 66 0.6× 54 0.5× 68 0.8× 48 874
Lauren Massingham United States 8 365 1.1× 295 1.4× 57 0.5× 110 1.0× 54 0.6× 19 845
Sachiko Nishina Japan 20 533 1.7× 230 1.1× 89 0.8× 112 1.0× 103 1.2× 82 1.2k
Pagon Ra United States 6 450 1.4× 260 1.2× 55 0.5× 49 0.4× 82 1.0× 291 791
Seher Başaran Türkiye 17 278 0.9× 305 1.4× 90 0.8× 215 1.9× 97 1.1× 73 814
Annalaura Torella Italy 18 697 2.2× 286 1.3× 60 0.5× 71 0.6× 103 1.2× 77 983
Joy B. Redman United States 17 301 0.9× 203 0.9× 31 0.3× 71 0.6× 119 1.4× 27 781
Cathy A. Stevens United States 21 467 1.5× 522 2.4× 352 3.0× 148 1.3× 50 0.6× 52 1.3k
Raoul Heller Germany 20 1.1k 3.3× 374 1.7× 329 2.8× 90 0.8× 83 1.0× 37 1.5k
Heidrun Holland Germany 18 304 0.9× 91 0.4× 226 1.9× 61 0.5× 33 0.4× 44 872

Countries citing papers authored by Andrea Accogli

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Accogli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Accogli

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Accogli. A scholar is included among the top collaborators of Andrea Accogli 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 Andrea Accogli. Andrea Accogli 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.
Schoch, Kelly, Sabine Uhrig, Saskia Biskup, et al.. (2024). A second hotspot for pathogenic exon-skipping variants in CDC45. European Journal of Human Genetics. 32(7). 786–794. 1 indexed citations
2.
Calevo, Maria Grazia, Anna Elsa Maria Allegri, Flavia Napoli, et al.. (2022). Clinical, Endocrine and Neuroimaging Findings in Girls With Central Precocious Puberty. The Journal of Clinical Endocrinology & Metabolism. 107(10). e4132–e4143. 5 indexed citations
3.
Severino, Mariasavina, Domenico Tortora, Sarà Uccella, et al.. (2022). Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts. Neuroradiology. 64(11). 2163–2177. 3 indexed citations
4.
Giacomini, Thea, Marcello Scala, Giulia Nobile, et al.. (2022). De novo POLR2A p.(Ile457Thr) variant associated with early-onset encephalopathy and cerebellar atrophy: expanding the phenotypic spectrum. Brain and Development. 44(7). 480–485. 4 indexed citations
5.
Accogli, Andrea, Christine Saint‐Martin, Irma López, et al.. (2021). PCDH12 variants are associated with basal ganglia anomalies and exudative vitreoretinopathy. European Journal of Medical Genetics. 65(2). 104405–104405. 3 indexed citations
6.
Imbrici, Paola, Andrea Accogli, Rikard Blunck, et al.. (2021). Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel. Biomedicines. 9(1). 75–75. 5 indexed citations
7.
Scala, Marcello, Bruno Reversade, Christelle Cabrol, et al.. (2020). Congenital posterior cervical spine malformation due to biallelic c.240‐4T>G RIPPLY2 variant: A discrete entity. American Journal of Medical Genetics Part A. 182(6). 1466–1472. 5 indexed citations
8.
Accogli, Andrea, et al.. (2020). Neurogenesis, neuronal migration, and axon guidance. Handbook of clinical neurology. 173. 25–42. 34 indexed citations
9.
Scarffe, Leslie A., et al.. (2020). The diagnostic yield of next generation sequencing panels for epilepsy in clinical practice (2229). Neurology. 94(15_supplement). 1 indexed citations
10.
Uccella, Sarà, Andrea Accogli, Domenico Tortora, et al.. (2019). Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development. Journal of Neurology. 266(5). 1167–1181. 9 indexed citations
11.
Scala, Marcello, Annalaura Torella, Mariasavina Severino, et al.. (2019). Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females. European Journal of Human Genetics. 27(8). 1254–1259. 36 indexed citations
12.
Accogli, Andrea, Marcello Scala, Annalisa Calcagno, et al.. (2018). CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations. European Journal of Medical Genetics. 62(3). 198–203. 22 indexed citations
13.
Pinto, Anna Maria, Eva Trevisson, Valeria Morbidoni, et al.. (2018). Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma. European Journal of Human Genetics. 26(7). 1026–1037. 16 indexed citations
14.
Scala, Marcello, Andrea Accogli, Anna Elsa Maria Allegri, et al.. (2018). Familial ROBO1 deletion associated with ectopic posterior pituitary, duplication of the pituitary stalk and anterior pituitary hypoplasia. Journal of Pediatric Endocrinology and Metabolism. 32(1). 95–99. 11 indexed citations
15.
Accogli, Andrea, Kether Guerrero, Daniela D’Agostino, et al.. (2018). Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease. Journal of Child Neurology. 34(2). 74–80. 8 indexed citations
16.
Accogli, Andrea, et al.. (2018). Diagnostic Yield of Intellectual Disability Gene Panels. Pediatric Neurology. 92. 32–36. 22 indexed citations
17.
Accogli, Andrea, Michele Iacomino, Alessandro Orsini, et al.. (2017). Novel AMPD2 mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities. Neurology Genetics. 3(5). e179–e179. 15 indexed citations
18.
Severino, Mariasavina, Andrea Accogli, Giorgio Gimelli, et al.. (2015). Clinico-radiological and molecular characterization of a child with ring chromosome 2 presenting growth failure, microcephaly, kidney and brain malformations. Molecular Cytogenetics. 8(1). 17–17. 15 indexed citations
19.
Tassano, Elisa, Andrea Accogli, Marco Pavanello, et al.. (2015). Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traits. European Journal of Medical Genetics. 59(1). 20–25. 11 indexed citations
20.
Tassano, Elisa, et al.. (2014). Phenotypic and genetic characterization of a patient with a de novo interstitial 14q24.1q24.3 deletion. Molecular Cytogenetics. 7(1). 49–49. 4 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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