Anna Capalbo

990 total citations
29 papers, 579 citations indexed

About

Anna Capalbo is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anna Capalbo has authored 29 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anna Capalbo's work include Genomic variations and chromosomal abnormalities (20 papers), Congenital heart defects research (9 papers) and Prenatal Screening and Diagnostics (7 papers). Anna Capalbo is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Congenital heart defects research (9 papers) and Prenatal Screening and Diagnostics (7 papers). Anna Capalbo collaborates with scholars based in Italy, United States and United Kingdom. Anna Capalbo's co-authors include Laura Bernardini, Antonio Novelli, Bruno Dallapiccola, Sara Loddo, Tiziana Filippi, Agatino Battaglia, John C. Carey, Viola Doccini, Rita Mingarelli and Irene Bottillo and has published in prestigious journals such as Scientific Reports, Gene and Human Mutation.

In The Last Decade

Anna Capalbo

27 papers receiving 530 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Capalbo Italy	16	389	244	112	77	59	29	579
Sara Loddo Italy	13	402 1.0×	277 1.1×	123 1.1×	59 0.8×	73 1.2×	39	639
Viola Alesi Italy	13	309 0.8×	263 1.1×	67 0.6×	37 0.5×	59 1.0×	59	558
Courtney Sebold United States	16	437 1.1×	216 0.9×	141 1.3×	97 1.3×	25 0.4×	27	616
Tadeusz Mazurczak Poland	17	444 1.1×	299 1.2×	102 0.9×	116 1.5×	49 0.8×	57	763
Aimee S. Spikes United States	9	452 1.2×	326 1.3×	79 0.7×	94 1.2×	32 0.5×	11	598
Nicole Maas Belgium	7	351 0.9×	191 0.8×	101 0.9×	120 1.6×	31 0.5×	13	455
JP Fryns Belgium	11	427 1.1×	284 1.2×	108 1.0×	107 1.4×	38 0.6×	14	563
Sophia Kitsiou‐Tzeli Greece	16	407 1.0×	422 1.7×	77 0.7×	69 0.9×	73 1.2×	39	656
Pietro Palumbo Italy	15	325 0.8×	314 1.3×	61 0.5×	40 0.5×	38 0.6×	64	620
Joanna Wiszniewska United States	12	360 0.9×	348 1.4×	106 0.9×	67 0.9×	36 0.6×	22	607

Countries citing papers authored by Anna Capalbo

Since Specialization

Citations

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

Fields of papers citing papers by Anna Capalbo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Capalbo

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

Fratoni, Stefano, Malgorzata Monika Trawinska, Anna Capalbo, et al.. (2022). Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangement. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 481(6). 975–979.

Bernardini, Laura, et al.. (2021). Koolen‐de Vries syndrome in a 63‐year‐old woman: Report of the oldest patient and a review of the adult phenotype. American Journal of Medical Genetics Part A. 188(2). 692–707. 3 indexed citations

Pontecorvi, Paola, Laura Bernardini, Anna Capalbo, et al.. (2021). Protein–protein interaction network analysis applied to DNA copy number profiling suggests new perspectives on the aetiology of Mayer–Rokitansky–Küster–Hauser syndrome. Scientific Reports. 11(1). 448–448. 15 indexed citations

Fontana, Paolo, Laura Bernardini, Cinzia Lombardi, et al.. (2020). De Novo Inverted Duplication Deletion of 4p in a 14-Week-Old Male Fetus Aborted Due to Multiple Anomalies. Journal of Pediatric Genetics. 10(3). 245–249.

Fratoni, Stefano, Pasquale Niscola, Luigi Maria Larocca, et al.. (2019). ALK-negative anaplastic large cell lymphoma with “Hodgkin-like” cytomorphology and nuclear expression of PAX5. Pathology - Research and Practice. 216(2). 152724–152724. 4 indexed citations

Capalbo, Anna, Bárbara Torres, Alice Traversa, et al.. (2019). Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings. European Journal of Medical Genetics. 63(4). 103772–103772. 9 indexed citations

Miolo, Gianmaria, Maria Grazia Giuffrida, Giuseppe Corona, et al.. (2018). A novel mosaic 1q32.1 microduplication identified through Chromosome Microarray Analysis: narrowing the smallest critical region including KDM5B gene found associated with neurodevelopmetal disorders. European Journal of Medical Genetics. 62(9). 103558–103558. 5 indexed citations

Battaglia, Agatino, Viola Doccini, Laura Bernardini, et al.. (2013). Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features. European Journal of Paediatric Neurology. 17(6). 589–599. 147 indexed citations

Ferraris, Alessandro, Laura Bernardini, Ginevra Zanni, et al.. (2013). Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. Orphanet Journal of Rare Diseases. 8(1). 75–75. 25 indexed citations

10.

Tarsitano, Marina, Antonio Novelli, Anna Capalbo, et al.. (2013). Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowth. Gene. 536(1). 213–216. 20 indexed citations

11.

Prontera, Paolo, Laura Bernardini, Gabriela Stangoni, et al.. (2011). Deletion 2p15–16.1 syndrome: Case report and review. American Journal of Medical Genetics Part A. 155(10). 2473–2478. 26 indexed citations

12.

Alesi, Viola, Giuseppe Barrano, Anna Capalbo, et al.. (2011). A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosis. American Journal of Medical Genetics Part A. 155(10). 2543–2551. 6 indexed citations

13.

Bernardini, Laura, Maria Grazia Giuffrida, Paola Francalanci, et al.. (2010). X chromosome monosomy restricted to the left ventricle is not a major cause of isolated hypoplastic left heart. American Journal of Medical Genetics Part A. 152A(8). 1967–1972. 2 indexed citations

14.

Digilio, M. Cristina, Laura Bernardini, Anna Capalbo, et al.. (2009). 16p subtelomeric duplication: a clinically recognizable syndrome. European Journal of Human Genetics. 17(9). 1135–1140. 16 indexed citations

15.

Bernardini, Laura, Lorenzo Sinibaldi, Anna Capalbo, et al.. (2009). HDR (Hypoparathyroidism, Deafness, Renal dysplasia) syndrome associated to GATA3 gene duplication. Clinical Genetics. 76(1). 117–119. 18 indexed citations

16.

Carbone, Angelo, Laura Bernardini, Irene Bottillo, et al.. (2008). Array‐based comparative genomic hybridization in early‐stage mycosis fungoides: Recurrent deletion of tumor suppressor genes BCL7A, SMAC/DIABLO, and RHOF. Genes Chromosomes and Cancer. 47(12). 1067–1075. 34 indexed citations

17.

Velinov, Milen, Antonio Novelli, Hong Gu, et al.. (2008). De-novo 2.15 Mb terminal Xq duplication involving MECP2 but not L1CAM gene in a male patient with mental retardation. Clinical Dysmorphology. 18(1). 9–12. 17 indexed citations

18.

Bernardini, Laura, Marco Castori, Anna Capalbo, et al.. (2007). Syndromic craniosynostosis due to complex chromosome 5 rearrangement andMSX2gene triplication. American Journal of Medical Genetics Part A. 143A(24). 2937–2943. 27 indexed citations

19.

Bernardini, Laura, Chiara Palka, Anna Capalbo, et al.. (2007). Complex rearrangement of chromosomes 7q21.13‐q22.1 confirms the ectrodactyly‐deafness locus and suggests new candidate genes. American Journal of Medical Genetics Part A. 146A(2). 238–244. 28 indexed citations

20.

Bernardini, Laura, Anna Capalbo, Isabella Torrente, et al.. (2006). Five cases of supernumerary small ring chromosomes 1: Heterogeneity and genotype–phenotype correlation. European Journal of Medical Genetics. 50(2). 94–102. 19 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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