Flavia Palombo

1.5k total citations
27 papers, 416 citations indexed

About

Flavia Palombo is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Flavia Palombo has authored 27 papers receiving a total of 416 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Flavia Palombo's work include Mitochondrial Function and Pathology (7 papers), Genomics and Rare Diseases (6 papers) and Metabolism and Genetic Disorders (4 papers). Flavia Palombo is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Genomics and Rare Diseases (6 papers) and Metabolism and Genetic Disorders (4 papers). Flavia Palombo collaborates with scholars based in Italy, United Kingdom and United States. Flavia Palombo's co-authors include Tommaso Pippucci, Marco Seri, Valério Carelli, Alberto Magi, Rocco Liguori, G. Cara Romeo, Alessandra Maresca, Gian Franco Gensini, Maria Lucia Valentino and Betti Giusti and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Bioinformatics.

In The Last Decade

Flavia Palombo

27 papers receiving 414 citations

Peers

Flavia Palombo

GENET

CMN

NEURO

HEMAT

Elisa Giorgio Italy

Sarah Vergult Belgium

Tarja Linnankivi Finland

Karin Writzl Slovenia

Suzanne C.E.H. Sallevelt Netherlands

Nisha Patel Saudi Arabia

Renske Oegema Netherlands

Davor Lessel Germany

Emmanuelle Ranza Switzerland

Shehla Mohammed United Kingdom

Elisa Giorgio Italy

Flavia Palombo

413 ×1.8

177 ×1.1

GENET

50 ×1.0

CMN

24 ×0.6

NEURO

14 ×0.4

HEMAT

Citations per year, relative to Flavia Palombo Flavia Palombo (= 1×) peers Elisa Giorgio

Countries citing papers authored by Flavia Palombo

Since Specialization

Citations

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

Fields of papers citing papers by Flavia Palombo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Flavia Palombo

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

Coccia, Emanuele, Stefania Calabrese, Flavia Palombo, et al.. (2024). Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily Practice. Clinical Genetics. 107(5). 570–575. 1 indexed citations

Bonfiglio, Ferdinando, Andrea Legati, Vito Alessandro Lasorsa, et al.. (2024). Best practices for germline variant and DNA methylation analysis of second- and third-generation sequencing data. Human Genomics. 18(1). 120–120. 5 indexed citations

Amore, Giulia, Martina Romagnoli, Michele Carbonelli, et al.. (2024). AFG3L2 and ACO2-Linked Dominant Optic Atrophy: Genotype–Phenotype Characterization Compared to OPA1 Patients. American Journal of Ophthalmology. 262. 114–124. 2 indexed citations

Palombo, Flavia, Danara Ormanbekova, Luca Morandi, et al.. (2024). Two more families supporting the existence of monogenic spinocerebellar ataxia 48. Neurogenetics. 25(3). 277–280. 4 indexed citations

Palombo, Flavia, Melania Giannotta, Monica Maffei, et al.. (2023). Expanding the Clinical Spectrum of UBTF -Related Neurodevelopmental Disorder. Neurology Genetics. 9(6). e200098–e200098. 2 indexed citations

Cascavilla, Maria Lucia, Chiara La Morgia, Marco Battista, et al.. (2023). Recessive MECR pathogenic variants cause an LHON-like optic neuropathy. Journal of Medical Genetics. 61(1). 93–101. 9 indexed citations

Slone, Jesse, Wensheng Liu, Stephanie Sacharow, et al.. (2023). Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population. SHILAP Revista de lepidopterología. 2. 100841–100841. 2 indexed citations

Marconi, Caterina, Alessandro Pecci, Flavia Palombo, et al.. (2022). Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup. Haematologica. 108(7). 1909–1919. 1 indexed citations

Palombo, Flavia, Leonardo Caporali, Angelo Iannielli, et al.. (2021). The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs. Stem Cell Reports. 16(8). 1953–1967. 8 indexed citations

10.

Palombo, Flavia, et al.. (2020). In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss. Journal of Genetic Engineering and Biotechnology. 18(1). 8–8. 6 indexed citations

11.

Graziano, Claudio, Flavia Palombo, Annio Posar, et al.. (2020). A New Homozygous CACNB2 Mutation has Functional Relevance and Supports a Role for Calcium Channels in Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 51(1). 377–381. 4 indexed citations

12.

Magi, Alberto, Tania Giangregorio, Roberto Semeraro, et al.. (2020). AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics. Computational and Structural Biotechnology Journal. 18. 1956–1967. 3 indexed citations

13.

Manitto, Maria Pia, Flavia Palombo, Leonardo Caporali, et al.. (2020). Combined Optic Atrophy and Rod–Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype. Journal of Neuro-Ophthalmology. 41(3). e290–e292. 7 indexed citations

14.

Harel, Tamar, John N. Griffin, Thomas Arbogast, et al.. (2020). Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies. Human Molecular Genetics. 29(9). 1489–1497. 7 indexed citations

15.

Marconi, Caterina, Christian A. Di Buduo, Serena Barozzi, et al.. (2018). Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia. Blood. 133(12). 1346–1357. 37 indexed citations

16.

Miccoli, Sara, Anna Prossomariti, Tommaso Pippucci, et al.. (2018). Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients. European Journal of Human Genetics. 26(3). 387–395. 25 indexed citations

17.

Palombo, Flavia, Guido Alberto Gnecchi‐Ruscone, Manuela Oppo, et al.. (2016). A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman. Journal of Human Genetics. 62(2). 259–264. 18 indexed citations

18.

Magi, Alberto, Romina D’Aurizio, Flavia Palombo, et al.. (2015). Characterization and identification of hidden rare variants in the human genome. BMC Genomics. 16(1). 340–340. 17 indexed citations

19.

Pippucci, Tommaso, Alessandra Maresca, Pamela Magini, et al.. (2015). Homozygous NOTCH 3 null mutation and impaired NOTCH 3 signaling in recessive early‐onset arteriopathy and cavitating leukoencephalopathy. EMBO Molecular Medicine. 7(6). 848–858. 41 indexed citations

20.

Magi, Alberto, Lorenzo Tattini, Flavia Palombo, et al.. (2014). H 3 M 2 : detection of runs of homozygosity from whole-exome sequencing data. Bioinformatics. 30(20). 2852–2859. 73 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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