Filomena Pirozzi

503 total citations
9 papers, 192 citations indexed

About

Filomena Pirozzi is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Filomena Pirozzi has authored 9 papers receiving a total of 192 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Filomena Pirozzi's work include Genetics and Neurodevelopmental Disorders (6 papers), Epigenetics and DNA Methylation (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Filomena Pirozzi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Epigenetics and DNA Methylation (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Filomena Pirozzi collaborates with scholars based in Italy, United States and Switzerland. Filomena Pirozzi's co-authors include Ghayda Mirzaa, Branden R. Nelson, Giovanni Neri, Elisabetta Tabolacci, Anthony Wynshaw‐Boris, Meixiang Zhang, Justine Ngo, F. Gasparini, Pietro Chiurazzi and Baltazar Gomez‐Mancilla and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Urology and Human Mutation.

In The Last Decade

Filomena Pirozzi

9 papers receiving 186 citations

Peers

Filomena Pirozzi

GENET

PPCH

SURGE

Andrea K. Vaags Canada

Marlene Stuempflen Austria

Devin M. Cox United States

Sanne Janssen Canada

Juliette Dupont Portugal

Charlly Kao United States

Hernán Guillermo Hernández Colombia

Aurora Arghir Romania

Margarida Venâncio Portugal

K. Naga Mohan India

Andrea K. Vaags Canada

Filomena Pirozzi

146 ×1.2

120 ×1.5

GENET

23 ×0.6

13 ×0.6

PPCH

46 ×2.3

SURGE

Citations per year, relative to Filomena Pirozzi Filomena Pirozzi (= 1×) peers Andrea K. Vaags

Countries citing papers authored by Filomena Pirozzi

Since Specialization

Citations

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

Fields of papers citing papers by Filomena Pirozzi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Filomena Pirozzi

This figure shows the co-authorship network connecting the top 25 collaborators of Filomena Pirozzi. A scholar is included among the top collaborators of Filomena Pirozzi 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 Filomena Pirozzi. Filomena Pirozzi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

Pirozzi, Filomena, Nicole Horsley, William B. Dobyns, et al.. (2021). Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes. American Journal of Medical Genetics Part A. 185(9). 2719–2738. 16 indexed citations

Zhang, Meixiang, et al.. (2018). Highly efficient methods to obtain homogeneous dorsal neural progenitor cells from human and mouse embryonic stem cells and induced pluripotent stem cells. Stem Cell Research & Therapy. 9(1). 67–67. 27 indexed citations

Fernández, Esperanza, Elena Di Gennaro, Filomena Pirozzi, et al.. (2018). FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene. Frontiers in Genetics. 9. 442–442. 8 indexed citations

Pirozzi, Filomena, Branden R. Nelson, & Ghayda Mirzaa. (2018). From microcephaly to megalencephaly: determinants of brain size. Dialogues in Clinical Neuroscience. 20(4). 267–282. 52 indexed citations

Tabolacci, Elisabetta, Filomena Pirozzi, Baltazar Gomez‐Mancilla, F. Gasparini, & Giovanni Neri. (2012). The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro. BMC Medical Genetics. 13(1). 13–13. 14 indexed citations

Barba, Marta, Filomena Pirozzi, N. Saulnier, et al.. (2012). Lim Mineralization Protein 3 Induces the Osteogenic Differentiation of Human Amniotic Fluid Stromal Cells through Kruppel-Like Factor-4 Downregulation and Further Bone-Specific Gene Expression. SHILAP Revista de lepidopterología. 2012. 1–11. 15 indexed citations

Pirozzi, Filomena, Francesco Guidi, Massimiliano Orsini, et al.. (2012). Bradeion (SEPT4) as a Urinary Marker of Transitional Cell Bladder Cancer: A Real-Time Polymerase Chain Reaction Study of Gene Expression. The Journal of Urology. 187(6). 2223–2227. 10 indexed citations

Pirozzi, Filomena, Elisabetta Tabolacci, & Giovanni Neri. (2011). The FRAXopathies: Definition, overview, and update. American Journal of Medical Genetics Part A. 155(8). 1803–1816. 33 indexed citations

Pirozzi, Filomena, Ginevra Zanni, Enrico Bertini, et al.. (2011). Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian family. Human Mutation. 32(11). E2294–E2307. 17 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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