G Filippi

942 total citations
37 papers, 695 citations indexed

About

G Filippi is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, G Filippi has authored 37 papers receiving a total of 695 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 13 papers in Molecular Biology. Recurrent topics in G Filippi's work include Neonatal Health and Biochemistry (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). G Filippi is often cited by papers focused on Neonatal Health and Biochemistry (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). G Filippi collaborates with scholars based in Italy, United States and United Kingdom. G Filippi's co-authors include M. Siniscalco, A Rinaldi, B Latte, Nicoletta Archidiacono, Mariano Rocchi, Mario C. Rattazzi, P. Meera Khan, Sergio Piomelli, Luigi F. Bernini and Vanna Pecile and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

G Filippi

35 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G Filippi Italy 16 313 311 179 105 72 37 695
Linda Beischel United States 18 248 0.8× 217 0.7× 162 0.9× 72 0.7× 123 1.7× 34 865
M D Crawfurd United Kingdom 18 290 0.9× 250 0.8× 129 0.7× 50 0.5× 25 0.3× 33 705
A Rinaldi Italy 12 191 0.6× 215 0.7× 128 0.7× 69 0.7× 25 0.3× 35 476
F Salamanca Mexico 15 287 0.9× 285 0.9× 89 0.5× 35 0.3× 35 0.5× 60 709
G. Bourrouillou France 14 398 1.3× 279 0.9× 146 0.8× 41 0.4× 36 0.5× 40 587
Jonathan J. Waters United Kingdom 17 439 1.4× 362 1.2× 410 2.3× 58 0.6× 127 1.8× 32 1.0k
Nicholas C. Bethlenfalvay United States 10 155 0.5× 153 0.5× 88 0.5× 165 1.6× 91 1.3× 28 451
Wayne H. Finley United States 15 199 0.6× 225 0.7× 130 0.7× 23 0.2× 26 0.4× 39 561
Simona Cavani Italy 16 393 1.3× 313 1.0× 160 0.9× 84 0.8× 142 2.0× 31 692
E. Boyd United Kingdom 22 804 2.6× 623 2.0× 233 1.3× 69 0.7× 74 1.0× 55 1.3k

Countries citing papers authored by G Filippi

Since Specialization
Citations

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

Fields of papers citing papers by G Filippi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Filippi

This figure shows the co-authorship network connecting the top 25 collaborators of G Filippi. A scholar is included among the top collaborators of G Filippi 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 G Filippi. G Filippi 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.
Maughan, Peter J., David E. Jarvis, Ramiro N. Curti, et al.. (2023). A chromosome‐scale reference of Chenopodium watsonii helps elucidate relationships within the North American A‐genome Chenopodium species and with quinoa. The Plant Genome. 16(3). e20349–e20349. 10 indexed citations
2.
Pecile, Vanna, et al.. (1990). Deficiency of distal 8p —: report of two cases and review of the literature. Clinical Genetics. 37(4). 271–278. 38 indexed citations
3.
Rocchi, Mariano, Nicoletta Archidiacono, A Rinaldi, et al.. (1990). Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.. PubMed. 46(4). 738–43. 14 indexed citations
4.
Filippi, G, Vanna Pecile, A Rinaldi, & M. Siniscalco. (1988). Fragile‐X mutation and Klinefelter syndrome: A reappraisal. American Journal of Medical Genetics. 30(1-2). 99–107. 11 indexed citations
5.
Purrello, Michele, Becky Alhadeff, K.E. Buckton, et al.. (1987). Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over. Cytogenetic and Genome Research. 44(1). 32–40. 21 indexed citations
6.
Archidiacono, Nicoletta, Mariano Rocchi, A Rinaldi, & G Filippi. (1987). X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families).. PubMed. 35(5). 381–98. 5 indexed citations
7.
Filippi, G. (1986). Klinefelter's syndrome in Sardinia. Clinical Genetics. 30(4). 276–284. 26 indexed citations
8.
Salvarani, Carlo, et al.. (1985). Neurologic involvement as first sign of Behcet's syndrome.. PubMed. 2(4). 353–4. 1 indexed citations
9.
Filippi, G, et al.. (1985). Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?. American Journal of Medical Genetics. 22(4). 821–824. 20 indexed citations
10.
Filippi, G, P.M. Mannucci, Rosa Coppola, et al.. (1984). Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.. PubMed. 36(1). 44–71. 14 indexed citations
11.
Purrello, Michele, Robert L. Nussbaum, A Rinaldi, et al.. (1984). Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm. Human Genetics. 65(3). 295–299. 6 indexed citations
12.
Szabó, Piroska E., Michele Purrello, Mariano Rocchi, et al.. (1984). Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.. Proceedings of the National Academy of Sciences. 81(24). 7855–7859. 62 indexed citations
13.
Filippi, G, et al.. (1983). X chromosome replication patterns in a case of X;9 balanced translocation.. Journal of Medical Genetics. 20(6). 467–468. 6 indexed citations
14.
Siniscalco, M., Piroska E. Szabó, G Filippi, & A Rinaldi. (1982). Combination of old and new strategies for the molecular mapping of the human X-chromosome.. PubMed. 103 Pt A. 103–24. 3 indexed citations
15.
Benatti, Umberto, A. Morelli, S. Pontremoli, et al.. (1981). Genetic variation in the quantitative levels of an NADP (H)-binding protein (FX) in human erythrocytes. Blood. 57(2). 209–217. 4 indexed citations
16.
Rinaldi, A, Nicoletta Archidiacono, Mariano Rocchi, & G Filippi. (1979). Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.. Journal of Medical Genetics. 16(3). 225–226. 11 indexed citations
17.
Filippi, G, et al.. (1968). Linkage studies on X-linked ichthyosis in Sardinia.. PubMed. 20(6). 564–9. 16 indexed citations
18.
Modiano, G., et al.. (1967). Studies on Red Cell Acid Phosphatases in Sardinia and Rome Absence of Correlation with Past Malarial Morbidity. Human Heredity. 17(1). 17–28. 32 indexed citations
19.
Siniscalco, M., G Filippi, B Latte, et al.. (1966). Failure to detect linkage between Xg and other X‐borne loci in Sardinians. Annals of Human Genetics. 29(3). 231–252. 24 indexed citations
20.
Filippi, G, et al.. (1966). Formation of a peculiar heme-protein fraction in plasmas containing hemoglobin. Cellular and Molecular Life Sciences. 22(1). 19–20.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026