G Filippi

942 citations
37 papers · 695 indexed · h-index 16
Topics
Neonatal Health and Biochemistry (8 papers)Genetics and Neurodevelopmental Disorders (8 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers)

In The Last Decade

G Filippi

35 papers receiving 622 citations

Peers

G Filippi
Comparison fields: 5 of 92
  • Genetics 313
  • Molecular Biology 311
  • Pediatrics, Perinatology and Child Health 179
  • Genetics 105
  • Hematology 72
Replace M D Crawfurd with:
M D Crawfurd United Kingdom
Kamal K. Naguib Kuwait
E. Boyd United Kingdom
Jos Dreesen Netherlands
Susan H. Black United States
Jodi D. Hoffman United States
A Rinaldi Italy
F Salamanca Mexico
Simona Cavani Italy
Linda Beischel United States
G Filippi relative to M D Crawfurd United Kingdom M D Crawfurd's profile →
Citations per field
00.5×
M D Crawfurd · 1×
Citations per year

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
#WorkIndexed citations
1 10
2 38
3 11
4 21
5 26
6 12
7
Neurologic involvement as first sign of Behcet's syndrome.
1
8 20
9
Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.
14
10 6
11 62
12 6
13
Combination of old and new strategies for the molecular mapping of the human X-chromosome.
3
14 11
15 9
16
Triplo-X constitution of mother explains apparent occurrence of two recombinants in sibship segregating at two closely X-linked loci (G6PD and deutan).
6
17
Characterization of glucose-6-phosphate dehydrogenase variants. I. Occurrence of a G6PD Seattle-like variant in Sardinia and its interaction with the G6PD Mediterranean variant.
20
18
Linkage studies on X-linked ichthyosis in Sardinia.
16
19 32
20 24

About G Filippi

G Filippi is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 37 papers that have together received 695 indexed citations. Recurring topics across this 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). The work is most often cited by research in Genetics (313 citations), Genetics (105 citations) and Pediatrics, Perinatology and Child Health (179 citations). G Filippi has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include M. Siniscalco, A Rinaldi, B Latte, Nicoletta Archidiacono, Mariano Rocchi, Mario C. Rattazzi, Sergio Piomelli, P. Meera Khan, Luigi F. Bernini and Vanna Pecile. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

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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