F. Giannelli

6.9k total citations
130 papers, 4.9k citations indexed

About

F. Giannelli is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, F. Giannelli has authored 130 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Molecular Biology, 51 papers in Hematology and 25 papers in Genetics. Recurrent topics in F. Giannelli's work include Hemophilia Treatment and Research (51 papers), Cancer-related gene regulation (42 papers) and DNA Repair Mechanisms (21 papers). F. Giannelli is often cited by papers focused on Hemophilia Treatment and Research (51 papers), Cancer-related gene regulation (42 papers) and DNA Repair Mechanisms (21 papers). F. Giannelli collaborates with scholars based in United Kingdom, Canada and United States. F. Giannelli's co-authors include Peter M. Green, Richard D. Bagnall, J.L. Hamerton, P. E. Polani, Naushin Waseem, J.A. Naylor, C. R. Rizza, G.G. Brownlee, D. R. Bentley and K.H. Andy Choo and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

F. Giannelli

126 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. Giannelli United Kingdom	40	3.2k	2.2k	1.1k	571	350	130	4.9k
Mark J. Pettenati United States	36	2.1k 0.7×	2.3k 1.0×	998 0.9×	620 1.1×	182 0.5×	148	5.1k
Helena Ayyub United Kingdom	27	2.7k 0.8×	429 0.2×	1.0k 0.9×	832 1.5×	329 0.9×	43	3.5k
Corinne D. Boehm United States	22	1.4k 0.4×	1.1k 0.5×	812 0.7×	1.6k 2.8×	223 0.6×	38	3.3k
Eric E. Bouhassira United States	41	3.7k 1.2×	1.7k 0.8×	1.2k 1.0×	1.6k 2.8×	311 0.9×	106	6.5k
Sandra Offner Switzerland	25	2.7k 0.8×	1.4k 0.6×	624 0.5×	459 0.8×	452 1.3×	37	4.5k
Mario Tosi France	38	2.1k 0.7×	580 0.3×	922 0.8×	1.3k 2.2×	148 0.4×	87	4.3k
Michael L. Mucenski United States	33	3.0k 1.0×	767 0.3×	830 0.7×	275 0.5×	93 0.3×	47	5.0k
D.G. Harnden United Kingdom	33	2.5k 0.8×	400 0.2×	1.6k 1.4×	338 0.6×	434 1.2×	90	4.8k
Maria Cristina Magli Italy	29	2.2k 0.7×	400 0.2×	814 0.7×	689 1.2×	92 0.3×	63	3.9k
David Vetrie United Kingdom	32	3.1k 1.0×	1.1k 0.5×	1.1k 1.0×	1.2k 2.0×	341 1.0×	59	5.7k

Countries citing papers authored by F. Giannelli

Since Specialization

Citations

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

Fields of papers citing papers by F. Giannelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Giannelli

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

Giannelli, F., Josephine R. Paris, Karen Bourgeois, et al.. (2025). Pervasive and recurrent hybridization prevents inbreeding in Europe’s most threatened seabird. Proceedings of the National Academy of Sciences. 122(34). e2427223122–e2427223122.

Trucchi, Emiliano, F. Giannelli, Joan Ferrer, et al.. (2025). High Gene Expression Predicts Extremely Low Segregation of Deleterious Mutations in Large Penguin Populations. Molecular Biology and Evolution. 42(6).

Casavecchia, Simona, F. Giannelli, Massimo Giovannotti, et al.. (2024). Morphological and Genomic Differences in the Italian Populations of Onopordum tauricum Willd.—A New Source of Vegetable Rennet. Plants. 13(5). 654–654. 2 indexed citations

Giannelli, F. & Peter M. Green. (2000). The X Chromosome and the Rate of Deleterious Mutations in Humans. The American Journal of Human Genetics. 67(2). 515–517. 15 indexed citations

Waseem, Naushin, et al.. (1997). Mutation Analysis and Genetic Service: The Construction and Use of National Confidential Databases of Mutations and Pedigrees. Genetic Testing. 1(3). 181–188. 5 indexed citations

Bagnall, Richard D., et al.. (1997). Mutational analysis of factor VIII transcripts in haemophilia A patients. UCL Discovery (University College London). 1 indexed citations

Morgan, Gareth, et al.. (1997). Further evidence for the importance of an androgen response element in the factor IX promoter. British Journal of Haematology. 98(1). 79–85. 16 indexed citations

Bentley, D. R., et al.. (1994). Mutation detection by fluorescent chemical cleavage: application to hemophilia B.. Genome Research. 3(5). 268–271. 23 indexed citations

Tuddenham, Edward G. D., R. Schwaab, David Millar, et al.. (1994). Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Research. 22(22). 4851–4868. 42 indexed citations

10.

Giannelli, F., Katherine A. High, M.‐C. Poon, et al.. (1993). Haemophilia B: database of point mutations and short additions and deletions—fourth edition, 1993. Nucleic Acids Research. 21(13). 3075–3087. 35 indexed citations

11.

McGraw, Adam P., et al.. (1993). Haemophilia B caused by a missense mutation in the prepeptide sequence of factor IX. Human Mutation. 2(2). 103–107. 6 indexed citations

12.

Giannelli, F., Sebastian-Patrick Sommer, Michael Ludwig, et al.. (1991). Haemophilia B: database of point mutations and short additions and deletions--second edition. Nucleic Acids Research. 19(suppl). 2193–2220. 98 indexed citations

13.

Green, Peter M., et al.. (1990). The incidence and distribution of CpG←Tpg transitions in the coagulation factor IX gene. A fresh look at CPG mutitional hospots. Nucleic Acids Research. 18(11). 3227–3231. 69 indexed citations

14.

Giannelli, F., et al.. (1988). UVA DOSE-RESPONSE OF NORMAL AND ACTINIC RETICULOID FIBROBLASTS - A STATISTICAL-ANALYSIS. UCL Discovery (University College London). 1 indexed citations

15.

Giannelli, F., et al.. (1969). The Genetical Society of Great Britain Abstracts of Papers read at the hundred and fifty-eighth meeting of the Society held on 8th and 9th November 1968, at the University College, London. Heredity. 24(1). 175–180. 1 indexed citations

16.

Giannelli, F., et al.. (1965). Cytogenetics of Down’s Syndrome (Mongolism) II. The Frequency of Interchange Trisomy in Patients Born at a Maternal Age of less than 30 Years. Cytogenetic and Genome Research. 4(3). 186–192. 28 indexed citations

17.

Hamerton, J.L., et al.. (1963). A Family Showing Transmission of a D/D Reciprocal Translocation and a Case of Regular 21-Trisomic Down’s Syndrome. Cytogenetic and Genome Research. 2(4-5). 194–207. 42 indexed citations

18.

Giannelli, F.. (1963). THE PATTERN OF X-CHROMOSOME DEOXYRIBONUCLEIC ACID SYNTHESIS IN TWO WOMEN WITH ABNORMAL SEX-CHROMOSOME COMPLEMENTS. The Lancet. 281(7286). 863–865. 54 indexed citations

19.

Hamerton, J.L., et al.. (1961). CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROME. The Lancet. 278(7206). 788–791. 84 indexed citations

20.

Hamerton, J.L., et al.. (1961). DIFFERENTIAL TRANSMISSION OF DOWN'S SYNDROME (MONGOLISM) THROUGH MALE AND FEMALE TRANSLOCATION CARRIERS. The Lancet. 278(7209). 956–958. 49 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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