F. Giannelli

6.9k citations

135 papers · 5.3k · h-index 41

Impact in

Hematology top 0.2%
- Hemophilia Treatment and Research
- Blood Coagulation and Thrombosis Mechanisms
- Platelet Disorders and Treatments
Genetics top 1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities

Papers in

Molecular Biology 84
- Cancer-related gene regulation 41
- DNA Repair Mechanisms 21
Hematology 53
- Hemophilia Treatment and Research 53
- Blood Coagulation and Thrombosis Mechanisms 19
- Platelet Disorders and Treatments 11

Co-authors: Peter M. Green (15 shared papers)Richard D. Bagnall (9 shared papers)J.L. Hamerton (11 shared papers)P. E. Polani (7 shared papers)C. R. Rizza (5 shared papers)J.A. Naylor (5 shared papers)Naushin Waseem (6 shared papers)G.G. Brownlee (4 shared papers)
Journals: Nucleic Acids Research (13 papers)The Lancet (10 papers)Nature (9 papers)Genomics (7 papers)Cytogenetic and Genome Research (6 papers)
Partner nations: United Kingdom Canada United States

In The Last Decade

F. Giannelli

128 papers receiving 4.8k citations

Peers

Replace Mark J. Pettenati with:

Mark J. Pettenati United States

Anna Jauch Germany

Ian D. Dubé Canada

Jay L. Hess United States

Michael L. Mucenski United States

Carol A. Wise United States

David Vetrie United Kingdom

James German United States

Eric Schoenmakers Belgium

Stephen M. Jane Australia

F. Giannelli relative to Mark J. Pettenati United States Mark J. Pettenati's profile →

Citations per field

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Mark J. Pettenati · 1×

×1.0 2k/2k

HEMAT

×1.0 583/584

GENET

×1.5 3k/2k

MB

×1.2 1k/1k

GENET

×1.8 377/209

CR

Citations per year

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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-authors

The 25 scholars most cited alongside F. Giannelli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with F. Giannelli Line = papers co-authored together F. Giannelli links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 135 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The gene structure of human anti‐haemophilic factor IX. The EMBO Journal ·D S Anson, K.H. Andy Choo, D. Jasper G. Rees, F. Giannelli, Keith G. Gould, Joyce A. Huddleston, G.G. Brownlee	1984	326
2	Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A Blood ·Richard D. Bagnall, Naushin Waseem, Peter M. Green, F. Giannelli	2002	283
3	Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions Human Molecular Genetics ·J.A. Naylor, Astrid Brinke, Shella Hassock, Peter M. Green, F. Giannelli	1993	197
4	Gene deletions in patients with haemophilia B and anti-factor IX antibodies Nature ·F. Giannelli, K.H. Andy Choo, D. Jasper G. Rees, Yvonne Boyd, C. R. Rizza, G.G. Brownlee	1983	168
5	Molecular pathology of haemophilia B. The EMBO Journal ·P. M. Green, D. R. Bentley, R. S. Mibashan, I. M. Nilsson, F. Giannelli	1989	161
6	Ultraviolet light sensitivity and delayed DNA-chain maturation in Bloom's syndrome fibroblasts Nature ·F. Giannelli, P. F. Benson, S. A. Pawsey, P. E. Polani	1977	151
7	Direct detection of point mutations by mismatch analysis: application to haemophilia B Nucleic Acids Research ·A.J. Montandon, P.M. Green, F. Giannelli, D.R. Bently	1989	144
8	Haemophilia B: database of point mutations and short additions and deletions--eighth edition Nucleic Acids Research ·F. Giannelli	1998	131
9	Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition Nucleic Acids Research ·Edward G. D. Tuddenham, R. Schwaab, J. Seehafer, David Millar, Jane Gitschier, Miyoko Higuchi, Sanjay I. Bidichandani, J. M. Connor, Leon W. Hoyer, Akira Yoshioka, I R Peake, K. Olek, H H Kazazian, J. M. Lavergne, F. Giannelli, Stylianos E. Antonarakis, D.N. Cooper	1994	125
10	CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY) The Lancet ·F. Giannelli, K.H. Andy Choo, Peter R. Winship, C. R. Rizza, D S Anson, Dai G., Nicolas Ferrari, G.G. Brownlee	1984	109
11	Haemophilia B: database of point mutations and short additions and deletions--second edition Nucleic Acids Research ·F. Giannelli, P. M. Green, (unknown), Sebastian-Patrick Sommer, (unknown), Michael Ludwig, (unknown), (unknown), M. Goossens, Akira Yoshioka, (unknown)	1991	101
12	Analyis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients Human Molecular Genetics ·J.A. Naylor, P.M. Green, C. R. Rizza, F. Giannelli	1993	100
13	Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene Nucleic Acids Research ·Edward G. D. Tuddenham, D.N. Cooper, Jane Gitschier, Miyoko Higuchi, Leon W. Hoyer, Akira Yoshioka, I. R. Peake, R. Schwaab, K. Olek, H H Kazazian, J. M. Lavergne, F. Giannelli, Stylianos E. Antonarakis	1991	94
14	CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROME The Lancet ·J.L. Hamerton, SusanM. Briggs, F. Giannelli, C.O. Carter	1961	93
15	Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach Genomics ·Alison J. Coffey, Roland G. Roberts, E D Green, C Cole, Rachel Butler, Rakesh Anand, F. Giannelli, David R. Bentley	1992	87
16	Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene The Lancet ·J.A. Naylor, P.M. Green, A.J. Montandon, F. Giannelli, C. R. Rizza	1991	85
17	Cytogenetics of Down’s Syndrome (Mongolism) I. Data on a Consecutive Series of Patients Referred for Genetic Counselling and Diagnosis Cytogenetic and Genome Research ·J.L. Hamerton, F. Giannelli, P. E. Polani	1965	81
18	Clinical, Genetic and DNA Repair Studies on a Consecutive Series of Patients with Xeroderma Pigmentosum QJM ·S. A. Pawsey, I.A. Magnus, Colin A. Ramsay, P. F. Benson, F. Giannelli	1979	79
19	Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) gene Human Molecular Genetics ·Rachel Flomen, Elizabeth P. Green, Peter M. Green, David Bentley, F. Giannelli	1993	73
20	The incidence and distribution of CpG←Tpg transitions in the coagulation factor IX gene. A fresh look at CPG mutitional hospots Nucleic Acids Research ·Peter M. Green, A.Jane Montandon, David Bentley, Rolf Ljung, Inga Marie Nilsson, F. Giannelli	1990	72

About F. Giannelli

F. Giannelli is a scholar working on Molecular Biology, Hematology, Genetics, Plant Science and Cancer Research, having authored 135 papers that have together received 5.3k indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (53 papers), Cancer-related gene regulation (41 papers), DNA Repair Mechanisms (21 papers), Blood Coagulation and Thrombosis Mechanisms (19 papers), Carcinogens and Genotoxicity Assessment (15 papers), Chromosomal and Genetic Variations (12 papers), Platelet Disorders and Treatments (11 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). The work is most often cited by research in Hematology (2.3k citations), Genetics (583 citations), Molecular Biology (3.2k citations), Genetics (1.2k citations) and Cancer Research (377 citations). F. Giannelli has collaborated with scholars based in United Kingdom, Canada and United States. Frequent co-authors include Peter M. Green, Richard D. Bagnall, J.L. Hamerton, P. E. Polani, C. R. Rizza, J.A. Naylor, Naushin Waseem, G.G. Brownlee, K.H. Andy Choo and D. R. Bentley. Their work appears in journals such as Nucleic Acids Research, The Lancet, Nature, Genomics and Cytogenetic and Genome Research.

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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