Vincent Ferretti

33.5k citations

42 papers · 2.8k indexed · 1 hit paper · h-index 21

Impact in

Cancer Research top 5%
- Cancer Genomics and Diagnostics
Molecular Biology top 5%
- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
- RNA modifications and cancer
- Bioinformatics and Genomic Networks
- Gene expression and cancer classification
- RNA and protein synthesis mechanisms

Papers in

Genetics 16
- Genome Rearrangement Algorithms 4
- Genetic Associations and Epidemiology 4
Cancer Research 6
- Cancer Genomics and Diagnostics 6

Co-authors: Robert L. Grossman Louis M. Staudt Allison P. Heath Warren A. Kibbe Douglas R. Lowy Harold Varmus Isabel Fortier Mark A. Jensen
Journals: International Journal of Epidemiology (4 papers)Cancer Research (3 papers)PLoS ONE (3 papers)Neuro-Oncology (2 papers)Bioinformatics (2 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Vincent Ferretti

41 papers receiving 2.8k citations

Hit Papers

align trajectories log scale

Toward a Shared Vision for Cancer Genomic Data 2016 · 1.1k citations

Peers

Countries citing papers authored by Vincent Ferretti

Since Specialization

Citations

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

Fields of papers citing papers by Vincent Ferretti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Vincent Ferretti, 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 Vincent Ferretti Line = papers co-authored together Vincent Ferretti links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Fostering population-based cohort data discovery: The Maelstrom Research cataloguing toolkit PLoS ONE ·ماجد نعمة, Dany Doiron, Yannick Marcon, Vincent Ferretti, Isabel Fortier	2018	27
2	Developing Cancer Informatics Applications and Tools Using the NCI Genomic Data Commons API Cancer Research ·K.R. Abbott, Michael Fitzsimons, Martin L. Ferguson, Allison P. Heath, Mark A. Jensen, N.V. Shestopalov, Mark W. Murphy, James J. Porter, Himanso Sahni, Louis M. Staudt, 翟祥军, Zhining Wang, Christine Yu, Junjun Zhang, Vincent Ferretti, Robert L. Grossman	2017	26
3	The NCI Genomic Data Commons as an engine for precision medicine Blood ·Mark A. Jensen, Vincent Ferretti, Robert L. Grossman, Louis M. Staudt	2017	180
4	Maelstrom Research guidelines for rigorous retrospective data harmonization International Journal of Epidemiology ·Isabel Fortier, Parminder Raina, Edwin R. van den Heuvel, Lauren E. Griffith, Camille Craig, Matilda Saliba, Dany Doiron, Ronald P. Stolk, Bartha Maria Knoppers, Vincent Ferretti, Peter Granda, Paul Burton	2016	147
5	Clinical genomics information management software linking cancer genome sequence and clinical decisions Genomics ·Stuart Watt, Wei Jiao, Andrew Brown, Teresa Petrocelli, Ben Tran, Tong Zhang, John D. McPherson, Suzanne Kamel‐Reid, Philippe L. Bédard, Nicole Onetto, Thomas J. Hudson, Janet Dancey, Lillian L. Siu, Lincoln Stein, Vincent Ferretti	2013	9
6	Observ-OM and Observ-TAB: Universal syntax solutions for the integration, search, and exchange of phenotype and genotype information Human Mutation ·Tomasz Adamusiak, Helen Parkinson, Juha Muilu, Mustafa Mohammed Mustafa, Quiroz-García David Leonor, Guðmundur Á. Þórisson, Antonin Finkelnburg, Chao Pang, H. J. Surendra, Vincent Ferretti, Hans L. Hillege, Anthony J. Brookes, Morris A. Swertz	2012	16
7	Securing the Data Economy: Translating Privacy and Enacting Security in the Development of DataSHIELD Public Health Genomics ·Madeleine J. Murtagh, İpek Demir, K. Neil Jenkings, Susan Wallace, 克雄間渕, Mathieu Boniol, Maria Bota, Philippe Laflamme, Paolo Boffetta, Vincent Ferretti, Paul R. Burton	2012	12
8	CaPSID: A bioinformatics platform for computational pathogen sequence identification in human genomes and transcriptomes BMC Bioinformatics ·Ivan Borozan, K.R. Abbott, Paola Blanchette, Philippe Laflamme, Stuart Watt, Paul M. Krzyzanowski, Fabrice Sircoulomb, Robert Rottapel, Philip E. Branton, Vincent Ferretti	2012	30
9	Is rigorous retrospective harmonization possible? Application of the DataSHaPER approach across 53 large studies International Journal of Epidemiology ·Isabel Fortier, Dany Doiron, Julian Little, Vincent Ferretti, Kui-wei Wang, Ronald P. Stolk, Bartha Maria Knoppers, Thomas J. Hudson, Paul R. Burton	2011	62
10	DataSHIELD: resolving a conflict in contemporary bioscience--performing a pooled analysis of individual-level data without sharing the data International Journal of Epidemiology ·Michael Wolfson, Susan Wallace, Nicholas G. D. Masca, Geoffrey M. Rowe, Nuala A. Sheehan, Vincent Ferretti, Philippe Laflamme, Martin D. Tobin, John Macleod, Julian Little, Isabel Fortier, Bartha Maria Knoppers, Paul R. Burton	2010	114
11	The Canadian Partnership for Tomorrow Project: building a pan-Canadian research platform for disease prevention Canadian Medical Association Journal ·Marilyn J. Borugian, Paula J. Robson, Isabel Fortier, Louise Parker, J. McLaughlin, Bartha Maria Knoppers, Karine Bédard, Richard P. Gallagher, Shane Sinclair, Vincent Ferretti, VC Mbachi, David W. Hoskin, John D. Potter	2010	49
12	Germline EPHB2 Receptor Variants in Familial Colorectal Cancer PLoS ONE ·George Zogopoulos, Claus Jørgensen, Julinor Bacani, Alexandre Montpetit, Patricia Lepage, Vincent Ferretti, Lauren Chad, Mehmet Sadık Aydin, Brent W. Zanke, Thomas J. Hudson, Tony Pawson, Steven Gallinger	2008	14
13	Genome-wide computational prediction of transcriptional regulatory modules reveals new insights into human gene expression Genome Research ·Mathieu Blanchette, Alain R. Bataille, Xiaoyu Chen, Christian Poitras, Josée Laganière, Céline Lefèbvre, Geneviève Deblois, Vincent Giguère, Vincent Ferretti, Dominique Bergeron, Benoit Coulombe, François Robert	2006	205
14	PReMod: a database of genome-wide mammalian cis-regulatory module predictions Nucleic Acids Research ·Vincent Ferretti, Christian Poitras, D Bergeron, Benoit Coulombe, François Robert, Mathieu Blanchette	2006	65
15	A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis Nature Genetics ·Matthew R. Lincoln, Alexandre Montpetit, M. Zameel Cader, Janna Saarela, David A. Dyment, 正井友里子, Vincent Ferretti, Pentti J. Tienari, A. Dessa Sadovnick, Leena Peltonen, George C. Ebers, Thomas J. Hudson	2005	236
16	Antimicrobial drug discovery through bacteriophage genomics Nature Biotechnology ·Jing Liu, Mohammed Dehbi, Greg Moeck, Francis F. Arhin, Pascale Bauda, Dominique Bergeron, Mario Callejo, Vincent Ferretti, Chen Xiaowei, Tony Kwan, John S. McCarty, Ramakrishnan Srikumar, Dan Williams, Jinzi J. Wu, Philippe Gros, N. Düzgüneşν, Michael S. DuBow	2004	175
17	Conserved segment identification David Sankoff, Vincent Ferretti, Joseph H. Nadeau	1997	21
18	Original Synteny Vincent Ferretti, Joseph H. Nadeau, David Sankoff	1996	21
19	Karyotype distributions in a stochastic model of reciprocal translocation. Genome Research ·David Sankoff, Vincent Ferretti	1996	15
20	Skewed Base Compositions, Asymmetric Transition Matrices, and Phylogenetic Invariants Journal of Computational Biology ·Vincent Ferretti, B. Franz Lang, David Sankoff	1994	7

About Vincent Ferretti

Vincent Ferretti is a scholar working on Genetics, Cancer Research, Health, Toxicology and Mutagenesis, Molecular Biology and Pathology and Forensic Medicine, having authored 42 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (12 papers), Cancer Genomics and Diagnostics (6 papers), RNA and protein synthesis mechanisms (5 papers), Health, Environment, Cognitive Aging (5 papers), Genome Rearrangement Algorithms (4 papers), Data-Driven Disease Surveillance (4 papers), Genetic Associations and Epidemiology (4 papers) and Ethics in Clinical Research (4 papers). The work is most often cited by research in Cancer Research (569 citations), Molecular Biology (1.5k citations), Health Informatics (24 citations), Pathology and Forensic Medicine (292 citations) and Genetics (434 citations). Vincent Ferretti has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Robert L. Grossman, Louis M. Staudt, Allison P. Heath, Warren A. Kibbe, Douglas R. Lowy, Harold Varmus, Isabel Fortier, Mark A. Jensen, David Sankoff and Ivan Borozan. Their work appears in journals such as International Journal of Epidemiology, Cancer Research, PLoS ONE, Neuro-Oncology and Bioinformatics.

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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