Virginie Saillour

530 total citations
10 papers, 191 citations indexed

About

Virginie Saillour is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, Virginie Saillour has authored 10 papers receiving a total of 191 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Public Health, Environmental and Occupational Health and 3 papers in Genetics. Recurrent topics in Virginie Saillour's work include Acute Lymphoblastic Leukemia research (3 papers), Epigenetics and DNA Methylation (3 papers) and Genomics and Rare Diseases (2 papers). Virginie Saillour is often cited by papers focused on Acute Lymphoblastic Leukemia research (3 papers), Epigenetics and DNA Methylation (3 papers) and Genomics and Rare Diseases (2 papers). Virginie Saillour collaborates with scholars based in Canada, France and United Kingdom. Virginie Saillour's co-authors include Daniel Sinnett, Jasmine Healy, Jean-François Spinella, Chantal Richer, Manon Ouimet, Ramón Vidal, Tomi Pastinen, Stephan Busche, Thomas Sontag and Mark D. Minden and has published in prestigious journals such as Cancer Research, BMC Bioinformatics and BMC Genomics.

In The Last Decade

Virginie Saillour

10 papers receiving 188 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Virginie Saillour Canada 7 116 65 55 46 38 10 191
Martina Mijušković United Kingdom 6 99 0.9× 53 0.8× 36 0.7× 29 0.6× 29 0.8× 8 179
Manon Ouimet Canada 11 198 1.7× 54 0.8× 65 1.2× 127 2.8× 46 1.2× 16 309
Thomas R. W. Oliver United Kingdom 5 119 1.0× 70 1.1× 29 0.5× 90 2.0× 20 0.5× 9 252
Nicholas Hickson United Kingdom 8 66 0.6× 54 0.8× 20 0.4× 54 1.2× 35 0.9× 10 185
Flávia S. Donaires Brazil 10 136 1.2× 27 0.4× 19 0.3× 41 0.9× 45 1.2× 25 251
Kristen E. Schratz United States 7 108 0.9× 40 0.6× 21 0.4× 29 0.6× 90 2.4× 10 272
Himalee S. Sabnis United States 8 123 1.1× 26 0.4× 19 0.3× 47 1.0× 85 2.2× 20 234
Kathrin Thomay Germany 7 81 0.7× 23 0.4× 32 0.6× 13 0.3× 65 1.7× 16 182
Robert J. Autry United States 6 68 0.6× 26 0.4× 26 0.5× 37 0.8× 15 0.4× 12 127
Marissa Rashkovan Canada 6 119 1.0× 19 0.3× 42 0.8× 38 0.8× 107 2.8× 7 210

Countries citing papers authored by Virginie Saillour

Since Specialization
Citations

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

Fields of papers citing papers by Virginie Saillour

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Virginie Saillour

This figure shows the co-authorship network connecting the top 25 collaborators of Virginie Saillour. A scholar is included among the top collaborators of Virginie Saillour 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 Virginie Saillour. Virginie Saillour is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Tusseau, Maud, Mélanie Eyries, Nicolas Chatron, et al.. (2024). Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families. European Journal of Medical Genetics. 68. 104919–104919. 3 indexed citations
2.
Rucheton, Benoît, Claire Ewenczyk, Pauline Gaignard, et al.. (2021). Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Impairments Caused by Biallelic SCO2 Variants. Neurology Genetics. 7(6). e630–e630. 1 indexed citations
3.
Ehresmann, Sophie, Julie Gauthier, Virginie Saillour, et al.. (2019). A variant of neonatal progeroid syndrome, or Wiedemann–Rautenstrauch syndrome, is associated with a nonsense variant in POLR3GL. European Journal of Human Genetics. 28(4). 461–468. 18 indexed citations
4.
Lopes, Fátima, J Gauthier, Virginie Saillour, et al.. (2018). Refining the phenotype associated with biallelic DNAJC21 mutations. Clinical Genetics. 94(2). 252–258. 26 indexed citations
5.
Spinella, Jean-François, Chantal Richer, Virginie Saillour, et al.. (2016). Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations. Oncotarget. 7(40). 65485–65503. 31 indexed citations
6.
Spinella, Jean-François, Ramón Vidal, Virginie Saillour, et al.. (2016). SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing. BMC Genomics. 17(1). 912–912. 42 indexed citations
7.
Spinella, Jean-François, Jasmine Healy, Virginie Saillour, et al.. (2015). Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes. BMC Cancer. 15(1). 539–539. 21 indexed citations
8.
Spinella, Jean-François, Philippe Rousseau, Claire Drullion, et al.. (2015). A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cells. BMC Cancer. 15(1). 621–621. 11 indexed citations
9.
Busche, Stephan, Bing Ge, Ramón Vidal, et al.. (2013). Integration of High-Resolution Methylome and Transcriptome Analyses to Dissect Epigenomic Changes in Childhood Acute Lymphoblastic Leukemia. Cancer Research. 73(14). 4323–4336. 34 indexed citations
10.
Bareke, Eric, Virginie Saillour, Jean-François Spinella, et al.. (2013). Joint genotype inference with germline and somatic mutations. BMC Bioinformatics. 14(S5). S3–S3. 4 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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