Vanessa Bruat

1.2k total citations
9 papers, 354 citations indexed

About

Vanessa Bruat is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Vanessa Bruat has authored 9 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Hematology. Recurrent topics in Vanessa Bruat's work include Genetic Associations and Epidemiology (3 papers), Evolution and Genetic Dynamics (3 papers) and Cancer Genomics and Diagnostics (2 papers). Vanessa Bruat is often cited by papers focused on Genetic Associations and Epidemiology (3 papers), Evolution and Genetic Dynamics (3 papers) and Cancer Genomics and Diagnostics (2 papers). Vanessa Bruat collaborates with scholars based in Canada, United Kingdom and United States. Vanessa Bruat's co-authors include Philip Awadalla, Elias Gbeha, Jean‐Christophe Grenier, Youssef Idaghdour, Alan Hodgkinson, Jean-Philippe Goulet, David Soave, Fabien C. Lamaze, Kimberly Skead and Mawussé Agbessi and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Vanessa Bruat

9 papers receiving 351 citations

Peers

Vanessa Bruat

MB

GENET

CR

IMMUN

PHEOH

Bernice Packer United States

Fangqin Lin China

C Marth Australia

Feixue Li China

Chengliang Xiong China

Cuong Nguyen Vietnam

Olya Yarychkivska United States

Juntae Kwon South Korea

Ran Gao China

Bernice Packer United States

Vanessa Bruat

294 ×1.7

MB

199 ×1.9

GENET

73 ×1.8

CR

70 ×1.7

IMMUN

33 ×0.8

PHEOH

Citations per year, relative to Vanessa Bruat Vanessa Bruat (= 1×) peers Bernice Packer

Countries citing papers authored by Vanessa Bruat

Since Specialization

Citations

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

Fields of papers citing papers by Vanessa Bruat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vanessa Bruat

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

All Works

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9 of 9 papers shown

1.

Alves, Isabel, Mawussé Agbessi, Vanessa Bruat, et al.. (2022). Recombination affects allele-specific expression of deleterious variants in human populations. Science Advances. 8(19). eabl3819–eabl3819. 4 indexed citations

2.

Skead, Kimberly, Sagi Abelson, Mawussé Agbessi, et al.. (2021). Interacting evolutionary pressures drive mutation dynamics and health outcomes in aging blood. Nature Communications. 12(1). 4921–4921. 12 indexed citations

3.

Lamaze, Fabien C., David Soave, Marie-Julie Favé, et al.. (2018). Aberrant PRDM9 expression impacts the pan-cancer genomic landscape. Genome Research. 28(11). 1611–1620. 27 indexed citations

4.

Favé, Marie‐Julie, Fabien C. Lamaze, David Soave, et al.. (2018). Gene-by-environment interactions in urban populations modulate risk phenotypes. Nature Communications. 9(1). 827–827. 80 indexed citations

5.

Peischl, Stephan, Isabelle Dupanloup, Adrien Foucal, et al.. (2017). Relaxed Selection During a Recent Human Expansion. Genetics. 208(2). 763–777. 42 indexed citations

6.

Troyanov, Stéphan, Guillaume Bollée, Sonia Youhanna, et al.. (2015). Clinical, Genetic, and Urinary Factors Associated with Uromodulin Excretion. Clinical Journal of the American Society of Nephrology. 11(1). 62–69. 33 indexed citations

7.

Quinlan, Jacklyn, Youssef Idaghdour, Jean-Philippe Goulet, et al.. (2014). Genomic architecture of sickle cell disease in West African children. Frontiers in Genetics. 5. 26–26. 12 indexed citations

8.

Hodgkinson, Alan, Youssef Idaghdour, Elias Gbeha, et al.. (2014). High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation. Science. 344(6182). 413–415. 74 indexed citations

9.

Idaghdour, Youssef, Jacklyn Quinlan, Jean-Philippe Goulet, et al.. (2012). Evidence for additive and interaction effects of host genotype and infection in malaria. Proceedings of the National Academy of Sciences. 109(42). 16786–16793. 70 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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