Thibaud Boutin

8.6k total citations
18 papers, 535 citations indexed

About

Thibaud Boutin is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Thibaud Boutin has authored 18 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Thibaud Boutin's work include Genetic Associations and Epidemiology (6 papers), Thyroid Disorders and Treatments (6 papers) and Growth Hormone and Insulin-like Growth Factors (4 papers). Thibaud Boutin is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Thyroid Disorders and Treatments (6 papers) and Growth Hormone and Insulin-like Growth Factors (4 papers). Thibaud Boutin collaborates with scholars based in United Kingdom, Croatia and France. Thibaud Boutin's co-authors include Pierre Capy, Arnaud Le Rouzic, Aurélie Hua‐Van, Jonathan Filée, Caroline Hayward, Andrew M. McIntosh, Ian J. Deary, Chris Haley, Yanni Zeng and Vesna Boraska Perica and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Thibaud Boutin

18 papers receiving 523 citations

Peers

Thibaud Boutin

GENET

EDM

PPCH

Kuo‐Wei Lee Taiwan

Arthur Gilly United Kingdom

Ryan M. Ames United Kingdom

Yagnesh Umrania United Kingdom

Lauren N. Booth United States

Nadezhda M. Belonogova Russia

Jennifer Crodian United States

O Wai‐Sum Hong Kong

Nadja Mannowetz United States

Adelheid Lempradl United States

Kuo‐Wei Lee Taiwan

Thibaud Boutin

214 ×0.7

662 ×2.2

39 ×0.3

GENET

6 ×0.3

EDM

16 ×0.7

PPCH

Citations per year, relative to Thibaud Boutin Thibaud Boutin (= 1×) peers Kuo‐Wei Lee

Countries citing papers authored by Thibaud Boutin

Since Specialization

Citations

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

Fields of papers citing papers by Thibaud Boutin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thibaud Boutin

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

All Works

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18 of 18 papers shown

Boutin, Thibaud, et al.. (2023). Colocalization of corneal resistance factor GWAS loci with GTEx e/sQTLs highlights plausible candidate causal genes for keratoconus postnatal corneal stroma weakening. Frontiers in Genetics. 14. 1171217–1171217. 1 indexed citations

Pleić, Nikolina, Mirjana Babić Leko, Ivana Gunjača, et al.. (2022). Genome-Wide Association Analysis and Genomic Prediction of Thyroglobulin Plasma Levels. International Journal of Molecular Sciences. 23(4). 2173–2173. 2 indexed citations

Boutin, Thibaud, Archie Campbell, Andrew M. McIntosh, et al.. (2022). SNP and Haplotype Regional Heritability Mapping (SNHap-RHM): Joint Mapping of Common and Rare Variation Affecting Complex Traits. Frontiers in Genetics. 12. 791712–791712. 4 indexed citations

Bretherick, Andrew D., Oriol Canela‐Xandri, Peter K. Joshi, et al.. (2020). Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits. PLoS Genetics. 16(7). e1008785–e1008785. 21 indexed citations

Pairo‐Castineira, Erola, et al.. (2020). Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants. Communications Biology. 3(1). 762–762. 7 indexed citations

Stevenson, Anna J., Daniel L. McCartney, Robert F. Hillary, et al.. (2020). Characterisation of an inflammation-related epigenetic score and its association with cognitive ability. Clinical Epigenetics. 12(1). 113–113. 41 indexed citations

Kerr, Shona M., Lucija Klarić, Mihail Halachev, et al.. (2019). An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. Scientific Reports. 9(1). 10964–10964. 16 indexed citations

Popović, Marijana, Thibaud Boutin, Vesela Torlak, et al.. (2019). Genetic Variants in the ST6GAL1 Gene Are Associated with Thyroglobulin Plasma Level in Healthy Individuals. Thyroid. 29(6). 886–893. 5 indexed citations

Gunjača, Ivana, Thibaud Boutin, Vesela Torlak, et al.. (2019). Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population. Journal of Human Genetics. 64(5). 473–480. 6 indexed citations

10.

Popović, Marijana, Vesela Torlak, Thibaud Boutin, et al.. (2019). Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone. Journal of Endocrinological Investigation. 42(10). 1171–1180. 9 indexed citations

11.

Boutin, Thibaud, Vesela Torlak, Ivana Gunjača, et al.. (2019). Genome-Wide Analysis Identifies Two Susceptibility Loci for Positive Thyroid Peroxidase and Thyroglobulin Antibodies. The Journal of Clinical Endocrinology & Metabolism. 105(3). 944–951. 4 indexed citations

12.

Howard, David M., Mark J. Adams, Jonathan D. Hafferty, et al.. (2019). THE IDENTIFICATION OF HETEROGENEOUS GENETIC SUBGROUPS FOR MAJOR DEPRESSIVE DISORDER. European Neuropsychopharmacology. 29. S846–S846. 1 indexed citations

13.

Hall, Lynsey S., Mark J. Adams, Aleix Arnau‐Soler, et al.. (2018). Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank. Translational Psychiatry. 8(1). 9–9. 53 indexed citations

14.

Torlak, Vesela, Thibaud Boutin, Marijana Popović, et al.. (2018). Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level. Molecular Medicine. 24(1). 15–15. 10 indexed citations

15.

Popović, Marijana, Thibaud Boutin, Vesela Torlak, et al.. (2018). Genome-wide meta-analysis identifies novel gender specific loci associated with thyroid antibodies level in Croatians. Genomics. 111(4). 737–743. 11 indexed citations

16.

Boutin, Thibaud, Arnaud Le Rouzic, & Pierre Capy. (2012). How does selfing affect the dynamics of selfish transposable elements?. Mobile DNA. 3(1). 5–5. 34 indexed citations

17.

Hua‐Van, Aurélie, Arnaud Le Rouzic, Thibaud Boutin, Jonathan Filée, & Pierre Capy. (2011). The struggle for life of the genome's selfish architects. Biology Direct. 6(1). 19–19. 184 indexed citations

18.

Rouzic, Arnaud Le, Thibaud Boutin, & Pierre Capy. (2007). Long-term evolution of transposable elements. Proceedings of the National Academy of Sciences. 104(49). 19375–19380. 126 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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