Yvan Labrie

1.4k total citations
43 papers, 1.1k citations indexed

About

Yvan Labrie is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Yvan Labrie has authored 43 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 20 papers in Genetics and 13 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Yvan Labrie's work include BRCA gene mutations in cancer (14 papers), Hormonal Regulation and Hypertension (11 papers) and DNA Repair Mechanisms (10 papers). Yvan Labrie is often cited by papers focused on BRCA gene mutations in cancer (14 papers), Hormonal Regulation and Hypertension (11 papers) and DNA Repair Mechanisms (10 papers). Yvan Labrie collaborates with scholars based in Canada, France and U.S. Virgin Islands. Yvan Labrie's co-authors include Francine Durocher, Jacques Simard, Claude Labrie, Geneviève Ouellette, Fernand Labrie, Jacques Couët, Carl Turgeon, Van Luu‐The, Fernand Labrie and Heng Qi and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Molecular Biology and Biochemical and Biophysical Research Communications.

In The Last Decade

Yvan Labrie

43 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yvan Labrie Canada 22 615 410 325 168 158 43 1.1k
Jacqueline Barra France 11 926 1.5× 528 1.3× 154 0.5× 150 0.9× 74 0.5× 13 1.6k
J.R. Puddefoot United Kingdom 20 453 0.7× 271 0.7× 450 1.4× 130 0.8× 82 0.5× 58 1.2k
Catherine K.L. Too Canada 22 625 1.0× 155 0.4× 196 0.6× 148 0.9× 163 1.0× 58 1.1k
J. Don Chen United States 15 1.4k 2.3× 801 2.0× 204 0.6× 245 1.5× 109 0.7× 17 1.9k
Ahmed Raafat United States 19 518 0.8× 430 1.0× 159 0.5× 569 3.4× 217 1.4× 40 1.1k
W Hoeck Switzerland 10 536 0.9× 282 0.7× 191 0.6× 139 0.8× 180 1.1× 11 931
W. E. C. Bradley Canada 21 1.0k 1.6× 497 1.2× 173 0.5× 168 1.0× 210 1.3× 54 1.3k
Rive Sarfstein Israel 26 899 1.5× 158 0.4× 471 1.4× 244 1.5× 388 2.5× 51 1.5k
Jean-Louis Danan France 22 559 0.9× 264 0.6× 96 0.3× 97 0.6× 169 1.1× 41 1.0k
Hetti Poukka Finland 13 1.1k 1.8× 629 1.5× 289 0.9× 251 1.5× 150 0.9× 15 1.5k

Countries citing papers authored by Yvan Labrie

Since Specialization
Citations

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

Fields of papers citing papers by Yvan Labrie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yvan Labrie

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

All Works

20 of 20 papers shown
1.
Laflamme, Nathalie, Baiba Lāce, Yvan Labrie, et al.. (2021). A Homozygous Deep Intronic Mutation Alters the Splicing of Nebulin Gene in a Patient With Nemaline Myopathy. Frontiers in Neurology. 12. 660113–660113. 6 indexed citations
2.
Picher‐Martel, Vincent, Yvan Labrie, Serge Rivest, Baiba Lāce, & Nicolas Chrestian. (2020). Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report. BMC Neurology. 20(1). 58–58. 6 indexed citations
3.
Labrie, Yvan, et al.. (2012). Polymorphic variations in the FANCA gene in high‐risk non‐BRCA1/2 breast cancer individuals from the French Canadian population. Molecular Oncology. 7(1). 85–100. 23 indexed citations
4.
Labrie, Yvan, et al.. (2012). Analysis of ZNF350/ZBRK1 promoter variants and breast cancer susceptibility in non-BRCA1/2 French Canadian breast cancer families. Journal of Human Genetics. 58(2). 59–66. 5 indexed citations
5.
Guénard, Frédéric, et al.. (2010). Evaluation of the Contribution of the Three Breast Cancer Susceptibility Genes CHEK2 , STK11 , and PALB2 in Non- BRCA1/2 French Canadian Families with High Risk of Breast Cancer. Genetic Testing and Molecular Biomarkers. 14(4). 515–526. 25 indexed citations
6.
Guénard, Frédéric, et al.. (2009). Genetic sequence variations of BRCA1-interacting genes AURKA, BAP1, BARD1 and DHX9 in French Canadian Families with high risk of breast cancer. Journal of Human Genetics. 54(3). 152–161. 42 indexed citations
7.
Desjardins, Sylvie, et al.. (2009). Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2French Canadian families with high risk of breast cancer. BMC Cancer. 9(1). 181–181. 32 indexed citations
8.
Labrie, Yvan, Ézéquiel Calvo, Pascal Belleau, et al.. (2008). Fine temporal analysis of DHT transcriptional modulation of the ATM/Gadd45g signaling pathways in the mouse uterus. Molecular Reproduction and Development. 76(3). 278–288. 9 indexed citations
9.
Guénard, Frédéric, Yvan Labrie, Geneviève Ouellette, et al.. (2008). Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families. Journal of Human Genetics. 53(7). 579–591. 27 indexed citations
10.
Desjardins, Sylvie, et al.. (2008). Analysis of GADD45A sequence variations in French Canadian families with high risk of breast cancer. Journal of Human Genetics. 53(6). 490–498. 8 indexed citations
11.
Durocher, Francine, et al.. (2007). Genetic sequence variations and ADPRT haplotype analysis in French Canadian families with high risk of breast cancer. Journal of Human Genetics. 52(12). 963–977. 10 indexed citations
12.
Desjardins, Sylvie, Pascal Belleau, Yvan Labrie, et al.. (2007). Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high‐risk non BRCA1/2 French Canadian breast and ovarian cancer families. International Journal of Cancer. 122(1). 108–116. 17 indexed citations
13.
Durocher, Francine, Rocío Sánchez, Marie‐Louise Ricketts, et al.. (2005). Characterization of the guinea pig 3β-hydroxysteroid dehydrogenase/Δ5–Δ4-isomerase expressed in the adrenal gland and gonads. The Journal of Steroid Biochemistry and Molecular Biology. 97(3). 289–298. 3 indexed citations
14.
Qi, Heng, et al.. (2001). Androgens induce expression of SPAK, a STE20/SPS1-related kinase, in LNCaP human prostate cancer cells. Molecular and Cellular Endocrinology. 182(2). 181–192. 34 indexed citations
15.
Simard, Jacques, Francine Durocher, Farida Mébarki, et al.. (1996). Molecular biology and genetics of the 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 isomerase gene family. Journal of Endocrinology. 150. 41 indexed citations
16.
Puy, Libertad A., Carl Turgeon, Donald Gagné, et al.. (1996). Localization and Regulation of Expression of the FAR-17A Gene in the Hamster Flank Organs. Journal of Investigative Dermatology. 107(1). 44–50. 14 indexed citations
17.
Valle, Luisa Dalla, Jacques Couët, Yvan Labrie, et al.. (1995). Occurrence of cytochrome P450c17 mRNA and dehydroepiandrosterone biosynthesis in the rat gastrointestinal tract. Molecular and Cellular Endocrinology. 111(1). 83–92. 38 indexed citations
18.
Durocher, Francine, Jean Morissette, Yvan Labrie, Fernand Labrie, & Jacques Simard. (1995). Mapping of the HSD17B2 gene encoding type II 17β-hydroxysteroid dehydrogenase close to D16S422 on chromosome 16q24.1–q24.2. Genomics. 25(3). 724–726. 21 indexed citations
19.
Luu‐The, Van, Y. Sugimoto, Libertad A. Puy, et al.. (1994). Characterization, Expression, and Immunohistochemical Localization of 5α-Reductase in Human Skin. Journal of Investigative Dermatology. 102(2). 221–226. 103 indexed citations
20.
Martel, Céline, Donald Gagné, Jacques Couët, et al.. (1994). Rapid modulation of ovarian 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 isomerase gene expression by prolactin and human chorionic gonadotropin in the hypophysectomized rat. Molecular and Cellular Endocrinology. 99(1). 63–71. 25 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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