Labrie Y - Search Results

1

A founder mutation in the PLPBP gene in families from Saguenay-Lac-St-Jean region affected by a pyridoxine-dependent epilepsy.

Pal M, Lace B, Labrie Y, Laflamme N, Rioux N, Setty ST, Dugas MA, Gosselin L, Droit A, Chrestian N, Rivest S. Pal M, et al. Among authors: labrie y. JIMD Rep. 2021 Feb 23;59(1):32-41. doi: 10.1002/jmd2.12196. eCollection 2021 May. JIMD Rep. 2021. PMID: 33977028 Free PMC article.

2

A Homozygous Deep Intronic Mutation Alters the Splicing of Nebulin Gene in a Patient With Nemaline Myopathy.

Laflamme N, Lace B, Thonta Setty S, Rioux N, Labrie Y, Droit A, Chrestian N, Rivest S. Laflamme N, et al. Among authors: labrie y. Front Neurol. 2021 Jun 15;12:660113. doi: 10.3389/fneur.2021.660113. eCollection 2021. Front Neurol. 2021. PMID: 34211429 Free PMC article.

3

Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report.

Picher-Martel V, Labrie Y, Rivest S, Lace B, Chrestian N. Picher-Martel V, et al. Among authors: labrie y. BMC Neurol. 2020 Feb 15;20(1):58. doi: 10.1186/s12883-020-01643-1. BMC Neurol. 2020. PMID: 32061250 Free PMC article.

4

Transcriptional signature of lymphoblastoid cell lines of BRCA1, BRCA2 and non-BRCA1/2 high risk breast cancer families.

Pouliot MC, Kothari C, Joly-Beauparlant C, Labrie Y, Ouellette G, Simard J, Droit A, Durocher F. Pouliot MC, et al. Among authors: labrie y. Oncotarget. 2017 Aug 12;8(45):78691-78712. doi: 10.18632/oncotarget.20219. eCollection 2017 Oct 3. Oncotarget. 2017. PMID: 29108258 Free PMC article.

5

Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families.

Guénard F, Labrie Y, Ouellette G, Joly Beauparlant C, Simard J; INHERIT BRCAs; Durocher F. Guénard F, et al. Among authors: labrie y. J Hum Genet. 2008;53(7):579. doi: 10.1007/s10038-008-0285-z. Epub 2008 Apr 15. J Hum Genet. 2008. PMID: 18414782

6

Identification of a gene signature for different stages of breast cancer development that could be used for early diagnosis and specific therapy.

Kothari C, Ouellette G, Labrie Y, Jacob S, Diorio C, Durocher F. Kothari C, et al. Among authors: labrie y. Oncotarget. 2018 Dec 21;9(100):37407-37420. doi: 10.18632/oncotarget.26448. eCollection 2018 Dec 21. Oncotarget. 2018. PMID: 30647841 Free PMC article.

7

Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.

Durocher F, Labrie Y, Soucy P, Sinilnikova O, Labuda D, Bessette P, Chiquette J, Laframboise R, Lépine J, Lespérance B, Ouellette G, Pichette R, Plante M, Tavtigian SV, Simard J. Durocher F, et al. Among authors: labrie y. BMC Cancer. 2006 Sep 29;6:230. doi: 10.1186/1471-2407-6-230. BMC Cancer. 2006. PMID: 17010193 Free PMC article.

8

Germline mutations in the breast cancer susceptibility gene PTEN are rare in high-risk non-BRCA1/2 French Canadian breast cancer families.

Guénard F, Labrie Y, Ouellette G, Beauparlant CJ, Bessette P, Chiquette J, Laframboise R, Lépine J, Lespérance B, Pichette R, Plante M, Durocher F; INHERIT BRCAs. Guénard F, et al. Among authors: labrie y. Fam Cancer. 2007;6(4):483-90. doi: 10.1007/s10689-007-9151-y. Epub 2007 Jul 17. Fam Cancer. 2007. PMID: 17636424

9

Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non BRCA1/2 French Canadian breast and ovarian cancer families.

Desjardins S, Belleau P, Labrie Y, Ouellette G, Bessette P, Chiquette J, Laframboise R, Lépine J, Lespérance B, Pichette R, Plante M; INHERIT BRCAs; Durocher F. Desjardins S, et al. Among authors: labrie y. Int J Cancer. 2008 Jan 1;122(1):108-16. doi: 10.1002/ijc.23058. Int J Cancer. 2008. PMID: 17764113

10

Genetic sequence variations and ADPRT haplotype analysis in French Canadian families with high risk of breast cancer.

Durocher F, Labrie Y, Ouellette G; INHERIT BRCAs; Simard J. Durocher F, et al. Among authors: labrie y. J Hum Genet. 2007;52(12):963-977. doi: 10.1007/s10038-007-0203-9. Epub 2007 Oct 18. J Hum Genet. 2007. PMID: 17943227

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