Ge B - Search Results

1

Radiation hybrid map of the mouse genome.

Van Etten WJ, Steen RG, Nguyen H, Castle AB, Slonim DK, Ge B, Nusbaum C, Schuler GD, Lander ES, Hudson TJ. Van Etten WJ, et al. Among authors: ge b. Nat Genet. 1999 Aug;22(4):384-7. doi: 10.1038/11962. Nat Genet. 1999. PMID: 10431245

2

Influence of human genome polymorphism on gene expression.

Pastinen T, Ge B, Hudson TJ. Pastinen T, et al. Among authors: ge b. Hum Mol Genet. 2006 Apr 15;15 Spec No 1:R9-16. doi: 10.1093/hmg/ddl044. Hum Mol Genet. 2006. PMID: 16651375 Review.

3

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.

Engert JC, Bérubé P, Mercier J, Doré C, Lepage P, Ge B, Bouchard JP, Mathieu J, Melançon SB, Schalling M, Lander ES, Morgan K, Hudson TJ, Richter A. Engert JC, et al. Among authors: ge b. Nat Genet. 2000 Feb;24(2):120-5. doi: 10.1038/72769. Nat Genet. 2000. PMID: 10655055

4

Mapping common regulatory variants to human haplotypes.

Pastinen T, Ge B, Gurd S, Gaudin T, Dore C, Lemire M, Lepage P, Harmsen E, Hudson TJ. Pastinen T, et al. Among authors: ge b. Hum Mol Genet. 2005 Dec 15;14(24):3963-71. doi: 10.1093/hmg/ddi420. Epub 2005 Nov 21. Hum Mol Genet. 2005. PMID: 16301213

5

Mapping cis-acting regulatory variation in recombinant congenic strains.

Lee PD, Ge B, Greenwood CM, Sinnett D, Fortin Y, Brunet S, Fortin A, Takane M, Skamene E, Pastinen T, Hallett M, Hudson TJ, Sladek R. Lee PD, et al. Among authors: ge b. Physiol Genomics. 2006 Apr 13;25(2):294-302. doi: 10.1152/physiolgenomics.00168.2005. Epub 2006 Jan 31. Physiol Genomics. 2006. PMID: 16449383

6

Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

Richter A, Rioux JD, Bouchard JP, Mercier J, Mathieu J, Ge B, Poirier J, Julien D, Gyapay G, Weissenbach J, Hudson TJ, Melançon SB, Morgan K. Richter A, et al. Among authors: ge b. Am J Hum Genet. 1999 Mar;64(3):768-75. doi: 10.1086/302274. Am J Hum Genet. 1999. PMID: 10053011 Free PMC article.

7

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.

Engert JC, Doré C, Mercier J, Ge B, Bétard C, Rioux JD, Owen C, Bérubé P, Devon K, Birren B, Melançon SB, Morgan K, Hudson TJ, Richter A. Engert JC, et al. Among authors: ge b. Genomics. 1999 Dec 1;62(2):156-64. doi: 10.1006/geno.1999.6003. Genomics. 1999. PMID: 10610707

8

Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci.

Lemire M, Zaidi SH, Ban M, Ge B, Aïssi D, Germain M, Kassam I, Wang M, Zanke BW, Gagnon F, Morange PE, Trégouët DA, Wells PS, Sawcer S, Gallinger S, Pastinen T, Hudson TJ. Lemire M, et al. Among authors: ge b. Nat Commun. 2015 Feb 26;6:6326. doi: 10.1038/ncomms7326. Nat Commun. 2015. PMID: 25716334 Free PMC article.

9

Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.

Serre D, Gurd S, Ge B, Sladek R, Sinnett D, Harmsen E, Bibikova M, Chudin E, Barker DL, Dickinson T, Fan JB, Hudson TJ. Serre D, et al. Among authors: ge b. PLoS Genet. 2008 Feb 29;4(2):e1000006. doi: 10.1371/journal.pgen.1000006. PLoS Genet. 2008. PMID: 18454203 Free PMC article.

10

Survey of allelic expression using EST mining.

Ge B, Gurd S, Gaudin T, Dore C, Lepage P, Harmsen E, Hudson TJ, Pastinen T. Ge B, et al. Genome Res. 2005 Nov;15(11):1584-91. doi: 10.1101/gr.4023805. Genome Res. 2005. PMID: 16251468 Free PMC article.

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