Bahlo M - Search Results

1

Candidate disease gene prediction using Gentrepid: application to a genome-wide association study on coronary artery disease.

Ballouz S, Liu JY, Oti M, Gaeta B, Fatkin D, Bahlo M, Wouters MA. Ballouz S, et al. Among authors: bahlo m. Mol Genet Genomic Med. 2014 Jan;2(1):44-57. doi: 10.1002/mgg3.40. Epub 2013 Nov 13. Mol Genet Genomic Med. 2014. PMID: 24498628 Free PMC article.

2

Analysis of genome-wide association study data using the protein knowledge base.

Ballouz S, Liu JY, Oti M, Gaeta B, Fatkin D, Bahlo M, Wouters MA. Ballouz S, et al. Among authors: bahlo m. BMC Genet. 2011 Nov 13;12:98. doi: 10.1186/1471-2156-12-98. BMC Genet. 2011. PMID: 22077927 Free PMC article.

3

Challenges of diagnostic exome sequencing in an inbred founder population.

Azmanov DN, Chamova T, Tankard R, Gelev V, Bynevelt M, Florez L, Tzoneva D, Zlatareva D, Guergueltcheva V, Bahlo M, Tournev I, Kalaydjieva L. Azmanov DN, et al. Among authors: bahlo m. Mol Genet Genomic Med. 2013 Jul;1(2):71-6. doi: 10.1002/mgg3.7. Epub 2013 Apr 22. Mol Genet Genomic Med. 2013. PMID: 24498604 Free PMC article.

4

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

Bahlo M, Stankovich J, Speed TP, Rubio JP, Burfoot RK, Foote SJ. Bahlo M, et al. Hum Genet. 2006 Mar;119(1-2):38-50. doi: 10.1007/s00439-005-0114-9. Epub 2005 Dec 14. Hum Genet. 2006. PMID: 16362347

5

X chromosome association testing in genome wide association studies.

Hickey PF, Bahlo M. Hickey PF, et al. Among authors: bahlo m. Genet Epidemiol. 2011 Nov;35(7):664-70. doi: 10.1002/gepi.20616. Epub 2011 Aug 4. Genet Epidemiol. 2011. PMID: 21818774

6

Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.

Smith KR, Dahl HH, Canafoglia L, Andermann E, Damiano J, Morbin M, Bruni AC, Giaccone G, Cossette P, Saftig P, Grötzinger J, Schwake M, Andermann F, Staropoli JF, Sims KB, Mole SE, Franceschetti S, Alexander NA, Cooper JD, Chapman HA, Carpenter S, Berkovic SF, Bahlo M. Smith KR, et al. Among authors: bahlo m. Hum Mol Genet. 2013 Apr 1;22(7):1417-23. doi: 10.1093/hmg/dds558. Epub 2013 Jan 7. Hum Mol Genet. 2013. PMID: 23297359 Free PMC article.

7

Dating rare mutations from small samples with dense marker data.

Gandolfo LC, Bahlo M, Speed TP. Gandolfo LC, et al. Among authors: bahlo m. Genetics. 2014 Aug;197(4):1315-27. doi: 10.1534/genetics.114.164616. Epub 2014 May 30. Genetics. 2014. PMID: 24879464 Free PMC article.

8

Using familial information for variant filtering in high-throughput sequencing studies.

Bahlo M, Tankard R, Lukic V, Oliver KL, Smith KR. Bahlo M, et al. Hum Genet. 2014 Nov;133(11):1331-41. doi: 10.1007/s00439-014-1479-4. Epub 2014 Aug 17. Hum Genet. 2014. PMID: 25129038 Free PMC article. Review.

9

Genome-wide analyses identify common variants associated with macular telangiectasia type 2.

Scerri TS, Quaglieri A, Cai C, Zernant J, Matsunami N, Baird L, Scheppke L, Bonelli R, Yannuzzi LA, Friedlander M; MacTel Project Consortium; Egan CA, Fruttiger M, Leppert M, Allikmets R, Bahlo M. Scerri TS, et al. Among authors: bahlo m. Nat Genet. 2017 Apr;49(4):559-567. doi: 10.1038/ng.3799. Epub 2017 Feb 27. Nat Genet. 2017. PMID: 28250457 Free article.

10

Multiple sclerosis: a haplotype association study.

Foote SJ, Rubio JP, Bahlo M, Kilpatrick TJ, Speed TP, Stankovich J, Burfoot R, Butzkueven H, Johnson L, Wilkinson C, Taylor B, Sale M, van der Mei IA, Dickinson JL, Groom P. Foote SJ, et al. Among authors: bahlo m. Novartis Found Symp. 2005;267:31-9; discussion 39-45. Novartis Found Symp. 2005. PMID: 15999799

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