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Results: 15

1.

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.

Dyment DA, Cader MZ, Chao MJ, Lincoln MR, Morrison KM, Disanto G, Morahan JM, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC, Ramagopalan SV.

Neurology. 2012 Jul 31;79(5):406-11. doi: 10.1212/WNL.0b013e3182616fc4. Epub 2012 Jun 27.

PMID:
22744673
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Molecular genetic studies of complex phenotypes.

Marian AJ.

Transl Res. 2012 Feb;159(2):64-79. doi: 10.1016/j.trsl.2011.08.001. Epub 2011 Aug 31. Review.

PMID:
22243791
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Exome sequencing and complex disease: practical aspects of rare variant association studies.

Do R, Kathiresan S, Abecasis GR.

Hum Mol Genet. 2012 Oct 15;21(R1):R1-9. Epub 2012 Sep 13. Review.

PMID:
22983955
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.

Wagner MJ.

Pharmacogenomics. 2013 Mar;14(4):413-24. doi: 10.2217/pgs.13.36. Review.

PMID:
23438888
[PubMed - indexed for MEDLINE]
5.

Exome versus transcriptome sequencing in identifying coding region variants.

Ku CS, Wu M, Cooper DN, Naidoo N, Pawitan Y, Pang B, Iacopetta B, Soong R.

Expert Rev Mol Diagn. 2012 Apr;12(3):241-51. doi: 10.1586/erm.12.10. Review.

PMID:
22468815
[PubMed - indexed for MEDLINE]
6.

Challenges in medical applications of whole exome/genome sequencing discoveries.

Marian AJ.

Trends Cardiovasc Med. 2012 Nov;22(8):219-23. doi: 10.1016/j.tcm.2012.08.001. Epub 2012 Aug 24. Review.

PMID:
22921985
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

The next generation of complex lung genetic studies.

Yang IV, Schwartz DA.

Am J Respir Crit Care Med. 2012 Dec 1;186(11):1087-94. doi: 10.1164/rccm.201207-1178PP. Epub 2012 Aug 30. Review.

PMID:
22936355
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Future possibilities in migraine genetics.

Rudkjobing LA, Esserlind AL, Olesen J.

J Headache Pain. 2012 Oct;13(7):505-11. doi: 10.1007/s10194-012-0481-2. Epub 2012 Sep 7. Review.

PMID:
22955452
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Inferring causality and functional significance of human coding DNA variants.

Sunyaev SR.

Hum Mol Genet. 2012 Oct 15;21(R1):R10-7. Epub 2012 Sep 17. Review.

PMID:
22990389
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Common vs. rare allele hypotheses for complex diseases.

Schork NJ, Murray SS, Frazer KA, Topol EJ.

Curr Opin Genet Dev. 2009 Jun;19(3):212-9. doi: 10.1016/j.gde.2009.04.010. Epub 2009 May 28. Review.

PMID:
19481926
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease.

Bras J, Guerreiro R, Hardy J.

Nat Rev Neurosci. 2012 Jun 20;13(7):453-64. doi: 10.1038/nrn3271. Review.

PMID:
22714018
[PubMed - indexed for MEDLINE]
12.

Whole exome sequencing of intracranial aneurysm.

Foroud T; FIA Study Investigators.

Stroke. 2013 Jun;44(6 Suppl 1):S26-8. doi: 10.1161/STROKEAHA.113.001174. Review. No abstract available.

PMID:
23709719
[PubMed - indexed for MEDLINE]
Free Article
13.

Genomic modulators of the immune response.

Knight JC.

Trends Genet. 2013 Feb;29(2):74-83. doi: 10.1016/j.tig.2012.10.006. Epub 2012 Nov 1. Review.

PMID:
23122694
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Genome-wide association studies: will we ever predict susceptibility to multiple sclerosis through genetics?

Dobson R, Ramagopalan SV, Giovannoni G.

Expert Rev Neurother. 2013 Mar;13(3):235-7. doi: 10.1586/ern.13.13. Review. No abstract available.

PMID:
23448211
[PubMed - indexed for MEDLINE]
15.

Understanding human glycosylation disorders: biochemistry leads the charge.

Freeze HH.

J Biol Chem. 2013 Mar 8;288(10):6936-45. doi: 10.1074/jbc.R112.429274. Epub 2013 Jan 17. Review.

PMID:
23329837
[PubMed - indexed for MEDLINE]
Free PMC Article

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