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Similar articles for PubMed (Select 20479773)

1.

Uncovering the roles of rare variants in common disease through whole-genome sequencing.

Cirulli ET, Goldstein DB.

Nat Rev Genet. 2010 Jun;11(6):415-25. doi: 10.1038/nrg2779. Review.

PMID:
20479773
2.

Discovery of rare variants via sequencing: implications for the design of complex trait association studies.

Li B, Leal SM.

PLoS Genet. 2009 May;5(5):e1000481. doi: 10.1371/journal.pgen.1000481. Epub 2009 May 15.

3.

Common genetic variation and human disease.

Orr N, Chanock S.

Adv Genet. 2008;62:1-32. doi: 10.1016/S0065-2660(08)00601-9. Review.

PMID:
19010252
4.

Design of association studies with pooled or un-pooled next-generation sequencing data.

Kim SY, Li Y, Guo Y, Li R, Holmkvist J, Hansen T, Pedersen O, Wang J, Nielsen R.

Genet Epidemiol. 2010 Jul;34(5):479-91. doi: 10.1002/gepi.20501.

PMID:
20552648
5.

Challenges in the identification and use of rare disease-associated predisposition variants.

Carvajal-Carmona LG.

Curr Opin Genet Dev. 2010 Jun;20(3):277-81. Review.

PMID:
20564784
6.

After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.

Gershon ES, Alliey-Rodriguez N, Liu C.

Am J Psychiatry. 2011 Mar;168(3):253-6. doi: 10.1176/appi.ajp.2010.10091340. Epub 2011 Feb 1. Review.

PMID:
21285144
7.

What can exome sequencing do for you?

Majewski J, Schwartzentruber J, Lalonde E, Montpetit A, Jabado N.

J Med Genet. 2011 Sep;48(9):580-9. doi: 10.1136/jmedgenet-2011-100223. Epub 2011 Jul 5. Review.

PMID:
21730106
8.

A neurologist's guide to genome-wide association studies.

Mullen SA, Crompton DE, Carney PW, Helbig I, Berkovic SF.

Neurology. 2009 Feb 10;72(6):558-65. doi: 10.1212/01.wnl.0000341942.29513.bd. Review.

PMID:
19204266
9.
10.

The genome-wide association study--a new era for common polygenic disorders.

Roberts R, Wells GA, Stewart AF, Dandona S, Chen L.

J Cardiovasc Transl Res. 2010 Jun;3(3):173-82. doi: 10.1007/s12265-010-9178-6. Epub 2010 Mar 27. Review.

PMID:
20560037
11.

Large-scale in silico mapping of complex quantitative traits in inbred mice.

Liu P, Vikis H, Lu Y, Wang D, You M.

PLoS One. 2007 Jul 25;2(7):e651.

12.

Genetic variants in association studies--review of strengths and weaknesses in study design and current knowledge of impact on cancer risk.

Andersson U, McKean-Cowdin R, Hjalmars U, Malmer B.

Acta Oncol. 2009;48(7):948-54. Review.

PMID:
19863254
13.

Strategies for identifying the genetic basis of dyslipidemia: genome-wide association studies vs. the resequencing of extremes.

Khor CC, Goh DL.

Curr Opin Lipidol. 2010 Apr;21(2):123-7. doi: 10.1097/MOL.0b013e328336eae9. Review.

PMID:
20125008
14.

Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.

Smith JG, Melander O, Lövkvist H, Hedblad B, Engström G, Nilsson P, Carlson J, Berglund G, Norrving B, Lindgren A.

Circ Cardiovasc Genet. 2009 Apr;2(2):159-64. doi: 10.1161/CIRCGENETICS.108.835173. Epub 2009 Feb 12.

15.

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.

16.

Bar-coded, multiplexed sequencing of targeted DNA regions using the Illumina Genome Analyzer.

Szelinger S, Kurdoglu A, Craig DW.

Methods Mol Biol. 2011;700:89-104. doi: 10.1007/978-1-61737-954-3_7.

PMID:
21204029
17.

Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation Ecotilling.

Marroni F, Pinosio S, Di Centa E, Jurman I, Boerjan W, Felice N, Cattonaro F, Morgante M.

Plant J. 2011 Aug;67(4):736-45. doi: 10.1111/j.1365-313X.2011.04627.x. Epub 2011 Jul 11. Erratum in: Plant J. 2012 Feb;69(3):564.

PMID:
21554453
18.

Genomic copy number variation, human health, and disease.

Wain LV, Armour JA, Tobin MD.

Lancet. 2009 Jul 25;374(9686):340-50. doi: 10.1016/S0140-6736(09)60249-X. Epub 2009 Jun 15. Review.

PMID:
19535135
19.

The discovery of human genetic variations and their use as disease markers: past, present and future.

Ku CS, Loy EY, Salim A, Pawitan Y, Chia KS.

J Hum Genet. 2010 Jul;55(7):403-15. doi: 10.1038/jhg.2010.55. Epub 2010 May 20. Review.

PMID:
20485443
20.

An evaluation of statistical approaches to rare variant analysis in genetic association studies.

Morris AP, Zeggini E.

Genet Epidemiol. 2010 Feb;34(2):188-93. doi: 10.1002/gepi.20450.

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