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Items: 1 to 20 of 98

1.

Linkage analysis in the next-generation sequencing era.

Bailey-Wilson JE, Wilson AF.

Hum Hered. 2011;72(4):228-36. doi: 10.1159/000334381. Epub 2011 Dec 23. Review.

2.

Identifying rare variants associated with complex traits via sequencing.

Li B, Liu DJ, Leal SM.

Curr Protoc Hum Genet. 2013 Jul;Chapter 1:Unit 1.26. doi: 10.1002/0471142905.hg0126s78. Review.

3.

Strategies to identify genes for complex disorders: a focus on bipolar disorder and chromosome 16p.

Byerley W, Badner JA.

Psychiatr Genet. 2011 Aug;21(4):173-82. doi: 10.1097/YPG.0b013e32833a21e3. Review.

PMID:
20453718
4.

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.

5.

In search of low-frequency and rare variants affecting complex traits.

Panoutsopoulou K, Tachmazidou I, Zeggini E.

Hum Mol Genet. 2013 Oct 15;22(R1):R16-21. doi: 10.1093/hmg/ddt376. Epub 2013 Aug 6. Review.

6.

[Exome sequencing and its application].

Zhang X, Li M, Zhang XJ.

Yi Chuan. 2011 Aug;33(8):847-56. Review. Chinese.

PMID:
21831801
7.

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
8.

Emerging trends in the search for genetic variants predisposing to human obesity.

Swarbrick MM, Vaisse C.

Curr Opin Clin Nutr Metab Care. 2003 Jul;6(4):369-75. Review.

PMID:
12806208
9.

Revisiting Mendelian disorders through exome sequencing.

Ku CS, Naidoo N, Pawitan Y.

Hum Genet. 2011 Apr;129(4):351-70. doi: 10.1007/s00439-011-0964-2. Epub 2011 Feb 18. Review.

PMID:
21331778
10.

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.

11.

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
12.

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.

13.

Narrowing the boundaries of the genetic architecture of schizophrenia.

Wray NR, Visscher PM.

Schizophr Bull. 2010 Jan;36(1):14-23. doi: 10.1093/schbul/sbp137. Epub 2009 Dec 8. Review.

14.

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.

15.

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

Visscher PM, Goddard ME, Derks EM, Wray NR.

Mol Psychiatry. 2012 May;17(5):474-85. doi: 10.1038/mp.2011.65. Epub 2011 Jun 14. Review.

PMID:
21670730
16.

Next-generation gene discovery for variants of large impact on lipid traits.

Rosenthal E, Blue E, Jarvik GP.

Curr Opin Lipidol. 2015 Apr;26(2):114-9. doi: 10.1097/MOL.0000000000000156. Review.

17.

Progress and promise of genome-wide association studies for human complex trait genetics.

Stranger BE, Stahl EA, Raj T.

Genetics. 2011 Feb;187(2):367-83. doi: 10.1534/genetics.110.120907. Epub 2010 Nov 29. Review.

18.

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
19.

Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data.

Cooper GM, Shendure J.

Nat Rev Genet. 2011 Aug 18;12(9):628-40. doi: 10.1038/nrg3046. Review.

PMID:
21850043
20.

Designs for linkage analysis and association studies of complex diseases.

Cui Y, Li G, Li S, Wu R.

Methods Mol Biol. 2010;620:219-42. doi: 10.1007/978-1-60761-580-4_6. Review.

PMID:
20652506
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