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Results: 15

Related Articles by Review for PubMed (Select 21325948)

1.

Global analysis of disease-related DNA sequence variation in 10 healthy individuals: implications for whole genome-based clinical diagnostics.

Moore B, Hu H, Singleton M, De La Vega FM, Reese MG, Yandell M.

Genet Med. 2011 Mar;13(3):210-7. doi: 10.1097/GIM.0b013e31820ed321.

2.

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
3.

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
4.

Medical DNA sequencing.

Marian AJ.

Curr Opin Cardiol. 2011 May;26(3):175-80. doi: 10.1097/HCO.0b013e3283459857. Review.

5.

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.

6.

Revealing the human mutome.

Chen JM, Férec C, Cooper DN.

Clin Genet. 2010 Oct;78(4):310-20. doi: 10.1111/j.1399-0004.2010.01474.x. Review.

PMID:
20569258
7.

Massive parallel sequencing in animal genetics: wherefroms and wheretos.

Pérez-Enciso M, Ferretti L.

Anim Genet. 2010 Dec;41(6):561-9. doi: 10.1111/j.1365-2052.2010.02057.x. Review.

PMID:
20477787
8.

The Human Genome Project--an overview.

Bentley DR.

Med Res Rev. 2000 May;20(3):189-96. Review.

PMID:
10797463
9.

The personal genome and the practice of cardiovascular medicine.

Marian AJ.

Methodist Debakey Cardiovasc J. 2010 Nov-2011 Jan;6(4):13-20. Review.

PMID:
21088654
10.

Whole genome sequencing.

Ng PC, Kirkness EF.

Methods Mol Biol. 2010;628:215-26. doi: 10.1007/978-1-60327-367-1_12. Review.

PMID:
20238084
11.

Accessing complex crop genomes with next-generation sequencing.

Edwards D, Batley J, Snowdon RJ.

Theor Appl Genet. 2013 Jan;126(1):1-11. doi: 10.1007/s00122-012-1964-x. Epub 2012 Sep 5. Review.

PMID:
22948437
12.

Rare-disease genetics in the era of next-generation sequencing: discovery to translation.

Boycott KM, Vanstone MR, Bulman DE, MacKenzie AE.

Nat Rev Genet. 2013 Oct;14(10):681-91. doi: 10.1038/nrg3555. Epub 2013 Sep 3. Review.

PMID:
23999272
13.

Identification of causal sequence variants of disease in the next generation sequencing era.

Kingsley CB.

Methods Mol Biol. 2011;700:37-46. doi: 10.1007/978-1-61737-954-3_3. Review.

PMID:
21204025
14.

Genetic contributions to clinical pain and analgesia: avoiding pitfalls in genetic research.

Kim H, Clark D, Dionne RA.

J Pain. 2009 Jul;10(7):663-93. doi: 10.1016/j.jpain.2009.04.001. Review.

15.

Radiogenomics helps to achieve personalized therapy by evaluating patient responses to radiation treatment.

Guo Z, Shu Y, Zhou H, Zhang W, Wang H.

Carcinogenesis. 2015 Mar;36(3):307-17. doi: 10.1093/carcin/bgv007. Epub 2015 Jan 20. Review.

PMID:
25604391
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