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Similar articles for PubMed (Select 21730106)

1.

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
2.

Genomic diagnosis by whole genome sequencing in a Korean family with atypical progeroid syndrome.

Lee S, Park SM, Kim HJ, Kim JW, Yu DS, Lee YB.

J Dermatol. 2015 Jun 29. doi: 10.1111/1346-8138.13005. [Epub ahead of print]

PMID:
26122271
3.

Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases.

Alkuraya FS; Saudi Mendeliome Group.

Genome Biol. 2015 Jun 26;16(1):134. [Epub ahead of print]

PMID:
26112015
4.

Genetic basis of hypersensitivity reactions to nonsteroidal anti-inflammatory drugs.

Gómez F, Perkins JR, García-Martín E, Canto G, Cornejo-García JA.

Curr Opin Allergy Clin Immunol. 2015 Aug;15(4):285-93. doi: 10.1097/ACI.0000000000000178.

PMID:
26110677
5.

From standard to new genome-based therapy of gastric cancer.

Lianos GD, Mangano A, Cho WC, Roukos DH.

Expert Rev Gastroenterol Hepatol. 2015 Jun 24:1-4. [Epub ahead of print]

PMID:
26108988
6.

Genetics: Whole-exome sequencing yields clinically useful information.

[No authors listed]

Nat Rev Clin Oncol. 2015 Jun 23. doi: 10.1038/nrclinonc.2015.116. [Epub ahead of print] No abstract available.

PMID:
26099987
7.

Genetic testing: Clinical whole-genome sequencing.

Bahcall OG.

Nat Rev Genet. 2015 Jun 18;16(7):377. doi: 10.1038/nrg3973. No abstract available.

PMID:
26084496
8.

From traditional to whole-genome sequencing biomarkers for gastric cancer.

Lianos GD, Bali CD, Katsios C, Roukos DH.

Biomark Med. 2015 Jun;9(6):559-62. doi: 10.2217/bmm.15.19. No abstract available.

9.

Management of Incidental Findings in the Era of Next-generation Sequencing.

Blackburn HL, Schroeder B, Turner C, Shriver CD, Ellsworth DL, Ellsworth RE.

Curr Genomics. 2015 Jun;16(3):159-74. doi: 10.2174/1389202916666150317232930.

PMID:
26069456
10.

Individualized Iterative Phenotyping for Genome-wide Analysis of Loss-of-Function Mutations.

Johnston JJ, Lewis KL, Ng D, Singh LN, Wynter J, Brewer C, Brooks BP, Brownell I, Candotti F, Gonsalves SG, Hart SP, Kong HH, Rother KI, Sokolic R, Solomon BD, Zein WM, Cooper DN, Stenson PD, Mullikin JC, Biesecker LG.

Am J Hum Genet. 2015 Jun 4;96(6):913-25. doi: 10.1016/j.ajhg.2015.04.013.

PMID:
26046366
11.

Interpretation of personal genome sequencing data in terms of disease ranks based on mutual information.

Na YJ, Sohn KA, Kim JH.

BMC Med Genomics. 2015;8 Suppl 2:S4. doi: 10.1186/1755-8794-8-S2-S4. Epub 2015 May 29.

12.

Gamut of Genetic Testing for Neonatal Care.

Ankala A, Hegde MR.

Clin Perinatol. 2015 Jun;42(2):217-226. doi: 10.1016/j.clp.2015.02.001. Epub 2015 Mar 31. Review.

PMID:
26042901
13.

Genetic Variation in Cardiomyopathy and Cardiovascular Disorders.

McNally EM, Puckelwartz MJ.

Circ J. 2015 Jun 25;79(7):1409-15. doi: 10.1253/circj.CJ-15-0536. Epub 2015 Jun 4.

14.

ERRATUM: A genome sequencing program for novel undiagnosed diseases.

[No authors listed]

Genet Med. 2015 Jun;17(6):515. doi: 10.1038/gim.2015.63. No abstract available.

PMID:
26035803
15.

Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies.

McCallum KJ, Ionita-Laza I.

Biometrics. 2015 Jun 1. doi: 10.1111/biom.12331. [Epub ahead of print]

PMID:
26033425
16.

Cardiovascular genetics: technological advancements and applicability for dilated cardiomyopathy.

Kummeling GJ, Baas AF, Harakalova M, van der Smagt JJ, Asselbergs FW.

Neth Heart J. 2015 Jun 2. [Epub ahead of print]

PMID:
26031632
17.

Diagnosis and treatment of cancer using genomics.

Vockley JG, Niederhuber JE.

BMJ. 2015 May 28;350:h1832. doi: 10.1136/bmj.h1832. Review.

18.

Clinical massively parallel sequencing for the diagnosis of myopathies.

Gorokhova S, Biancalana V, Lévy N, Laporte J, Bartoli M, Krahn M.

Rev Neurol (Paris). 2015 Jun-Jul;171(6-7):558-71. doi: 10.1016/j.neurol.2015.02.019. Epub 2015 May 26.

PMID:
26022190
19.

Clinical application of whole-genome sequencing in patients with primary immunodeficiency.

Mousallem T, Urban TJ, McSweeney KM, Kleinstein SE, Zhu M, Adeli M, Parrott RE, Roberts JL, Krueger B, Buckley RH, Goldstein DB.

J Allergy Clin Immunol. 2015 May 13. pii: S0091-6749(15)00428-5. doi: 10.1016/j.jaci.2015.02.040. [Epub ahead of print] No abstract available.

PMID:
25981738
20.

Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions.

Lelieveld SH, Spielmann M, Mundlos S, Veltman JA, Gilissen C.

Hum Mutat. 2015 May 14. doi: 10.1002/humu.22813. [Epub ahead of print]

PMID:
25973577
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