Similar articles for PMID: 18846217

Year	Number of Results
1986	1
1988	1
1993	1
1997	1
2000	2
2001	2
2004	2
2005	7
2006	4
2007	2
2008	5
2009	4
2010	8
2011	3
2012	1
2013	3
2014	2
2015	4
2016	2
2017	2
2018	1
2019	1
2020	1
2024	0

1

Genome wide identification of recessive cancer genes by combinatorial mutation analysis.

Volinia S, Mascellani N, Marchesini J, Veronese A, Ormondroyd E, Alder H, Palatini J, Negrini M, Croce CM. Volinia S, et al. PLoS One. 2008;3(10):e3380. doi: 10.1371/journal.pone.0003380. Epub 2008 Oct 10. PLoS One. 2008. PMID: 18846217 Free PMC article.

2

Signs of positive selection of somatic mutations in human cancers detected by EST sequence analysis.

Babenko VN, Basu MK, Kondrashov FA, Rogozin IB, Koonin EV. Babenko VN, et al. BMC Cancer. 2006 Feb 9;6:36. doi: 10.1186/1471-2407-6-36. BMC Cancer. 2006. PMID: 16469093 Free PMC article.

3

[Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].

Zhang DL, Ji L, Li YD. Zhang DL, et al. Yi Chuan Xue Bao. 2004 May;31(5):431-43. Yi Chuan Xue Bao. 2004. PMID: 15478601 Chinese.

4

Zoom-in array comparative genomic hybridization (aCGH) to detect germline rearrangements in cancer susceptibility genes.

Staaf J, Borg A. Staaf J, et al. Methods Mol Biol. 2010;653:221-35. doi: 10.1007/978-1-60761-759-4_13. Methods Mol Biol. 2010. PMID: 20721746 Review.

5

Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosa.

Clark GR, Crowe P, Muszynska D, O'Prey D, O'Neill J, Alexander S, Willoughby CE, McKay GJ, Silvestri G, Simpson DA. Clark GR, et al. Ophthalmology. 2010 Nov;117(11):2169-77.e3. doi: 10.1016/j.ophtha.2010.02.029. Epub 2010 Jun 29. Ophthalmology. 2010. PMID: 20591486

6

Genome-wide mutational spectra analysis reveals significant cancer-specific heterogeneity.

Tan H, Bao J, Zhou X. Tan H, et al. Sci Rep. 2015 Jul 27;5:12566. doi: 10.1038/srep12566. Sci Rep. 2015. PMID: 26212640 Free PMC article.

7

The use of denaturing high performance liquid chromatography (DHPLC) for mutation scanning of hereditary cancer genes.

Marsh DJ, Howell VM. Marsh DJ, et al. Methods Mol Biol. 2010;653:133-45. doi: 10.1007/978-1-60761-759-4_8. Methods Mol Biol. 2010. PMID: 20721741 Review.

8

Signatures of mutation and selection in the cancer genome.

Bignell GR, Greenman CD, Davies H, Butler AP, Edkins S, Andrews JM, Buck G, Chen L, Beare D, Latimer C, Widaa S, Hinton J, Fahey C, Fu B, Swamy S, Dalgliesh GL, Teh BT, Deloukas P, Yang F, Campbell PJ, Futreal PA, Stratton MR. Bignell GR, et al. Nature. 2010 Feb 18;463(7283):893-8. doi: 10.1038/nature08768. Nature. 2010. PMID: 20164919 Free PMC article.

9

Mutations and deletions of the CBP gene in human lung cancer.

Kishimoto M, Kohno T, Okudela K, Otsuka A, Sasaki H, Tanabe C, Sakiyama T, Hirama C, Kitabayashi I, Minna JD, Takenoshita S, Yokota J. Kishimoto M, et al. Clin Cancer Res. 2005 Jan 15;11(2 Pt 1):512-9. Clin Cancer Res. 2005. PMID: 15701835

10

Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays.

Karaman MW, Groshen S, Lee CC, Pike BL, Hacia JG. Karaman MW, et al. Nucleic Acids Res. 2005 Feb 18;33(3):e33. doi: 10.1093/nar/gni034. Nucleic Acids Res. 2005. PMID: 15722479 Free PMC article.

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