Similar articles for PMID: 21781308

Year	Number of Results
1994	1
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1998	2
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2004	1
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2013	8
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2015	6
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2017	4
2018	1
2019	8
2020	4
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2022	2
2023	1
2024	0

1

Ranking insertion, deletion and nonsense mutations based on their effect on genetic information.

Zia A, Moses AM. Zia A, et al. BMC Bioinformatics. 2011 Jul 22;12:299. doi: 10.1186/1471-2105-12-299. BMC Bioinformatics. 2011. PMID: 21781308 Free PMC article.

2

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.

Montgomery SB, Goode DL, Kvikstad E, Albers CA, Zhang ZD, Mu XJ, Ananda G, Howie B, Karczewski KJ, Smith KS, Anaya V, Richardson R, Davis J; 1000 Genomes Project Consortium; MacArthur DG, Sidow A, Duret L, Gerstein M, Makova KD, Marchini J, McVean G, Lunter G. Montgomery SB, et al. Genome Res. 2013 May;23(5):749-61. doi: 10.1101/gr.148718.112. Epub 2013 Mar 11. Genome Res. 2013. PMID: 23478400 Free PMC article.

3

Distribution and effects of nonsense polymorphisms in human genes.

Yamaguchi-Kabata Y, Shimada MK, Hayakawa Y, Minoshima S, Chakraborty R, Gojobori T, Imanishi T. Yamaguchi-Kabata Y, et al. PLoS One. 2008;3(10):e3393. doi: 10.1371/journal.pone.0003393. Epub 2008 Oct 14. PLoS One. 2008. PMID: 18852891 Free PMC article.

4

Nonsynonymous, synonymous and nonsense mutations in human cancer-related genes undergo stronger purifying selections than expectation.

Chu D, Wei L. Chu D, et al. BMC Cancer. 2019 Apr 16;19(1):359. doi: 10.1186/s12885-019-5572-x. BMC Cancer. 2019. PMID: 30991970 Free PMC article.

5

Predicting the functional effect of amino acid substitutions and indels.

Choi Y, Sims GE, Murphy S, Miller JR, Chan AP. Choi Y, et al. PLoS One. 2012;7(10):e46688. doi: 10.1371/journal.pone.0046688. Epub 2012 Oct 8. PLoS One. 2012. PMID: 23056405 Free PMC article.

6

An analysis of substitution, deletion and insertion mutations in cancer genes.

Iengar P. Iengar P. Nucleic Acids Res. 2012 Aug;40(14):6401-13. doi: 10.1093/nar/gks290. Epub 2012 Apr 9. Nucleic Acids Res. 2012. PMID: 22492711 Free PMC article.

7

Serum starvation enhances nonsense mutation readthrough.

Wittenstein A, Caspi M, David Y, Shorer Y, Nadar-Ponniah PT, Rosin-Arbesfeld R. Wittenstein A, et al. J Mol Med (Berl). 2019 Dec;97(12):1695-1710. doi: 10.1007/s00109-019-01847-0. Epub 2019 Nov 15. J Mol Med (Berl). 2019. PMID: 31786671

8

Identifying the Impact of Inframe Insertions and Deletions on Protein Function in Cancer.

Baeissa HM, Pearl FMG. Baeissa HM, et al. J Comput Biol. 2020 May;27(5):786-795. doi: 10.1089/cmb.2018.0192. Epub 2019 Aug 28. J Comput Biol. 2020. PMID: 31460787

9

DDIG-in: detecting disease-causing genetic variations due to frameshifting indels and nonsense mutations employing sequence and structural properties at nucleotide and protein levels.

Folkman L, Yang Y, Li Z, Stantic B, Sattar A, Mort M, Cooper DN, Liu Y, Zhou Y. Folkman L, et al. Bioinformatics. 2015 May 15;31(10):1599-606. doi: 10.1093/bioinformatics/btu862. Epub 2015 Jan 7. Bioinformatics. 2015. PMID: 25573915

10

Deep sequencing of Danish Holstein dairy cattle for variant detection and insight into potential loss-of-function variants in protein coding genes.

Das A, Panitz F, Gregersen VR, Bendixen C, Holm LE. Das A, et al. BMC Genomics. 2015 Dec 9;16:1043. doi: 10.1186/s12864-015-2249-y. BMC Genomics. 2015. PMID: 26645365 Free PMC article.

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