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Items: 1 to 20 of 65

1.

Single-nucleotide variations in cardiac arrhythmias: prospects for genomics and proteomics based biomarker discovery and diagnostics.

Abunimer A, Smith K, Wu TJ, Lam P, Simonyan V, Mazumder R.

Genes (Basel). 2014 Mar 27;5(2):254-69. doi: 10.3390/genes5020254.

2.

Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.

Dingerdissen H, Motwani M, Karagiannis K, Simonyan V, Mazumder R.

FEBS J. 2013 Mar;280(6):1542-62. doi: 10.1111/febs.12155. Epub 2013 Feb 24.

3.

Proteome-wide analysis of single-nucleotide variations in the N-glycosylation sequon of human genes.

Mazumder R, Morampudi KS, Motwani M, Vasudevan S, Goldman R.

PLoS One. 2012;7(5):e36212. doi: 10.1371/journal.pone.0036212. Epub 2012 May 7.

4.

SNVDis: a proteome-wide analysis service for evaluating nsSNVs in protein functional sites and pathways.

Karagiannis K, Simonyan V, Mazumder R.

Genomics Proteomics Bioinformatics. 2013 Apr;11(2):122-6. doi: 10.1016/j.gpb.2012.10.003. Epub 2012 Dec 5.

5.

Non-synonymous variations in cancer and their effects on the human proteome: workflow for NGS data biocuration and proteome-wide analysis of TCGA data.

Cole C, Krampis K, Karagiannis K, Almeida JS, Faison WJ, Motwani M, Wan Q, Golikov A, Pan Y, Simonyan V, Mazumder R.

BMC Bioinformatics. 2014 Jan 27;15:28. doi: 10.1186/1471-2105-15-28.

6.

Collective judgment predicts disease-associated single nucleotide variants.

Capriotti E, Altman RB, Bromberg Y.

BMC Genomics. 2013;14 Suppl 3:S2. doi: 10.1186/1471-2164-14-S3-S2. Epub 2013 May 28.

7.

Human germline and pan-cancer variomes and their distinct functional profiles.

Pan Y, Karagiannis K, Zhang H, Dingerdissen H, Shamsaddini A, Wan Q, Simonyan V, Mazumder R.

Nucleic Acids Res. 2014 Oct;42(18):11570-88. doi: 10.1093/nar/gku772. Epub 2014 Sep 17.

8.

Prioritizing single-nucleotide variations that potentially regulate alternative splicing.

Teng M, Wang Y, Wang G, Jung J, Edenberg HJ, Sanford JR, Liu Y.

BMC Proc. 2011 Nov 29;5 Suppl 9:S40. doi: 10.1186/1753-6561-5-S9-S40.

9.

Biventricular pacing (cardiac resynchronization therapy): an evidence-based analysis.

Health Quality Ontario.

Ont Health Technol Assess Ser. 2005;5(13):1-60. Epub 2005 Sep 1.

10.

Identifying potential functional impact of mutations and polymorphisms: linking heart failure, increased risk of arrhythmias and sudden cardiac death.

Jagu B, Charpentier F, Toumaniantz G.

Front Physiol. 2013 Sep 20;4:254. doi: 10.3389/fphys.2013.00254. Review.

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13.

Impact of germline and somatic missense variations on drug binding sites.

Yan C, Pattabiraman N, Goecks J, Lam P, Nayak A, Pan Y, Torcivia-Rodriguez J, Voskanian A, Wan Q, Mazumder R.

Pharmacogenomics J. 2016 Jan 26. doi: 10.1038/tpj.2015.97. [Epub ahead of print]

PMID:
26810135
14.

[Development of antituberculous drugs: current status and future prospects].

Tomioka H, Namba K.

Kekkaku. 2006 Dec;81(12):753-74. Review. Japanese.

PMID:
17240921
15.

Genomics and cardiac arrhythmias.

Roberts R.

J Am Coll Cardiol. 2006 Jan 3;47(1):9-21. Epub 2005 Dec 15. Review.

16.

Genetics of arrhythmia: disease pathways beyond ion channels.

Perez MV, Wheeler M, Ho M, Pavlovic A, Wang P, Ashley EA.

J Cardiovasc Transl Res. 2008 Jun;1(2):155-65. doi: 10.1007/s12265-008-9030-4. Epub 2008 May 15. Review.

PMID:
20559910
17.

Biomarkers in atrial fibrillation, ventricular arrhythmias, and sudden cardiac death.

Mountantonakis S, Deo R.

Cardiovasc Ther. 2012 Apr;30(2):e74-80. doi: 10.1111/j.1755-5922.2010.00238.x. Epub 2010 Nov 11. Review.

PMID:
21070616
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19.

[Detection of patients at risk for sudden heart death by long-term ECG. The role of life-threatening ventricular arrhythmias].

Hombach V, Höpp HW, Osterspey A, Winter U, Deutsch H, Hilger HH.

Herz. 1984 Feb;9(1):6-25. German.

PMID:
6200415
20.

SNVHMM: predicting single nucleotide variants from next generation sequencing.

Bian J, Liu C, Wang H, Xing J, Kachroo P, Zhou X.

BMC Bioinformatics. 2013 Jul 15;14:225. doi: 10.1186/1471-2105-14-225.

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