91 related articles for article (PubMed ID: 29217828)
1. Frequently used bioinformatics tools overestimate the damaging effect of allelic variants.
Andersen LL; Terczyńska-Dyla E; Mørk N; Scavenius C; Enghild JJ; Höning K; Hornung V; Christiansen M; Mogensen TH; Hartmann R
Genes Immun; 2019 Jan; 20(1):10-22. PubMed ID: 29217828
[TBL] [Abstract][Full Text] [Related]
2. Computational Analysis of Missense Variants of G Protein-Coupled Receptors Involved in the Neuroendocrine Regulation of Reproduction.
Min L; Nie M; Zhang A; Wen J; Noel SD; Lee V; Carroll RS; Kaiser UB
Neuroendocrinology; 2016; 103(3-4):230-9. PubMed ID: 26088945
[TBL] [Abstract][Full Text] [Related]
3. [Evaluation of performance of five bioinformatics software for the prediction of missense mutations].
Chen Q; Dai C; Zhang Q; Du J; Li W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):625-8. PubMed ID: 27577208
[TBL] [Abstract][Full Text] [Related]
4. [Clinical characteristics, prognosis and genetic susceptibility of herpes simplex encephalitis in children].
Feng W; Chen T; Hu B; Wan J; Liu G
Zhonghua Er Ke Za Zhi; 2015 Sep; 53(9):701-6. PubMed ID: 26757972
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of computational techniques for predicting non-synonymous single nucleotide variants pathogenicity.
Hassan MS; Shaalan AA; Dessouky MI; Abdelnaiem AE; ElHefnawi M
Genomics; 2019 Jul; 111(4):869-882. PubMed ID: 29842949
[TBL] [Abstract][Full Text] [Related]
6. Proteomics in immunity and herpes simplex encephalitis.
Pérez de Diego R; Mulvey C; Casanova JL; Godovac-Zimmermann J
Expert Rev Proteomics; 2014 Feb; 11(1):21-9. PubMed ID: 24351021
[TBL] [Abstract][Full Text] [Related]
7. Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations.
Flanagan SE; Patch AM; Ellard S
Genet Test Mol Biomarkers; 2010 Aug; 14(4):533-7. PubMed ID: 20642364
[TBL] [Abstract][Full Text] [Related]
8. Assessment of the predictive accuracy of five in silico prediction tools, alone or in combination, and two metaservers to classify long QT syndrome gene mutations.
Leong IU; Stuckey A; Lai D; Skinner JR; Love DR
BMC Med Genet; 2015 May; 16():34. PubMed ID: 25967940
[TBL] [Abstract][Full Text] [Related]
9. Functional IRF3 deficiency in a patient with herpes simplex encephalitis.
Andersen LL; Mørk N; Reinert LS; Kofod-Olsen E; Narita R; Jørgensen SE; Skipper KA; Höning K; Gad HH; Østergaard L; Ørntoft TF; Hornung V; Paludan SR; Mikkelsen JG; Fujita T; Christiansen M; Hartmann R; Mogensen TH
J Exp Med; 2015 Aug; 212(9):1371-9. PubMed ID: 26216125
[TBL] [Abstract][Full Text] [Related]
10. A computational approach for detecting physiological homogeneity in the midst of genetic heterogeneity.
Zhang P; Cobat A; Lee YS; Wu Y; Bayrak CS; Boccon-Gibod C; Matuozzo D; Lorenzo L; Jain A; Boucherit S; Vallée L; Stüve B; Chabrier S; Casanova JL; Abel L; Zhang SY; Itan Y
Am J Hum Genet; 2021 Jun; 108(6):1012-1025. PubMed ID: 34015270
[TBL] [Abstract][Full Text] [Related]
11. Mutations in the TLR3 signaling pathway and beyond in adult patients with herpes simplex encephalitis.
Mørk N; Kofod-Olsen E; Sørensen KB; Bach E; Ørntoft TF; Østergaard L; Paludan SR; Christiansen M; Mogensen TH
Genes Immun; 2015 Dec; 16(8):552-66. PubMed ID: 26513235
[TBL] [Abstract][Full Text] [Related]
12. [Genetic susceptibility to herpes simplex encephalitis].
Rozenberg F
Pathol Biol (Paris); 2013 Jan; 61(1):21-7. PubMed ID: 23399415
[TBL] [Abstract][Full Text] [Related]
13. IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variants.
Knecht C; Mort M; Junge O; Cooper DN; Krawczak M; Caliebe A
Nucleic Acids Res; 2017 Feb; 45(3):e13. PubMed ID: 28180317
[TBL] [Abstract][Full Text] [Related]
14. Effect of genome-wide genotyping and reference panels on rare variants imputation.
Zheng HF; Ladouceur M; Greenwood CM; Richards JB
J Genet Genomics; 2012 Oct; 39(10):545-50. PubMed ID: 23089364
[TBL] [Abstract][Full Text] [Related]
15. Inborn errors underlying herpes simplex encephalitis: From TLR3 to IRF3.
Zhang SY; Casanova JL
J Exp Med; 2015 Aug; 212(9):1342-3. PubMed ID: 26304982
[No Abstract] [Full Text] [Related]
16. Unraveling the molecular mechanism governing the tissue specific expression of IFNλR1.
Akhtar H; Hamming OJ; Jan SU; Akhtar S; Terczyn' ska-Dyla E; Siupka P; Shafique A; Hartmann R; Sadia H
Pak J Pharm Sci; 2016 May; 29(3):795-9. PubMed ID: 27166550
[TBL] [Abstract][Full Text] [Related]
17. Computational Analysis of Breast Cancer GWAS Loci Identifies the Putative Deleterious Effect of STXBP4 and ZNF404 Gene Variants.
Masoodi TA; Banaganapalli B; Vaidyanathan V; Talluri VR; Shaik NA
J Cell Biochem; 2017 Dec; 118(12):4296-4307. PubMed ID: 28422318
[TBL] [Abstract][Full Text] [Related]
18. Three novel variants (p.Glu178Lys, p.Val245Met, p.Ser250Phe) of the phenylalanine hydroxylase (PAH) gene impair protein expression and function in vitro.
Zong Y; Liu N; Ma S; Bai Y; Guan F; Kong X
Gene; 2018 Aug; 668():135-139. PubMed ID: 29653233
[TBL] [Abstract][Full Text] [Related]
19. Machine learning classifier for identification of damaging missense mutations exclusive to human mitochondrial DNA-encoded polypeptides.
Martín-Navarro A; Gaudioso-Simón A; Álvarez-Jarreta J; Montoya J; Mayordomo E; Ruiz-Pesini E
BMC Bioinformatics; 2017 Mar; 18(1):158. PubMed ID: 28270093
[TBL] [Abstract][Full Text] [Related]
20. A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.
Bacchelli E; Cainazzo MM; Cameli C; Guerzoni S; Martinelli A; Zoli M; Maestrini E; Pini LA
J Headache Pain; 2016 Dec; 17(1):114. PubMed ID: 27957625
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
