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For: Arshad M, Bhatti A, John P. Identification and in silico analysis of functional SNPs of human TAGAP protein: A comprehensive study. PLoS One 2018;13:e0188143. [PMID: 29329296 DOI: 10.1371/journal.pone.0188143] [Cited by in Crossref: 26] [Cited by in F6Publishing: 19] [Article Influence: 6.5] [Reference Citation Analysis]
Number Citing Articles
1 Avsar O. Analysis of missense SNPs in the SLC47A1 and SLC47A2 genes affecting the pharmacokinetics of metformin: Computational approach. Egypt J Med Hum Genet 2022;23. [DOI: 10.1186/s43042-022-00306-9] [Reference Citation Analysis]
2 Panchal NK, Bhale A, Verma VK, Beevi SS. Computational and molecular dynamics simulation approach to analyze the impactof XPD gene mutation on protein stability and function. Molecular Simulation 2020;46:1200-19. [DOI: 10.1080/08927022.2020.1810852] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Das SS, Chakravorty N. Identification of deleterious SNPs and their effects on BCL11A, the master regulator of fetal hemoglobin expression. Genomics 2020;112:397-403. [PMID: 30853596 DOI: 10.1016/j.ygeno.2019.03.002] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
4 Hossain MS, Roy AS, Islam MS. In silico analysis predicting effects of deleterious SNPs of human RASSF5 gene on its structure and functions. Sci Rep 2020;10:14542. [PMID: 32884013 DOI: 10.1038/s41598-020-71457-1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
5 Hasan MA, Hakim FT, Islam Shovon MT, Islam MM, Islam MS, Islam MA. The investigation of nonsynonymous SNPs of human SLC6A4 gene associated with depression: An in silico approach. Heliyon 2021;7:e07815. [PMID: 34466701 DOI: 10.1016/j.heliyon.2021.e07815] [Reference Citation Analysis]
6 Rangasamy N, Senthil Kumar N, K.s. S. Computational analysis of missense variants in MMP2 gene linked with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis reveals structural shift in protein-protein and protein-ligand complexes. Meta Gene 2021;29:100931. [DOI: 10.1016/j.mgene.2021.100931] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Kaman T, Karasakal ÖF, Özkan Oktay E, Ulucan K, Konuk M. In silico approach to the analysis of SNPs in the human APAF1 gene. Turk J Biol 2019;43:371-81. [PMID: 31892812 DOI: 10.3906/biy-1905-18] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
8 Rutkowska L, Salachna D, Lewandowski K, Lewiński A, Gach A. Familial Partial Lipodystrophy—Literature Review and Report of a Novel Variant in PPARG Expanding the Spectrum of Disease-Causing Alterations in FPLD3. Diagnostics 2022;12:1122. [DOI: 10.3390/diagnostics12051122] [Reference Citation Analysis]
9 Namvar A, Bolhassani A, Javadi G, Noormohammadi Z. In silico/In vivo analysis of high-risk papillomavirus L1 and L2 conserved sequences for development of cross-subtype prophylactic vaccine. Sci Rep 2019;9:15225. [PMID: 31645650 DOI: 10.1038/s41598-019-51679-8] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
10 Alzahrani FA, Ahmed F, Sharma M, Rehan M, Mahfuz M, Baeshen MN, Hawsawi Y, Almatrafi A, Alsagaby SA, Kamal MA, Warsi MK, Choudhry H, Jamal MS. Investigating the pathogenic SNPs in BLM helicase and their biological consequences by computational approach. Sci Rep 2020;10:12377. [PMID: 32704157 DOI: 10.1038/s41598-020-69033-8] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
11 Ammar A, Cavill R, Evelo C, Willighagen E. PSnpBind: a database of mutated binding site protein-ligand complexes constructed using a multithreaded virtual screening workflow. J Cheminform 2022;14:8. [PMID: 35227289 DOI: 10.1186/s13321-021-00573-5] [Reference Citation Analysis]
12 Avsar O. Investigation of Putative Functional SNPs of Human HAT1 Protein: A Comprehensive “in silico” Study. Cytol Genet 2022;56:98-107. [DOI: 10.3103/s0095452722010029] [Reference Citation Analysis]
13 Khoruddin NA, Noorizhab MN, Teh LK, Mohd Yusof FZ, Salleh MZ. Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays. Sci Rep 2021;11:16158. [PMID: 34373545 DOI: 10.1038/s41598-021-95618-y] [Reference Citation Analysis]
14 Bhattacharya S, Ray S. In silico screening and exploration into phenotypic alterations of deleterious oncogenic single nucleotide polymorphisms in HSPB1 gene. Genomics 2021;113:2812-25. [PMID: 34129932 DOI: 10.1016/j.ygeno.2021.06.017] [Reference Citation Analysis]
15 Stalin A, Lin D, Josephine Princy J, Feng Y, Xiang H, Ignacimuthu S, Chen Y. Computational analysis of single nucleotide polymorphisms (SNPs) in PPAR gamma associated with obesity, diabetes and cancer. Journal of Biomolecular Structure and Dynamics. [DOI: 10.1080/07391102.2020.1835724] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
16 Wang L, Tu H, Zeng L, Gao R, Luo S, Xiong C. Identification and in silico Analysis of Nonsense SNPs of Human Colorectal Cancer Protein. J Oleo Sci 2022;71:363-70. [PMID: 35236796 DOI: 10.5650/jos.ess21313] [Reference Citation Analysis]
17 Khalid Z, Almaghrabi O. Mutational analysis on predicting the impact of high-risk SNPs in human secretary phospholipase A2 receptor (PLA2R1). Sci Rep 2020;10:11750. [PMID: 32678193 DOI: 10.1038/s41598-020-68696-7] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
18 Akhtar M, Jamal T, Jamal H, Din JU, Jamal M, Arif M, Arshad M, Jalil F. Identification of most damaging nsSNPs in human CCR6 gene: In silico analyses. Int J Immunogenet 2019;46:459-71. [PMID: 31364806 DOI: 10.1111/iji.12449] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.7] [Reference Citation Analysis]
19 Hosen SMZ, Dash R, Junaid M, Mitra S, Absar N. Identification and structural characterization of deleterious non-synonymous single nucleotide polymorphisms in the human SKP2 gene. Comput Biol Chem 2019;79:127-36. [PMID: 30802828 DOI: 10.1016/j.compbiolchem.2019.02.003] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
20 Pandey S, Dhusia K, Katara P, Singh S, Gautam B. An in silico analysis of deleterious single nucleotide polymorphisms and molecular dynamics simulation of disease linked mutations in genes responsible for neurodegenerative disorder. Journal of Biomolecular Structure and Dynamics 2020;38:4259-72. [DOI: 10.1080/07391102.2019.1682047] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
21 Soltani I, Bahia W, Radhouani A, Mahdhi A, Ferchichi S, Almawi WY. Comprehensive in-silico analysis of damage associated SNPs in hOCT1 affecting Imatinib response in chronic myeloid leukemia. Genomics 2021;113:755-66. [PMID: 33075481 DOI: 10.1016/j.ygeno.2020.10.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
22 Miao L, Wang B, Ji J, Wan L, Yin L, Zhu B, Zhang J, Pu Y. CARD8 polymorphism rs2043211 protects against noise-induced hearing loss by causing the dysfunction of CARD8 protein. Environ Sci Pollut Res 2021;28:8626-36. [DOI: 10.1007/s11356-020-11193-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Al-Kindi MN, Al-Khabouri MJ, Al-Lamki KA, Palombo F, Pippucci T, Romeo G, Al-Wardy NM. In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss. J Genet Eng Biotechnol 2020;18:8. [PMID: 32115674 DOI: 10.1186/s43141-020-0021-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
24 Khalid Z, Sezerman OU. A comprehensive study on identifying the structural and functional SNPs of human neuronal membrane glycoprotein M6A (GPM6A). J Biomol Struct Dyn 2021;39:2693-701. [PMID: 32248748 DOI: 10.1080/07391102.2020.1751712] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
25 Yazar M, Özbek P. In Silico Tools and Approaches for the Prediction of Functional and Structural Effects of Single-Nucleotide Polymorphisms on Proteins: An Expert Review. OMICS 2021;25:23-37. [PMID: 33058752 DOI: 10.1089/omi.2020.0141] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
26 Arifuzzaman M, Mitra S, Das R, Hamza A, Absar N, Dash R. In silico analysis of nonsynonymous single-nucleotide polymorphisms (nsSNPs) of the SMPX gene. Ann Hum Genet 2020;84:54-71. [PMID: 31583691 DOI: 10.1111/ahg.12350] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
27 Lim SW, Tan KJ, Azuraidi OM, Sathiya M, Lim EC, Lai KS, Yap WS, Afizan NARNM. Functional and structural analysis of non-synonymous single nucleotide polymorphisms (nsSNPs) in the MYB oncoproteins associated with human cancer. Sci Rep 2021;11:24206. [PMID: 34921182 DOI: 10.1038/s41598-021-03624-x] [Reference Citation Analysis]
28 Li Y, Wang W, Li Z, Wang N, Xiao F, Gao H, Guo H, Li H, Wang S. Integration of association and computational methods reveals functional variants of LEPR gene for abdominal fat content in chickens. Journal of Integrative Agriculture 2021;20:2734-48. [DOI: 10.1016/s2095-3119(20)63575-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Safder I, Shao G, Sheng Z, Hu P, Tang S. Identification of SNPs in rice GPAT genes and in silico analysis of their functional impact on GPAT proteins. Not Bot Horti Agrobo 2021;49:12346. [DOI: 10.15835/nbha49312346] [Reference Citation Analysis]
30 Hussain M, Arshad N, Ujan R, Saeed A, Channar PA, Perveen F, Larik FA, Farooqi SI, Hussain Z, Hökelek T, Kaur M, Jasinski JP. Synthesis, structure elucidation and surface analysis of a new single crystal N-((2-(benzo [4,5]imidazo [1,2-c]quinazolin-6-yl)phenyl)carbamothioyl)heptanamide: Theoretical and experimental DNA binding studies. Journal of Molecular Structure 2020;1205:127496. [DOI: 10.1016/j.molstruc.2019.127496] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
31 Abarna R, Dutta D, Sneha P, George Priya Doss C, Anbalagan M. Identification of novel heterozygous Apex 1 gene variant (Glu87Gln) in patients with head and neck cancer of Indian origin. J Cell Biochem 2018;119:8851-61. [PMID: 30076617 DOI: 10.1002/jcb.27138] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
32 Oktay EO. Bioinformatics Analysis of Functional SNPs in Human ASAH1 Gene Related to Farber Disease. Russ J Genet 2022;58:109-15. [DOI: 10.1134/s1022795422010070] [Reference Citation Analysis]