Kong L, Chen Z, Jia Z, Deng Q, Zhu P, Xu Y
BMC Genomics. 2025; 26(1):184.
PMID: 39994554
PMC: 11849188.
DOI: 10.1186/s12864-025-11373-8.
Liu Q, Archilla I, Lopez-Prades S, Torres F, Camps J, Cuatrecasas M
Cancer Med. 2025; 14(2):e70621.
PMID: 39840720
PMC: 11751872.
DOI: 10.1002/cam4.70621.
Kong L, Chen Z, Jia Z, Deng Q, Zhu P, Xu Y
Res Sq. 2025; .
PMID: 39764131
PMC: 11702833.
DOI: 10.21203/rs.3.rs-5097219/v1.
Hasan M, Sarker M, Jabin T, Sarker S, Ahmed S, Abdullah-Al-Shoeb M
Curr Res Struct Biol. 2024; 8:100159.
PMID: 39698059
PMC: 11653153.
DOI: 10.1016/j.crstbi.2024.100159.
Davletgildeeva A, Kuznetsov N
Biomolecules. 2024; 14(9).
PMID: 39334883
PMC: 11430729.
DOI: 10.3390/biom14091117.
Unraveling the potential effects of non-synonymous single nucleotide polymorphisms (nsSNPs) on the Protein structure and function of the human gene on type 2 diabetes and colorectal cancer: An approach.
Uddin M, Hossain M, Hossain M, Ahsan A, Shamim K, Hossen M
Heliyon. 2024; 10(17):e37280.
PMID: 39296124
PMC: 11408818.
DOI: 10.1016/j.heliyon.2024.e37280.
A comprehensive in silico investigation into the pathogenic SNPs in the RTEL1 gene and their biological consequences.
Tanshee R, Mahmud Z, Nabi A, Sayem M
PLoS One. 2024; 19(9):e0309713.
PMID: 39240887
PMC: 11379182.
DOI: 10.1371/journal.pone.0309713.
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy.
Weber J, Czisch L, Pereira Sena P, Fath F, Huridou C, Schwarz N
Acta Neuropathol. 2024; 148(1):14.
PMID: 39088078
PMC: 11294389.
DOI: 10.1007/s00401-024-02762-6.
Prediction of Deleterious Single Amino Acid Polymorphisms with a Consensus Holdout Sampler.
Alvarez-Machancoses O, Faraggi E, deAndres-Galiana E, Fernandez-Martinez J, Kloczkowski A
Curr Genomics. 2024; 25(3):171-184.
PMID: 39086995
PMC: 11288160.
DOI: 10.2174/0113892029236347240308054538.
Decoding the genetic landscape of juvenile dermatomyositis: insights from phosphorylation-associated single nucleotide polymorphisms.
Zhang H, Zhang Z, Fan K, Chen H, Guo Y, Mo X
Immunogenetics. 2024; 76(5-6):291-304.
PMID: 39085621
DOI: 10.1007/s00251-024-01350-y.
Identifying Oncogenic Missense Single Nucleotide Polymorphisms in Human SAT1 Gene Using Computational Algorithms and Molecular Dynamics Tools.
Mozibullah M, Khatun M, Sikder M, Islam M, Sharmin M
Cancer Rep (Hoboken). 2024; 7(7):e2130.
PMID: 39041636
PMC: 11264109.
DOI: 10.1002/cnr2.2130.
Missense variants in CYP4B1 associated with increased risk of lung cancer among Chinese Han population.
Yang Y, Yuan S, Yan S, Dong K, Yang Y
World J Surg Oncol. 2023; 21(1):352.
PMID: 37950293
PMC: 10638751.
DOI: 10.1186/s12957-023-03223-2.
Genetic Variations in the Purinergic P2X7 Receptor Are Associated with the Immune Response to Ocular Toxoplasmosis in Colombia.
Naranjo-Galvis C, McLeod R, Gomez-Marin J, de-la-Torre A, Rocha-Roa C, Cardona N
Microorganisms. 2023; 11(10).
PMID: 37894166
PMC: 10609425.
DOI: 10.3390/microorganisms11102508.
In silico prediction of deleterious non-synonymous SNPs in .
Ajith A, Subbiah U
Asian Biomed (Res Rev News). 2023; 17(4):185-199.
PMID: 37860678
PMC: 10584383.
DOI: 10.2478/abm-2023-0059.
Impact of highly deleterious non-synonymous polymorphisms on GRIN2A protein's structure and function.
Ahammad I, Jamal T, Bhattacharjee A, Chowdhury Z, Rahman S, Hassan M
PLoS One. 2023; 18(6):e0286917.
PMID: 37319252
PMC: 10270607.
DOI: 10.1371/journal.pone.0286917.
Deep Learning Framework for Complex Disease Risk Prediction Using Genomic Variations.
Alzoubi H, Alzubi R, Ramzan N
Sensors (Basel). 2023; 23(9).
PMID: 37177642
PMC: 10181706.
DOI: 10.3390/s23094439.
Strong Cumulative Evidence of Associations of 6 Single Nucleotide Polymorphisms with Ovarian Cancer Risk: An Umbrella Review.
Huo Y, Li X, Zhang M, Gao C, Xiao Q, Zhao Y
J Clin Med. 2023; 12(5).
PMID: 36902812
PMC: 10004083.
DOI: 10.3390/jcm12052025.
Addressing Noise and Estimating Uncertainty in Biomedical Data through the Exploration of Chemical Space.
deAndres-Galiana E, Fernandez-Martinez J, Fernandez-Brillet L, Cernea A, Kloczkowski A
Int J Mol Sci. 2022; 23(21).
PMID: 36361765
PMC: 9656407.
DOI: 10.3390/ijms232112975.
Identification of N7-methylguanosine related subtypes and construction of prognostic model in gastric cancer.
Li X, Dong H, Chen L, Wang Y, Hao Z, Zhang Y
Front Immunol. 2022; 13:984149.
PMID: 36300121
PMC: 9589367.
DOI: 10.3389/fimmu.2022.984149.
Missplicing suppressor alleles of Arabidopsis PRE-MRNA PROCESSING FACTOR 8 increase splicing fidelity by reducing the use of novel splice sites.
Cabezas-Fuster A, Micol-Ponce R, Fontcuberta-Cervera S, Ponce M
Nucleic Acids Res. 2022; 50(10):5513-5527.
PMID: 35639749
PMC: 9177961.
DOI: 10.1093/nar/gkac338.
