A citation-based method for searching scientific literature




Biao Li, Vidhya G Krishnan, Matthew E Mort, Fuxiao Xin, Kishore K Kamati, David N Cooper, Sean D Mooney, Predrag Radivojac. Bioinformatics 2009
Times Cited: 535




List of shared articles



Times cited


Identification and in silico Analysis of Nonsense SNPs of Human Colorectal Cancer Protein.
Lu Wang, Huiyang Tu, Lingzhi Zeng, Ruichen Gao, Sumei Luo, Chao Xiong. J Oleo Sci 2022
0

Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy.
Sheh Wen Kuan, Kek Heng Chua, E-Wei Tan, Lay Koon Tan, Alexander Loch, Boon Pin Kee. PeerJ 2022
0

Genome interpretation using in silico predictors of variant impact.
Panagiotis Katsonis, Kevin Wilhelm, Amanda Williams, Olivier Lichtarge. Hum Genet 2022
0

Exploring the Structural and Functional Effects of Nonsynonymous SNPs in the Human Serotonin Transporter Gene Through In Silico Approaches.
Md Arzo Mia, Md Nasir Uddin, Yasmin Akter, Jesmin, Lolo Wal Marzan. Bioinform Biol Insights 2022
0


A comprehensive in silico analysis of the deleterious nonsynonymous SNPs of human FOXP2 protein.
Mahmuda Akter, Sumaiya Farah Khan, Abu Ashfaqur Sajib, Fahmida Sultana Rima. PLoS One 2022
0


Exploring Single Nucleotide Polymorphisms in ITGAV for Gastric, Pancreatic and Liver Malignancies: An Approach Towards the Discovery of Biomarker.
Shreya Bhattacharya, Pragati Prasad Sah, Arundhati Banerjee, Sujay Ray. Comb Chem High Throughput Screen 2021
0

Comprehensive in-silico analysis of damage associated SNPs in hOCT1 affecting Imatinib response in chronic myeloid leukemia.
Ismael Soltani, Wael Bahia, Assala Radhouani, Abdelkarim Mahdhi, Salima Ferchichi, Wassim Y Almawi. Genomics 2021
3

Novel rare variants in FGFR1 and clinical characteristics analysis in a series of congenital hypogonadotropic hypogonadism patients.
Min Nie, Bingqing Yu, Rongrong Chen, Bang Sun, Jiangfeng Mao, Xi Wang, Hongbing Zhang, Xueyan Wu. Clin Endocrinol (Oxf) 2021
3

In silico screening and identification of deleterious missense SNPs along with their effects on CD-209 gene: An insight to CD-209 related-diseases.
Mohib Ullah Kakar, Muhammad Matloob, Rongji Dai, Yulin Deng, Kifayat Ullah, Ihsan Ullah Kakar, Ghulam Khaliq, Muhammad Umer, Zhoaib Ahmed Bhutto, Sarfarz Ali Fazlani,[...]. PLoS One 2021
2

Structural effects driven by rare point mutations in amylin hormone, the type II diabetes-associated peptide.
Wendy S Mendes, Octavio L Franco, Sergio A Alencar, William F Porto. Biochim Biophys Acta Gen Subj 2021
0


Characterization of Rheumatoid Arthritis Risk-Associated SNPs and Identification of Novel Therapeutic Sites Using an In-Silico Approach.
Mehran Akhtar, Yasir Ali, Zia-Ul Islam, Maria Arshad, Mamoona Rauf, Muhammad Ali, Saleh N Maodaa, Saleh A Al-Farraj, Hamed A El-Serehy, Fazal Jalil. Biology (Basel) 2021
0

Computational Insights into the Deleterious Impacts of Missense Variants on N-Acetyl-d-glucosamine Kinase Structure and Function.
Raju Dash, Sarmistha Mitra, Yeasmin Akter Munni, Ho Jin Choi, Md Chayan Ali, Largess Barua, Tae Jung Jang, Il Soo Moon. Int J Mol Sci 2021
3

Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays.
Nurul Ain Khoruddin, Mohd NurFakhruzzaman Noorizhab, Lay Kek Teh, Farida Zuraina Mohd Yusof, Mohd Zaki Salleh. Sci Rep 2021
2

The investigation of nonsynonymous SNPs of human SLC6A4 gene associated with depression: An in silico approach.
Md Amit Hasan, Fuad Taufiqul Hakim, Md Tanjil Islam Shovon, Md Mirajul Islam, Md Samiul Islam, Md Asadul Islam. Heliyon 2021
0

Towards Understanding the Pathogenicity of DROSHA Mutations in Oncohematology.
Dmitrii S Bug, Artem V Tishkov, Ivan S Moiseev, Yuri B Porozov, Natalia V Petukhova. Cells 2021
0