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– Vadapalli, S., Abdelhalim, H., Zeeshan, S., Ahmed, Z. (2022). Artificial intelligence & machine learning approaches using gene expression and variant data for personalized medicine.Briefings in Bioinformatics. [Online ahead of print]. PMID: 35595537. (Oxford)

– Ahmed Z. (2022). Precision medicine with multi-omics strategies, deep phenotyping, and predictive analysis. Progress in Molecular Biology and Translational Science (PMBTS): Precision Medicine. 190, 10. [Advance online publication, In Press]. (Elsevier)

– Ahmed Z., Renart., E., Zeeshan, S. (2022). Investigating underlying human immunity genes, implicated diseases, and their relationship with the COVID-19. Personalized Medicine. [Advance online publication]. PMID: 35261286

– Ahmed Z. (2022). Multi-omics strategies for personalized and predictive medicine: past, current, and future translational opportunities. Emerging Topics in Life Sciences. PMID: 35234253. (Portland Press, Biochemical Society and the Royal Society of Biology)

Ahmed, Z., Zeeshan, S., & Liang, B. T. (2021). RNA-seq driven expression and enrichment analysis to investigate CVD genes with associated phenotypes among high-risk Heart Failure patients. Human Genomics. 15, 67. PMID: 34774109. (BMC, Springer Nature, Human Genome Organization)

Ahmed, Z. (2021).Intelligent health system for investigation and consenting COVID-19 patients and precision medicine. Personalized Medicine. 18(6), 573–582. PMID: 34619976

 Ahmed, Z., Renart., E., Mishra, D., & Zeeshan, S. (2021). JWES: A new pipeline for whole genome/exome sequence data processing, management, and gene-variant discovery, annotation, prediction, and genotyping. FEBS Open Bio. 11(9):2441-2452. PMID: 34370400. (Wiley, Federation of European Biochemical Societies)

Ahmed, Z., Renart, E. G., Zeeshan, S., & Dong, X. (2021). Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis. Human Genomics. 15(1), 37. PMID: 34174938. (BMC, Springer Nature, Human Genome Organization)

Ahmed, Z., Renart., E., & Zeeshan, S.(2021). Genomics pipelines to investigate susceptibility in whole genome and exome sequenced data for variant discovery, annotation, prediction, and genotyping. PeerJ Life and Environment. 9:e11724. PMID: 34395068. (PeerJ)

Ahmed, Z., Zeeshan, S., Foran, D. J., Kleinman, L. C., Wondisford, F. E., & Dong, XQ. (2021). Integrative Clinical, Genomics and Metabolomics Data Analysis for Mainstream Precision Medicine to Investigate COVID-19. BMJ Innovations. 7, 6-10. (BMJ)

Ahmed, Z. (2020). Practicing precision medicine with intelligently integrative clinical and multi-omics data analysis. Human Genomics. 14(1), 35. PMID: 33008459. (BMC, Springer Nature)

 Ahmed, Z., Zeeshan, S., Mendhe, D., & Dong, X. (2020). Human gene and disease associations for clinical-genomics and precision medicine research. Clinical and Translational Medicine. 10(1), 297–318. PMID: 32508008. (Wiley)

Ahmed, Z., Mohamed, K., Zeeshan, S., & Dong, X. (2020). Artificial intelligence with multi-functional machine learning platform development for better healthcare and precision medicine. Database : the journal of biological databases and curation, 2020, baaa010. PMID: 32185396. (Oxford)

Zeeshan, S., Xiong, R., Liang, B. T., & Ahmed, Z. (2020). 100 Years of evolving gene-disease complexities and scientific debutants. Briefings in Bioinformatics. 21(3), 885–905. PMID: 30972412. (Oxford)

Ahmed, Z., Kim, M., & Liang, B. T. (2019). MAV-clic: management, analysis, and visualization of clinical data. JAMIA open. 2(1), 23–28. PMID: 31984341. (Oxford)

Ahmed, Z., Zeeshan, S., Xiong, R., & Liang, B. T. (2019). Debutant iOS app and gene-disease complexities in clinical genomics and precision medicine. Clinical and Translational medicine. 8(1), 26. PMID: 31586224. (Wiley)

Ahmed, Z., & Dandekar, T. (2018). MSL: Facilitating automatic and physical analysis of published sci-entific literature in PDF format. F1000Research. 4, 1453. PMID: 29721305. (Faculty of 1000)

Ahmed, Z., & Ucar, D. (2017). I-ATAC: Interactive pipeline tool for the management and pre-processing of ATAC-seq samples. PeerJ Life and Environment, 5:e4040. PMID: 29181276. (PeerJ)

Ahmed, Z., Saman, Z., & Dandekar, T. (2016). Mining Biomedical Images towards Valuable Information Retrieval in Biomedical and Life Sciences. Database: The Journal of Biological Databases and Curation, baw118. PMID: 27538578. (Oxford)

Ahmed, Z., Bolisetty, M., Saman, Z., Anguiano, E., Ucar, D. (2016). MAV-seq: An interactive platform for the Management, Analysis, and Visualization of Sequence Data. Human Genomics. PMID: 27294413. (BMC, Springer Nature, Human Genome Organization)

Ahmed, Z., Michel, M., Saman, Z., Dandekar, T., Mueller, M., & Fekete, A. (2015). Lipid-Pro: A computational lipid identification solution for untargeted lipidomics on data-independent acquisition tan-dem mass spectrometry platforms. Bioinformatics. 31, 1150-1153. PMID: 25433698. (Oxford)

Ahmed, Z., Saman, Z., Huber, C., Hensel, M., Schomburg, D., Münch, R., Eylert, E., Eisenreich. W, & Dandekar, T. (2014). Isotopo Database and Tool for Facile Analysis and Management of Mass Isotopomer Data. Database: The Journal of Biological Databases and Curation. 2014. PMID: 25204646. (Oxford)

Dandekar, T., Fieselmann, A., Saman, M., & Ahmed, Z. (2014). Software Applications toward Quantitative Metabolic Flux Analysis and Visualization. Briefings in Bioinformatics. 15, 91-107. PMID: 23142828. (Oxford)

Ahmed, Z., Zeeshan, S., & Dandekar, T. (2014). Developing sustainable software solutions for bioinformatics by the ” Butterfly” paradigm. F1000Research, 3, 71. PMID: 25383181. (Faculty of 1000)

Ahmed, Z., Saman, Z., Huber, C., Hensel, M., Schomburg, D., Münch, R., Eisenreich. W, & Dandekar, T. (2013). Software LS-MIDA for efficient Mass Isotopomer Distribution Analysis. BMC Bioinformatics. 14: 218. PMID: 23837681. (BMC, Springer Nature)

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