| Discovering biomarkers associated and predicting cardiovascular disease with high accuracy using a novel nexus of machine learning techniques for precision medicine W DeGroat, H Abdelhalim, K Patel, D Mendhe, S Zeeshan, Z Ahmed Scientific reports 14 (1), 1, 2024 | 31 | 2024 |
| Deciphering genomic signatures associating human dental oral craniofacial diseases with cardiovascular diseases using machine learning approaches Z Ahmed, W Degroat, H Abdelhalim, S Zeeshan, D Fine Clinical oral investigations 28 (1), 52, 2024 | 2 | 2024 |
| IntelliGenes: a novel machine learning pipeline for biomarker discovery and predictive analysis using multi-genomic profiles W DeGroat, D Mendhe, A Bhusari, H Abdelhalim, S Zeeshan, Z Ahmed Bioinformatics 39 (12), btad755, 2023 | 13 | 2023 |
| Role of genome-wide association studies, polygenic risk score and AI/ML using big data for personalized treatment to the patients with cardiovascular disease H Abdelhalim, RM Hunter, W DeGroat, D Mendhe, S Zeeshan, Z Ahmed Future Medicine AI, FMAI10, 2023 | 2 | 2023 |
| Genomic approaches to identify and investigate genes associated with atrial fibrillation and heart failure susceptibility KK Patel, C Venkatesan, H Abdelhalim, S Zeeshan, Y Arima, ... Human genomics 17 (1), 47, 2023 | 12 | 2023 |
| Investigating genes associated with cardiovascular disease among heart failure patients for translational research and precision medicine Z Ahmed, S Zeeshan, N Persaud, W Degroat, H Abdelhalim, BT Liang Clinical and Translational Discovery 3 (3), e206, 2023 | 2 | 2023 |
| Artificial intelligence for personalized and predictive genomics data analysis Z Ahmed, S Zeeshan, D Lee Frontiers in genetics 14, 1162869, 2023 | 7 | 2023 |
| Investigating genes associated with heart failure, atrial fibrillation, and other cardiovascular diseases, and predicting disease using machine learning techniques for … V Venkat, H Abdelhalim, W DeGroat, S Zeeshan, Z Ahmed Genomics 115 (2), 110584, 2023 | 20 | 2023 |
| Investigating variant and expression of CVD genes associated phenotypes among high-risk Heart Failure patients Z Ahmed, S Zeeshan, N Persaud, BT Liang bioRxiv, 2023.01. 24.525457, 2023 | | 2023 |
| Inhibition of Mtorc1/2 and DNA-PK via CC-115 Synergizes with Carboplatin and Paclitaxel in Lung Squamous Cell Carcinoma GM Castellano, S Zeeshan, OB Garbuzenko, HE Sabaawy, J Malhotra, ... Molecular cancer therapeutics 21 (9), 1381-1392, 2022 | | 2022 |
| Artificial intelligence and machine learning approaches using gene expression and variant data for personalized medicine S Vadapalli, H Abdelhalim, S Zeeshan, Z Ahmed Briefings in bioinformatics 23 (5), bbac191, 2022 | 44 | 2022 |
| RNA‐seq‐driven expression analysis to investigate cardiovascular disease genes with associated phenotypes among atrial fibrillation patients A Berber, H Abdelhalim, S Zeeshan, S Vadapalli, B von Oehsen, ... Clinical and translational medicine 12 (7), 2022 | 3 | 2022 |
| Investigating underlying human immunity genes, implicated diseases and their relationship to COVID-19 Z Ahmed, EG Renart, S Zeeshan Personalized medicine 19 (3), 229-250, 2022 | 2 | 2022 |
| Global profiling of alternative splicing in non-small cell lung cancer reveals novel histological and population differences S Zeeshan, RA Mendelez, A Zingone, H Khiabanian, SR Pine, BM Ryan | | 2022 |
| RNA-seq driven expression and enrichment analysis to investigate CVD genes with associated phenotypes among high-risk heart failure patients Z Ahmed, S Zeeshan, BT Liang Human genomics 15, 1-18, 2021 | 11 | 2021 |
| Targeting the immune microenvironment during immunotherapy for solid tumors A Sabaawy, S Zeeshan Molecular & Cellular Oncology 8 (5), 1994327, 2021 | 3 | 2021 |
| JWES: a new pipeline for whole genome/exome sequence data processing, management, and gene‐variant discovery, annotation, prediction, and genotyping Z Ahmed, EG Renart, D Mishra, S Zeeshan FEBS Open bio 11 (9), 2441-2452, 2021 | 14 | 2021 |
| Genomics pipelines to investigate susceptibility in whole genome and exome sequenced data for variant discovery, annotation, prediction and genotyping Z Ahmed, EG Renart, S Zeeshan PeerJ 9, e11724, 2021 | 11 | 2021 |
| Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis Z Ahmed, EG Renart, S Zeeshan, XQ Dong Human genomics 15 (1), 37, 2021 | 19 | 2021 |
| RNA-seq driven expression and enrichment analysis to investigate CVD genes with associated phenotypes among high-risk heart failure patients A Zeeshan, Z Saman, B T Liang Human Genomics (Web) 15 (1), 1-18, 2021 | | 2021 |
