| A systematic review of extreme phenotype strategies to search for rare variants in genetic studies of complex disorders S Amanat, T Requena, JA Lopez-Escamez Genes 11 (9), 987, 2020 | 53 | 2020 |
| Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI W Schlee, S Schoisswohl, S Staudinger, A Schiller, A Lehner, B Langguth, ... Progress in brain research 260, 441-451, 2021 | 48 | 2021 |
| Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study S Amanat, A Gallego-Martinez, J Sollini, P Perez-Carpena, ... EBioMedicine 66, 2021 | 35 | 2021 |
| Multidisciplinary tinnitus research: challenges and future directions from the perspective of early stage researchers JP Simoes, E Daoud, M Shabbir, S Amanat, K Assouly, R Biswas, ... Frontiers in aging neuroscience 13, 647285, 2021 | 31 | 2021 |
| Heritability and genetics contribution to tinnitus JA Lopez-Escamez, S Amanat Otolaryngologic Clinics of North America 53 (4), 501-513, 2020 | 21 | 2020 |
| Genetic inheritance and its contribution to tinnitus S Amanat, A Gallego-Martinez, JA Lopez-Escamez The Behavioral Neuroscience of Tinnitus, 29-47, 2020 | 12 | 2020 |
| Video retrieval system for meniscal surgery to improve health care services S Amanat, M Idrees, MUG Khan, Z Rehman, H Chang, I Mehmood, ... Journal of Sensors 2018 (1), 4390703, 2018 | 10 | 2018 |
| A systematic review of extreme phenotype strategies to search for rare variants in genetic studies of complex disorders. Genes 11 S Amanat, T Requena, JA Lopez-Escamez E987, 2020 | 8 | 2020 |
| Burden of rare variants in synaptic genes in patients with severe tinnitus: an exome based extreme phenotype study. EBioMedicine. 2021; 66: 103309 S Amanat, A Gallego-Martinez, J Sollini, P Perez-Carpena, ... | 5 | 2021 |
| Corrigendum: multidisciplinary tinnitus research: challenges and future directions from the perspective of early stage researchers JP Simoes, E Daoud, M Shabbir, S Amanat, K Assouly, R Biswas, ... Frontiers in Aging Neuroscience 13, 730758, 2021 | 4 | 2021 |
| Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions QQ Huang, EM Wigdor, P Campbell, DS Malawsky, KE Samocha, ... medRxiv, 2024.03. 05.24303772, 2024 | 3 | 2024 |
| An Agent-based CBIR system for medical images MU Ghani, PI Khan, KH Asif, A Nasir, MJ Arshad, S Amanat Journal of Faculty of Engineering & Technology 21 (2), 39-45, 2014 | 2 | 2014 |
| A Computational Framework for Unified Biological Databank to Overcome Heterogeneity of Biological Data Format MUG Khan, S Amanat, A Nasir, R Iqbal, M Idrees PAKISTAN ACADEMY OF SCIENCES 91, 2015 | 1 | 2015 |
| Examining the role of common variants in rare neurodevelopmental conditions QQ Huang, EM Wigdor, DS Malawsky, P Campbell, KE Samocha, ... Nature, 1-8, 2024 | | 2024 |
| Genetic Contribution to Tinnitus and Tinnitus Disorder CR Cederroth, N Trpchevska, S Amanat, A Gallego-Martinez, ... Textbook of Tinnitus, 49-58, 2024 | | 2024 |
| Ultrarare structural variation across the genome contributes to severe tinnitus phenotype A Gallego-Martinez, S Amanat, N Trpchevska, CR Cederroth, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 302-302, 2022 | | 2022 |
| Burden of rare variants in ANK2, AKAP9 and TSC2 genes supports membrane trafficking and cytoskeletal protein binding as biological processes in patients with severe tinnitus S Amanat, A Gallego-Martinez, J Sollini, P Perez-Carpena, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 301-302, 2022 | | 2022 |
| Corrigendum: Multidisciplinary Tinnitus Research: Challenges and Future Directions From the Perspective of Early Stage Researchers D Ortuño-Sahagún, E Genitsaridi, JP Simoes, M Shabbir, E Daoud, ... | | 2021 |
| A Systematic Review of Extreme Phenotype Strategies to Search for Rare Variants in Genetic Studies of Complex Disorders JA López Escámez, S Amanat, T Requena MDPI, 2020 | | 2020 |
| Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study JM Espinosa-Sanchez, JA Lopez-Escamez, CR Cederroth, B Canlon, ... EBioMedicine 66, 0 | | |
