| Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases B Zurek, K Ellwanger, LELM Vissers, R Schüle, M Synofzik, A Töpf, ... European journal of human genetics 29 (9), 1325-1331, 2021 | 67 | 2021 |
| Solving patients with rare diseases through programmatic reanalysis of genome-phenome data L Matalonga, C Hernández-Ferrer, D Piscia, R Schüle, M Synofzik, A Töpf, ... European Journal of Human Genetics 29 (9), 1337-1347, 2021 | 42 | 2021 |
| A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing AS Denommé-Pichon, L Matalonga, E de Boer, A Jackson, E Benetti, ... Genetics in Medicine 25 (4), 100018, 2023 | 6 | 2023 |
| Hypergraph Computation Q Dai, Y Gao Springer Nature, 2023 | 6 | 2023 |
| Solving unsolved rare neurological diseases—a Solve-RD viewpoint R Schüle, D Timmann, CE Erasmus, J Reichbauer, M Wayand, ... European Journal of Human Genetics 29 (9), 1332-1336, 2021 | 6 | 2021 |
| Trusted autonomous vehicles: An interactive exhibit HLS Araujo, CDN Damasceno, R Dimitrova, G Kefalidou, M Mehtarizadeh, ... 2019 IEEE International Conferences on Ubiquitous Computing & Communications …, 2019 | 4 | 2019 |
| Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 A Jackson, SJ Lin, EA Jones, KE Chandler, D Orr, C Moss, Z Haider, ... Human Genetics and Genomics Advances 4 (2), 2023 | 2 | 2023 |
| Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases B Zurek, K Ellwanger, LELM Vissers, R Schüle, M Synofzik, A Töpf, ... European Journal of Human Genetics 29 (9), 1459-1461, 2021 | 1 | 2021 |
| An ensemble of deep semantic representation for medical x-ray image classification MR Zare, M Mehtarizadeh 2021 55th Annual Conference on Information Sciences and Systems (CISS), 1-6, 2021 | 1 | 2021 |
| Automatic Inference of Smart Data Discovery Interfaces for Rare Disease Datasets A Boronat, A Ademeyo, M Mehtarizadeh, S Zschaler University of Leicester, 2023 | | 2023 |
| Medical Compound Figure Detection Using Inductive Transfer and Ensemble Learning M Mehtarizadeh, M Reza Zare International Conference on Computational & Experimental Engineering and …, 2022 | | 2022 |
| Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data L Matalonga, C Hernández-Ferrer, D Piscia, R Schüle, M Synofzik, A Töpf, ... European Journal of Human Genetics 29 (9), 1466-1469, 2021 | | 2021 |
| Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases LELM Vissers, R Schüle, M Synofzik, A Töpf, L Matalonga, C Gilissen, ... Springer International Publishing, 2021 | | 2021 |
| Solving unsolved rare neurological diseases—a Solve-RD viewpoint R Schule, D Timmann, CE Erasmus, J Reichbauer, M Wayand, J Baets, ... European Journal of Human Genetics 29 (9), 1332-1336, 2021 | | 2021 |
| Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics,(2021), 10.1038/s41431-021-00901-1) R Schule, D Timmann, CE Erasmus, J Reichbauer, J Baets, P Chinnery, ... European Journal of Human Genetics, 2021 | | 2021 |
| Solving unsolved rare neurological diseases-a Solve-RD viewpoint L Matalonga, D Timmann, CE Erasmus, J Reichbauer, M Wayand, ... European Journal of Human Genetics. 2021; 29: 1332-6, 2021 | | 2021 |
| Chi, Yongsheng 621 Choi, Won-Ho 218 Dai, Xuwen 202 Damasceno, Carlos Diego N. 386 J Deng, MAA Al-Qaness, X An, Z An, HLS Araujo, M Badawy, Y Bai, Y Bai, ... | | |
