Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome T Zemojtel, S Köhler, L Mackenroth, M Jäger, J Hecht, P Krawitz, ... Science translational medicine 6 (252), 252ra123-252ra123, 2014 | 196 | 2014 |
eXtasy: variant prioritization by genomic data fusion A Sifrim, D Popovic, LC Tranchevent, A Ardeshirdavani, R Sakai, ... Nature methods 10 (11), 1083-1084, 2013 | 139 | 2013 |
Candidate gene prioritization with Endeavour LC Tranchevent, A Ardeshirdavani, S ElShal, D Alcaide, J Aerts, ... Nucleic acids research 44 (W1), W117-W121, 2016 | 70 | 2016 |
NGS-Logistics: federated analysis of NGS sequence variants across multiple locations A Ardeshirdavani, E Souche, L Dehaspe, J Van Houdt, JR Vermeesch, ... Genome medicine 6 (9), 1-11, 2014 | 24 | 2014 |
Beegle: from literature mining to disease-gene discovery S ElShal, LC Tranchevent, A Sifrim, A Ardeshirdavani, J Davis, Y Moreau Nucleic acids research 44 (2), e18-e18, 2016 | 21 | 2016 |
Towards practical privacy-preserving genome-wide association study C Bonte, E Makri, A Ardeshirdavani, J Simm, Y Moreau, F Vercauteren BMC bioinformatics 19 (1), 1-12, 2018 | 15 | 2018 |
Privacy-Preserving Genome-Wide Association Study is Practical. C Bonte, E Makri, A Ardeshirdavani, J Simm, Y Moreau, F Vercauteren IACR Cryptol. ePrint Arch. 2017, 955, 2017 | 12 | 2017 |
pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion AA Kumar, L Van Laer, M Alaerts, A Ardeshirdavani, Y Moreau, ... Bioinformatics 34 (13), 2254-2262, 2018 | 11 | 2018 |
Galahad: a web server for drug effect analysis from gene expression G Laenen, A Ardeshirdavani, Y Moreau, L Thorrez Nucleic acids research 43 (W1), W208-W212, 2015 | 11 | 2015 |
HiVA: an integrative wet-and dry-lab platform for haplotype and copy number analysis of single-cell genomes MZ Esteki, A Ardeshirdavani, D Alcaide, H Masset, J Ding, A Sifrim, ... bioRxiv, 564914, 2019 | 3 | 2019 |
NGS-Logistics: data infrastructure for efficient analysis of NGS sequence variants across multiple centers A Ardeshirdavani, E Souche, L Dehaspe, J Van Houdt, JR Vermeesch, ... BMC Bioinformatics 16 (2), 1-3, 2015 | 3 | 2015 |
First results of the COVID-19 in MS Global Data Sharing Initiative suggest anti-CD20 DMTs are associated with worse COVID-19 outcomes S Simpson-Yap, E De Brouwer, T Kalincik, N Rijke, J Hillert, C Walton, ... Multiple Sclerosis Journal 26 (3_SUPPL), 48-49, 2020 | 2 | 2020 |
Clinical population genetic analysis of variants in the SARS-CoV-2 receptor ACE2 A Ardeshirdavani, P Zakeri, A Mehrtash, SM Hosseini, G Li, ... medRxiv, 2020 | 2 | 2020 |
Multiple Sclerosis Data Alliance–A global multi-stakeholder collaboration to scale-up real world data research LM Peeters, T Parciak, D Kalra, Y Moreau, E Kasilingam, P van Galen, ... Multiple sclerosis and related disorders 47, 102634, 2021 | 1 | 2021 |
Associations of DMT therapies with COVID-19 severity in multiple sclerosis S Simpson-Yap, E De Brouwer, T Kalincik, N Rijke, J Hillert, C Walton, ... medRxiv, 2021 | | 2021 |
Associations of DMT Therapies with COVID-19 Severity in Multiple Sclerosis: An International Cohort Study S Simpson-Yap, E De Brouwer, T Kalincik, N Rijke, J Hillert, C Walton, ... | | 2020 |
HiVA: a web platform for haplotyping and copy number analysis of single-cell genomes A Ardeshirdavani, M Zamani Esteki, D Alcaide, H Masset, J Ding, A Sifrim, ... European Journal Of Human Genetics 27, 1703-1703, 2019 | | 2019 |
WiNGS: Widely integrated NGS platform for whole genome sequencing A Ardeshirdavani, H Chizari, E Souche, N Sattanathan, N Shabani Lalani, ... 19th annual BeSHG meeting: Precision Medicine: Application of Genetics in …, 2019 | | 2019 |
A Development Framework for Data Analytics in Genomics A Ardeshirdavani | | 2017 |
Single-cell genome sequencing to characterize chromosome instability in human cleavage stage embryos E Fernandez Gallardo, M Zamani Esteki, N Van der Aa, C Szanto, ... Abstract book, 101-101, 2017 | | 2017 |