Amin Ardeshirdavani
Amin Ardeshirdavani
Department of Electrical Engineering, STADIUS Center for Dynamical Systems, Signal Processing and
Geverifieerd e-mailadres voor esat.kuleuven.be
Titel
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Jaar
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
2022014
eXtasy: variant prioritization by genomic data fusion
A Sifrim, D Popovic, LC Tranchevent, A Ardeshirdavani, R Sakai, ...
Nature methods 10 (11), 1083-1084, 2013
1412013
Candidate gene prioritization with Endeavour
LC Tranchevent, A Ardeshirdavani, S ElShal, D Alcaide, J Aerts, ...
Nucleic acids research 44 (W1), W117-W121, 2016
772016
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
242014
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
222016
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
162018
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
132020
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
122017
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
112018
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
112015
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
52021
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
32021
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
32020
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
32019
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
32015
Clinical Whole-Exome Sequencing Analysis Reveals a Novel Missense COL11A1 Mutation Resulting in an 18-Week Iranian Male Aborted Fetus with Fibrochondrogenesis 1: A Case Report
H Mirtavoos-Mahyari, S Ajami, A Mehrtash, SM Marashiyan, F Bahreini, ...
2021
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples
P Paluoja, H Teder, A Ardeshirdavani, B Bayindir, J Vermeesch, ...
bioRxiv, 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
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Artikelen 1–20