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Amin Ardeshirdavani
Amin Ardeshirdavani
Department of Electrical Engineering, STADIUS Center for Dynamical Systems, Signal Processing and
Verified email at esat.kuleuven.be
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Cited by
Year
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
2822014
eXtasy: variant prioritization by genomic data fusion
A Sifrim, D Popovic, LC Tranchevent, A Ardeshirdavani, R Sakai, ...
Nature methods 10 (11), 1083-1084, 2013
1852013
Candidate gene prioritization with Endeavour
LC Tranchevent, A Ardeshirdavani, S ElShal, D Alcaide, J Aerts, ...
Nucleic acids research 44 (W1), W117-W121, 2016
1212016
Recommendations for whole genome sequencing in diagnostics for rare diseases
E Souche, S Beltran, E Brosens, JW Belmont, M Fossum, O Riess, ...
European Journal of Human Genetics 30 (9), 1017-1021, 2022
672022
Towards practical privacy-preserving genome-wide association study
C Bonte, E Makri, A Ardeshirdavani, J Simm, Y Moreau, F Vercauteren
BMC bioinformatics 19, 1-12, 2018
482018
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
292018
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
292016
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, 1-11, 2014
282014
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
H Masset, J Ding, E Dimitriadou, A Ardeshirdavani, S Debrock, O Tšuiko, ...
Nucleic Acids Research 50 (11), e63-e63, 2022
192022
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
192020
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
172021
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
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
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples
P Paluoja, H Teder, A Ardeshirdavani, B Bayindir, J Vermeesch, ...
PLoS Computational Biology 17 (12), e1009684, 2021
102021
Clinical population genetic analysis of variants in the SARS-CoV-2 receptor ACE2
A Ardeshirdavani, P Zakeri, A Mehrtash, SM Hosseini, G Li, ...
medRxiv, 2020.05. 27.20115071, 2020
52020
HiVA: an integrative wet-and dry-lab platform for haplotype and copy number analysis of single-cell genomes
M Zamani Esteki, A Ardeshirdavani, D Alcaide, H Masset, J Ding, A Sifrim, ...
42019
1298Associations of DMT therapies with COVID-19 severity in multiple sclerosis.
S Simpson-Yap, ED Brouwer, T Kalincik, N Rijke, J Hillert, C Walton, ...
International Journal of Epidemiology 50, 2021
32021
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, 1-3, 2015
32015
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome. Sci Transl Med. 2014; 6 (252): 252–123
T Zemojtel, S Köhler, L Mackenroth, M Jäger, J Hecht, P Krawitz, ...
2
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