Author

Amin Ardeshirdavani

Observed names: A. Ardeshirdavani, Amin ArdeshirDavani, Ardeshirdavani, A, Ardeshirdavani, A., Ardeshirdavani, Amin

Observed institutions: University of Technology Sydney, University of Freiburg, The University of Melbourne, University Medical Center Freiburg, iMinds, Agilent Technologies (Belgium), Iran Khodro (Iran), IMEC, KU Leuven

ORCID: 0000-0002-7226-7324

Observed ORCID: 0000-0002-7226-7324

OpenAlex ID: A5046353002

Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome

2014 · Tomasz Zemojtel, Sebastian Köhler, et al. · Science Translational Medicine · 255

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eXtasy: variant prioritization by genomic data fusion

2013 · Alejandro Sifrim, Dusan Popovic, et al. · Nature Methods · 163

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Recommendations for whole genome sequencing in diagnostics for rare diseases

2022 · Erika Souche, Sergi Beltran, et al. · European Journal of Human Genetics · 126

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Candidate gene prioritization with Endeavour

2016 · Léon-Charles Tranchevent, Amin Ardeshirdavani, et al. · Nucleic Acids Research · 115

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Beegle: from literature mining to disease-gene discovery

2015 · Sarah ElShal, Léon-Charles Tranchevent, et al. · Nucleic Acids Research · 61

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Towards practical privacy-preserving genome-wide association study

2018 · Charlotte Bonte, Eleftheria Makri, et al. · BMC Bioinformatics · 53

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Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing

2022 · Heleen Masset, Jia Ding, et al. · Nucleic Acids Research · 39

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pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion

2018 · Ajay Anand Kumar, Lut Van Laer, et al. · Bioinformatics · 33

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Associations of DMT therapies with COVID-19 severity in multiple sclerosis

2021 · Steve Simpson-Yap, Edward De Brouwer, et al. · medRxiv · 27

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Multiple Sclerosis Data Alliance – A global multi-stakeholder collaboration to scale-up real world data research

2020 · Liesbet M. Peeters, Tina Parciak, et al. · Multiple Sclerosis and Related Disorders · 23

NGS-Logistics : Federated analysis of NGS sequence variants across multiple locations

2014 · Amin Ardeshirdavani, Erika Souche, et al. · Genome Medicine · 23

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples

2021 · Priit Paluoja, Hindrek Teder, et al. · PLoS Computational Biology · 18

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Galahad: a web server for drug effect analysis from gene expression

2015 · Griet Laenen, Amin Ardeshirdavani, et al. · Nucleic Acids Research · 9

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1298Associations of DMT therapies with COVID-19 severity in multiple sclerosis

2021 · Steve Simpson-Yap, Edward De Brouwer, et al. · International Journal of Epidemiology · 7

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Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies

2024 · Parisa Vaseghi, Laleh Habibi, et al. · European Journal of Human Genetics · 6

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First results of the COVID-19 in MS global data sharing initiative suggest anti-CD20 dmts are associated with worse covid-19 outcomes

2020 · Simpson-Yap, S., de Brouwer, E., et al. · HAL (Le Centre pour la Communication Scientifique Directe) · 6

Privacy-Preserving Genome-Wide Association Study is Practical.

2017 · Charlotte Bonte, Eleftheria Makri, et al. · IACR Cryptology ePrint Archive · 6

Clinical population genetic analysis of variants in the SARS-CoV-2 receptor ACE2

2020 · Amin Ardeshirdavani, Pooya Zakeri, et al. · medRxiv · 5

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HiVA: an integrative wet- and dry-lab platform for haplotype and copy number analysis of single-cell genomes

2019 · Masoud Zamani Esteki, Amin Ardeshirdavani, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 5

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MINDDS-connect: a federated data platform integrating biobanks for meta cohort building and analysis

2025 · Benjamin Huremagic, Nishkala Sattanathan, et al. · European Journal of Human Genetics · 4

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NGS-Logistics: data infrastructure for efficient analysis of NGS sequence variants across multiple centers

2015 · Amin Ardeshirdavani, Erika Souche, et al. · BMC Bioinformatics · 4

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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

2022 · Hanifeh Mirtavoos‐Mahyari, Sanaz Ajami, et al. · Clinical Case Reports · 2

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WiNGS: Widely integrated NGS platform for federated genome analysis

2022 · Haleh Chizari, Nishkala Sattanathan, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 2

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Associations of DMT Therapies with COVID-19 Severity in Multiple Sclerosis: An International Cohort Study

2020 · Steve Simpson-Yap, Edward De Brouwer, et al. · SSRN Electronic Journal · 2

Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII

2024 · Amir Hossein Ebrahimi, Manzar Bolhassani, et al. · Archives of Iranian Medicine · 1

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Works count: 38

Citation count: 995

H-index: 12

I10-index: 12