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Author Details
Full Name
Amin Ardeshirdavani
Affiliation
STADIUS Center for Dynamical Systems
ORCID
Career Start Year
2013
Papers
12
H Index
9
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36397853
Clinical whole-exome sequencing analysis reveals a novel missense COL11A1 mutation resulting in an 18-week Iranian male aborted fetus with Fibrochondrogenesis 1: AÂ case report.
Clin Case Rep
2022
35577938
Recommendations for whole genome sequencing in diagnostics for rare diseases.
Eur J Hum Genet
2022
33278741
Multiple Sclerosis Data Alliance - A global multi-stakeholder collaboration to scale-up real world data research.
Mult Scler Relat Disord
2021
34928946
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples.
PLoS Comput Biol
2021
29452392
pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion.
Bioinformatics
2018
30572817
Towards practical privacy-preserving genome-wide association study.
BMC Bioinformatics
2018
27131783
Candidate gene prioritization with Endeavour.
Nucleic Acids Res
2016
26384564
Beegle: from literature mining to disease-gene discovery.
Nucleic Acids Res
2016
25940630
Galahad: a web server for drug effect analysis from gene expression.
Nucleic Acids Res
2015
25186178
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome.
Sci Transl Med
2014
25328540
NGS-Logistics: federated analysis of NGS sequence variants across multiple locations.
Genome Med
2014
24076761
eXtasy: variant prioritization by genomic data fusion.
Nat Methods
2013
1 - 12 of 12
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