Alistair Ward

Sanford Health — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

16h-index63.4kcitations34works2.82yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genomics and Rare Diseases(19), Genomics and Phylogenetic Studies(10), Genomic variations and chromosomal abnormalities(9), Biomedical Text Mining and Ontologies(7), Genetic Associations and Epidemiology(5)

Publications23 total

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser
Genome Medicine·2025· 5 citedOpen Access
An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser
2025· 1 citedOpen Access
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit
npj Genomic Medicine·2025· 1 citedOpen Access
Author Correction: Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization
Scientific Reports·2022Open Access
eP415: Team-based genome diagnostics made possible with intuitive web-based iobio tools
Genetics in Medicine·2022
Clin.iobio: A Collaborative Diagnostic Workflow to Enable Team-Based Precision Genomics
Journal of Personalized Medicine·2022· 3 citedOpen Access
Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization
Scientific Reports·2021· 15 citedOpen Access
gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization
Research Square (Research Square)·2021Open Access
gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization
2020· 2 citedOpen Access
Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists
BMC Medical Genomics·2019· 10 citedOpen Access
Human-specific tandem repeat expansion and differential gene expression during primate evolution
Proceedings of the National Academy of Sciences·2019· 153 citedOpen Access
genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists
2019· 6 citedOpen Access
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Nature Communications·2019· 983 citedOpen Access
MOESM1 of Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists
Figshare·2019Open Access
Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy
npj Genomic Medicine·2018· 83 citedOpen Access
Rapid clinical diagnostic variant investigation of genomic patient sequencing data with <i>iobio</i> web tools
Journal of Clinical and Translational Science·2017· 7 citedOpen Access
Multi-platform discovery of haplotype-resolved structural variation in human genomes
2017· 157 citedOpen Access
2278
Journal of Clinical and Translational Science·2017Open Access
2097
Journal of Clinical and Translational Science·2017Open Access
2254
Journal of Clinical and Translational Science·2017Open Access
page 1 of 2Next →

Frequent Co-authors

Gábor Marth(21), Matt Velinder(11), Chase Miller(8), 義行 高橋(8), Aditya Ekawade(8), Tonya DiSera(5), Tonya Di Sera(5), John C. Carey(5), Ashley Andrews(5), Mark Chaisson(4), David Porubský(4), Peter A. Audano(4), Laura Clarke(4), Andrew Farrell(4), Xiangqun Zheng-Bradley(4), Paul Flicek(4), Stephanie Georges(4), Anders Pitman(4), Will Richards(4), David Viskochil(4)