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Adam C. English

Baylor University · US
Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genomics and Phylogenetic Studies, Genomics and Rare Diseases, Chromosomal and Genetic Variations, and Genomic variations and chromosomal abnormalities.
h-index
25
citations
4,837
works
107
NIH funding
primary concept
email

Recent publications

Sixth Annual BCM Hackathon on Structural Variation and Pangenomics
F1000Research 2025cited by 1position: middledoi
Characterization and visualization of tandem repeats at genome scale
Nature Biotechnology 2024cited by 122position: middledoi
Analysis and benchmarking of small and large genomic variants across tandem repeats
Nature Biotechnology 2024cited by 66position: firstdoi
Truvari: refined structural variant comparison preserves allelic diversity
Genome biology 2022cited by 223position: firstdoi
A robust benchmark for detection of germline large deletions and insertions
Nature Biotechnology 2020cited by 478position: middledoi
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2
Cell 2019cited by 85position: middledoi
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
Nature Communications 2018cited by 252position: middledoi
Sooty mangabey genome sequence provides insight into AIDS resistance in a natural SIV host
Nature 2018cited by 141position: middledoi
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease
Neurology Genetics 2018cited by 28position: middledoi
Improved annotation of the insect vector of citrus greening disease: biocuration by a diverse genomics community
Database 2017cited by 76position: middledoi
Assessing structural variation in a personal genome—towards a human reference diploid genome
BMC Genomics 2015cited by 179position: firstdoi
The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma
Cancer Cell 2014cited by 852position: middledoi
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
BMC Bioinformatics 2014cited by 232position: middledoi
PBHoney: identifying genomic variants via long-read discordance and interrupted mapping
BMC Bioinformatics 2014cited by 173position: firstdoi
Mind the Gap: Upgrading Genomes with Pacific Biosciences RS Long-Read Sequencing Technology
PLoS ONE 2012cited by 991position: firstdoi

Grants

No grants ingested yet.

Frequent collaborators

Fritz J. Sedlazeck · Baylor College of Medicine3 papers (2022–2024)Jeffrey G. Reid · Regeneron (United States)3 papers (2012–2014)Richard A. Gibbs · Baylor College of Medicine3 papers (2012–2022)William Salerno · Regeneron (United States)2 papers (2014–2014)Egor Dolzhenko · Pacific Biosciences (United States)2 papers (2024–2024) · 2 papers (2024–2024)Donna M. Muzny · Baylor College of Medicine2 papers (2012–2014)Heng Li · Xijing Hospital1 papers (2018–2018)Min Wang · Jingdezhen Ceramic Institute1 papers (2012–2012)David L. Nelson · Smithsonian Conservation Biology Institute1 papers (2024–2024)Xiang Qin · Zhejiang Chinese Medical University1 papers (2012–2012)Simon White · University of Connecticut1 papers (2014–2014) · 1 papers (2024–2024)Fuli Yu · East China University of Science and Technology1 papers (2014–2014) · 1 papers (2024–2024) · 1 papers (2014–2014)Stephan Züchner · Harvard University1 papers (2024–2024)Khi Pin Chua · Nanyang Technological University1 papers (2024–2024)Will Salerno · Baylor College of Medicine1 papers (2018–2018)Verónica Martínez-Cerdeño · Shriners Hospitals for Children - Erie1 papers (2024–2024)