Author

Neil E. Lamb

HudsonAlpha Institute for Biotechnology

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:statistical model· 2 Research Focus:database / resource· 1 Organism:human· 1 Assay:protein structure· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adam C. UnderwoodiD· 1 shared Amy S. Nesmith· 1 shared Austin Frisch· 1 shared Benjamin T. Weaver· 1 shared Bruce D. UhaliD· 1 shared Caleb P. BuppiD· 1 shared Candice R. FinnilaiD· 1 shared Carla A. RichiD· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetics

Adam C. UnderwoodORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

SARS-CoV2 (COVID-19) Structural/Evolution Dynamicome: Insights into functional evolution and human genomics.

Ruchir Gupta, Jacob G. Charron, Cynthia L. Stenger, Jared Painter, Hunter Steward, Taylor W. Cook, William Faber, Austin Frisch, Eric Lind, Jacob M. Bauss, Xiaopeng Li, Olivia L. Sirpilla, Xavier Soehnlen, Adam C. Underwood, David Hinds, , Jeremy W. Prokop

The paper presents VIStEDD, a database of SARS-CoV-2 structural and evolutionary dynamics, highlighting conserved amino acids and variants in ACE2/SLC6A19/TMPRSS2 linked to pandemic susceptibility.

bioRxiv · May 15, 2020 · PreprintGenetics

Genomic diagnosis for children with intellectual disability and/or developmental delay

Kevin M. Bowling, Michelle L. Thompson, Michelle D. Amaral, Candice R. Finnila, Susan M. Hiatt, Krysta L. Engel, J. Nicholas Cochran, Kyle Bertram Brothers, Kelly M. East, David E. Gray, Whitley V. Kelley, Neil E. Lamb, Edward J. Lose, Carla A. Rich, Shirley Simmons, , Gregory M. Cooper

This study analyzes genomic data from 371 children with intellectual disability or developmental delay to identify pathogenic variants and assess diagnostic utility.

Genome Medicine · May 17, 2017Peer-reviewedGenomics