Author

Ryan E. Lamont

University of CalgaryORCID 0000-0002-7720-068XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Assay:bulk RNA-seq· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Allan Micheil InnesiD· 2 shared François P. BernieriD· 2 shared Jillian S. Parboosingh· 2 shared Adam J. Cornish· 1 shared Amanda V. Tyndall· 1 shared Caitlin Goedhart· 1 shared Claudia VivoriiD· 1 shared Danielle BlackwelliD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersDevelopmental Biology

Allan Micheil InnesORCID

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2 papers

Recent·Most cited

Developmental BiologyG3 Genes Genomes GeneticsPeer-reviewedMar 23, 2022

Hnrnpul1 loss of function affects skeletal and limb development

Danielle Blackwell, Sherri D. Fraser, Oana Caluseriu…·Sarah J. Childs

This study shows Hnrnpul1 loss of function in zebrafish causes skeletal and limb defects and links it to human congenital limb malformations.

12 citations

zebrafishbulk RNA-seq

𝕏 PostBluesky

Molecular BiologyLife Science AlliancePeer-reviewedMar 11, 2019

PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts and white matter changes

Tian Zhao, Caitlin Goedhart, Pingdewinde N. Sam…·Timothy E. Shutt

The paper identifies PISD as a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes through exome sequencing and functional analysis of patient fibroblasts.

69 citations

humanwhole-exome sequencing

𝕏 PostBluesky