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BMC Biotechnology|June 8, 2017
Somatic cell selection for chlorsulfuron-resistant mutants in potato: identification of point mutations in the acetohydroxyacid synthase genePhilippa J Barrell, Julie M Latimer, Samantha J Baldwin, et al.
Disease Models & Mechanisms|December 7, 2013
TorsinA rescues ER-associated stress and locomotive defects in C. elegans models of ALSMichelle L Thompson, Pan Chen, Xiaohui Yan, et al.
Pain|May 21, 2015
Targeting cells of the myeloid lineage attenuates pain and disease progression in a prostate model of bone cancerMichelle L Thompson, Juan M Jimenez-Andrade, Stephane Chartier, et al.
The Journal of Molecular Diagnostics : JMD|July 24, 2025
Survey of Demographics, Training, Duties, and Professional Development for Variant Scientists in Genomic MedicineAlexa Dickson, Kelsey R Cone, Barbara K Fortini, et al.
Plos Genetics|September 1, 2017
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamusPatricia Blanchet, Martina Bebin, Shaam Bruet, et al.
Genome Medicine|November 22, 2022
Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencingKevin M Bowling, Michelle L Thompson, Melissa A Kelly, et al.
Science (New York, N.Y.)|October 26, 2013
Yeast reveal a "druggable" Rsp5/Nedd4 network that ameliorates α-synuclein toxicity in neuronsDaniel F Tardiff, Nathan T Jui, Vikram Khurana, et al.
Neurology. Genetics|November 23, 2016
De novo FGF12 mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
American Journal of Human Genetics|April 25, 2020
Non-coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative DiseasesJ Nicholas Cochran, Ethan G Geier, Luke W Bonham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2020
Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfallsKevin M Bowling, Michelle L Thompson, David E Gray, et al.
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