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The Journal of Cell Biology|April 18, 2007
The UNC-45 chaperone mediates sarcomere assembly through myosin degradation in Caenorhabditis elegansMegan L Landsverk, Shumin Li, Alex H Hutagalung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2012
Diagnostic approaches to apparent homozygosityMegan L Landsverk, Ganka V Douglas, Sha Tang, et al.
The Journal of Biological Chemistry|August 20, 2011
Ubiquilin-1 is a molecular chaperone for the amyloid precursor proteinEmily S Stieren, Amina El Ayadi, Yao Xiao, et al.
Molecular Genetics and Metabolism|March 19, 2011
Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutationGary Fruhman, Megan L Landsverk, Timothy E Lotze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 10, 2012
An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory's experienceJing Wang, Eric S Schmitt, Megan L Landsverk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2013
Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disordersHong Cui, Fangyuan Li, David Chen, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 24, 2015
Mutation in GM2A Leads to a Progressive Chorea-dementia SyndromeMustafa A Salih, Mohammed Z Seidahmed, Heba Y El Khashab, et al.
Human Molecular Genetics|January 14, 2009
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophyMegan L Landsverk, Elizabeth K Ruzzo, Heather C Mefford, et al.
JCO Precision Oncology|February 9, 2022
Delivering Precision Oncology in a Community Cancer Program: Results From a Prospective Observational StudySteven F Powell, Elie G Dib, Jonathan S Bleeker, et al.
Neurology. Genetics|June 14, 2019
Loss-of-function mutations in Lysyl-tRNA synthetase cause various leukoencephalopathy phenotypesChong Sun, Jie Song, Yanjun Jiang, et al.
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