Megan Landsverk - Concepedia

Author

Megan Landsverk

Also Known As

Landsverk, Megan L., M L Landsverk, M. L. Landsverk, M. Landsverk, M.L. Landsverk, Megan L Landsverk, Megan L. Landsverk, Megan Landsverk, Megan Landsverk⁎

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine University of Washington Sanford Health Sanford Research The University of Texas Medical Branch at Galveston

About

Megan Landsverk is an author at Baylor College of Medicine specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	717
2	Natural Sciences	4	4	363
3	Public Health	2	2	84
4	Social Sciences	1	1	33
5	Biochemistry	1	1	88

Megan Landsverk

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing Yaping Yang, Donna M. Muzny, Fan Xia, JAMA	2014	1.4K
Two mammalian UNC-45 isoforms are related to distinct cytoskeletal and muscle-specific functions Maureen G. Price, Megan Landsverk, José M. Barral, Journal of Cell Science	2002	194
Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders Hong Cui, Fangyuan Li, David Chen, Genetics in Medicine Mitochondrial MyopathyDnaMendelian DisorderMitochondrial FunctionNatural Sciences	2013	131
The UNC-45 chaperone mediates sarcomere assembly through myosin degradation in <i>Caenorhabditis elegans</i> Megan Landsverk, Shumin Li, Alex H. Hutagalung, The Journal of Cell Biology	2007	95
Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects Sha Tang, Jing Wang, Victor Wei Zhang, Human Mutation GeneticsMolecular BiologyPathologyMolecular GeneticsDisease Gene Identification	2013	88
Ubiquilin-1 Is a Molecular Chaperone for the Amyloid Precursor Protein Emily S. Stieren, Amina El Ayadi, Yao Xiao, Journal of Biological Chemistry Protein AssemblyGeneticsMolecular BiologyAmyloid Precursor ProteinAlzheimer's Disease	2011	88
Interpretation of mitochondrial tRNA variants Lee‐Jun C. Wong, Ting Chen, Jing Wang, Genetics in Medicine	2020	61
<i>SEPT9</i> gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy Mark Hannibal, Elizabeth K. Ruzzo, Lauren Miller, Neurology	2009	60
Clinical delineation of the <i>PACS1</i>‐related syndrome—Report on 19 patients Janneke Schuurs-Hoeijmakers, Megan Landsverk, Nicola Foulds, American Journal of Medical Genetics Part A Neurodevelopmental DisordersDown SyndromeDevelopmental AnomalySpecific MutationDevelopmental Biology	2016	58
Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes Bekim Sadiković, Jing Wang, Ayman W. El‐Hattab, PLoS ONE GeneticsMolecular BiologyPathologyMolecular GeneticsDisease Gene Identification	2010	56

Page 1