Megan Landsverk

2.9k total citations
33 papers, 967 citations indexed

About

Megan Landsverk is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Megan Landsverk has authored 33 papers receiving a total of 967 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Clinical Biochemistry. Recurrent topics in Megan Landsverk's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (7 papers) and RNA modifications and cancer (6 papers). Megan Landsverk is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (7 papers) and RNA modifications and cancer (6 papers). Megan Landsverk collaborates with scholars based in United States, Saudi Arabia and Germany. Megan Landsverk's co-authors include Henry F. Epstein, José M. Barral, Maureen G. Price, Lee‐Jun C. Wong, Victor Wei Zhang, Alex H. Hutagalung, Jing Wang, Eric Schmitt, William J. Craigen and Brett H. Graham and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Megan Landsverk

32 papers receiving 950 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Megan Landsverk United States 18 750 201 141 140 135 33 967
Marco Crimi Italy 18 930 1.2× 383 1.9× 27 0.2× 138 1.0× 35 0.3× 33 1.3k
Helen Tuppen United Kingdom 20 1.5k 2.0× 721 3.6× 36 0.3× 125 0.9× 30 0.2× 34 1.7k
Olga S. Koutsopoulos Australia 6 884 1.2× 245 1.2× 61 0.4× 33 0.2× 183 1.4× 6 1.0k
Emélie Braschi Canada 6 1.5k 2.0× 262 1.3× 30 0.2× 40 0.3× 211 1.6× 7 1.8k
Pirjo Isohanni Finland 22 1.4k 1.9× 812 4.0× 32 0.2× 179 1.3× 68 0.5× 45 1.7k
Friedrich P. Thinnes Germany 21 911 1.2× 136 0.7× 25 0.2× 53 0.4× 137 1.0× 50 1.2k
Christian Hamel France 20 1.2k 1.7× 141 0.7× 20 0.1× 265 1.9× 203 1.5× 39 1.5k
Victor Venegas United States 9 329 0.4× 74 0.4× 21 0.1× 29 0.2× 56 0.4× 9 657
Arcangela Iuso Germany 15 720 1.0× 307 1.5× 30 0.2× 79 0.6× 44 0.3× 28 974
Ana Fernández‐Marmiesse Spain 17 460 0.6× 233 1.2× 70 0.5× 219 1.6× 43 0.3× 33 842

Countries citing papers authored by Megan Landsverk

Since Specialization
Citations

This map shows the geographic impact of Megan Landsverk's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Megan Landsverk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Megan Landsverk more than expected).

Fields of papers citing papers by Megan Landsverk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Megan Landsverk. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Megan Landsverk. The network helps show where Megan Landsverk may publish in the future.

Co-authorship network of co-authors of Megan Landsverk

This figure shows the co-authorship network connecting the top 25 collaborators of Megan Landsverk. A scholar is included among the top collaborators of Megan Landsverk based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Megan Landsverk. Megan Landsverk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Weimer, Jill M., et al.. (2021). Novel variants identified in CKAP2L in two siblings with Filippi Syndrome. Molecular Case Studies. 8(2). mcs.a006130–mcs.a006130.
2.
Wong, Lee‐Jun C., Ting Chen, Jing Wang, et al.. (2020). Interpretation of mitochondrial tRNA variants. Genetics in Medicine. 22(5). 917–926. 37 indexed citations
3.
Johnson, Tyler B., Jacob T. Cain, Stephen R. Braddock, et al.. (2018). Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1. Scientific Reports. 8(1). 16161–16161. 6 indexed citations
4.
Landsverk, Megan, Victor Wei Zhang, Lee‐Jun C. Wong, & Hans C. Andersson. (2014). A SUCLG1 mutation in a patient with mitochondrial DNA depletion and congenital anomalies. Molecular Genetics and Metabolism Reports. 1. 451–454. 14 indexed citations
5.
Tang, Sha, Jing Wang, Victor Wei Zhang, et al.. (2013). Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects. Human Mutation. 34(6). 882–893. 70 indexed citations
6.
Wang, Jing, Eric Schmitt, Megan Landsverk, et al.. (2012). An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory’s experience. Genetics in Medicine. 14(6). 620–626. 30 indexed citations
7.
Landsverk, Megan, Sha Tang, Victor Wei Zhang, et al.. (2012). Diagnostic approaches to apparent homozygosity. Genetics in Medicine. 14(10). 877–882. 31 indexed citations
8.
Landsverk, Megan, Timothy Lotze, Jill V. Hunter, et al.. (2011). Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation. Molecular Genetics and Metabolism. 103(2). 153–160. 20 indexed citations
9.
Landsverk, Megan, et al.. (2011). Sequence Analysis of the Whole Mitochondrial Genome and Nuclear Genes Causing Mitochondrial Disorders. Methods in molecular biology. 837. 281–300. 6 indexed citations
10.
Stieren, Emily S., Amina El Ayadi, Yao Xiao, et al.. (2011). Ubiquilin-1 Is a Molecular Chaperone for the Amyloid Precursor Protein. Journal of Biological Chemistry. 286(41). 35689–35698. 75 indexed citations
11.
Landsverk, Megan, Jing Wang, Eric Schmitt, Amber N. Pursley, & Lee‐Jun C. Wong. (2011). Utilization of targeted array comparative genomic hybridization, MitoMet®, in prenatal diagnosis of metabolic disorders. Molecular Genetics and Metabolism. 103(2). 148–152. 8 indexed citations
12.
Landsverk, Megan, Douglas C. Weiser, Mark Hannibal, & David Kimelman. (2010). Alternative Splicing of sept9a and sept9b in Zebrafish Produces Multiple mRNA Transcripts Expressed Throughout Development. PLoS ONE. 5(5). e10712–e10712. 11 indexed citations
13.
Sadiković, Bekim, Jing Wang, Ayman W. El‐Hattab, et al.. (2010). Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes. PLoS ONE. 5(12). e15687–e15687. 41 indexed citations
14.
Collie, Angela M. B., Megan Landsverk, Elizabeth K. Ruzzo, et al.. (2009). Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy. Journal of Medical Genetics. 47(9). 601–607. 35 indexed citations
15.
Hannibal, Mark, Elizabeth K. Ruzzo, Jillian G. Buchan, et al.. (2009). SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy. Neurology. 72(20). 1755–1759. 40 indexed citations
16.
Landsverk, Megan, Elizabeth K. Ruzzo, Heather C. Mefford, et al.. (2009). Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Human Molecular Genetics. 18(7). 1200–1208. 22 indexed citations
17.
Landsverk, Megan, et al.. (2008). Requirement of Inositol 1,4,5-Trisphosphate Receptors for Tumor-mediated Lymphocyte Apoptosis. Journal of Biological Chemistry. 283(20). 13506–13509. 20 indexed citations
18.
Landsverk, Megan, Shumin Li, Alex H. Hutagalung, et al.. (2007). The UNC-45 chaperone mediates sarcomere assembly through myosin degradation in Caenorhabditis elegans. The Journal of Cell Biology. 177(2). 205–210. 81 indexed citations
19.
Miller, Rachel K., Hiroshi Qadota, Megan Landsverk, et al.. (2006). UNC-98 links an integrin-associated complex to thick filaments in Caenorhabditis elegans muscle. The Journal of Cell Biology. 175(6). 853–859. 28 indexed citations
20.
Landsverk, Megan & Henry F. Epstein. (2005). Genetic analysis of myosin II assembly and organization in model organisms. Cellular and Molecular Life Sciences. 62(19-20). 2270–2282. 37 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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