Megan Martin

600 total citations
28 papers, 418 citations indexed

About

Megan Martin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Megan Martin has authored 28 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 6 papers in Molecular Biology. Recurrent topics in Megan Martin's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (8 papers) and Genomics and Rare Diseases (7 papers). Megan Martin is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (8 papers) and Genomics and Rare Diseases (7 papers). Megan Martin collaborates with scholars based in United States, Italy and Australia. Megan Martin's co-authors include Gregory S. Berns, Rena Vanzo, Sarah T. South, Caroline F. Zink, Kurt Wiesenfeld, Giuseppe Pagnoni, Mukeshwar Dhamala, Charles H. Hensel, E. Robert Wassman and Karen S. Ho and has published in prestigious journals such as JAMA, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Megan Martin

27 papers receiving 399 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 Martin United States 12 194 165 84 53 43 28 418
Maarten Van Den Bossche Belgium 11 146 0.8× 83 0.5× 160 1.9× 15 0.3× 93 2.2× 33 470
Diane C. Lanham United States 11 349 1.8× 425 2.6× 181 2.2× 107 2.0× 88 2.0× 16 717
Emma Viscidi United States 10 216 1.1× 292 1.8× 105 1.3× 21 0.4× 125 2.9× 15 513
Aurore Curie France 14 290 1.5× 304 1.8× 227 2.7× 88 1.7× 58 1.3× 29 690
Fabrizio Pizzagalli United States 9 113 0.6× 173 1.0× 91 1.1× 33 0.6× 41 1.0× 18 330
Eline van Hugte Netherlands 9 69 0.4× 99 0.6× 175 2.1× 69 1.3× 20 0.5× 11 424
K Murakawa Japan 4 168 0.9× 263 1.6× 79 0.9× 46 0.9× 55 1.3× 7 324
Yohan Yee Canada 10 85 0.4× 129 0.8× 127 1.5× 56 1.1× 11 0.3× 17 415
Matthieu Raveau Japan 10 229 1.2× 99 0.6× 232 2.8× 39 0.7× 70 1.6× 13 535

Countries citing papers authored by Megan Martin

Since Specialization
Citations

This map shows the geographic impact of Megan Martin'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 Martin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Megan Martin more than expected).

Fields of papers citing papers by Megan Martin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Megan Martin. 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 Martin. The network helps show where Megan Martin may publish in the future.

Co-authorship network of co-authors of Megan Martin

This figure shows the co-authorship network connecting the top 25 collaborators of Megan Martin. A scholar is included among the top collaborators of Megan Martin 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 Martin. Megan Martin 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.
Narayan, Sanjiv M., et al.. (2025). Addressing contemporary threats in anonymised healthcare data using privacy engineering. npj Digital Medicine. 8(1). 145–145. 11 indexed citations
2.
Martin, Megan, et al.. (2023). P510: Validation of parent of origin detection for de novo events identified on SNP microarray in a postnatal population. SHILAP Revista de lepidopterología. 1(1). 100557–100557. 1 indexed citations
3.
Davis, Kyle, Colleen G. Bilancia, Megan Martin, et al.. (2022). NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system. Scientific Reports. 12(1). 5427–5427. 1 indexed citations
4.
Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2019). Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing. Scientific Reports. 9(1). 15315–15315. 8 indexed citations
5.
Vanzo, Rena, Karen S. Ho, Aparna Prasad, et al.. (2018). Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders. European Journal of Medical Genetics. 62(1). 15–20. 13 indexed citations
6.
Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2017). Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions. PLoS Currents. 9. 7 indexed citations
7.
Ho, Karen S., E. Robert Wassman, Charles H. Hensel, et al.. (2016). Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders. International Journal of Molecular Sciences. 17(12). 2070–2070. 50 indexed citations
8.
Ho, Karen S., Sarah T. South, Charles H. Hensel, et al.. (2016). Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome. Journal of Medical Genetics. 53(4). 256–263. 29 indexed citations
9.
Zanotti, Giovanni, et al.. (2016). Treatment and Patient Burden in ER+ HER2- Metastatic Breast Cancer: Results From a Physician Survey in the United States. Value in Health. 19(3). A171–A171. 1 indexed citations
10.
Peabody, John, Megan Martin, Lisa DeMaria, et al.. (2016). Clinical Utility of a Comprehensive, Whole Genome CMA Testing Platform in Pediatrics: A Prospective Randomized Controlled Trial of Simulated Patients in Physician Practices. PLoS ONE. 11(12). e0169064–e0169064. 5 indexed citations
11.
Martin, Megan, et al.. (2015). Mosaic deletion of 20pter due to rescue by somatic recombination. American Journal of Medical Genetics Part A. 170(1). 243–248. 19 indexed citations
12.
Martin, Megan, et al.. (2015). Variants of unknown significance on chromosomal microarray analysis: parental perspectives. Journal of Community Genetics. 6(4). 343–349. 28 indexed citations
13.
Vanzo, Rena, Megan Martin, Erin E. Baldwin, et al.. (2014). Clinical Utility of Chromosomal Microarray Analysis of DNA from Buccal Cells: Detection of Mosaicism in Three Patients. Journal of Genetic Counseling. 23(6). 922–927. 13 indexed citations
14.
Vanzo, Rena, et al.. (2013). Familial KANK1 deletion that does not follow expected imprinting pattern. European Journal of Medical Genetics. 56(5). 256–259. 19 indexed citations
15.
Vanzo, Rena, et al.. (2013). SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot. American Journal of Medical Genetics Part A. 164(2). 554–556. 7 indexed citations
16.
Gasparini, Roberto, Carlo Lucioni, Filippo Ansaldi, et al.. (2007). Studio costo-efficacia della vaccinazione influenzale per gli italiani di età compresa tra 50 e 64 anni. 9(2). 91–101. 5 indexed citations
17.
Dhamala, Mukeshwar, Giuseppe Pagnoni, Kurt Wiesenfeld, et al.. (2003). Neural correlates of the complexity of rhythmic finger tapping. NeuroImage. 20(2). 918–926. 94 indexed citations
18.
Berns, Gregory S., et al.. (2002). Limbic Hyperreactivity in Bipolar II Disorder. American Journal of Psychiatry. 159(2). 304–306. 38 indexed citations
19.
Schoop, W, Megan Martin, & Emily P. Zeitler. (1969). The effect of intravenous streptokinase on arterial stenosis in the limbs.. PubMed. 14(7). 347–53 passim. 1 indexed citations
20.
Martin, Megan. (1963). Preparation for Psychological Aspects of Nuclear Disaster. JAMA. 183(5). 197–197. 1 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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