Matthew Bower

1.2k total citations
29 papers, 535 citations indexed

About

Matthew Bower is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Matthew Bower has authored 29 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Matthew Bower's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (5 papers). Matthew Bower is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (5 papers). Matthew Bower collaborates with scholars based in United States, United Kingdom and Canada. Matthew Bower's co-authors include Bonnie S. LeRoy, Patricia McCarthy Veach, Dianne M. Bartels, Bharat Thyagarajan, Kevin A.T. Silverstein, Getiria Onsongo, Xinjing Wang, Dimitre R. Simeonov, Juergen Scharner and Yuri V. Sergeev and has published in prestigious journals such as PLoS ONE, Human Mutation and Genetics in Medicine.

In The Last Decade

Matthew Bower

28 papers receiving 527 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew Bower United States 14 260 161 109 58 55 29 535
Moeenaldeen AlSayed Saudi Arabia 15 254 1.0× 183 1.1× 84 0.8× 52 0.9× 25 0.5× 49 737
Erik-Jan Kamsteeg Netherlands 15 425 1.6× 320 2.0× 76 0.7× 64 1.1× 66 1.2× 21 874
Jiddeke M. van de Kamp Netherlands 15 222 0.9× 196 1.2× 172 1.6× 74 1.3× 29 0.5× 24 786
Morad Khayat Israel 16 422 1.6× 162 1.0× 73 0.7× 57 1.0× 18 0.3× 50 664
Wenqi Zeng United States 12 277 1.1× 187 1.2× 60 0.6× 50 0.9× 101 1.8× 19 607
Josef Ekstein United States 12 407 1.6× 193 1.2× 122 1.1× 59 1.0× 48 0.9× 27 851
Nathalie Van der Aa Belgium 19 412 1.6× 388 2.4× 89 0.8× 38 0.7× 25 0.5× 26 809
Séverine Drunat France 21 581 2.2× 443 2.8× 160 1.5× 144 2.5× 37 0.7× 57 1.1k
Hamad Alzaidan Saudi Arabia 14 283 1.1× 173 1.1× 45 0.4× 66 1.1× 15 0.3× 39 578
Marc D’Hooghe Belgium 12 337 1.3× 63 0.4× 44 0.4× 103 1.8× 45 0.8× 18 580

Countries citing papers authored by Matthew Bower

Since Specialization
Citations

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

Fields of papers citing papers by Matthew Bower

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Bower

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Bower. A scholar is included among the top collaborators of Matthew Bower 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 Matthew Bower. Matthew Bower 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.
Sen, Siddhartha, Alec Victorsen, Todd P. Knutson, et al.. (2025). Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis. Frontiers in Genetics. 16. 1499456–1499456. 1 indexed citations
2.
Peters, Samuel T., David R. Deyle, Matthew Bower, et al.. (2020). Case Report: Early-Onset Behavioral Variant Frontotemporal Dementia in Patient With Retrotransposed Full-Length Transcript of Matrin-3 Variant 5. Frontiers in Neurology. 11. 600468–600468. 5 indexed citations
3.
Tolar, Jakub, Megan Riddle, Douglas R. Keene, et al.. (2019). A homozygous frameshift variant in the KRT5 gene is compatible with life and results in severe recessive epidermolysis bullosa simplex. JAAD Case Reports. 5(7). 576–579. 1 indexed citations
4.
Sarafoglou, Kyriakie, et al.. (2018). Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: a case report. BMC Medical Genetics. 19(1). 100–100. 11 indexed citations
5.
Onsongo, Getiria, Linda B. Baughn, Matthew Bower, et al.. (2016). CNV-RF Is a Random Forest–Based Copy Number Variation Detection Method Using Next-Generation Sequencing. Journal of Molecular Diagnostics. 18(6). 872–881. 24 indexed citations
6.
Yohe, Sophia, Matthew Bower, Getiria Onsongo, et al.. (2015). Clinical Validation of Targeted Next-Generation Sequencing for Inherited Disorders. Archives of Pathology & Laboratory Medicine. 139(2). 204–210. 43 indexed citations
7.
Nelson, Andrew C., Matthew Bower, Linda B. Baughn, et al.. (2015). Criteria for Clinical Reporting of Variants from a Broad Target Capture NGS Assay without Sanger Verification. University of Minnesota Digital Conservancy (University of Minnesota). 2(1). 12 indexed citations
8.
Veach, Patricia McCarthy, et al.. (2014). Ethical and Professional Challenges Encountered by Laboratory Genetic Counselors. Journal of Genetic Counseling. 24(4). 580–596. 12 indexed citations
9.
Liu, Jilin, Karen N. McFarland, Samuel S. Wu, et al.. (2014). Identifying novel interruption motifs in spinocerebellar ataxia type 10 expansions. Neurology and Clinical Neuroscience. 2(2). 38–43. 3 indexed citations
10.
Onsongo, Getiria, John Chilton, Kenneth B. Beckman, et al.. (2014). Implementation of Cloud based Next Generation Sequencing data analysis in a clinical laboratory. BMC Research Notes. 7(1). 314–314. 18 indexed citations
11.
Simeonov, Dimitre R., Xinjing Wang, Chen Wang, et al.. (2013). DNA Variations in Oculocutaneous Albinism: An Updated Mutation List and Current Outstanding Issues in Molecular Diagnostics. Human Mutation. 34(6). 827–835. 102 indexed citations
12.
Bushara, Khalaf, Matthew Bower, Jilin Liu, et al.. (2013). Expansion of the Spinocerebellar Ataxia Type 10 (SCA10) Repeat in a Patient with Sioux Native American Ancestry. PLoS ONE. 8(11). e81342–e81342. 26 indexed citations
13.
Zhang, Ying, John Chilton, Getiria Onsongo, et al.. (2012). CLIA-certified next-generation sequencing analysis in the cloud. BMC Proceedings. 6(S6). 3 indexed citations
14.
Brown, Charlotte A., Juergen Scharner, Kevin J. Felice, et al.. (2011). Novel and recurrent EMD mutations in patients with Emery–Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot. Journal of Human Genetics. 56(8). 589–594. 26 indexed citations
15.
Bower, Matthew, Michael R. Eccles, Laurence Heidet, & Lisa A. Schimmenti. (2011). Clinical utility gene card for: renal coloboma (Papillorenal) syndrome. European Journal of Human Genetics. 19(9). 1017–1017. 5 indexed citations
16.
Scharner, Juergen, Charlotte A. Brown, Matthew Bower, et al.. (2010). Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations. Human Mutation. 32(2). 152–167. 55 indexed citations
17.
Thyagarajan, Bharat, et al.. (2008). A novel polymorphism in the FMR1 gene: implications for clinical testing of fragile X syndrome.. PubMed. 132(1). 95–8. 2 indexed citations
18.
Tuite, Paul, H. Brent Clark, Catherine Bergeron, et al.. (2005). Clinical and Pathologic Evidence of Corticobasal Degeneration and Progressive Supranuclear Palsy in Familial Tauopathy. Archives of Neurology. 62(9). 1453–1453. 23 indexed citations
19.
Levine, John E., Robert Ruiz, Wendy Kohlmann, et al.. (2005). Malignant triton tumor in a patient with Li‐Fraumeni syndrome and a novel TP53 mutation. Pediatric Blood & Cancer. 49(7). 1000–1004. 15 indexed citations
20.
Bower, Matthew, et al.. (2003). Role of the geneticist in testing and counseling for inherited thrombophilia. Genetics in Medicine. 5(3). 133–143. 42 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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