Mathew Wallis

2.2k total citations
18 papers, 319 citations indexed

About

Mathew Wallis is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Mathew Wallis has authored 18 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Oncology and 4 papers in Genetics. Recurrent topics in Mathew Wallis's work include Genomics and Rare Diseases (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Prenatal Screening and Diagnostics (2 papers). Mathew Wallis is often cited by papers focused on Genomics and Rare Diseases (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Prenatal Screening and Diagnostics (2 papers). Mathew Wallis collaborates with scholars based in Australia, Germany and France. Mathew Wallis's co-authors include I. Schreer, Thomas Helbich, Damien F. Hudson, Paul Kalitsis, Tao Zhang, Vida Petrovic, Xicheng Mao, Andreas W. Kuß, Baozhi Chen and Petro Starokadomskyy and has published in prestigious journals such as Journal of Clinical Investigation, Movement Disorders and European Radiology.

In The Last Decade

Mathew Wallis

17 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathew Wallis Australia 8 126 77 66 57 42 18 319
Chun Qiu China 11 172 1.4× 18 0.2× 142 2.2× 43 0.8× 24 0.6× 25 371
Natsumi Maehara Japan 8 164 1.3× 23 0.3× 79 1.2× 17 0.3× 21 0.5× 15 384
Janusz Jaszczyński Poland 7 73 0.6× 24 0.3× 58 0.9× 36 0.6× 30 0.7× 14 213
Katharina Buser Switzerland 7 108 0.9× 40 0.5× 58 0.9× 75 1.3× 35 0.8× 10 342
Yi Qu China 11 167 1.3× 20 0.3× 87 1.3× 51 0.9× 19 0.5× 25 330
Μαρία Παναγοπούλου Greece 12 256 2.0× 32 0.4× 155 2.3× 13 0.2× 48 1.1× 29 401
Eric Mukherjee United States 11 142 1.1× 121 1.6× 19 0.3× 33 0.6× 27 0.6× 17 411
Leigh J. Hodson Australia 7 79 0.6× 15 0.2× 76 1.2× 28 0.5× 28 0.7× 9 321
Huan-Chang Liang Austria 4 74 0.6× 23 0.3× 44 0.7× 103 1.8× 8 0.2× 5 255
Ewa Zembala‐Nożyńska Poland 11 135 1.1× 33 0.4× 41 0.6× 20 0.4× 22 0.5× 45 345

Countries citing papers authored by Mathew Wallis

Since Specialization
Citations

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

Fields of papers citing papers by Mathew Wallis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathew Wallis

This figure shows the co-authorship network connecting the top 25 collaborators of Mathew Wallis. A scholar is included among the top collaborators of Mathew Wallis 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 Mathew Wallis. Mathew Wallis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Collins, Felicity, Susan M. White, Mathew Wallis, et al.. (2024). Assessing the unmet needs of genomic testing in Australia: a geospatial exploration. European Journal of Human Genetics. 33(4). 496–503. 1 indexed citations
2.
Charlesworth, Jac, et al.. (2024). Measuring the impact of rare diseases in Tasmania, Australia. Orphanet Journal of Rare Diseases. 19(1). 399–399.
3.
Parmar, J., Melina Ellis, Samantha J. Bryen, et al.. (2024). A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing. Journal of the Peripheral Nervous System. 29(2). 262–274. 1 indexed citations
4.
Ye, Zimeng, Sufang Lin, Mathew Wallis, et al.. (2023). Are Germline Mosaic TSC1/2 Variants Present in Controls? Implications for Diagnosis. Pediatric Neurology. 150. 37–39. 1 indexed citations
5.
Wallis, Mathew, et al.. (2021). Cryopyrin-associated periodic syndrome: a treatable genetic inflammatory condition. Practical Neurology. 21(5). 424–426. 1 indexed citations
6.
Ramchand, Jay, Mathew Wallis, Ivan Macciocca, et al.. (2020). Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy. Journal of the American Heart Association. 9(2). e013346–e013346. 26 indexed citations
7.
Rafehi, Haloom, David J. Szmulewicz, Kate Pope, et al.. (2020). Rapid Diagnosis of Spinocerebellar Ataxia 36 in a Three‐Generation Family Using Short‐Read Whole‐Genome Sequencing Data. Movement Disorders. 35(9). 1675–1679. 7 indexed citations
8.
Wallis, Mathew, et al.. (2020). Lymphedema distichiasis syndrome may be caused by FOXC2 promoter‐enhancer dissociation and disruption of a topological associated domain. American Journal of Medical Genetics Part A. 185(1). 150–156. 2 indexed citations
9.
Wallis, Mathew, Amber Boys, Elisa Tassano, & Martin B. Delatycki. (2019). Small interstitial 9p24.3 deletions principally involving KANK1 are likely benign copy number variants. European Journal of Medical Genetics. 63(1). 103618–103618. 3 indexed citations
10.
Zhang, Tao, et al.. (2019). Loss of TOP3B leads to increased R-loop formation and genome instability. Open Biology. 9(12). 190222–190222. 49 indexed citations
11.
Wallis, Mathew, Alessandra Baumer, Imane Cherkaoui Jaouad, et al.. (2017). Surprisingly good outcome in antenatal diagnosis of severe hydrocephalus related to CCDC88C deficiency. European Journal of Medical Genetics. 61(4). 189–196. 10 indexed citations
12.
Stevens, Hannah, et al.. (2016). Fanconi anemia in 55‐year‐old identical twins first presenting as fatal post‐chemotherapy pancytopenia. American Journal of Hematology. 91(12). 1273–1276. 2 indexed citations
13.
Wallis, Mathew, Yoshinori Tsurusaki, Trent Burgess, et al.. (2015). Dual genetic diagnoses: Atypical hand‐foot‐genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1. American Journal of Medical Genetics Part A. 170(3). 717–724. 10 indexed citations
14.
Larkins, Nicholas, Mathew Wallis, Barbara McGillivray, & Cherry Mammen. (2014). A severe phenotype of Gitelman syndrome with increased prostaglandin excretion and favorable response to indomethacin. Clinical Kidney Journal. 7(3). 306–310. 15 indexed citations
15.
Starokadomskyy, Petro, Nathan Gluck, Haiying Li, et al.. (2013). CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling. Journal of Clinical Investigation. 123(5). 2244–2256. 77 indexed citations
16.
Wallis, Mathew, et al.. (2006). Guidelines from the European Society of Breast Imaging for diagnostic interventional breast procedures. European Radiology. 17(2). 581–588. 93 indexed citations
17.
Wallis, Mathew, A. Tardivon, Thomas H. Helbich, & I. Schreer. (2006). Guidelines from the European Society of Breast Imaging for diagnostic interventional breast procedures. European Radiology. 17(2). 589–589. 6 indexed citations
18.
Wallis, Mathew. (1971). Chemistry of Proteins. BMJ. 2(5759). 476.1–476. 15 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Chun Qiu Breakdown of academic impact, for papers by Natsumi Maehara Breakdown of academic impact, for papers by Janusz Jaszczyński Breakdown of academic impact, for papers by Katharina Buser Breakdown of academic impact, for papers by Yi Qu Breakdown of academic impact, for papers by Μαρία Παναγοπούλου Breakdown of academic impact, for papers by Eric Mukherjee Breakdown of academic impact, for papers by Leigh J. Hodson Breakdown of academic impact, for papers by Huan-Chang Liang Breakdown of academic impact, for papers by Ewa Zembala‐Nożyńska
Rankless by CCL
2026