David Mowat

9.9k total citations
69 papers, 2.4k citations indexed

About

David Mowat is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, David Mowat has authored 69 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 20 papers in Surgery and 20 papers in Genetics. Recurrent topics in David Mowat's work include Congenital gastrointestinal and neural anomalies (15 papers), Muscle Physiology and Disorders (11 papers) and Tuberous Sclerosis Complex Research (8 papers). David Mowat is often cited by papers focused on Congenital gastrointestinal and neural anomalies (15 papers), Muscle Physiology and Disorders (11 papers) and Tuberous Sclerosis Complex Research (8 papers). David Mowat collaborates with scholars based in Australia, United States and France. David Mowat's co-authors include Meredith Wilson, Elizabeth E. Palmer, Michel Goossens, John A. Lawson, Bronwyn Kerr, Florence Dastot‐Le Moal, Seán Kennedy, Stewart Einfeld, Nicole Chia and Michael F. Buckley and has published in prestigious journals such as PLoS ONE, Neurology and PEDIATRICS.

In The Last Decade

David Mowat

68 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Mowat Australia 27 1.3k 644 621 300 264 69 2.4k
Young Min Choi South Korea 32 1.5k 1.2× 390 0.6× 407 0.7× 286 1.0× 191 0.7× 227 4.0k
Shin Yong Moon South Korea 32 2.1k 1.7× 376 0.6× 473 0.8× 280 0.9× 172 0.7× 171 3.9k
Dusica Babovic‐Vuksanovic United States 27 863 0.7× 540 0.8× 294 0.5× 144 0.5× 138 0.5× 99 2.2k
Kwame Anyane‐Yeboa United States 26 1.3k 1.0× 1.2k 1.9× 277 0.4× 361 1.2× 127 0.5× 66 2.3k
Susan Holder United Kingdom 21 1.1k 0.9× 1.2k 1.8× 525 0.8× 265 0.9× 100 0.4× 43 2.2k
Craig B. Woda United States 17 1.4k 1.1× 329 0.5× 275 0.4× 111 0.4× 187 0.7× 21 2.4k
Jean‐Louis Blouin Switzerland 27 1.0k 0.8× 1.1k 1.7× 221 0.4× 280 0.9× 156 0.6× 75 2.4k
David Geneviève France 24 1.3k 1.1× 1.1k 1.7× 285 0.5× 202 0.7× 88 0.3× 80 2.3k
Aldo Giannotti Italy 31 1.9k 1.5× 1.0k 1.6× 512 0.8× 210 0.7× 147 0.6× 104 3.0k
Kim L. McBride United States 30 1.3k 1.1× 807 1.3× 267 0.4× 209 0.7× 266 1.0× 108 2.7k

Countries citing papers authored by David Mowat

Since Specialization
Citations

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

Fields of papers citing papers by David Mowat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Mowat

This figure shows the co-authorship network connecting the top 25 collaborators of David Mowat. A scholar is included among the top collaborators of David Mowat 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 David Mowat. David Mowat 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.
Chan, Denise, Vanessa Sarkozy, Elise Farley, et al.. (2025). Diagnosis and Management of Children With Tuberous Sclerosis Complex. Journal of Paediatrics and Child Health.
2.
Bournazos, Adam, Vanessa Sarkozy, John A. Lawson, et al.. (2024). Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex “No Mutations Identified” Cohort. Molecular Genetics & Genomic Medicine. 12(10). e70017–e70017. 1 indexed citations
3.
Kelada, Lauren, Claire E. Wakefield, David Armstrong, et al.. (2022). Genomic testing for children with interstitial and diffuse lung disease (chILD): parent satisfaction, understanding and health-related quality of life. BMJ Open Respiratory Research. 9(1). e001139–e001139. 2 indexed citations
4.
Fennell, Andrew, Samuel F. Berkovic, Carolyn Ellaway, et al.. (2022). The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome. American Journal of Medical Genetics Part A. 188(12). 3432–3447. 12 indexed citations
5.
6.
Jones, Hannah, Samantha J. Bryen, Leigh B. Waddell, et al.. (2019). Importance of muscle biopsy to establish pathogenicity of DMD missense and splice variants. Neuromuscular Disorders. 29(12). 913–919. 11 indexed citations
7.
Pinner, Jason, Cheng Yee Chan, Lucy Bowyer, et al.. (2019). Fetal diagnosis of Mowat‐Wilson syndrome by whole exome sequencing. American Journal of Medical Genetics Part A. 179(10). 2152–2157. 4 indexed citations
8.
Oei, Ju Lee, Kei Lui, Meredith Ward, et al.. (2017). Antenatal gastrointestinal anomalies in neonates subsequently found to have alveolar capillary dysplasia. Clinical Case Reports. 5(5). 559–566. 7 indexed citations
9.
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
10.
Drew, Alexander P., Manoj P. Menezes, Monique M. Ryan, et al.. (2016). Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3. PLoS Genetics. 12(7). e1006177–e1006177. 27 indexed citations
11.
Palmer, Elizabeth E. & David Mowat. (2014). Agenesis of the corpus callosum: A clinical approach to diagnosis. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(2). 184–197. 70 indexed citations
12.
Cardamone, Michael, Danny Flanagan, David Mowat, et al.. (2014). Mammalian Target of Rapamycin Inhibitors for Intractable Epilepsy and Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex. The Journal of Pediatrics. 164(5). 1195–1200. 101 indexed citations
13.
Palmer, Elizabeth E., H. J. L. Speirs, Peter J. Taylor, et al.. (2013). Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability. American Journal of Medical Genetics Part A. 164(2). 377–385. 33 indexed citations
14.
Tsurusaki, Yoshinori, Nobuhiko Okamoto, Hirofumi Ohashi, et al.. (2013). Coffin–Siris syndrome is a SWI/SNF complex disorder. Clinical Genetics. 85(6). 548–554. 103 indexed citations
15.
Monagle, Paul, David Mowat, Susan Russell, et al.. (2011). Australian Paediatric Surveillance Unit study of haemoglobinopathies in Australian children. Journal of Paediatrics and Child Health. 48(4). 356–360. 4 indexed citations
16.
Ng, Bernard, Ellie Mulyadi, J K Pereira, et al.. (2006). Familial cerebral cavernous haemangioma diagnosed in an infant with a rapidly growing cerebral lesion. Australasian Radiology. 50(6). 583–590. 13 indexed citations
17.
McGaughran, Julie, et al.. (2005). Recurrence of Mowat–Wilson syndrome in siblings with the same proven mutation. American Journal of Medical Genetics Part A. 137A(3). 302–304. 32 indexed citations
18.
Pingault, Véronique, Mathilde Girard, Nadège Bondurand, et al.. (2002). SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism. Human Genetics. 111(2). 198–206. 95 indexed citations
19.
Partington, M. W., David Mowat, Stewart Einfeld, Bruce J. Tonge, & Gillian Turner. (2000). Genes on the X chromosome are important in undiagnosed mental retardation. American Journal of Medical Genetics. 92(1). 57–61. 26 indexed citations
20.
Mowat, David, et al.. (1999). Respiratory chain complex III deficiency with pruritus: A novel vitamin responsive clinical feature. The Journal of Pediatrics. 134(3). 352–354. 18 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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