David Coman

3.3k total citations
79 papers, 1.2k citations indexed

About

David Coman is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, David Coman has authored 79 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 24 papers in Genetics and 22 papers in Clinical Biochemistry. Recurrent topics in David Coman's work include Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (15 papers) and Glycosylation and Glycoproteins Research (9 papers). David Coman is often cited by papers focused on Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (15 papers) and Glycosylation and Glycoproteins Research (9 papers). David Coman collaborates with scholars based in Australia, United States and United Kingdom. David Coman's co-authors include Avihu Boneh, Joy Yaplito‐Lee, Peter Lewindon, Jaak Jaeken, Pekka Kannus, Jeremy Rajanayagam, David Cartwright, James McGill, Sophie Calvert and Eileen P. Treacy and has published in prestigious journals such as SHILAP Revista de lepidopterología, Molecular and Cellular Biology and The American Journal of Human Genetics.

In The Last Decade

David Coman

78 papers receiving 1.2k 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 Coman Australia 20 583 302 302 227 149 79 1.2k
Diana Ballhausen Switzerland 19 546 0.9× 356 1.2× 347 1.1× 167 0.7× 158 1.1× 46 1.1k
Ali Dursun Türkiye 17 434 0.7× 438 1.5× 215 0.7× 145 0.6× 165 1.1× 97 995
Callum Wilson New Zealand 21 956 1.6× 495 1.6× 293 1.0× 241 1.1× 174 1.2× 58 1.6k
Tomáš Honzík Czechia 23 1.1k 1.8× 524 1.7× 233 0.8× 225 1.0× 217 1.5× 102 1.6k
György Fekete Hungary 18 530 0.9× 184 0.6× 196 0.6× 322 1.4× 93 0.6× 94 1.3k
Christine Barnérias France 20 704 1.2× 236 0.8× 113 0.4× 283 1.2× 146 1.0× 73 1.4k
Carolina Fischinger Moura de Souza Brazil 19 507 0.9× 362 1.2× 427 1.4× 183 0.8× 279 1.9× 110 1.2k
Ayşegül Tokatlı Türkiye 17 610 1.0× 575 1.9× 249 0.8× 116 0.5× 184 1.2× 101 1.3k
Judit García‐Villoria Spain 24 673 1.2× 511 1.7× 189 0.6× 135 0.6× 218 1.5× 73 1.3k
Chantal Tallaksen Norway 29 604 1.0× 207 0.7× 175 0.6× 151 0.7× 140 0.9× 77 2.3k

Countries citing papers authored by David Coman

Since Specialization
Citations

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

Fields of papers citing papers by David Coman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Coman

This figure shows the co-authorship network connecting the top 25 collaborators of David Coman. A scholar is included among the top collaborators of David Coman 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 Coman. David Coman 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.
Coman, David, Michèl A.A.P. Willemsen, Margherita Doria, et al.. (2025). Biomarkers in Ataxia-Telangiectasia: a Systematic Review. Journal of Neurology. 272(2). 110–110. 2 indexed citations
2.
Anderson, Erin M., James Harraway, Anna Stewart, et al.. (2022). WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review. Pediatric Nephrology. 37(10). 2369–2374. 3 indexed citations
3.
Riley, Lisa G., Mark J. Cowley, Velimir Gayevskiy, et al.. (2020). The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease. Genetics in Medicine. 22(7). 1254–1261. 45 indexed citations
4.
Yeo, Abrey J., Kok Leong Chong, Magtouf Gatei, et al.. (2020). Impaired endoplasmic reticulum-mitochondrial signaling in ataxia-telangiectasia. iScience. 24(1). 101972–101972. 22 indexed citations
5.
Moravej, Hossein, Ruqaiah Altassan, Jaak Jaeken, et al.. (2019). Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients. JIMD Reports. 51(1). 76–81. 10 indexed citations
6.
Munoz, Marcia A., Julie Jurczyluk, Anna Simon, et al.. (2019). Defective Protein Prenylation in a Spectrum of Patients With Mevalonate Kinase Deficiency. Frontiers in Immunology. 10. 1900–1900. 16 indexed citations
7.
Cardinal, John, et al.. (2018). SYNE1-related Autosomal Recessive Cerebellar Ataxia, Congenital Cerebellar Hypoplasia, and Cognitive Impairment. SHILAP Revista de lepidopterología. 8(3). 1071–1071. 9 indexed citations
8.
Coman, David, Lisenka E.L.M. Vissers, Lisa G. Riley, et al.. (2018). Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis. The American Journal of Human Genetics. 103(1). 125–130. 23 indexed citations
9.
Coman, David, Peter Lewindon, Peter T. Clayton, & Kate Riney. (2015). PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?. JIMD Reports. 25. 71–75. 17 indexed citations
10.
Arvier, John, et al.. (2015). Septic Arthritis of the Temporomandibular Joint in an Infant. SHILAP Revista de lepidopterología. 5(2). 736–736. 7 indexed citations
11.
Lewis, Fiona M., et al.. (2012). Differential Phonological Awareness Skills in Children with Classic Galactosemia: A Descriptive Study of Four Cases. JIMD Reports. 10. 45–52. 5 indexed citations
12.
13.
Coss, Karen P., Jennifer C. Byrne, David Coman, et al.. (2011). IgG N-glycans as potential biomarkers for determining galactose tolerance in Classical Galactosaemia. Molecular Genetics and Metabolism. 105(2). 212–220. 52 indexed citations
14.
Malhotra, Anil K., et al.. (2009). Prenatal Cardiac Ultrasound Finding in Congenital Disorder of Glycosylation Type 1a. Fetal Diagnosis and Therapy. 25(1). 54–57. 17 indexed citations
15.
Coman, David, et al.. (2009). Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age–a sibling control study. Clinical Genetics. 77(5). 492–498. 134 indexed citations
16.
Hildebrand, Michael S., et al.. (2008). A novel splice site mutation in EYA4 causes DFNA10 hearing loss (vol 143, pg 1599, 2007). American Journal of Medical Genetics Part A. 2 indexed citations
17.
Coman, David, Amber Boys, Duncan B. Sparrow, et al.. (2008). Spondylocostal dysostosis in a pregnancy complicated by confined placental mosaicism for tetrasomy 9p. American Journal of Medical Genetics Part A. 146A(15). 1972–1976. 3 indexed citations
18.
Coman, David, James McGill, R. MacDonald, et al.. (2007). Congenital disorder of glycosylation type 1a: Three siblings with a mild neurological phenotype. Journal of Clinical Neuroscience. 14(7). 668–672. 28 indexed citations
19.
Coman, David, et al.. (2006). Carbamyl phosphate synthase deficiency: Diagnosed during pregnancy in a 41-year-old. Journal of Clinical Neuroscience. 13(6). 702–706. 18 indexed citations
20.
Coman, David, Jianping Huang, Steven McTaggart, et al.. (2005). Renal transplantation in a 14-year-old girl with vitamin B12-responsive cblA-type methylmalonic acidaemia. Pediatric Nephrology. 21(2). 270–273. 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 Diana Ballhausen Breakdown of academic impact, for papers by Ali Dursun Breakdown of academic impact, for papers by Callum Wilson Breakdown of academic impact, for papers by Tomáš Honzík Breakdown of academic impact, for papers by György Fekete Breakdown of academic impact, for papers by Christine Barnérias Breakdown of academic impact, for papers by Carolina Fischinger Moura de Souza Breakdown of academic impact, for papers by Ayşegül Tokatlı Breakdown of academic impact, for papers by Judit García‐Villoria Breakdown of academic impact, for papers by Chantal Tallaksen
Rankless by CCL
2026