David Coman

3.3k citations

79 papers · 1.2k indexed · h-index 20

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Physiology top 10%
- Lysosomal Storage Disorders Research
- Diet and metabolism studies

Papers in ⓘ

Clinical Biochemistry 22
- Metabolism and Genetic Disorders 22
Genetics 24
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 6

Co-authors: Joy Yaplito‐Lee (1 shared paper)Avihu Boneh (2 shared papers)Peter Lewindon (3 shared papers)Jaak Jaeken (6 shared papers)Pekka Kannus (3 shared papers)Sophie Calvert (3 shared papers)James McGill (7 shared papers)Jeremy Rajanayagam (1 shared paper)
Journals: Pediatric Nephrology (3 papers)Journal of Inherited Metabolic Disease (3 papers)Molecular Genetics and Metabolism (3 papers)Fetal Diagnosis and Therapy (2 papers)Clinical Genetics (2 papers)
Partner nations: Australia United States United Kingdom

In The Last Decade

David Coman

78 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside David Coman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David Coman Line = papers co-authored together David Coman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 79 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age–a sibling control study Clinical Genetics ·JJ McGill, AC Inwood, David Coman, ML Lipke, Danny de Lore, SJ Swiedler, JJ Hopwood	2009	134
2	New indications and controversies in arginine therapy Clinical Nutrition ·David Coman, Joy Yaplito‐Lee, Avihu Boneh	2008	71
3	IgG N-glycans as potential biomarkers for determining galactose tolerance in Classical Galactosaemia Molecular Genetics and Metabolism ·Karen P. Coss, Jennifer C. Byrne, David Coman, B Adamczyk, Jodie L. Abrahams, Radka Saldova, Andrew Brown, Olivia Walsh, Una Hendroff, C. Carolan, Pauline M. Rudd, Eileen P. Treacy	2011	52
4	Galactosemia, a Single Gene Disorder With Epigenetic Consequences Pediatric Research ·David Coman, David W. Murray, Jennifer C. Byrne, Pauline M. Rudd, Paola M Bagaglia, Peter Doran, Eileen P. Treacy	2010	52
5	Pediatric acute liver failure: Etiology, outcomes, and the role of serial pediatric end‐stage liver disease scores Pediatric Transplantation ·Jeremy Rajanayagam, David Coman, David Cartwright, Peter Lewindon	2013	50
6	The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease Genetics in Medicine ·Lisa G. Riley, Mark J. Cowley, Velimir Gayevskiy, André E. Minoche, Clare Puttick, David R. Thorburn, Rocío Rius, Alison G. Compton, Minal Menezes, Kaustuv Bhattacharya, David Coman, Carolyn Ellaway, Ian E. Alexander, Louisa Adams, Maina Kava, Jacqui Robinson, Carolyn M. Sue, Shanti Balasubramaniam, John Christodoulou	2020	45
7	Seizures, ataxia, developmental delay and the general paediatrician: Glucose transporter 1 deficiency syndrome Journal of Paediatrics and Child Health ·David Coman, KG Sinclair, CJ Burke, DB Appleton, J. T. Pelekanos, CM O’Neil, Geoff Wallace, FG Bowling, D Wang, DC De Vivo, JJ McGill	2006	38
8	The skeletal manifestations of the congenital disorders of glycosylation Clinical Genetics ·David Coman, Melita Irving, Pekka Kannus, Jaak Jaeken, Ravi Savarirayan	2008	36
9	A novel splice site mutation in EYA4 causes DFNA10 hearing loss American Journal of Medical Genetics Part A ·Michael S. Hildebrand, David Coman, Tao Yang, R. J McKinlay Gardner, Elizabeth Rose, Richard J. Smith, Melanie Bahlo, Hans‐Henrik M. Dahl	2007	34
10	Long-term follow-up of patients with idiopathic infantile hypercalcaemia Pediatric Nephrology ·Jianping Huang, David Coman, Steven McTaggart, John R. Burke	2006	31
11	Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division PubMed ·Cheryl Shoubridge, May H. Tan, Tod Fullston, Desiree Cloosterman, David Coman, George McGillivray, Grazia M.S. Mancini, Tjitske Kleefstra, Jozef Gécz	2010	31
12	Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome European Journal of Human Genetics ·Gabrielle R. Wilson, Jasmine Sunley, Katherine R. Smith, Kate Pope, Catherine Bromhead, Elizabeth Fitzpatrick, Maja Di Rocco, Maurice A. M. Van Steensel, David Coman, Richard J. Leventer, Martin B. Delatycki, David J. Amor, Melanie Bahlo, Paul J. Lockhart	2013	30
13	Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation British Journal of Dermatology ·S.E. Clements, Tanasit Techanukul, David Coman, Jemima E. Mellerio, John A. McGrath	2009	29
14	Congenital disorder of glycosylation type 1a: Three siblings with a mild neurological phenotype Journal of Clinical Neuroscience ·David Coman, James McGill, R. MacDonald, Danna K. Morris, Sandra Klingberg, Jaak Jaeken, D. Barry Appleton	2007	28
15	Trisomy 16 Mosaicism at Chorionic Villus Sampling and Amniocentesis with a Normal Physical and Intellectual Outcome Fetal Diagnosis and Therapy ·David Coman, R. J McKinlay Gardner, Mark D. Pertile, Pekka Kannus	2010	24
16	Glucose transporter 1 deficiency syndrome and hemiplegic migraines as a dominant presenting clinical feature Journal of Paediatrics and Child Health ·Shekeeb S. Mohammad, David Coman, Sophie Calvert	2014	24
17	Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis The American Journal of Human Genetics ·David Coman, Lisenka E.L.M. Vissers, Lisa G. Riley, Michael Kwint, Roxanna Hauck, Janet Koster, Sinje Geuer, Sarah Hopkins, Barbra Hallinan, Larry Sweetman, Udo F. H. Engelke, T. Burrow, John Cardinal, James McGill, Anita Inwood, Christine Gurnsey, Hans R. Waterham, John Christodoulou, Ron A. Wevers, James Pitt	2018	23
18	Impaired endoplasmic reticulum-mitochondrial signaling in ataxia-telangiectasia iScience ·Abrey J. Yeo, Kok Leong Chong, Magtouf Gatei, Dongxiu Zou, Romal Stewart, Sarah Withey, Ernst J. Wolvetang, Robert G. Parton, Adam Brown, Michael B. Kastan, David Coman, Martin F. Lavin	2020	22
19	Normal Neurodevelopmental Outcomes in PNPO Deficiency: A Case Series and Literature Review JIMD Reports ·Joshua Hatch, David Coman, Peter T. Clayton, Philippa B. Mills, Sophie Calvert, Richard Webster, Kate Riney	2015	22
20	Persistent Hyperinsulinism in Kabuki Syndrome 2: Case Report and Literature Review SHILAP Revista de lepidopterología ·Hobia Gole, Raymond Chuk, David Coman	2016	21

About David Coman

David Coman is a scholar working on Clinical Biochemistry, Genetics, Biochemistry, Pediatrics, Perinatology and Child Health and Sensory Systems, having authored 79 papers that have together received 1.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (15 papers), Glycosylation and Glycoproteins Research (9 papers), Neonatal Health and Biochemistry (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Diet and metabolism studies (6 papers) and Genomics and Rare Diseases (6 papers). The work is most often cited by research in Clinical Biochemistry (302 citations), Physiology (302 citations), Biochemistry (79 citations), Rheumatology (149 citations) and Molecular Biology (583 citations). David Coman has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Joy Yaplito‐Lee, Avihu Boneh, Peter Lewindon, Jaak Jaeken, Pekka Kannus, Sophie Calvert, James McGill, Jeremy Rajanayagam, David Cartwright and Pauline M. Rudd. Their work appears in journals such as Pediatric Nephrology, Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Fetal Diagnosis and Therapy and Clinical Genetics.

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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