David Coman

3.4k citations
80 papers · 1.2k · h-index 20

Impact in

Papers in

    • Mitochondrial Function and Pathology 14
    • Glycosylation and Glycoproteins Research 9
    • Genomic variations and chromosomal abnormalities 6
    • Genetics and Neurodevelopmental Disorders 5

David Coman

78 papers receiving 1.2k citations

Peers

David Coman
Comparison fields: 5 of 90
  • Clinical Biochemistry 270
  • Physiology 275
  • Biochemistry 69
  • Molecular Biology 521
  • Rheumatology 104
Replace Adel Shalata with:
Adel Shalata Israel
Amel Karaa United States
Elżbieta Ciara Poland
Filippo Pinto e Vairo Brazil
Ewa Pronicka Poland
Ali Dursun Türkiye
Annette Feigenbaum Canada
Carolina Fischinger Moura de Souza Brazil
Chantal Tallaksen Norway
Brendan C. Lanpher United States
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Citations per field
00.5×2.8×
Adel Shalata · 1×
Citations per year

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

20 of 20 papers shown

Showing the 20 most-cited of 80 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2009134
2 200872
3 201152
4 201052
5 201350
6 202046
7 200638
8 200836
9 200734
10 201032
11 200631
12 200930
13 201330
14 200728
15 201424
16 201024
17 202023
18 201823
19 201522
20 201621

About David Coman

David Coman is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Physiology and Pediatrics, Perinatology and Child Health, having authored 80 papers that have together received 1.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (20 papers), Mitochondrial Function and Pathology (14 papers), Glycosylation and Glycoproteins Research (9 papers), Neonatal Health and Biochemistry (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Galectins and Cancer Biology (5 papers), Lysosomal Storage Disorders Research (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Clinical Biochemistry (270 citations), Physiology (275 citations), Biochemistry (69 citations), Molecular Biology (521 citations) and Rheumatology (104 citations). David Coman has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Avihu Boneh, Joy Yaplito‐Lee, Peter Lewindon, Jaak Jaeken, Pekka Kannus, Jeremy Rajanayagam, David Cartwright, Sophie Calvert, James McGill and Pauline M. Rudd. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Pediatric Nephrology, Clinical Genetics and European Journal of Human 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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