D. M. Danks
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Genetics top 0.5%
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
Papers in
-
- Metabolism and Genetic Disorders 26
-
- Biochemical and Molecular Research 8
- Renal and related cancers 4
- Co-authors
- David Sillence (2 shared papers)P Kincaid-Smith (2 shared papers)David Ravine (2 shared papers)Robert N. Gibson (2 shared papers)Denise M. Kirby (3 shared papers)Richard G.H. Cotton (9 shared papers)H H Dahl (4 shared papers)C.W. Chow (2 shared papers)
- Journals
- The Lancet (12 papers)Archives of Disease in Childhood (7 papers)Journal of Inherited Metabolic Disease (5 papers)Journal of Medical Genetics (5 papers)Biochemical Journal (4 papers)
- Partner nations
- AustraliaUnited StatesGermany
In The Last Decade
D. M. Danks
69 papers receiving 4.5k citations
D. M. Danks's Hit Papers
Peers
Comparison fields: 5 of 129
- Clinical Biochemistry 967
- Genetics 2.5k
- Rheumatology 753
- Biochemistry 212
- Nutrition and Dietetics 421
Countries citing papers authored by D. M. Danks
This map shows the geographic impact of D. M. Danks'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 D. M. Danks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. M. Danks more than expected).
Fields of papers citing papers by D. M. Danks
This network shows the impact of papers produced by D. M. Danks. 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 D. M. Danks. The network helps show where D. M. Danks may publish in the future.
Co-authors
The 25 scholars most cited alongside D. M. Danks, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic heterogeneity in osteogenesis imperfecta. Hit paper breakdown → | 1979 | 1771 |
| 2 | Leigh syndrome: Clinical features and biochemical and DNA abnormalities Hit paper breakdown → | 1996 | 617 |
| 3 | 1994 | 462 | |
| 4 | MENKES' KINKY-HAIR SYNDROME Hit paper breakdown → | 1972 | 353 |
| 5 | 1992 | 146 | |
| 6 | 1976 | 139 | |
| 7 | Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity. | 1979 | 133 |
| 8 | 1978 | 87 | |
| 9 | 1988 | 83 | |
| 10 | 1976 | 69 | |
| 11 | 1966 | 57 | |
| 12 | 1981 | 48 | |
| 13 | 1962 | 44 | |
| 14 | 1979 | 44 | |
| 15 | 1994 | 40 | |
| 16 | 1976 | 35 | |
| 17 | 1984 | 34 | |
| 18 | 1973 | 34 | |
| 19 | 1974 | 33 | |
| 20 | 1966 | 33 |
About D. M. Danks
D. M. Danks is a scholar working on Clinical Biochemistry, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 72 papers that have together received 4.9k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (26 papers), Neonatal Health and Biochemistry (9 papers), Biochemical and Molecular Research (8 papers), Amino Acid Enzymes and Metabolism (7 papers), Liver Disease Diagnosis and Treatment (5 papers), Trace Elements in Health (5 papers), Pediatric Hepatobiliary Diseases and Treatments (5 papers) and Renal and related cancers (4 papers). The work is most often cited by research in Clinical Biochemistry (967 citations), Genetics (2.5k citations), Rheumatology (753 citations), Biochemistry (212 citations) and Nutrition and Dietetics (421 citations). D. M. Danks has collaborated with scholars based in Australia, United States and Germany. Frequent co-authors include David Sillence, P Kincaid-Smith, David Ravine, Robert N. Gibson, Denise M. Kirby, Richard G.H. Cotton, H H Dahl, C.W. Chow, Rozanne B. Blok and John Christodoulou. Their work appears in journals such as The Lancet, Archives of Disease in Childhood, Journal of Inherited Metabolic Disease, Journal of Medical Genetics and Biochemical Journal.
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.