David Millar
Impact in
- Hematology top 1%
- Blood Coagulation and Thrombosis Mechanisms
- Hemophilia Treatment and Research
- Molecular Biology top 2%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics
Papers in
-
- Neonatal Respiratory Health Research 18
- Respiratory Support and Mechanisms 6
- Hematology 21
- Blood Coagulation and Thrombosis Mechanisms 13
- Hemophilia Treatment and Research 12
- Platelet Disorders and Treatments 5
- Co-authors
- Peter L. Molloy (1 shared paper)Christina M. Collis (1 shared paper)Cheryl Paul (1 shared paper)G. W. GRIGG (1 shared paper)Marianne Frommer (1 shared paper)Fujiko Watt (1 shared paper)D.N. Cooper (24 shared papers)Haresh Kirpalani (15 shared papers)
- Journals
- Human Genetics (11 papers)Cochrane Database of Systematic Reviews (5 papers)Thrombosis and Haemostasis (4 papers)Nucleic Acids Research (3 papers)Human Mutation (2 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
David Millar
58 papers receiving 4.8k citations
David Millar's Hit Papers
Peers
Comparison fields: 5 of 133
- Hematology 787
- Molecular Biology 2.9k
- Genetics 897
- Internal Medicine 101
- Cancer Research 315
Countries citing papers authored by David Millar
This map shows the geographic impact of David Millar'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 Millar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Millar more than expected).
Fields of papers citing papers by David Millar
This network shows the impact of papers produced by David Millar. 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 Millar. The network helps show where David Millar may publish in the future.
Co-authors
The 25 scholars most cited alongside David Millar, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Hit paper breakdown → | 1992 | 2461 |
| 2 | The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting Hit paper breakdown → | 2020 | 435 |
| 3 | 1997 | 308 | |
| 4 | 1997 | 193 | |
| 5 | 2013 | 169 | |
| 6 | 1994 | 120 | |
| 7 | 1997 | 115 | |
| 8 | 2000 | 106 | |
| 9 | 2003 | 88 | |
| 10 | 1998 | 62 | |
| 11 | 1997 | 50 | |
| 12 | 1994 | 44 | |
| 13 | 2008 | 44 | |
| 14 | 2010 | 42 | |
| 15 | 2006 | 38 | |
| 16 | 2014 | 36 | |
| 17 | 1990 | 34 | |
| 18 | 1985 | 33 | |
| 19 | 1985 | 32 | |
| 20 | 1985 | 31 |
About David Millar
David Millar is a scholar working on Pulmonary and Respiratory Medicine, Hematology, Molecular Biology, Genetics and Surgery, having authored 60 papers that have together received 4.9k indexed citations. Recurring topics across this work include Neonatal Respiratory Health Research (18 papers), Blood Coagulation and Thrombosis Mechanisms (13 papers), Hemophilia Treatment and Research (12 papers), Cancer-related gene regulation (7 papers), Respiratory Support and Mechanisms (6 papers), Platelet Disorders and Treatments (5 papers), Growth Hormone and Insulin-like Growth Factors (5 papers) and Congenital Diaphragmatic Hernia Studies (5 papers). The work is most often cited by research in Hematology (787 citations), Molecular Biology (2.9k citations), Genetics (897 citations), Internal Medicine (101 citations) and Cancer Research (315 citations). David Millar has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Peter L. Molloy, Christina M. Collis, Cheryl Paul, G. W. GRIGG, Marianne Frommer, Fujiko Watt, D.N. Cooper, Haresh Kirpalani, Clare Stirzaker and Susan J. Clark. Their work appears in journals such as Human Genetics, Cochrane Database of Systematic Reviews, Thrombosis and Haemostasis, Nucleic Acids Research and Human Mutation.
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.