David Fitzpatrick
Impact in
- Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Ocular Disorders and Treatments
- Cleft Lip and Palate Research
- Immunology top 0.5%
- Immune Cell Function and Interaction
- T-cell and B-cell Immunology
Papers in
-
- Genomics and Chromatin Dynamics 15
- Genetics 106
- Genomic variations and chromosomal abnormalities 33
- Genomics and Rare Diseases 25
- Ocular Disorders and Treatments 21
- Genetics and Neurodevelopmental Disorders 19
- Congenital Ear and Nasal Anomalies 18
- Cleft Lip and Palate Research 15
- Co-authors
- Anne Kelso (12 shared papers)Helen V. Firth (15 shared papers)Christopher Wilson (5 shared papers)Caroline F. Wright (11 shared papers)Kathleen A. Williamson (15 shared papers)Veronica van Heyningen (15 shared papers)Helle Bielefeldt‐Ohmann (17 shared papers)Karen W. Makar (3 shared papers)
- Journals
- The American Journal of Human Genetics (16 papers)Journal of Medical Genetics (11 papers)European Journal of Human Genetics (9 papers)Human Molecular Genetics (7 papers)Nature Genetics (6 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
David Fitzpatrick
270 papers receiving 14.6k citations
David Fitzpatrick's Hit Papers
Peers
Comparison fields: 5 of 183
- Genetics 5.3k
- Immunology 2.6k
- Molecular Biology 6.6k
- Genetics 811
- Cancer Research 837
Countries citing papers authored by David Fitzpatrick
This map shows the geographic impact of David Fitzpatrick'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 Fitzpatrick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Fitzpatrick more than expected).
Fields of papers citing papers by David Fitzpatrick
This network shows the impact of papers produced by David Fitzpatrick. 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 Fitzpatrick. The network helps show where David Fitzpatrick may publish in the future.
Co-authors
The 25 scholars most cited alongside David Fitzpatrick, 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 278 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A Critical Role for Dnmt1 and DNA Methylation in T Cell Development, Function, and Survival Hit paper breakdown → | 2001 | 1037 |
| 2 | 2004 | 469 | |
| 3 | 2003 | 427 | |
| 4 | 2003 | 375 | |
| 5 | Paediatric genomics: diagnosing rare disease in children Hit paper breakdown → | 2018 | 362 |
| 6 | 2001 | 303 | |
| 7 | 2007 | 274 | |
| 8 | 2008 | 259 | |
| 9 | 2007 | 255 | |
| 10 | 2005 | 252 | |
| 11 | 1990 | 238 | |
| 12 | 2003 | 235 | |
| 13 | 1996 | 222 | |
| 14 | 2005 | 208 | |
| 15 | 2002 | 206 | |
| 16 | 2018 | 202 | |
| 17 | 2007 | 201 | |
| 18 | 2018 | 199 | |
| 19 | 2005 | 190 | |
| 20 | 2013 | 184 |
About David Fitzpatrick
David Fitzpatrick is a scholar working on Molecular Biology, Genetics, Immunology, Genetics and Surgery, having authored 278 papers that have together received 15.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Genomics and Rare Diseases (25 papers), Ocular Disorders and Treatments (21 papers), Genetics and Neurodevelopmental Disorders (19 papers), Congenital Ear and Nasal Anomalies (18 papers), Cleft Lip and Palate Research (15 papers), Genomics and Chromatin Dynamics (15 papers) and Immune Cell Function and Interaction (15 papers). The work is most often cited by research in Genetics (5.3k citations), Immunology (2.6k citations), Molecular Biology (6.6k citations), Genetics (811 citations) and Cancer Research (837 citations). David Fitzpatrick has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Anne Kelso, Helen V. Firth, Christopher Wilson, Caroline F. Wright, Kathleen A. Williamson, Veronica van Heyningen, Helle Bielefeldt‐Ohmann, Karen W. Makar, Lorne A. Babiuk and William M. Weaver. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, European Journal of Human Genetics, Human Molecular Genetics and Nature 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.