Daniel N. Murphy
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
- Neurogenetic and Muscular Disorders Research
Papers in ⓘ
-
- Metabolism and Genetic Disorders 1
- Genetics 4
- Genomics and Rare Diseases 4
- Co-authors
- Deborah M. Lambert (3 shared papers)Stéphanie Nguengang Wakap (1 shared paper)Charlotte Rodwell (1 shared paper)Yann Le Cam (1 shared paper)Annie Olry (1 shared paper)Ana Rath (1 shared paper)Valérie Serrière-Lanneau (1 shared paper)Aoife McLysaght (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)Journal of Autism and Developmental Disorders (1 paper)eLife (1 paper)Orphanet Journal of Rare Diseases (1 paper)PLoS ONE (1 paper)
- Partner nations
- IrelandUnited KingdomFrance
In The Last Decade
Daniel N. Murphy
8 papers receiving 1.1k citations
Hit Papers
Peers
Comparison fields: 5 of 119
- Genetics 573
- Aging 13
- Molecular Biology 496
- Genetics 73
- Cancer Research 94
Countries citing papers authored by Daniel N. Murphy
This map shows the geographic impact of Daniel N. Murphy'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 Daniel N. Murphy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel N. Murphy more than expected).
Fields of papers citing papers by Daniel N. Murphy
This network shows the impact of papers produced by Daniel N. Murphy. 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 Daniel N. Murphy. The network helps show where Daniel N. Murphy may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel N. Murphy, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database Hit paper breakdown → | 2019 | 833 |
| 2 | 2017 | 220 | |
| 3 | 2012 | 39 | |
| 4 | 2020 | 18 | |
| 5 | 2022 | 11 | |
| 6 | 2022 | 6 | |
| 7 | 2022 | 6 | |
| 8 | 2019 | 6 |
About Daniel N. Murphy
Daniel N. Murphy is a scholar working on Clinical Biochemistry, Genetics, Economics and Econometrics, Cancer Research and Rheumatology, having authored 8 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Health Systems, Economic Evaluations, Quality of Life (2 papers), RNA Research and Splicing (2 papers), Metabolism and Genetic Disorders (1 paper), MicroRNA in disease regulation (1 paper), Cystic Fibrosis Research Advances (1 paper), Neonatal Health and Biochemistry (1 paper) and RNA and protein synthesis mechanisms (1 paper). The work is most often cited by research in Genetics (573 citations), Aging (13 citations), Molecular Biology (496 citations), Genetics (73 citations) and Cancer Research (94 citations). Daniel N. Murphy has collaborated with scholars based in Ireland, United Kingdom and France. Frequent co-authors include Deborah M. Lambert, Stéphanie Nguengang Wakap, Charlotte Rodwell, Yann Le Cam, Annie Olry, Ana Rath, Valérie Serrière-Lanneau, Aoife McLysaght, Elisabeth M. Busch‐Nentwich and Christopher M. Dooley. Their work appears in journals such as European Journal of Human Genetics, Journal of Autism and Developmental Disorders, eLife, Orphanet Journal of Rare Diseases and PLoS ONE.
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.