Daniel Ward
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Genetic and phenotypic traits in livestock
- Genetic Mapping and Diversity in Plants and Animals
- Hematology top 10%
- Acute Myeloid Leukemia Research
Papers in
- Genetics 7
- Myeloproliferative Neoplasms: Diagnosis and Treatment 3
- Genetic and phenotypic traits in livestock 2
- Genetic Mapping and Diversity in Plants and Animals 2
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Sarah Ennis (5 shared papers)Anna Murray (1 shared paper)Amy V. Jones (3 shared papers)Andrew Chase (3 shared papers)Nicholas C.P. Cross (4 shared papers)C. Mattocks (5 shared papers)Joannah Score (2 shared papers)Frank Stegelmann (2 shared papers)
- Journals
- Scientific Reports (3 papers)Blood (2 papers)Clinical Chemistry (1 paper)European Journal of Human Genetics (1 paper)Molecular Ecology (1 paper)
- Partner nations
- United KingdomGermanyGreece
In The Last Decade
Daniel Ward
14 papers receiving 549 citations
Peers
Comparison fields: 5 of 60
- Genetics 279
- Hematology 108
- Genetics 100
- Immunology 97
- Cognitive Neuroscience 75
Countries citing papers authored by Daniel Ward
This map shows the geographic impact of Daniel Ward'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 Ward with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Ward more than expected).
Fields of papers citing papers by Daniel Ward
This network shows the impact of papers produced by Daniel Ward. 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 Ward. The network helps show where Daniel Ward may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel Ward, 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 | 2005 | 130 | |
| 2 | 2011 | 125 | |
| 3 | 2003 | 58 | |
| 4 | 2017 | 46 | |
| 5 | 2014 | 46 | |
| 6 | 2017 | 45 | |
| 7 | 2004 | 44 | |
| 8 | 2021 | 16 | |
| 9 | 2017 | 15 | |
| 10 | 2010 | 10 | |
| 11 | 2020 | 9 | |
| 12 | 2005 | 9 | |
| 13 | 2019 | 7 | |
| 14 | 2011 | 4 |
About Daniel Ward
Daniel Ward is a scholar working on Molecular Biology, Genetics, Genetics, Hematology and Immunology, having authored 14 papers that have together received 564 indexed citations. Recurring topics across this work include Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers), Acute Myeloid Leukemia Research (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers), Genetic and phenotypic traits in livestock (2 papers), T-cell and B-cell Immunology (2 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genomics and Rare Diseases (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (279 citations), Hematology (108 citations), Genetics (100 citations), Immunology (97 citations) and Cognitive Neuroscience (75 citations). Daniel Ward has collaborated with scholars based in United Kingdom, Germany and Greece. Frequent co-authors include Sarah Ennis, Anna Murray, Amy V. Jones, Andrew Chase, Nicholas C.P. Cross, C. Mattocks, Joannah Score, Frank Stegelmann, Katerina Zoi and Nils Winkelmann. Their work appears in journals such as Scientific Reports, Blood, Clinical Chemistry, European Journal of Human Genetics and Molecular Ecology.
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.