Ros Hastings
- Genetics top 2%
- Genomics and Rare Diseases 13
- Genomic variations and chromosomal abnormalities 9
- BRCA gene mutations in cancer 6
- Hematology top 5%
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- Prenatal Screening and Diagnostics 10
- Fetal and Pediatric Neurological Disorders 5
- Cancer Research top 10%
- Cancer Genomics and Diagnostics 9
- Genetics top 10%
- Genomics and Rare Diseases 13
- Genomic variations and chromosomal abnormalities 9
- BRCA gene mutations in cancer 6
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- Ethics in Clinical Research 3
- Acute Lymphoblastic Leukemia research 3
- Co-authors
- Lisa G. ShafferA. SimonsMartina C. CornelWybo DondorpCarla van ElHeidi HowardFlorence FellmannAnne Cambon‐Thomsen
- Partner nations
- United KingdomNetherlandsUnited States
In The Last Decade
Ros Hastings
28 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 90
- Genetics 906
- Hematology 221
- Pediatrics, Perinatology and Child Health 363
- Cancer Research 270
- Genetics 151
Countries citing papers authored by Ros Hastings
This map shows the geographic impact of Ros Hastings'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 Ros Hastings with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ros Hastings more than expected).
Fields of papers citing papers by Ros Hastings
This network shows the impact of papers produced by Ros Hastings. 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 Ros Hastings. The network helps show where Ros Hastings may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Ros Hastings, 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 | 2025 | 2 | |
| 2 | 2024 | 7 | |
| 3 | 2023 | 13 | |
| 4 | 2021 | 98 | |
| 5 | 2020 | 35 | |
| 6 | 2020 | 82 | |
| 7 | 2019 | 85 | |
| 8 | 2018 | 92 | |
| 9 | 2015 | 56 | |
| 10 | 2013 | 256 | |
| 11 | 2013 | 70 | |
| 12 | 2013 | 180 | |
| 13 | Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. | 2013 | 270 |
| 14 | 2012 | 28 | |
| 15 | 2012 | 83 | |
| 16 | 2012 | 53 | |
| 17 | 2010 | 8 | |
| 18 | 2010 | 11 | |
| 19 | 2007 | 33 | |
| 20 | ECA Permanent working group for cytogenetics and society: Cytogenetic guidelines and quality assurance. A common framework for quality assessment for constitutional and acquired cytogenetic investigations | 2006 | 5 |
About Ros Hastings
Ros Hastings is a scholar working on Genetics, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 28 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Prenatal Screening and Diagnostics (10 papers), Cancer Genomics and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (9 papers), BRCA gene mutations in cancer (6 papers), Fetal and Pediatric Neurological Disorders (5 papers), Ethics in Clinical Research (3 papers) and Acute Lymphoblastic Leukemia research (3 papers). The work is most often cited by research in Genetics (906 citations), Hematology (221 citations) and Pediatrics, Perinatology and Child Health (363 citations). Ros Hastings has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Lisa G. Shaffer, A. Simons, Martina C. Cornel, Wybo Dondorp, Carla van El, Heidi Howard, Florence Fellmann, Anne Cambon‐Thomsen, Pascal Borry and Hans Scheffer.
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.