Helen Dolling
- Genetics
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Pulmonary and Respiratory Medicine
- Clinical Biochemistry
- Co-authors
- Alba Sanchis‐JuanOlga ShamardinaF. Lucy RaymondCourtney E. FrenchStephen AbbsSarah BowdinTopun AustinDavid H. Rowitch
- Topics
- Genomics and Rare Diseases (3 papers)Genomic variations and chromosomal abnormalities (1 paper)Genetics and Neurodevelopmental Disorders (1 paper)
- Journals
- Intensive Care MedicineEuropean Journal of Human GeneticsHuman Genetics and Genomics Advances
- Partner nations
- United KingdomPortugalUnited States
In The Last Decade
Helen Dolling
2 papers receiving 157 citations
Peers
Comparison fields: 5 of 32
- Genetics 130
- Molecular Biology 52
- Pediatrics, Perinatology and Child Health 32
- Pulmonary and Respiratory Medicine 28
- Clinical Biochemistry 26
Countries citing papers authored by Helen Dolling
This map shows the geographic impact of Helen Dolling'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 Helen Dolling with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Helen Dolling more than expected).
Fields of papers citing papers by Helen Dolling
This network shows the impact of papers produced by Helen Dolling. 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 Helen Dolling. The network helps show where Helen Dolling may publish in the future.
Co-authorship network of co-authors of Helen Dolling
This figure shows the co-authorship network connecting the top 25 collaborators of Helen Dolling. A scholar is included among the top collaborators of Helen Dolling based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Helen Dolling. Helen Dolling is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 10 | |
| 3 | 149 |
About Helen Dolling
Helen Dolling is a scholar working on Clinical Biochemistry, Genetics and Pediatrics, Perinatology and Child Health, having authored 3 papers that have together received 159 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (130 citations), Clinical Biochemistry (26 citations) and Pediatrics, Perinatology and Child Health (32 citations). Helen Dolling has collaborated with scholars based in United Kingdom, Portugal and United States. Frequent co-authors include Alba Sanchis‐Juan, Olga Shamardina, F. Lucy Raymond, Courtney E. French, Stephen Abbs, Sarah Bowdin, Topun Austin, David H. Rowitch, Ricardo Garcia Branco and Helen V. Firth. Their work appears in journals such as Intensive Care Medicine, European Journal of Human Genetics and Human Genetics and Genomics Advances.
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.