Louise E Docherty
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Diabetes and associated disorders
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 6
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 1
-
- Epigenetics and DNA Methylation 4
- Co-authors
- I. Karen Temple (8 shared papers)Deborah Mackay (8 shared papers)Rebecca Poole (6 shared papers)Anna Lehmann (3 shared papers)Sian Ellard (1 shared paper)Sarah E. Flanagan (1 shared paper)Steven Ndugwa Kabwama (1 shared paper)Andrew T. Hattersley (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Diabetologia (2 papers)Clinical Epigenetics (1 paper)Journal of Medical Genetics (1 paper)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Louise E Docherty
8 papers receiving 416 citations
Peers
Comparison fields: 5 of 33
- Genetics 343
- Pediatrics, Perinatology and Child Health 178
- Molecular Biology 242
- Endocrinology, Diabetes and Metabolism 52
- Surgery 106
Countries citing papers authored by Louise E Docherty
This map shows the geographic impact of Louise E Docherty'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 Louise E Docherty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Louise E Docherty more than expected).
Fields of papers citing papers by Louise E Docherty
This network shows the impact of papers produced by Louise E Docherty. 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 Louise E Docherty. The network helps show where Louise E Docherty may publish in the future.
Co-authors
The 25 scholars most cited alongside Louise E Docherty, 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 | 2013 | 120 | |
| 2 | 2010 | 78 | |
| 3 | 2014 | 60 | |
| 4 | 2013 | 59 | |
| 5 | 2011 | 55 | |
| 6 | 2011 | 32 | |
| 7 | 2010 | 28 | |
| 8 | 2015 | 13 |
About Louise E Docherty
Louise E Docherty is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Infectious Diseases, having authored 8 papers that have together received 445 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (4 papers), Prenatal Screening and Diagnostics (3 papers), Pancreatic function and diabetes (2 papers) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Genetics (343 citations), Pediatrics, Perinatology and Child Health (178 citations), Molecular Biology (242 citations), Endocrinology, Diabetes and Metabolism (52 citations) and Surgery (106 citations). Louise E Docherty has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include I. Karen Temple, Deborah Mackay, Rebecca Poole, Anna Lehmann, Sian Ellard, Sarah E. Flanagan, Steven Ndugwa Kabwama, Andrew T. Hattersley, Claire Turner and L. Harrison. Their work appears in journals such as European Journal of Human Genetics, Diabetologia, Clinical Epigenetics, Journal of Medical Genetics and American Journal of Medical Genetics Part A.
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.