Zoe Docherty
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
-
- DNA Repair Mechanisms 4
- Co-authors
- Caroline Mackie Ogilvie (16 shared papers)Kathy Mann (9 shared papers)Celia Donaghue (5 shared papers)Paul N. Scriven (2 shared papers)Stephen Abbs (1 shared paper)Shu C. Yau (1 shared paper)P Ramani (1 shared paper)Chris Bennett (1 shared paper)
- Journals
- Journal of Medical Genetics (8 papers)Prenatal Diagnosis (4 papers)European Journal of Human Genetics (2 papers)Heredity (2 papers)Molecular Cytogenetics (2 papers)
- Partner nations
- United KingdomCanadaHungary
In The Last Decade
Zoe Docherty
36 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 65
- Genetics 787
- Pediatrics, Perinatology and Child Health 540
- Reproductive Medicine 51
- Developmental Biology 12
- Molecular Biology 378
Countries citing papers authored by Zoe Docherty
This map shows the geographic impact of Zoe 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 Zoe Docherty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zoe Docherty more than expected).
Fields of papers citing papers by Zoe Docherty
This network shows the impact of papers produced by Zoe 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 Zoe Docherty. The network helps show where Zoe Docherty may publish in the future.
Co-authors
The 25 scholars most cited alongside Zoe 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
Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 160 | |
| 2 | 1993 | 124 | |
| 3 | 2004 | 112 | |
| 4 | 2005 | 76 | |
| 5 | 2010 | 57 | |
| 6 | 2000 | 57 | |
| 7 | 2005 | 52 | |
| 8 | 2005 | 45 | |
| 9 | 2010 | 38 | |
| 10 | 2001 | 37 | |
| 11 | 2007 | 37 | |
| 12 | 2009 | 32 | |
| 13 | 2003 | 28 | |
| 14 | 2007 | 27 | |
| 15 | 1983 | 21 | |
| 16 | 1989 | 20 | |
| 17 | 2006 | 19 | |
| 18 | 1997 | 19 | |
| 19 | 2000 | 17 | |
| 20 | 1999 | 17 |
About Zoe Docherty
Zoe Docherty is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Cognitive Neuroscience, having authored 36 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (13 papers), Chromosomal and Genetic Variations (12 papers), Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), DNA Repair Mechanisms (4 papers) and Fetal and Pediatric Neurological Disorders (3 papers). The work is most often cited by research in Genetics (787 citations), Pediatrics, Perinatology and Child Health (540 citations), Reproductive Medicine (51 citations), Developmental Biology (12 citations) and Molecular Biology (378 citations). Zoe Docherty has collaborated with scholars based in United Kingdom, Canada and Hungary. Frequent co-authors include Caroline Mackie Ogilvie, Kathy Mann, Celia Donaghue, Paul N. Scriven, Stephen Abbs, Shu C. Yau, P Ramani, Chris Bennett, S. Robb and J. Ross Hawkins. Their work appears in journals such as Journal of Medical Genetics, Prenatal Diagnosis, European Journal of Human Genetics, Heredity and Molecular Cytogenetics.
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.