Zoe Docherty
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
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- Prenatal Screening and Diagnostics 12
- Co-authors
- Caroline Mackie Ogilvie (16 shared papers)Kathy Mann (9 shared papers)Celia Donaghue (5 shared papers)Paul N. Scriven (2 shared papers)Shu C. Yau (1 shared paper)Stephen Abbs (1 shared paper)P Ramani (1 shared paper)J. Ross Hawkins (1 shared paper)
- Journals
- Journal of Medical Genetics (8 papers)Prenatal Diagnosis (4 papers)Heredity (2 papers)European Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)
- Partner nations
- United KingdomCanadaHungary
In The Last Decade
Zoe Docherty
36 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 59
- Pediatrics, Perinatology and Child Health 531
- Genetics 644
- Reproductive Medicine 57
- Molecular Biology 347
- Developmental Biology 11
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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 167 | |
| 2 | 1993 | 137 | |
| 3 | 2004 | 117 | |
| 4 | 2005 | 94 | |
| 5 | 2000 | 62 | |
| 6 | 2010 | 57 | |
| 7 | 2005 | 55 | |
| 8 | 2005 | 49 | |
| 9 | 2003 | 44 | |
| 10 | 2010 | 39 | |
| 11 | 2007 | 38 | |
| 12 | 2001 | 38 | |
| 13 | 2009 | 32 | |
| 14 | 2007 | 28 | |
| 15 | 2006 | 27 | |
| 16 | 1999 | 22 | |
| 17 | 1983 | 21 | |
| 18 | 1989 | 20 | |
| 19 | 2006 | 19 | |
| 20 | 1997 | 19 |
About Zoe Docherty
Zoe Docherty is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Cognitive Neuroscience, having authored 37 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (12 papers), Chromosomal and Genetic Variations (10 papers), Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), DNA Repair Mechanisms (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (531 citations), Genetics (644 citations), Reproductive Medicine (57 citations), Molecular Biology (347 citations) and Developmental Biology (11 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, Shu C. Yau, Stephen Abbs, P Ramani, J. Ross Hawkins, David Grant and S. Robb. Their work appears in journals such as Journal of Medical Genetics, Prenatal Diagnosis, Heredity, European Journal of Human Genetics and Clinical Genetics.
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.