Kate Baker
Impact in
- Genetics top 5%
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Cognitive Neuroscience top 5%
- Functional Brain Connectivity Studies
- Autism Spectrum Disorder Research
Papers in
-
- Congenital heart defects research 6
- Genetics 12
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Philip L. Beales (2 shared papers)David Skuse (4 shared papers)Duncan E. Astle (12 shared papers)Torsten Baldeweg (6 shared papers)Jessica Barnes (6 shared papers)Mark W. Woolrich (4 shared papers)F. Lucy Raymond (8 shared papers)Giles L. Colclough (2 shared papers)
- Journals
- Journal of Neurodevelopmental Disorders (3 papers)Journal of Neuroscience (2 papers)Journal of Pain (2 papers)Current Opinion in Neurology (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Kate Baker
40 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 105
- Genetics 496
- Cognitive Neuroscience 266
- Equine 19
- Molecular Biology 672
- Psychiatry and Mental health 119
Countries citing papers authored by Kate Baker
This map shows the geographic impact of Kate Baker'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 Kate Baker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kate Baker more than expected).
Fields of papers citing papers by Kate Baker
This network shows the impact of papers produced by Kate Baker. 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 Kate Baker. The network helps show where Kate Baker may publish in the future.
Co-authors
The 25 scholars most cited alongside Kate Baker, 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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 254 | |
| 2 | 2005 | 140 | |
| 3 | 2005 | 113 | |
| 4 | 2015 | 104 | |
| 5 | 2015 | 72 | |
| 6 | 2001 | 64 | |
| 7 | 1983 | 64 | |
| 8 | 2012 | 50 | |
| 9 | 2014 | 46 | |
| 10 | 2010 | 43 | |
| 11 | 2020 | 39 | |
| 12 | 2011 | 32 | |
| 13 | 2020 | 32 | |
| 14 | 2016 | 29 | |
| 15 | 2015 | 28 | |
| 16 | 2023 | 24 | |
| 17 | 2015 | 24 | |
| 18 | 2020 | 24 | |
| 19 | 2010 | 23 | |
| 20 | 2019 | 22 |
About Kate Baker
Kate Baker is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Clinical Psychology and Cellular and Molecular Neuroscience, having authored 47 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (6 papers), Autism Spectrum Disorder Research (4 papers), Genomics and Rare Diseases (4 papers), Functional Brain Connectivity Studies (4 papers), Pain Management and Opioid Use (2 papers), Cellular transport and secretion (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (496 citations), Cognitive Neuroscience (266 citations), Equine (19 citations), Molecular Biology (672 citations) and Psychiatry and Mental health (119 citations). Kate Baker has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Philip L. Beales, David Skuse, Duncan E. Astle, Torsten Baldeweg, Jessica Barnes, Mark W. Woolrich, F. Lucy Raymond, Giles L. Colclough, Jacob Vorstman and Peter Scambler. Their work appears in journals such as Journal of Neurodevelopmental Disorders, Journal of Neuroscience, Journal of Pain, Current Opinion in Neurology and European Journal of Human 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.