Laura Whitton
Impact in
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- Phonetics and Phonology Research
Papers in
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- Congenital heart defects research 2
- Epigenetics and DNA Methylation 2
- Genomics and Chromatin Dynamics 2
- Ubiquitin and proteasome pathways 1
- Genetics 6
- Genetics and Neurodevelopmental Disorders 5
- Genetic Associations and Epidemiology 3
- Co-authors
- Derek W. Morris (10 shared papers)Gary Donohoe (9 shared papers)Jason Brenier (2 shared papers)Georg Dechant (3 shared papers)Ani Nenkova (2 shared papers)David Beaver (2 shared papers)Dan Jurafsky (2 shared papers)Stephen Rea (2 shared papers)
- Journals
- American Journal of Medical Genetics Part B Neuropsychiatric Genetics (3 papers)PLoS Genetics (2 papers)Human Molecular Genetics (2 papers)Genes Brain & Behavior (1 paper)European Neuropsychopharmacology (1 paper)
- Partner nations
- IrelandUnited StatesUnited Kingdom
In The Last Decade
Laura Whitton
14 papers receiving 248 citations
Peers
Comparison fields: 5 of 59
- Biological Psychiatry 19
- Experimental and Cognitive Psychology 34
- Virology 11
- Genetics 64
- Neurology 18
Countries citing papers authored by Laura Whitton
This map shows the geographic impact of Laura Whitton'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 Laura Whitton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura Whitton more than expected).
Fields of papers citing papers by Laura Whitton
This network shows the impact of papers produced by Laura Whitton. 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 Laura Whitton. The network helps show where Laura Whitton may publish in the future.
Co-authors
The 25 scholars most cited alongside Laura Whitton, 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 | 2016 | 41 | |
| 2 | 1984 | 40 | |
| 3 | To Memorize or to Predict: Prominence labeling in Conversational Speech | 2007 | 38 |
| 4 | 2018 | 31 | |
| 5 | 2020 | 22 | |
| 6 | 2020 | 19 | |
| 7 | 2019 | 12 | |
| 8 | 2019 | 10 | |
| 9 | 2006 | 10 | |
| 10 | 2023 | 9 | |
| 11 | 2019 | 9 | |
| 12 | 2020 | 8 | |
| 13 | 2018 | 8 | |
| 14 | 2019 | 1 |
About Laura Whitton
Laura Whitton is a scholar working on Molecular Biology, Genetics, Artificial Intelligence, Immunology and Virology, having authored 14 papers that have together received 258 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genetic Associations and Epidemiology (3 papers), Congenital heart defects research (2 papers), Speech and dialogue systems (2 papers), Epigenetics and DNA Methylation (2 papers), Complement system in diseases (2 papers), Genomics and Chromatin Dynamics (2 papers) and Ubiquitin and proteasome pathways (1 paper). The work is most often cited by research in Biological Psychiatry (19 citations), Experimental and Cognitive Psychology (34 citations), Virology (11 citations), Genetics (64 citations) and Neurology (18 citations). Laura Whitton has collaborated with scholars based in Ireland, United States and United Kingdom. Frequent co-authors include Derek W. Morris, Gary Donohoe, Jason Brenier, Georg Dechant, Ani Nenkova, David Beaver, Dan Jurafsky, Stephen Rea, Galina Apostolova and Denise Harold. Their work appears in journals such as American Journal of Medical Genetics Part B Neuropsychiatric Genetics, PLoS Genetics, Human Molecular Genetics, Genes Brain & Behavior and European Neuropsychopharmacology.
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.