Bryan Lynch
Impact in
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
Papers in
-
- Ion channel regulation and function 5
- RNA modifications and cancer 3
- Genetics 11
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 8
- Neurogenetic and Muscular Disorders Research 3
- Co-authors
- Mary D. King (12 shared papers)Sally Ann Lynch (10 shared papers)Amre Shahwan (9 shared papers)Judith Conroy (5 shared papers)Nicholas M. Allen (6 shared papers)Sean Ennis (5 shared papers)Tiago R. Magalhães (1 shared paper)Sérgio D.J. Pena (1 shared paper)
- Journals
- Developmental Medicine & Child Neurology (4 papers)Epilepsia (3 papers)European Journal of Paediatric Neurology (2 papers)Neuromuscular Disorders (2 papers)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- IrelandUnited KingdomUnited States
In The Last Decade
Bryan Lynch
28 papers receiving 649 citations
Peers
Comparison fields: 5 of 61
- Psychiatry and Mental health 170
- Clinical Biochemistry 57
- Immunology and Allergy 49
- Genetics 217
- Cellular and Molecular Neuroscience 141
Countries citing papers authored by Bryan Lynch
This map shows the geographic impact of Bryan Lynch'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 Bryan Lynch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bryan Lynch more than expected).
Fields of papers citing papers by Bryan Lynch
This network shows the impact of papers produced by Bryan Lynch. 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 Bryan Lynch. The network helps show where Bryan Lynch may publish in the future.
Co-authors
The 25 scholars most cited alongside Bryan Lynch, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 133 | |
| 2 | 2015 | 123 | |
| 3 | 2014 | 60 | |
| 4 | 2012 | 54 | |
| 5 | 2010 | 39 | |
| 6 | 2013 | 34 | |
| 7 | 2014 | 30 | |
| 8 | 2015 | 26 | |
| 9 | 2017 | 23 | |
| 10 | 2016 | 15 | |
| 11 | 1994 | 15 | |
| 12 | 2020 | 15 | |
| 13 | 2015 | 13 | |
| 14 | 2021 | 12 | |
| 15 | 2017 | 11 | |
| 16 | 2014 | 11 | |
| 17 | 2017 | 8 | |
| 18 | 2022 | 8 | |
| 19 | 2016 | 7 | |
| 20 | 2019 | 5 |
About Bryan Lynch
Bryan Lynch is a scholar working on Molecular Biology, Genetics, Psychiatry and Mental health, Genetics and Cellular and Molecular Neuroscience, having authored 32 papers that have together received 659 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (8 papers), Epilepsy research and treatment (5 papers), Ion channel regulation and function (5 papers), Metabolism and Genetic Disorders (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), RNA modifications and cancer (3 papers) and Sleep and Wakefulness Research (3 papers). The work is most often cited by research in Psychiatry and Mental health (170 citations), Clinical Biochemistry (57 citations), Immunology and Allergy (49 citations), Genetics (217 citations) and Cellular and Molecular Neuroscience (141 citations). Bryan Lynch has collaborated with scholars based in Ireland, United Kingdom and United States. Frequent co-authors include Mary D. King, Sally Ann Lynch, Amre Shahwan, Judith Conroy, Nicholas M. Allen, Sean Ennis, Tiago R. Magalhães, Sérgio D.J. Pena, Dara McCreary and Heinz Jungbluth. Their work appears in journals such as Developmental Medicine & Child Neurology, Epilepsia, European Journal of Paediatric Neurology, Neuromuscular Disorders and Journal of Inherited Metabolic Disease.
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.