Judith Conroy
Impact in
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment
- Attention Deficit Hyperactivity Disorder
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
-
- RNA and protein synthesis mechanisms 3
- Mitochondrial Function and Pathology 3
- Genetics 15
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Sean Ennis (18 shared papers)Sally Ann Lynch (12 shared papers)Mary D. King (10 shared papers)Ricardo Segurado (4 shared papers)Michael Gill (6 shared papers)Michael Fitzgerald (4 shared papers)Nicholas M. Allen (7 shared papers)Bryan Lynch (5 shared papers)
- Journals
- American Journal of Medical Genetics Part B Neuropsychiatric Genetics (3 papers)Epilepsia (3 papers)GeroScience (2 papers)European Journal of Human Genetics (2 papers)Nature Genetics (1 paper)
- Partner nations
- IrelandUnited StatesItaly
In The Last Decade
Judith Conroy
31 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 91
- Psychiatry and Mental health 251
- Genetics 404
- Transplantation 31
- Cellular and Molecular Neuroscience 160
- Clinical Biochemistry 59
Countries citing papers authored by Judith Conroy
This map shows the geographic impact of Judith Conroy'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 Judith Conroy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judith Conroy more than expected).
Fields of papers citing papers by Judith Conroy
This network shows the impact of papers produced by Judith Conroy. 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 Judith Conroy. The network helps show where Judith Conroy may publish in the future.
Co-authors
The 25 scholars most cited alongside Judith Conroy, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 123 | |
| 2 | 2014 | 115 | |
| 3 | 2005 | 75 | |
| 4 | 2012 | 68 | |
| 5 | 2011 | 64 | |
| 6 | 2005 | 63 | |
| 7 | 2005 | 61 | |
| 8 | 2014 | 60 | |
| 9 | 2004 | 58 | |
| 10 | 2013 | 56 | |
| 11 | 2014 | 41 | |
| 12 | 2021 | 38 | |
| 13 | 2013 | 37 | |
| 14 | 2021 | 34 | |
| 15 | 2015 | 27 | |
| 16 | 2009 | 17 | |
| 17 | 2016 | 15 | |
| 18 | 2013 | 14 | |
| 19 | 2015 | 13 | |
| 20 | 2014 | 12 |
About Judith Conroy
Judith Conroy is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Epidemiology and Psychiatry and Mental health, having authored 31 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Microscopic Colitis (3 papers), RNA and protein synthesis mechanisms (3 papers), Mitochondrial Function and Pathology (3 papers) and Nutrition and Health in Aging (3 papers). The work is most often cited by research in Psychiatry and Mental health (251 citations), Genetics (404 citations), Transplantation (31 citations), Cellular and Molecular Neuroscience (160 citations) and Clinical Biochemistry (59 citations). Judith Conroy has collaborated with scholars based in Ireland, United States and Italy. Frequent co-authors include Sean Ennis, Sally Ann Lynch, Mary D. King, Ricardo Segurado, Michael Gill, Michael Fitzgerald, Nicholas M. Allen, Bryan Lynch, Amre Shahwan and Louise Gallagher. Their work appears in journals such as American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Epilepsia, GeroScience, European Journal of Human Genetics and Nature 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.