PJ Morrison
Impact in
-
- Genetic Neurodegenerative Diseases
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- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
Papers in
- Genetics 3
- Neurogenetic and Muscular Disorders Research 1
- BRCA gene mutations in cancer 1
- Genetic Syndromes and Imprinting 1
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- Epigenetics and DNA Methylation 1
- Co-authors
- Vivienne McConnell (2 shared papers)Theodore M. Brown (1 shared paper)W Henry Smithson (1 shared paper)Ellen Campbell (1 shared paper)John Craig (1 shared paper)Linda M. Parsons (1 shared paper)N Delanty (1 shared paper)Rebecca Bromley (1 shared paper)
- Journals
- Clinical Genetics (2 papers)Seizure (1 paper)The Lancet (1 paper)Clinical Dysmorphology (2 papers)
- Partner nations
- United KingdomIreland
In The Last Decade
PJ Morrison
6 papers receiving 125 citations
Peers
Comparison fields: 5 of 30
- Cellular and Molecular Neuroscience 64
- Neurology 28
- Pediatrics, Perinatology and Child Health 26
- Psychiatry and Mental health 12
- Genetics 23
Countries citing papers authored by PJ Morrison
This map shows the geographic impact of PJ Morrison'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 PJ Morrison with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites PJ Morrison more than expected).
Fields of papers citing papers by PJ Morrison
This network shows the impact of papers produced by PJ Morrison. 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 PJ Morrison. The network helps show where PJ Morrison may publish in the future.
Co-authors
The 16 scholars most cited alongside PJ Morrison, 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 | 2010 | 81 | |
| 2 | 2021 | 18 | |
| 3 | 1998 | 11 | |
| 4 | 1998 | 9 | |
| 5 | 2003 | 8 | |
| 6 | 2004 | 1 |
About PJ Morrison
PJ Morrison is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Genetics, having authored 6 papers that have together received 128 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (2 papers), Amyotrophic Lateral Sclerosis Research (1 paper), Pharmacological Effects and Toxicity Studies (1 paper), Epigenetics and DNA Methylation (1 paper), Fibromyalgia and Chronic Fatigue Syndrome Research (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), BRCA gene mutations in cancer (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (64 citations), Neurology (28 citations), Pediatrics, Perinatology and Child Health (26 citations), Psychiatry and Mental health (12 citations) and Genetics (23 citations). PJ Morrison has collaborated with scholars based in United Kingdom and Ireland. Frequent co-authors include Vivienne McConnell, Theodore M. Brown, W Henry Smithson, Ellen Campbell, John Craig, Linda M. Parsons, N Delanty, Rebecca Bromley, B. Irwin and Jim Morrow. Their work appears in journals such as Clinical Genetics, Seizure, The Lancet and Clinical Dysmorphology.
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.