Mark A. Pook
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Molecular Biology top 5%
- Mitochondrial Function and Pathology
- Epigenetics and DNA Methylation
- Ion Transport and Channel Regulation
- DNA Repair Mechanisms
Papers in
-
- Genetic Neurodegenerative Diseases 53
- Hereditary Neurological Disorders 3
- Genetics 11
- Genetic Associations and Epidemiology 5
- Genetic Mapping and Diversity in Plants and Animals 4
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Sahar Al‐Mahdawi (30 shared papers)Chiranjeevi Sandi (15 shared papers)Ricardo Mouro Pinto (7 shared papers)Rajesh V. Thakker (7 shared papers)Dhaval Varshney (3 shared papers)Sara Anjomani Virmouni (9 shared papers)Carol Wooding (4 shared papers)Sanjay I. Bidichandani (6 shared papers)
- Journals
- PLoS ONE (9 papers)Human Molecular Genetics (8 papers)Genomics (4 papers)Human Genetics (3 papers)Annals of Neurology (3 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Mark A. Pook
68 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 90
- Cellular and Molecular Neuroscience 1.8k
- Molecular Biology 1.1k
- Neurology 121
- Nephrology 132
- Genetics 265
Countries citing papers authored by Mark A. Pook
This map shows the geographic impact of Mark A. Pook'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 Mark A. Pook with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark A. Pook more than expected).
Fields of papers citing papers by Mark A. Pook
This network shows the impact of papers produced by Mark A. Pook. 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 Mark A. Pook. The network helps show where Mark A. Pook may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark A. Pook, 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 69 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 224 | |
| 2 | 2006 | 200 | |
| 3 | 2008 | 198 | |
| 4 | 2013 | 145 | |
| 5 | 1993 | 131 | |
| 6 | 2016 | 110 | |
| 7 | 2011 | 100 | |
| 8 | 2007 | 99 | |
| 9 | 2014 | 89 | |
| 10 | 1993 | 87 | |
| 11 | 2004 | 84 | |
| 12 | 1993 | 83 | |
| 13 | 2013 | 76 | |
| 14 | 1996 | 74 | |
| 15 | 2014 | 72 | |
| 16 | 2007 | 71 | |
| 17 | 2013 | 67 | |
| 18 | 1996 | 65 | |
| 19 | 2015 | 64 | |
| 20 | 2001 | 63 |
About Mark A. Pook
Mark A. Pook is a scholar working on Cellular and Molecular Neuroscience, Genetics, Molecular Biology, Physiology and Immunology, having authored 69 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (53 papers), Epigenetics and DNA Methylation (5 papers), Genetic Associations and Epidemiology (5 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers), Mitochondrial Function and Pathology (4 papers), Hereditary Neurological Disorders (3 papers), Lysosomal Storage Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.8k citations), Molecular Biology (1.1k citations), Neurology (121 citations), Nephrology (132 citations) and Genetics (265 citations). Mark A. Pook has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Sahar Al‐Mahdawi, Chiranjeevi Sandi, Ricardo Mouro Pinto, Rajesh V. Thakker, Dhaval Varshney, Sara Anjomani Virmouni, Carol Wooding, Sanjay I. Bidichandani, Irene De Biase and Vahid Ezzatizadeh. Their work appears in journals such as PLoS ONE, Human Molecular Genetics, Genomics, Human Genetics and Annals of Neurology.
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.