John David Brook
Impact in
- Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Genetic Neurodegenerative Diseases 41
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- Congenital heart defects research 34
- Mitochondrial Function and Pathology 22
- Ubiquitin and proteasome pathways 8
- Co-authors
- David E. Housman (6 shared papers)Ian D. Young (3 shared papers)Duncan J. Shaw (28 shared papers)Marina A. Dominguez-Steglich (3 shared papers)Silvana Guioli (3 shared papers)Jamie W. Foster (3 shared papers)Sahar Mansour (2 shared papers)Cheni Kwok (2 shared papers)
- Journals
- Human Genetics (13 papers)Genomics (13 papers)Human Molecular Genetics (9 papers)Nucleic Acids Research (7 papers)Nature Genetics (6 papers)
- Partner nations
- United KingdomUnited StatesBelgium
In The Last Decade
John David Brook
121 papers receiving 11.1k citations
John David Brook's Hit Papers
Peers
Comparison fields: 5 of 137
- Cellular and Molecular Neuroscience 4.0k
- Genetics 3.5k
- Molecular Biology 8.4k
- Neurology 1.2k
- Cardiology and Cardiovascular Medicine 1.0k
Countries citing papers authored by John David Brook
This map shows the geographic impact of John David Brook'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 John David Brook with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John David Brook more than expected).
Fields of papers citing papers by John David Brook
This network shows the impact of papers produced by John David Brook. 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 John David Brook. The network helps show where John David Brook may publish in the future.
Co-authors
The 25 scholars most cited alongside John David Brook, 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 126 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member Hit paper breakdown → | 1992 | 2371 |
| 2 | Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene Hit paper breakdown → | 1994 | 1350 |
| 3 | Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family Hit paper breakdown → | 1997 | 735 |
| 4 | Targeted integration of adeno‐associated virus (AAV) into human chromosome 19. Hit paper breakdown → | 1991 | 644 |
| 5 | 1992 | 634 | |
| 6 | 1991 | 348 | |
| 7 | 2016 | 336 | |
| 8 | Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. | 1993 | 328 |
| 9 | 2012 | 254 | |
| 10 | 2005 | 231 | |
| 11 | 2005 | 182 | |
| 12 | Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal. | 1995 | 172 |
| 13 | 1992 | 168 | |
| 14 | 2014 | 150 | |
| 15 | 2019 | 144 | |
| 16 | 2010 | 128 | |
| 17 | 1984 | 127 | |
| 18 | 2007 | 127 | |
| 19 | 2013 | 126 | |
| 20 | 1997 | 116 |
About John David Brook
John David Brook is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Neurology and Epidemiology, having authored 126 papers that have together received 11.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (41 papers), Congenital heart defects research (34 papers), Mitochondrial Function and Pathology (22 papers), Congenital Heart Disease Studies (17 papers), Genomic variations and chromosomal abnormalities (12 papers), Cardiomyopathy and Myosin Studies (11 papers), Chromosomal and Genetic Variations (9 papers) and Ubiquitin and proteasome pathways (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (4.0k citations), Genetics (3.5k citations), Molecular Biology (8.4k citations), Neurology (1.2k citations) and Cardiology and Cardiovascular Medicine (1.0k citations). John David Brook has collaborated with scholars based in United Kingdom, United States and Belgium. Frequent co-authors include David E. Housman, Ian D. Young, Duncan J. Shaw, Marina A. Dominguez-Steglich, Silvana Guioli, Jamie W. Foster, Sahar Mansour, Cheni Kwok, William Reardon and Shelley A. Rundle. Their work appears in journals such as Human Genetics, Genomics, Human Molecular Genetics, Nucleic Acids Research 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.