J. David Brook
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Virus-based gene therapy research
Papers in
-
- Mitochondrial Function and Pathology 20
- Congenital heart defects research 19
- Ubiquitin and proteasome pathways 8
-
- Genetic Neurodegenerative Diseases 39
- Co-authors
- David E. Housman (6 shared papers)I D Young (3 shared papers)Duncan J. Shaw (27 shared papers)Jamie W. Foster (3 shared papers)Silvana Guioli (3 shared papers)M. Dominguez-Steglich (3 shared papers)Cheni Kwok (2 shared papers)Sahar Mansour (2 shared papers)
- Journals
- Human Genetics (13 papers)Genomics (13 papers)Nucleic Acids Research (6 papers)Human Molecular Genetics (6 papers)Journal of Medical Genetics (5 papers)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
J. David Brook
99 papers receiving 7.1k citations
J. David Brook's Hit Papers
Peers
Comparison fields: 5 of 124
- Cellular and Molecular Neuroscience 2.0k
- Genetics 2.6k
- Molecular Biology 5.3k
- Neurology 616
- Reproductive Medicine 324
Countries citing papers authored by J. David Brook
This map shows the geographic impact of J. 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 J. 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 J. David Brook more than expected).
Fields of papers citing papers by J. David Brook
This network shows the impact of papers produced by J. 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 J. David Brook. The network helps show where J. David Brook may publish in the future.
Co-authors
The 25 scholars most cited alongside J. 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 102 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene Hit paper breakdown → | 1994 | 1241 |
| 2 | Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family Hit paper breakdown → | 1997 | 666 |
| 3 | Targeted integration of adeno‐associated virus (AAV) into human chromosome 19. Hit paper breakdown → | 1991 | 602 |
| 4 | Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy Hit paper breakdown → | 1992 | 589 |
| 5 | 1991 | 339 | |
| 6 | Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. | 1993 | 303 |
| 7 | 2005 | 195 | |
| 8 | 2005 | 161 | |
| 9 | Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal. | 1995 | 158 |
| 10 | 1992 | 143 | |
| 11 | 2007 | 115 | |
| 12 | 2010 | 114 | |
| 13 | 1984 | 114 | |
| 14 | 1997 | 111 | |
| 15 | 2009 | 101 | |
| 16 | 2018 | 94 | |
| 17 | 1985 | 90 | |
| 18 | Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. | 1991 | 80 |
| 19 | 2007 | 75 | |
| 20 | 2011 | 71 |
About J. David Brook
J. David Brook is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Cardiology and Cardiovascular Medicine, having authored 102 papers that have together received 7.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (39 papers), Mitochondrial Function and Pathology (20 papers), Congenital heart defects research (19 papers), Cardiomyopathy and Myosin Studies (11 papers), Chromosomal and Genetic Variations (9 papers), Ubiquitin and proteasome pathways (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Parkinson's Disease Mechanisms and Treatments (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.0k citations), Genetics (2.6k citations), Molecular Biology (5.3k citations), Neurology (616 citations) and Reproductive Medicine (324 citations). J. David Brook has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include David E. Housman, I D Young, Duncan J. Shaw, Jamie W. Foster, Silvana Guioli, M. Dominguez-Steglich, Cheni Kwok, Sahar Mansour, Alan Buckler and William Reardon. Their work appears in journals such as Human Genetics, Genomics, Nucleic Acids Research, Human Molecular Genetics and Journal of Medical 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.