N.J. Barton
Impact in
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Hemoglobinopathies and Related Disorders
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- Renal and related cancers
Papers in
- Genetics 9
- Genetic and Kidney Cyst Diseases 7
- Genetic Syndromes and Imprinting 3
- Genomic variations and chromosomal abnormalities 2
- Hemoglobinopathies and Related Disorders 1
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- Renal and related cancers 5
- Hedgehog Signaling Pathway Studies 3
- Biochemical and Molecular Research 1
- Co-authors
- Stephen T. Reeders (8 shared papers)Peter C. Harris (4 shared papers)Andrew O.M. Wilkie (3 shared papers)Janette Lamb (3 shared papers)Douglas R. Higgs (3 shared papers)Veronica J. Buckle (2 shared papers)R H Lindenbaum (2 shared papers)Gregory G. Germino (4 shared papers)
- Journals
- Genomics (3 papers)Cytogenetic and Genome Research (1 paper)The Lancet (1 paper)Contributions to nephrology (1 paper)PubMed (3 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
N.J. Barton
8 papers receiving 436 citations
Peers
Comparison fields: 5 of 53
- Genetics 303
- Genetics 53
- Molecular Biology 264
- Hepatology 27
- Pediatrics, Perinatology and Child Health 51
Countries citing papers authored by N.J. Barton
This map shows the geographic impact of N.J. Barton'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 N.J. Barton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N.J. Barton more than expected).
Fields of papers citing papers by N.J. Barton
This network shows the impact of papers produced by N.J. Barton. 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 N.J. Barton. The network helps show where N.J. Barton may publish in the future.
Co-authors
The 25 scholars most cited alongside N.J. Barton, 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 | Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3. | 1990 | 110 |
| 2 | 1989 | 71 | |
| 3 | 1992 | 65 | |
| 4 | Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16. | 1990 | 61 |
| 5 | Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1). | 1994 | 49 |
| 6 | 1995 | 48 | |
| 7 | 1990 | 43 | |
| 8 | 1990 | 5 | |
| 9 | Linkage studies of autosomal dominant polycystic kidney disease pkd1 and a genetic map of chromosome 16 based on 40 rflp markers | 1987 | 1 |
| 10 | 2015 | 0 |
About N.J. Barton
N.J. Barton is a scholar working on Genetics, Molecular Biology, Genetics, Pulmonary and Respiratory Medicine and Plant Science, having authored 10 papers that have together received 453 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (7 papers), Renal and related cancers (5 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetic Syndromes and Imprinting (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Cystic Fibrosis Research Advances (1 paper), Hemoglobinopathies and Related Disorders (1 paper) and Biochemical and Molecular Research (1 paper). The work is most often cited by research in Genetics (303 citations), Genetics (53 citations), Molecular Biology (264 citations), Hepatology (27 citations) and Pediatrics, Perinatology and Child Health (51 citations). N.J. Barton has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Stephen T. Reeders, Peter C. Harris, Andrew O.M. Wilkie, Janette Lamb, Douglas R. Higgs, Veronica J. Buckle, R H Lindenbaum, Gregory G. Germino, Debra Weinstat‐Saslow and Michael Schneider. Their work appears in journals such as Genomics, Cytogenetic and Genome Research, The Lancet, Contributions to nephrology and PubMed.
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.