J.K. Nancarrow
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 11
- Genetics and Neurodevelopmental Disorders 8
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 2
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- Genomics and Chromatin Dynamics 3
- Epigenetics and DNA Methylation 2
- CRISPR and Genetic Engineering 2
- Co-authors
- Robert I. Richards (8 shared papers)G.R. Sutherland (5 shared papers)K. Holman (4 shared papers)Elizabeth Baker (5 shared papers)Eric J. Kremer (2 shared papers)John C. Mulley (2 shared papers)Michael Lynch (1 shared paper)Stephen T. Warren (1 shared paper)
- Journals
- Genomics (6 papers)Science (2 papers)Human Molecular Genetics (1 paper)The Lancet (1 paper)PubMed (2 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
J.K. Nancarrow
13 papers receiving 1.2k citations
J.K. Nancarrow's Hit Papers
Peers
Comparison fields: 5 of 64
- Genetics 860
- Cognitive Neuroscience 335
- Molecular Biology 773
- Cellular and Molecular Neuroscience 164
- Hematology 48
Countries citing papers authored by J.K. Nancarrow
This map shows the geographic impact of J.K. Nancarrow'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.K. Nancarrow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.K. Nancarrow more than expected).
Fields of papers citing papers by J.K. Nancarrow
This network shows the impact of papers produced by J.K. Nancarrow. 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.K. Nancarrow. The network helps show where J.K. Nancarrow may publish in the future.
Co-authors
The 25 scholars most cited alongside J.K. Nancarrow, 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 | Fragile X Genotype Characterized by an Unstable Region of DNA Hit paper breakdown → | 1991 | 644 |
| 2 | 1994 | 117 | |
| 3 | Chromosomal fragile site FRA16D and DNA instability in cancer. | 2000 | 103 |
| 4 | 1994 | 88 | |
| 5 | 1992 | 44 | |
| 6 | Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12. | 1991 | 39 |
| 7 | 1992 | 36 | |
| 8 | 1991 | 35 | |
| 9 | 1995 | 33 | |
| 10 | 1994 | 28 | |
| 11 | 1994 | 17 | |
| 12 | 1991 | 13 | |
| 13 | Studies of fragile sites on human chromosome 16 / Julie Nancarrow. | 1998 | 1 |
About J.K. Nancarrow
J.K. Nancarrow is a scholar working on Genetics, Molecular Biology, Plant Science, Cognitive Neuroscience and Neurology, having authored 13 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (3 papers), Autism Spectrum Disorder Research (2 papers), Epigenetics and DNA Methylation (2 papers), Genomics and Rare Diseases (2 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Genetics (860 citations), Cognitive Neuroscience (335 citations), Molecular Biology (773 citations), Cellular and Molecular Neuroscience (164 citations) and Hematology (48 citations). J.K. Nancarrow has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Robert I. Richards, G.R. Sutherland, K. Holman, Elizabeth Baker, Eric J. Kremer, John C. Mulley, Michael Lynch, Stephen T. Warren, Melanie Pritchard and David Schlessinger. Their work appears in journals such as Genomics, Science, Human Molecular Genetics, The Lancet 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.