K. Holman
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
-
- DNA Repair Mechanisms 3
- Genomics and Chromatin Dynamics 2
- RNA modifications and cancer 2
- Genetics 10
- Genetics and Neurodevelopmental Disorders 8
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Robert I. Richards (15 shared papers)G.R. Sutherland (11 shared papers)Eric J. Kremer (4 shared papers)Shuancang Yu (3 shared papers)Michael Lynch (3 shared papers)Melanie Pritchard (3 shared papers)Elizabeth Baker (3 shared papers)Stephen T. Warren (2 shared papers)
- Journals
- Genomics (3 papers)Nucleic Acids Research (3 papers)Science (3 papers)Human Molecular Genetics (3 papers)Biological Psychiatry (1 paper)
- Partner nations
- AustraliaUnited StatesFrance
In The Last Decade
K. Holman
17 papers receiving 2.0k citations
K. Holman's Hit Papers
Peers
Comparison fields: 5 of 73
- Genetics 1.5k
- Cognitive Neuroscience 567
- Cellular and Molecular Neuroscience 403
- Molecular Biology 1.4k
- Neurology 74
Countries citing papers authored by K. Holman
This map shows the geographic impact of K. Holman'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 K. Holman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Holman more than expected).
Fields of papers citing papers by K. Holman
This network shows the impact of papers produced by K. Holman. 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 K. Holman. The network helps show where K. Holman may publish in the future.
Co-authors
The 25 scholars most cited alongside K. Holman, 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 | Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n Hit paper breakdown → | 1991 | 738 |
| 2 | Fragile X Genotype Characterized by an Unstable Region of DNA Hit paper breakdown → | 1991 | 641 |
| 3 | 1991 | 120 | |
| 4 | 1994 | 118 | |
| 5 | 1997 | 112 | |
| 6 | 1993 | 104 | |
| 7 | 1992 | 83 | |
| 8 | 1991 | 45 | |
| 9 | Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers. | 1991 | 38 |
| 10 | 1995 | 34 | |
| 11 | Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies. | 1993 | 25 |
| 12 | 1991 | 13 | |
| 13 | 1991 | 8 | |
| 14 | 1994 | 4 | |
| 15 | 1991 | 3 | |
| 16 | 1994 | 1 | |
| 17 | 1996 | 1 |
About K. Holman
K. Holman is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Plant Science and Pediatrics, Perinatology and Child Health, having authored 17 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Autism Spectrum Disorder Research (4 papers), DNA Repair Mechanisms (3 papers), Chromosomal and Genetic Variations (2 papers), Genomics and Chromatin Dynamics (2 papers), RNA modifications and cancer (2 papers) and Alzheimer's disease research and treatments (1 paper). The work is most often cited by research in Genetics (1.5k citations), Cognitive Neuroscience (567 citations), Cellular and Molecular Neuroscience (403 citations), Molecular Biology (1.4k citations) and Neurology (74 citations). K. Holman has collaborated with scholars based in Australia, United States and France. Frequent co-authors include Robert I. Richards, G.R. Sutherland, Eric J. Kremer, Shuancang Yu, Michael Lynch, Melanie Pritchard, Elizabeth Baker, Stephen T. Warren, David Schlessinger and John C. Mulley. Their work appears in journals such as Genomics, Nucleic Acids Research, Science, Human Molecular Genetics and Biological Psychiatry.
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.