K. Holman
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 7
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research 4
- Molecular Biology top 5%
- DNA Repair Mechanisms 3
- RNA modifications and cancer 2
- Ubiquitin and proteasome pathways 2
- RNA Research and Splicing 2
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- Chromosomal and Genetic Variations 2
- Co-authors
- Robert I. RichardsG.R. SutherlandEric J. KremerMelanie PritchardShuancang YuMichael LynchElizabeth BakerDavid Schlessinger
- Partner nations
- AustraliaUnited StatesJapan
In The Last Decade
K. Holman
19 papers receiving 2.1k citations
Hit Papers
Peers
Comparison fields: 5 of 75
- Genetics 1.6k
- Cognitive Neuroscience 616
- Cellular and Molecular Neuroscience 414
- Molecular Biology 1.5k
- Neurology 78
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-authorship network
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 | 1997 | 112 | |
| 2 | 1996 | 1 | |
| 3 | 1995 | 33 | |
| 4 | 1994 | 1 | |
| 5 | 1994 | 31 | |
| 6 | 1994 | 117 | |
| 7 | 1994 | 4 | |
| 8 | 1993 | 104 | |
| 9 | Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies. | 1993 | 25 |
| 10 | 1992 | 21 | |
| 11 | 1992 | 82 | |
| 12 | 1991 | 3 | |
| 13 | 1991 | 45 | |
| 14 | 1991 | 13 | |
| 15 | 1991 | 8 | |
| 16 | 1991 | 120 | |
| 17 | Fragile X Genotype Characterized by an Unstable Region of DNAbreakdown → | 1991 | 644 |
| 18 | Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) nbreakdown → | 1991 | 738 |
| 19 | Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers. | 1991 | 38 |
About K. Holman
K. Holman is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology, having authored 19 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Autism Spectrum Disorder Research (4 papers), DNA Repair Mechanisms (3 papers), RNA modifications and cancer (2 papers), Ubiquitin and proteasome pathways (2 papers), Chromosomal and Genetic Variations (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Genetics (1.6k citations), Cognitive Neuroscience (616 citations) and Cellular and Molecular Neuroscience (414 citations). K. Holman has collaborated with scholars based in Australia, United States and Japan. Frequent co-authors include Robert I. Richards, G.R. Sutherland, Eric J. Kremer, Melanie Pritchard, Shuancang Yu, Michael Lynch, Elizabeth Baker, David Schlessinger, John C. Mulley and Stephen T. Warren. Their work appears in journals such as Human Molecular Genetics, Science, Nucleic Acids Research, Genomics 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.