H.M. Kozman
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Muscle Physiology and Disorders
- Ubiquitin and proteasome pathways
- RNA modifications and cancer
Papers in
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- Genomics and Chromatin Dynamics 3
- RNA regulation and disease 3
- Ubiquitin and proteasome pathways 2
- Genetics 13
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Co-authors
- John C. Mulley (10 shared papers)Robert I. Richards (7 shared papers)G.R. Sutherland (8 shared papers)K. Holman (3 shared papers)David F. Callen (8 shared papers)Ági K. Gedeon (6 shared papers)Michael Lynch (2 shared papers)Melanie Pritchard (1 shared paper)
- Journals
- Genomics (8 papers)Human Molecular Genetics (1 paper)The American Journal of Human Genetics (1 paper)Nucleic Acids Research (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
H.M. Kozman
21 papers receiving 701 citations
Peers
Comparison fields: 5 of 58
- Genetics 350
- Molecular Biology 468
- Cardiology and Cardiovascular Medicine 112
- Genetics 52
- Cell Biology 77
Countries citing papers authored by H.M. Kozman
This map shows the geographic impact of H.M. Kozman'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 H.M. Kozman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.M. Kozman more than expected).
Fields of papers citing papers by H.M. Kozman
This network shows the impact of papers produced by H.M. Kozman. 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 H.M. Kozman. The network helps show where H.M. Kozman may publish in the future.
Co-authors
The 25 scholars most cited alongside H.M. Kozman, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1991 | 122 | |
| 2 | Autosomal dominant distal myopathy: linkage to chromosome 14. | 1995 | 104 |
| 3 | 1989 | 54 | |
| 4 | Refined genetic localization for central core disease. | 1993 | 46 |
| 5 | 1991 | 45 | |
| 6 | 1993 | 44 | |
| 7 | Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers. | 1991 | 38 |
| 8 | 1992 | 31 | |
| 9 | 1994 | 29 | |
| 10 | 1994 | 29 | |
| 11 | 1995 | 29 | |
| 12 | 1994 | 28 | |
| 13 | 1994 | 26 | |
| 14 | 1991 | 25 | |
| 15 | 1994 | 23 | |
| 16 | 1994 | 16 | |
| 17 | 1996 | 13 | |
| 18 | 1992 | 10 | |
| 19 | 1989 | 4 | |
| 20 | 1991 | 3 |
About H.M. Kozman
H.M. Kozman is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Cognitive Neuroscience and Epidemiology, having authored 23 papers that have together received 720 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Chromatin Dynamics (3 papers), RNA regulation and disease (3 papers), Trypanosoma species research and implications (2 papers), Ubiquitin and proteasome pathways (2 papers), Skin and Cellular Biology Research (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (350 citations), Molecular Biology (468 citations), Cardiology and Cardiovascular Medicine (112 citations), Genetics (52 citations) and Cell Biology (77 citations). H.M. Kozman has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include John C. Mulley, Robert I. Richards, G.R. Sutherland, K. Holman, David F. Callen, Ági K. Gedeon, Michael Lynch, Melanie Pritchard, Shuancang Yu and Andrew Thompson. Their work appears in journals such as Genomics, Human Molecular Genetics, The American Journal of Human Genetics, Nucleic Acids Research 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.