H.M. Kozman
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
-
- Muscle Physiology and Disorders
- Ubiquitin and proteasome pathways
- RNA modifications and cancer
Papers in
-
- Genomics and Chromatin Dynamics 3
- RNA regulation and disease 3
- 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)Michael Lynch (2 shared papers)Ági K. Gedeon (6 shared papers)Andrew Thompson (5 shared papers)
- Journals
- Genomics (8 papers)Cytogenetic and Genome Research (2 papers)The American Journal of Human Genetics (1 paper)Science (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
H.M. Kozman
23 papers receiving 695 citations
Peers
Comparison fields: 5 of 63
- Genetics 356
- Molecular Biology 483
- Cardiology and Cardiovascular Medicine 112
- Genetics 51
- 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 | 120 | |
| 2 | Autosomal dominant distal myopathy: linkage to chromosome 14. | 1995 | 96 |
| 3 | 1989 | 54 | |
| 4 | 1991 | 45 | |
| 5 | 1993 | 43 | |
| 6 | Refined genetic localization for central core disease. | 1993 | 38 |
| 7 | Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers. | 1991 | 38 |
| 8 | 1992 | 31 | |
| 9 | 1995 | 30 | |
| 10 | 1994 | 29 | |
| 11 | 1994 | 28 | |
| 12 | 1994 | 27 | |
| 13 | 1994 | 26 | |
| 14 | 1991 | 23 | |
| 15 | 1994 | 18 | |
| 16 | 1994 | 13 | |
| 17 | 1993 | 12 | |
| 18 | 1996 | 12 | |
| 19 | 1992 | 10 | |
| 20 | 1993 | 5 |
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 706 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), Skin and Cellular Biology Research (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Autism Spectrum Disorder Research (2 papers) and Lysosomal Storage Disorders Research (2 papers). The work is most often cited by research in Genetics (356 citations), Molecular Biology (483 citations), Cardiology and Cardiovascular Medicine (112 citations), Genetics (51 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, Michael Lynch, Ági K. Gedeon, Andrew Thompson, Eric J. Kremer and Shuancang Yu. Their work appears in journals such as Genomics, Cytogenetic and Genome Research, The American Journal of Human Genetics, Science and Human Molecular 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.