HR Slater
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Plant Science top 10%
- Chromosomal and Genetic Variations
Papers in
- Genetics 8
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 1
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- RNA regulation and disease 2
- Epigenetics and DNA Methylation 1
- Co-authors
- Vida Petrovic (2 shared papers)Lucille Voullaire (1 shared paper)K. H. Andy Choo (1 shared paper)Danuta Z. Loesch (4 shared papers)Richard Huggins (1 shared paper)Trent Burgess (2 shared papers)Alison Venn (1 shared paper)Andrew Evans (1 shared paper)
In The Last Decade
HR Slater
8 papers receiving 394 citations
Peers
Comparison fields: 5 of 36
- Genetics 243
- Plant Science 206
- Cell Biology 69
- Molecular Biology 252
- Cognitive Neuroscience 70
Countries citing papers authored by HR Slater
This map shows the geographic impact of HR Slater'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 HR Slater with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites HR Slater more than expected).
Fields of papers citing papers by HR Slater
This network shows the impact of papers produced by HR Slater. 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 HR Slater. The network helps show where HR Slater may publish in the future.
Co-authors
The 25 scholars most cited alongside HR Slater, 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 | A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere? | 1993 | 233 |
| 2 | 2009 | 55 | |
| 3 | 2013 | 29 | |
| 4 | Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring. | 1995 | 24 |
| 5 | 1988 | 18 | |
| 6 | 2004 | 16 | |
| 7 | 2012 | 14 | |
| 8 | 2016 | 12 |
About HR Slater
HR Slater is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 8 papers that have together received 401 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Autism Spectrum Disorder Research (4 papers), RNA regulation and disease (2 papers), Epigenetics and DNA Methylation (1 paper), Prenatal Screening and Diagnostics (1 paper), Genomics and Rare Diseases (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Genetics (243 citations), Plant Science (206 citations), Cell Biology (69 citations), Molecular Biology (252 citations) and Cognitive Neuroscience (70 citations). HR Slater has collaborated with scholars based in Australia, Iran and Canada. Frequent co-authors include Vida Petrovic, Lucille Voullaire, K. H. Andy Choo, Danuta Z. Loesch, Richard Huggins, Trent Burgess, Alison Venn, Andrew Evans, Wendyl D’Souza and Justin P. Rubio. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, BJOG An International Journal of Obstetrics & Gynaecology, Translational Psychiatry 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.