A.E. Retief
Impact in
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Reproductive Medicine top 5%
- Sperm and Testicular Function
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genetics and Neurodevelopmental Disorders 4
-
- Genomics and Chromatin Dynamics 7
- Co-authors
- W.A. Van Niekerk (4 shared papers)Maritha J. Kotze (17 shared papers)E. Langenhoven (10 shared papers)Louise Warnich (15 shared papers)L. du Plessis (7 shared papers)E. Dietzsch (8 shared papers)H. F. H. Weich (3 shared papers)E. Retief (2 shared papers)
- Journals
- Nucleic Acids Research (10 papers)Human Genetics (8 papers)Journal of Medical Genetics (5 papers)Genomics (3 papers)Prenatal Diagnosis (1 paper)
- Partner nations
- South AfricaUnited StatesFrance
In The Last Decade
A.E. Retief
45 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 86
- Genetics 544
- Reproductive Medicine 118
- Cancer Research 144
- Surgery 355
- Molecular Biology 569
Countries citing papers authored by A.E. Retief
This map shows the geographic impact of A.E. Retief'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 A.E. Retief with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.E. Retief more than expected).
Fields of papers citing papers by A.E. Retief
This network shows the impact of papers produced by A.E. Retief. 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 A.E. Retief. The network helps show where A.E. Retief may publish in the future.
Co-authors
The 25 scholars most cited alongside A.E. Retief, 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 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1981 | 153 | |
| 2 | 1993 | 106 | |
| 3 | 1979 | 96 | |
| 4 | 1984 | 84 | |
| 5 | 1991 | 76 | |
| 6 | 2001 | 56 | |
| 7 | 1990 | 54 | |
| 8 | 1985 | 53 | |
| 9 | 1987 | 52 | |
| 10 | A DNA polymorphism in the human low-density lipoprotein receptor gene. | 1986 | 50 |
| 11 | The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia. | 1989 | 42 |
| 12 | 1989 | 36 | |
| 13 | 1993 | 31 | |
| 14 | 1984 | 28 | |
| 15 | 1992 | 28 | |
| 16 | 1977 | 28 | |
| 17 | 1989 | 26 | |
| 18 | 1987 | 23 | |
| 19 | 1986 | 20 | |
| 20 | Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor gene. | 1989 | 18 |
About A.E. Retief
A.E. Retief is a scholar working on Genetics, Molecular Biology, Surgery, Cancer Research and Plant Science, having authored 48 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Lipoproteins and Cardiovascular Health (9 papers), Genomics and Chromatin Dynamics (7 papers), Chromosomal and Genetic Variations (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Prenatal Screening and Diagnostics (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Cancer, Lipids, and Metabolism (4 papers). The work is most often cited by research in Genetics (544 citations), Reproductive Medicine (118 citations), Cancer Research (144 citations), Surgery (355 citations) and Molecular Biology (569 citations). A.E. Retief has collaborated with scholars based in South Africa, United States and France. Frequent co-authors include W.A. Van Niekerk, Maritha J. Kotze, E. Langenhoven, Louise Warnich, L. du Plessis, E. Dietzsch, H. F. H. Weich, E. Retief, M. Iqbal Parker and Roelof Menkveld. Their work appears in journals such as Nucleic Acids Research, Human Genetics, Journal of Medical Genetics, Genomics and Prenatal Diagnosis.
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.