H.G. Close
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- N. Maclean (3 shared papers)J.A. Strong (3 shared papers)W.M. Court Brown (3 shared papers)D.G. Harnden (3 shared papers)PatriciaA. Jacobs (2 shared papers)Jackie Goldstein (2 shared papers)Tara MacGregor (2 shared papers)M. Sandler (1 shared paper)
- Journals
- The Lancet (4 papers)Obstetrical & Gynecological Survey (1 paper)Clinical Genetics (1 paper)Cytogenetic and Genome Research (1 paper)PubMed (1 paper)
- Partner nations
- United KingdomSouth Africa
In The Last Decade
H.G. Close
8 papers receiving 259 citations
Peers
Comparison fields: 5 of 51
- Genetics 203
- Developmental Biology 13
- Reproductive Medicine 30
- Gender Studies 22
- Molecular Biology 133
Countries citing papers authored by H.G. Close
This map shows the geographic impact of H.G. Close'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.G. Close with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.G. Close more than expected).
Fields of papers citing papers by H.G. Close
This network shows the impact of papers produced by H.G. Close. 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.G. Close. The network helps show where H.G. Close may publish in the future.
Co-authors
The 13 scholars most cited alongside H.G. Close, 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 | 1960 | 134 | |
| 2 | 1962 | 102 | |
| 3 | 1963 | 24 | |
| 4 | 1959 | 23 | |
| 5 | 1968 | 17 | |
| 6 | 1975 | 10 | |
| 7 | 1961 | 8 | |
| 8 | 1978 | 1 |
About H.G. Close
H.G. Close is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Hematology, having authored 8 papers that have together received 319 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Prenatal Screening and Diagnostics (1 paper), Gestational Trophoblastic Disease Studies (1 paper), Cancer, Hypoxia, and Metabolism (1 paper), Blood groups and transfusion (1 paper), Cancer Research and Treatments (1 paper), Cancer, Lipids, and Metabolism (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (203 citations), Developmental Biology (13 citations), Reproductive Medicine (30 citations), Gender Studies (22 citations) and Molecular Biology (133 citations). H.G. Close has collaborated with scholars based in United Kingdom and South Africa. Frequent co-authors include N. Maclean, J.A. Strong, W.M. Court Brown, D.G. Harnden, PatriciaA. Jacobs, Jackie Goldstein, Tara MacGregor, M. Sandler, J Mcbride and A.G. Baikie. Their work appears in journals such as The Lancet, Obstetrical & Gynecological Survey, Clinical Genetics, Cytogenetic and Genome Research 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.