H.G. Close

536 total citations
8 papers, 319 citations indexed

About

H.G. Close is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H.G. Close has authored 8 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in H.G. Close's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Cancer, Lipids, and Metabolism (1 paper) and Sexual Differentiation and Disorders (1 paper). H.G. Close is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Cancer, Lipids, and Metabolism (1 paper) and Sexual Differentiation and Disorders (1 paper). H.G. Close collaborates with scholars based in United Kingdom and South Africa. H.G. Close's co-authors include D.G. Harnden, N. Maclean, W.M. Court Brown, J.A. Strong, PatriciaA. Jacobs, Tara MacGregor, Jackie Goldstein, M. Sandler, A.G. Baikie and J Mcbride and has published in prestigious journals such as The Lancet, Obstetrical & Gynecological Survey and Cytogenetic and Genome Research.

In The Last Decade

H.G. Close

8 papers receiving 259 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
H.G. Close United Kingdom	7	203	133	34	30	28	8	319
Jackie Goldstein United Kingdom	3	111 0.5×	76 0.6×	15 0.4×	12 0.4×	18 0.6×	4	178
G. H. Valentine Canada	10	160 0.8×	97 0.7×	108 3.2×	11 0.4×	34 1.2×	22	336
A. Kleczkowska Belgium	11	282 1.4×	114 0.9×	109 3.2×	17 0.6×	89 3.2×	33	329
Kenneth W. Dumars United States	12	170 0.8×	138 1.0×	96 2.8×	17 0.6×	42 1.5×	25	357
Kim Freriks Netherlands	10	194 1.0×	145 1.1×	27 0.8×	32 1.1×	19 0.7×	14	279
M Osztovics United States	8	92 0.5×	56 0.4×	99 2.9×	11 0.4×	28 1.0×	34	207
George F. Koepf United States	6	150 0.7×	122 0.9×	17 0.5×	26 0.9×	33 1.2×	8	286
Natalie Blagowidow United States	6	157 0.8×	190 1.4×	22 0.6×	17 0.6×	25 0.9×	10	253
L Cifuentes Chile	10	127 0.6×	64 0.5×	32 0.9×	14 0.5×	12 0.4×	41	254
Sorrell H. Waxman United States	13	217 1.1×	132 1.0×	143 4.2×	34 1.1×	50 1.8×	19	387

Countries citing papers authored by H.G. Close

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of H.G. Close

This figure shows the co-authorship network connecting the top 25 collaborators of H.G. Close. A scholar is included among the top collaborators of H.G. Close based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with H.G. Close. H.G. Close is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Close, H.G., et al.. (1978). Buccal smears and numerical sex chromosome anomalies.. PubMed. 54(14). 557–61. 1 indexed citations

2.

Close, H.G., et al.. (1975). Down's syndrome with additional XYY aneuploidy. Clinical Genetics. 8(1). 55–58. 10 indexed citations

3.

Close, H.G., et al.. (1968). The incidence of sex chromosomal abnormalities in mentally subnormal males. Cytogenetic and Genome Research. 7(4). 277–285. 17 indexed citations

4.

Close, H.G.. (1963). TWO APPARENTLY NORMAL TRIPLE-X FEMALES. The Lancet. 282(7322). 1358–1359. 24 indexed citations

5.

Maclean, N., D.G. Harnden, PatriciaA. Jacobs, et al.. (1962). A SURVEY OF SEX-CHROMOSOME ABNORMALITIES AMONG 4514 MENTAL DEFECTIVES. The Lancet. 279(7224). 293–296. 102 indexed citations

6.

Jacobs, Patricia A., D.G. Harnden, W.M. Court Brown, et al.. (1961). ABNORMALITIES INVOLVING THE X CHROMOSOME IN WOMEN. Obstetrical & Gynecological Survey. 16(1). 140–142. 8 indexed citations

7.

Jacobs, PatriciaA., D.G. Harnden, W.M. Court Brown, et al.. (1960). ABNORMALITIES INVOLVING THE X CHROMOSOME IN WOMEN. The Lancet. 275(7136). 1213–1216. 134 indexed citations

8.

Sandler, M. & H.G. Close. (1959). BIOCHEMICAL EFFECT OF PHENYLACETIC ACID IN A PATIENT WITH 5-HYDROXYTRYPTOPHANSECRETING CARCINOID TUMOUR. The Lancet. 274(7098). 316–318. 23 indexed citations

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.

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