H.J. Eyre

673 total citations
16 papers, 487 citations indexed

About

H.J. Eyre is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, H.J. Eyre has authored 16 papers receiving a total of 487 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Plant Science. Recurrent topics in H.J. Eyre's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers) and RNA Research and Splicing (4 papers). H.J. Eyre is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers) and RNA Research and Splicing (4 papers). H.J. Eyre collaborates with scholars based in Australia, United States and Germany. H.J. Eyre's co-authors include G.R. Sutherland, Toni Antalis, D. C. Gotley, Michael A. McGuckin, CR Kjeldsberg, David F. Callen, Steve D. Wilton, Nigel G. Laing, P. Anthony Akkari and Elizabeth Baker and has published in prestigious journals such as Blood, Journal of Medical Genetics and American Journal of Medical Genetics.

In The Last Decade

H.J. Eyre

16 papers receiving 473 citations

Peers

H.J. Eyre

IMMUN

GENET

SURGE

ONCOL

N Takami Japan

Jutta Renkonen Finland

K Hochstrasser Germany

Ling Yin China

Walter L. Henley United States

Patrick T. Hennessey United States

H. van Someren Netherlands

T Seguchi Japan

Bosco Shang Wang United States

Wagner R. Montor Brazil

N Takami Japan

H.J. Eyre

312 ×1.0

77 ×0.6

IMMUN

65 ×0.8

GENET

61 ×1.0

SURGE

60 ×1.0

ONCOL

Citations per year, relative to H.J. Eyre H.J. Eyre (= 1×) peers N Takami

Countries citing papers authored by H.J. Eyre

Since Specialization

Citations

This map shows the geographic impact of H.J. Eyre'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.J. Eyre with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.J. Eyre more than expected).

Fields of papers citing papers by H.J. Eyre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.J. Eyre. 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.J. Eyre. The network helps show where H.J. Eyre may publish in the future.

Co-authorship network of co-authors of H.J. Eyre

This figure shows the co-authorship network connecting the top 25 collaborators of H.J. Eyre. A scholar is included among the top collaborators of H.J. Eyre 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.J. Eyre. H.J. Eyre is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Yu, Shuancang, Elizabeth Baker, H.J. Eyre, et al.. (2005). Frequency of truly cryptic subtelomere abnormalities – a study of 534 patients and literature review. Clinical Genetics. 68(5). 436–441. 12 indexed citations

McGuckin, Michael A., et al.. (1999). Two novel mucin genes down-regulated in colorectal cancer identified by differential display.. PubMed. 59(16). 4083–9. 263 indexed citations

Callen, David F., et al.. (1997). Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics. Chromosome Research. 5(2). 81–85. 6 indexed citations

Fang, Yuqiang, Sharon Bain, Eric Haan, et al.. (1997). High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome. American Journal of Medical Genetics. 71(4). 453–457. 18 indexed citations

Wilton, Steve D., et al.. (1996). Assignment of the human α-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridization. Cytogenetic and Genome Research. 72(4). 294–296. 8 indexed citations

Sturm, Richard A., H.J. Eyre, Elizabeth Baker, & G.R. Sutherland. (1995). The human OTF1 locus which overlaps the CD3Z gene is located at 1q22→q23. Cytogenetic and Genome Research. 68(3-4). 231–232. 6 indexed citations

Eyre, H.J., et al.. (1995). Assignment of the human skeletal muscle α-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization. Cytogenetic and Genome Research. 69(1-2). 15–17. 16 indexed citations

Eyre, H.J., P. Anthony Akkari, S.M. Dorosz, et al.. (1995). Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation. Cytogenetic and Genome Research. 71(1). 94–95. 6 indexed citations

Wilton, Steve D., et al.. (1995). Assignment of the human α-tropomyosin gene TPM3 to 1q22→q23 by fluorescence in situ hybridisation. Cytogenetic and Genome Research. 68(1-2). 122–124. 19 indexed citations

10.

Akkari, P. Anthony, H.J. Eyre, Steve D. Wilton, et al.. (1994). Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation. Cytogenetic and Genome Research. 65(4). 265–267. 9 indexed citations

11.

Romain, D R, et al.. (1991). A rare heteromorphism of chromosome 20 and reproductive loss.. Journal of Medical Genetics. 28(7). 477–478. 3 indexed citations

12.

Callen, David F., et al.. (1990). A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308. Clinical Genetics. 37(2). 81–83. 4 indexed citations

13.

Eyre, H.J., et al.. (1981). Hereditary myeloperoxidase deficiency. Blood. 57(5). 888–893. 5 indexed citations

14.

Eyre, H.J., et al.. (1981). Hereditary myeloperoxidase deficiency. Blood. 57(5). 888–893. 74 indexed citations

15.

Kjeldsberg, CR, et al.. (1977). Evidence for intracellular amyloid formation in myeloma. Blood. 50(3). 493–504. 36 indexed citations

16.

Kjeldsberg, CR, et al.. (1977). Evidence for intracellular amyloid formation in myeloma. Blood. 50(3). 493–504. 2 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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