H.J. Eyre

Women's and Children's Hospital — Australia

Biochemistry, Genetics and Molecular Biology · Life Sciences

10h-index673citations19works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(7), Chromosomal and Genetic Variations(5), RNA Research and Splicing(4), Cardiomyopathy and Myosin Studies(4), RNA modifications and cancer(3)

Publications19 total

Frequency of truly cryptic subtelomere abnormalities – a study of 534 patients and literature review
Clinical Genetics·2005· 20 citedOpen Access
Two novel mucin genes down-regulated in colorectal cancer identified by differential display.
PubMed·1999· 300 cited
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·1997· 25 cited
Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics
Chromosome Research·1997· 7 cited
Assignment of the human α-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridization
Cytogenetic and Genome Research·1996· 10 cited
Dr. John L. Hamerton steps-down from the Associate Editorship
Cytogenetic and Genome Research·1995Open Access
The human OTF1 locus which overlaps the CD3Z gene is located at 1q22→q23
Cytogenetic and Genome Research·1995· 6 cited
Assignment of the human skeletal muscle α-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization
Cytogenetic and Genome Research·1995· 20 cited
Inherited diseases of skeletal and cardiac muscle associated with contractile proteins
Murdoch Research Repository (Murdoch University)·1995
Assignment of the human α-tropomyosin gene TPM3 to 1q22→q23 by fluorescence in situ hybridisation
Cytogenetic and Genome Research·1995· 24 cited
Localization of the tropomyosin genes
Murdoch Research Repository (Murdoch University)·1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation
Cytogenetic and Genome Research·1995· 8 cited
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation
Cytogenetic and Genome Research·1994· 11 cited
A rare heteromorphism of chromosome 20 and reproductive loss.
Journal of Medical Genetics·1991· 46 citedOpen Access
A dicentric variant of chromosome 6: characterization by use of <i>in situ</i> hybridisation with the biotinylated probe p308
Clinical Genetics·1990· 41 cited
Hereditary myeloperoxidase deficiency
Blood·1981· 99 citedOpen Access
Hereditary myeloperoxidase deficiency
Blood·1981· 8 citedOpen Access
Evidence for intracellular amyloid formation in myeloma
Blood·1977· 2 citedOpen Access
Evidence for intracellular amyloid formation in myeloma
Blood·1977· 46 citedOpen Access

Frequent Co-authors

David F. Callen(9), Steve D. Wilton(8), Nigel G. Laing(8), P. Anthony Akkari(7), D.C. Callen(3), S.M. Dorosz(3), G.R. Sutherland(2), M Kitahara(2), Y Simonian(2), CL Atkin(2), SJ Hasstedt(2), CR Kjeldsberg(2), H Totzke(2), Hugh Watkins(2), Caitlin MacRae(2), Elizabeth Baker(2), Elizabeth Baker(2), Stephanie J. Williams(1), Michael A. McGuckin(1), D. C. Gotley(1)