R.T. Taggart

Biochemistry, Genetics and Molecular Biology · Life Sciences

26h-index2.6kcitations72works0.02yr avg
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Research Topics

Glycosylation and Glycoproteins Research(15), Helicobacter pylori-related gastroenterology studies(10), RNA and protein synthesis mechanisms(10), Molecular Biology Techniques and Applications(7), Monoclonal and Polyclonal Antibodies Research(5)

Publications68 total

07 - D EVELOPMENT OF THE SURFACE WATER FLOOD MAP FOR NORTHERN IRELAND
2010
Genetic Hearing Loss With No Associated Abnormalities
2004· 10 cited
GJB2: The spectrum of deafness-causing allele variants and their phenotype
Human Mutation·2004· 87 citedOpen Access
Environmentally induced hearing impairment: the impact of genetics
Current Opinion in Otolaryngology & Head & Neck Surgery·2002· 1 cited
A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene
Molecular Genetics and Metabolism·2000· 57 cited
Novel mutations associated with carnitine palmitoyltransferase II deficiency
Human Mutation·1999· 6 cited
Age-Gender Influence on the Rate-Corrected QT Interval and the QT-Heart Rate Relation in Families With Genotypically Characterized Long QT Syndrome
Journal of the American College of Cardiology·1997· 192 cited
Expression of cathepsin E in pancreas: A possible tumor marker for pancreas, a preliminary report
International Journal of Cancer·1996· 33 citedOpen Access
Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.
Circulation·1994· 83 cited
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
Nature Genetics·1994· 271 cited
T wave “humps” as a potential electrocardiographic marker of the long QT syndrome
Journal of the American College of Cardiology·1994· 119 cited
Multiple endocrine neoplasia type I (MEN1): Identification of informative polymorphic markers and candidate genes
The American Journal of Human Genetics·1994
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.
PubMed·1994· 61 cited
Human gastric adenocarcinoma cathepsin B: isolation and sequencing of full-length cDNAs and polymorphisms of the gene
Gene·1994· 55 cited
Isolation and characterization of recombinant human cathepsin E expressed in Chinese hamster ovary cells.
Journal of Biological Chemistry·1993· 43 citedOpen Access
Pepsinogen C gene polymorphisms associated with gastric body ulcer.
Gut·1993· 8 citedOpen Access
D11S970 CATT polymorphism (RC29) located near the MEN1 locus at 11q13
Human Molecular Genetics·1993· 6 cited
D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13
Human Molecular Genetics·1993· 5 cited
MOLECULAR-GENETIC MAPPING OF 13 MARKERS FROM CHROMOSOME-11Q13 IN 33 FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1
Oxford University Research Archive (ORA) (University of Oxford)·1993· 1 cited
Detection of a polymorphism within the pepsinogen C gene with PCR: Construction of a linkage map around PGC from 6p11–6p21.3
Genomics·1992· 4 cited
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Frequent Co-authors

Takeshi Azuma(12), I. Michael Samloff(9), T. Mohandas(5), Gerard Pals(5), Uta Francke(5), Michael H. Lehmann(4), A. Bowcock(4), Jeffrey A. Towbin(3), Peter J. Schwartz(3), Arthur J. Moss(3), Tadashi Shiraishi(3), William A. Reid(3), G I Bell(3), Graeme I. Bell(3), Katherine W. Timothy(2), G. Michael Vincent(2), Debra Frankovich(2), Barbara S. Fromm(2), T. Branch(2), RH Heath(2)