S.A. Rundle

Cardiff University — United Kingdom

Neuroscience · Life Sciences

13h-index4.3kcitations23works0.02yr avg
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Research Topics

Genetic Neurodegenerative Diseases(13), Mitochondrial Function and Pathology(6), Cancer-related molecular mechanisms research(3), Genomic variations and chromosomal abnormalities(3), Parkinson's Disease Mechanisms and Treatments(2)

Publications23 total

Pinolenic acid exhibits anti-inflammatory and anti-atherogenic effects in peripheral blood-derived monocytes from patients with rheumatoid arthritis
Scientific Reports·2022· 10 citedOpen Access
Pinolenic acid exhibits Anti-inflammatory and Anti-atherogenic effects in Peripheral blood-derived Monocytes from patients with Rheumatoid Arthritis
Research Square (Research Square)·2022Open Access
Pinolenic acid Mediated Anti-inflammatory and Immunometabolic Effects in Peripheral blood-derived Monocytes from patients with Rheumatoid Arthritis is Associated with Modulation of miRNA expression
Research Square (Research Square)·2022Open Access
Genomic organization and transcriptional units at the myotonic dystrophy locus
Genomics·1993· 73 cited
Cataract and myotonic dystrophy: the role of molecular diagnosis.
British Journal of Ophthalmology·1993· 18 citedOpen Access
A study of DNA methylation in myotonic dystrophy.
Journal of Medical Genetics·1993· 37 citedOpen Access
Minimal expression of myotonic dystrophy: a clinical and molecular analysis.
Journal of Medical Genetics·1992· 31 citedOpen Access
Radiation-reduced hybrids for the myotonic dystrophy locus
Genomics·1992· 17 cited
Unstable DNA sequence in myotonic dystrophy
The Lancet·1992· 201 cited
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
Nature·1992· 727 cited
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
Cell·1992· 2.8k cited
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19
Cytogenetic and Genome Research·1992· 9 cited
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat
Human Molecular Genetics·1992· 11 cited
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.
PubMed·1991· 92 cited
Identification of new DNA markers close to the myotonic dystrophy locus.
Journal of Medical Genetics·1991· 23 citedOpen Access
The promoter of the latency-associated transcripts of herpes simplex virus type 1 contains a functional cAMP-response element: role of the latency-associated transcripts and cAMP in reactivation of viral latency.
Proceedings of the National Academy of Sciences·1991· 145 citedOpen Access
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments
Human Genetics·1991· 13 cited
Localisation of the myotonic dystrophy locus to 19q13.2?19q13.3 and its relationship to twelve polymorphic loci on 19q
Human Genetics·1991· 32 cited
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.
PubMed·1990· 48 cited
A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)
Nucleic Acids Research·1990· 3 citedOpen Access
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Frequent Co-authors

H G Harley(18), J. David Brook(16), Duncan J. Shaw(14), K.V. Walsh(8), Steve Crow(7), Peter S. Harper(7), David E. Housman(4), William Reardon(4), Alan Buckler(3), Jessica L. Buxton(3), Keith Johnson(3), Michael J. Siciliano(3), Rabaa Takala(3), Dipak P. Ramji(3), Robert Andrews(3), You Zhou(3), Farhat Mustafa(3), Ernest Choy(3), Mila E. McCurrach(2), Robert Sohn(2)