Carol Paterson

Biochemistry, Genetics and Molecular Biology · Life Sciences

10h-index904citations16works0.02yr avg
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Research Topics

Peroxisome Proliferator-Activated Receptors(3), Cancer Genomics and Diagnostics(3), Congenital heart defects research(3), DNA Repair Mechanisms(2), Epigenetics and DNA Methylation(2)

Publications16 total

Editorial: Non-invasive physiological measurements: from discovery to implementation
UNC Libraries·2024Open Access
A Multifactorial Likelihood Model for MMR Gene Variant Classification Incorporating Probabilities Based on Sequence Bioinformatics and Tumor Characteristics: A Report from the Colon Cancer Family Registry
Human Mutation·2012· 92 citedOpen Access
Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants
Hereditary Cancer in Clinical Practice·2012· 1 citedOpen Access
Blimp1 regulates development of the posterior forelimb, caudal pharyngeal arches, heart and sensory vibrissae in mice
Development·2007· 131 citedOpen Access
Regulation of the <i>Atm</i> promoter in vivo
Genes Chromosomes and Cancer·2005· 24 cited
Analysis of allelic choice of Xist transcription in X inactivation
Mechanisms of Development·2005
<i>Tyrosinase‐Cre</i> mice for tissue‐specific gene ablation in neural crest and neuroepithelial‐derived tissues
genesis·2003· 48 cited
<i>Pex13</i>Inactivation in the Mouse Disrupts Peroxisome Biogenesis and Leads to a Zellweger Syndrome Phenotype
Molecular and Cellular Biology·2003· 112 citedOpen Access
Pex13 conditional inactivation in the mouse: A model for the peroxisome biogenesis disorders.
Griffith Research Online (Griffith University, Queensland, Australia)·2003
Targeting and conditional inactivation of the murine <i>Men1</i> locus using the Cre recombinase: <i>loxP</i> System
genesis·2002· 22 citedOpen Access
Conditional inactivation of the peroxisome biogenesis <i>Pex13</i> gene by Cre‐<i>loxP</i> excision
genesis·2002· 13 citedOpen Access
Mouse models of the peroxisome biogenesis disorders through conditional inactivation of Pex13
Griffith Research Online (Griffith University, Queensland, Australia)·2002
Atm knock-in mice harboring an in-frame deletion corresponding to the human ATM 7636del9 common mutation exhibit a variant phenotype.
PubMed·2001· 68 cited
Mice Lacking the Vascular Endothelial Growth Factor-B Gene ( <i>Vegfb</i> ) Have Smaller Hearts, Dysfunctional Coronary Vasculature, and Impaired Recovery From Cardiac Ischemia
Circulation Research·2000· 326 citedOpen Access
Bisulfite Genomic Sequencing-Derived Methylation Profile of theXistGene throughout Early Mouse Development
Genomics·1998· 66 cited
Imperforate Cardiac Septal Defect in a Dog
Journal of the American Veterinary Medical Association·1970· 1 cited

Frequent Co-authors

Graham F. Kay(11), Ian D. Tonks(8), Megan Maxwell(4), Jonas Björkman(4), Denis I. Crane(4), John Finnie(3), Barbara C. Paton(3), Michael G. Gartside(2), Arne W. Mould(2), Nicholas K. Hayward(2), Tam Nguyen(2), P. Sharp(2), Bryony A. Thompson(2), David E. Goldgar(2), Mark Clendenning(2), Rhiannon Walters(2), Michael T. Parsons(2), John L. Hopper(2), Mark A. Jenkins(2), Joanne Young(2)