C. Potter

发表

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Simon C. Potter, P. Donnelly, C. Spencer, 2007, Nature.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Simon C. Potter, David M. Evans, P. Donnelly, 2007, Nature Genetics.

Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

Samuel E. Jones, David M. Evans, M. Jarvelin, 2018, Human molecular genetics.

Maternal Red Blood Cell Folate and Infant Vitamin B12 Status Influence Methylation of Genes Associated with Childhood Acute Lymphoblastic Leukemia

C. Potter, J. Mathers, C. Relton, 2018, Molecular nutrition & food research.

Influence of DNMT Genotype on Global and Site Specific DNA Methylation Patterns in Neonates and Pregnant Women

C. Potter, J. Mathers, C. Relton, 2013, PloS one.

Investigation of the MHC2TA gene, associated with rheumatoid arthritis in a Swedish population, in a UK rheumatoid arthritis cohort.

D. Strachan, S. Ring, A. Barton, 2006, Arthritis and rheumatism.

Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

David M. Evans, K. Lunetta, J. Murabito, 2018, Human molecular genetics.

Polymorphisms spanning the TNFR2 and TACE genes do not contribute towards variable anti-TNF treatment response.

A. Barton, C. Potter, H. Cordell, 2010, Pharmacogenetics and genomics.

Bioinformatic selection of putative epigenetically regulated loci associated with obesity using gene expression data.

C. Potter, M. Pearce, V. Turcot, 2012, Gene.

Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment

Anne Barton, John D Isaacs, A. Barton, 2010, Annals of the rheumatic diseases.

Postnatal Growth and DNA Methylation Are Associated With Differential Gene Expression of the TACSTD2 Gene and Childhood Fat Mass

Mark S. Pearce, John C. Mathers, George Davey Smith, 2012, Diabetes.

Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations.

David A Mackey, Carmel Toomes, Katherine V Towns, 2007, American journal of ophthalmology.

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

Samuel E. Jones, David M. Evans, K. Lunetta, 2017, bioRxiv.

Maternal genome-wide association study identifies a fasting glucose variant associated with offspring birth weight

Samuel E. Jones, David M. Evans, M. Jarvelin, 2015 .

Genome-Wide Association Study of Genetic Predictors of Anti–Tumor Necrosis Factor Treatment Efficacy in Rheumatoid Arthritis Identifies Associations with Polymorphisms at Seven Loci

A. Barton, C. Potter, J. Bowes, 2011, Arthritis and rheumatism.

Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5–CHRNA3–CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

Paul C. D. Johnson, M. Jarvelin, A. Hofman, 2012, Human molecular genetics.

Investigation of association between the TRAF family genes and RA susceptibility

A. Barton, S. Eyre, C. Potter, 2007, Annals of the rheumatic diseases.

Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?

A. Barton, S. Eyre, C. Potter, 2006, Arthritis research & therapy.

Genetic and Non-Genetic Influences during Pregnancy on Infant Global and Site Specific DNA Methylation: Role for Folate Gene Variants and Vitamin B12

C. Potter, J. Mathers, C. Relton, 2012, PloS one.

Global LINE-1 DNA methylation is associated with blood glycaemic and lipid profiles

C. Potter, M. Pearce, L. Parker, 2012, International journal of epidemiology.

Association of rheumatoid factor and anti-cyclic citrullinated peptide positivity, but not carriage of shared epitope or PTPN22 susceptibility variants, with anti-tumour necrosis factor response in rheumatoid arthritis

A. Barton, C. Potter, D. Symmons, 2008 .

Baseline serum MMP-3 levels in patients with Rheumatoid Arthritis are still independently predictive of radiographic progression in a longitudinal observational cohort at 8 years follow up

C. Potter, J. Isaacs, I. Griffiths, 2012, Arthritis Research & Therapy.

Investigation of genetic variants within candidate genes of the TNFRSF1B signalling pathway on the response to anti-TNF agents in a UK cohort of rheumatoid arthritis patients

A. Barton, C. Potter, Jane Worthington, 2009, Pharmacogenetics and genomics.

Association of the tumour necrosis factor-308 variant with differential response to anti-TNF agents in the treatment of rheumatoid arthritis.

Anne Barton, John D Isaacs, Jane Worthington, 2008, Human molecular genetics.

Association between anti-tumour necrosis factor treatment response and genetic variants within the TLR and NFκB signalling pathways

Anne Barton, John D Isaacs, Heather J Cordell, 2010, Annals of the rheumatic diseases.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

P. Donnelly, C. Spencer, A. Silman, 2007, Nature genetics.

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Simon C. Potter, C. Spencer, A. Silman, 2007, Nature.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

P. Donnelly, C. Spencer, A. Silman, 2007, Nature Genetics.

C. Potter, D. Symmons, W. Thomson, 2008 .

C. Potter, K. Hyrich, D. Plant, 2008, Annals of the rheumatic diseases.

Newcastle University E-prints Citation for Item: Baseline Serum Mmp-3 Levels in Patients with Rheumatoid Arthritis Are Still Independently Predictive of Radiographic Progression in a Longitudinal Observational Cohort at 8 Years Follow Up

C. Potter, J. Isaacs, I. Griffiths, 2022 .