Publications by authors named "Matthew Simmonds"

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Alterations in calreticulin and CD47 expression dynamics in myeloid malignancies: therapeutic and prognostic implications in myelodysplastic syndromes and myeloproliferative neoplasms.
Kristian Boasman, Claire L Walker, Matthew J Simmonds, Ciro R Rinaldi

Haematologica· September 2025

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Using PU.1 and Jun dimerization protein 2 transcription factor expression in myelodysplastic syndromes to predict treatment response and leukaemia transformation.
Kristian Boasman, Matthew James Simmonds, Ciaren Graham, Yogen Saunthararajah, Ciro Roberto Rinaldi

Ann Hematol· June 2019

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Genetic predictors of long-term graft function in kidney and pancreas transplant patients.
Claire E Duff, Matthew J Simmonds

Brief Funct Genomics· July 2017

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Caveolin-1 single-nucleotide polymorphism and arterial stiffness in non-dialysis chronic kidney disease.
Sourabh Chand, Nicola C Edwards, Colin D Chue, Mark Jesky, Stephanie Stringer, Matthew J Simmonds

Nephrol Dial Transplant· July 2016

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Using Genetic Variation to Predict and Extend Long-term Kidney Transplant Function.
Matthew J Simmonds

Transplantation· October 2015

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Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease.
Sourabh Chand, Colin D Chue, Nicola C Edwards, James Hodson, Matthew J Simmonds

PLoS One· September 2015

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Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe.
Alexander Hamilton, Paul R Newby, Jacqueline D Carr-Smith, Giulio Disanto, Amit Allahabadia, Matthew J Simmonds

J Clin Endocrinol Metab· August 2014

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Caveolin-1 single nucleotide polymorphism in antineutrophil cytoplasmic antibody associated vasculitis.
Sourabh Chand, Julia U Holle, Marc Hilhorst, Matthew J Simmonds, Stuart Smith

PLoS One· March 2014

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Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
Marco Medici, Eleonora Porcu, Giorgio Pistis, Alexander Teumer, Suzanne J Brown, Matthew J Simmonds

PLoS Genet· February 2014

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Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: an association study and meta-analysis.
Matthew J Simmonds, Fotini K Kavvoura, Oliver J Brand, Paul R Newby, Laura E Jackson

J Clin Endocrinol Metab· January 2014

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Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
Karen A Hunt, Vanisha Mistry, Nicholas A Bockett, Tariq Ahmad, Maria Ban, Matthew J Simmonds

Nature· June 2013

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GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.
Matthew J Simmonds

Nat Rev Endocrinol· May 2013

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Skewing of female X-chromosome inactivation: an epigenetic risk factor for kidney transplantation outcome.
Matthew J Simmonds, David Benavente, Oliver J Brand, Jason Moore, Simon Ball

Transplantation· March 2013

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Seven newly identified loci for autoimmune thyroid disease.
Jason D Cooper, Matthew J Simmonds, Neil M Walker, Oliver Burren, Oliver J Brand

Hum Mol Genet· December 2012

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Donor ABCB1 variant associates with increased risk for kidney allograft failure.
Jason Moore, Amy Jayne McKnight, Bernd Döhler, Matthew J Simmonds, Aisling E Courtney

J Am Soc Nephrol· November 2012

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Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.
Karen A Hunt, Deborah J Smyth, Tobias Balschun, Maria Ban, Vanisha Mistry, Matthew J Simmonds

Nat Genet· December 2011

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Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.
Vincent Plagnol, Joanna M M Howson, Deborah J Smyth, Neil Walker, Jason P Hafler, Matthew J Simmonds

PLoS Genet· August 2011

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The search for the genetic contribution to autoimmune thyroid disease: the never ending story?
Matthew J Simmonds, Stephen C L Gough

Brief Funct Genomics· March 2011

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Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3.
Matthew J Simmonds, Oliver J Brand, Jeffrey C Barrett, Paul R Newby, Jayne A Franklyn

Clin Endocrinol (Oxf)· November 2010

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Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.
Rafał Płoski, Oliver J Brand, Beata Jurecka-Lubieniecka, Maria Franaszczyk, Dorota Kula, Matthew J Simmonds

PLoS One· November 2010

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Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study.
Paul R Newby, Oliver J Pickles, Samaresh Mazumdar, Oliver J Brand, Jaqueline D Carr-Smith, Matthew J Simmonds

Eur J Hum Genet· September 2010

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Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression.
Kadija Yesmin, Chantal Hargreaves, Paul R Newby, Oliver J Brand, Joanne M Heward, Matthew J Simmonds

Clin Endocrinol (Oxf)· July 2010

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Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease.
Matthew J Simmonds, Kadija Yesmin, Paul R Newby, Oliver J Brand, Jayne A Franklyn

Thyroid· April 2010

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.

Nature· April 2010

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Association of caveolin-1 gene polymorphism with kidney transplant fibrosis and allograft failure.
Jason Moore, Amy Jayne McKnight, Matthew J Simmonds, Aisling E Courtney, Rajesh Hanvesakul

JAMA· April 2010

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