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Other IDs

Scopus Author ID: 9846749100

Keywords

Autoimmunity, Transplantation, Genetics, Type 1 Diabetes, Autoimmune Thyroid Disease

Countries

United Kingdom

Activities

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Employment (6)

University of Lincoln: Lincoln, Lincolnshire, GB

2016-02-01 to present | Senior Lecturer in Biosciences (School of Life Sciences)
Employment
Source: Self-asserted source
Matt Simmonds

University of Oxford: Oxford, Oxfordshire, GB

2015-04 to 2016-01 | University Research Lecturer & Diabetes Research and Wellness Foundation (DRWF) Non-Clinical Fellow (Oxford Centre for Diabetes, Endocrinology & Metabolism)
Employment
Source: Self-asserted source
Matt Simmonds

University of Oxford: Oxford, Oxfordshire, GB

2012-10 to 2015-03 | Diabetes Research and Wellness Foundation (DRWF) Non-Clinical Fellow (Oxford Centre for Diabetes, Endocrinology and Metabolism )
Employment
Source: Self-asserted source
Matt Simmonds

University of Oxford: Oxford, Oxfordshire, GB

2011-10 to 2012-09 | European Foundation for the Study of Diabetes (EFSD)/Lilly Postdoctoral Research Fellow (Oxford Centre for Diabetes, Endocrinology and Metabolism )
Employment
Source: Self-asserted source
Matt Simmonds

University of Oxford: Oxford, Oxfordshire, GB

2010-03 to 2011-09 | Senior Postdoctoral Research Fellow (Oxford Centre for Diabetes, Endocrinology and Metabolism )
Employment
Source: Self-asserted source
Matt Simmonds

University of Birmingham: Birmingham, West Midlands, GB

2005-07 to 2010-03 | Postdoctoral Research Fellow (Centre for Endocrinology, Diabetes and Metabolism)
Employment
Source: Self-asserted source
Matt Simmonds

Education and qualifications (2)

University of Birmingham: Birmingham, West Midlands, GB

2001-10 to 2005-07 | PhD in Genetics of Autoimmune Disease (Department of Medicine)
Education
Source: Self-asserted source
Matt Simmonds

University of Essex: Colchester, Essex, GB

1998-10 to 2001-07 | BSc. Cell and Molecular Biology with Honours
Education
Source: Self-asserted source
Matt Simmonds

Funding (11)

Is Science for Me? Sixth Form Students Careers Event

2015 to 2015 | Grant
Society for Endocrinology (Bristol, GB)
Source: Self-asserted source
Matt Simmonds

Innovators in Diabetes (IDia) Course

2014 to 2016 | Award
Diabetes UK (London, GB)
Source: Self-asserted source
Matt Simmonds

Extending whole pancreas transplant function in type 1 diabetics

2014 to 2015 | Grant
Diabetes Research & Wellness Foundation (Hayling Island, GB)
Source: Self-asserted source
Matt Simmonds

Role of type 1 diabetes (T1D) susceptibility genes in predicting long term pancreas transplant function in T1D patients: pilot study

2014 to 2015 | Grant
Novo Nordisk UK Research Foundation (Gatwick, GB)
Source: Self-asserted source
Matt Simmonds

Unravelling the Mysteries of Diabetes

2014 to 2014 | Grant
Society for Endocrinology (Bristol, GB)
Source: Self-asserted source
Matt Simmonds

Identifying genetic predictors of graft function to enable pancreas transplantation to become a lifelong cure for type 1 diabetes

2012 to 2015 | Salary award
Diabetes Research & Wellness Foundation (Hayling Island, GB)
Source: Self-asserted source
Matt Simmonds

Identifying genetic predictors of graft function in whole organ pancreas transplantation

2011 to 2012 | Salary award
European Foundation for the Study of Diabetes (Düsseldorf, DE)
Source: Self-asserted source
Matt Simmonds

Screening the HDLBP region for association with Graves’ disease

2008 to 2008 | Grant
Society for Endocrinology (Bristol, GB)
Source: Self-asserted source
Matt Simmonds

Sense about Science: Media Training Workshop

2008 to 2008 | Award
Society for Endocrinology (Bristol, GB)
Source: Self-asserted source
Matt Simmonds

Identification of the Graves’ disease associated DNA variant located within FCRL5

2007 to 2008 | Grant
Society for Endocrinology (Bristol, GB)
Source: Self-asserted source
Matt Simmonds

Examining the expression of different isoforms of the thyroid stimulating hormone receptor (TSHR) in peripheral blood lymphocytes (PBLs) and thyroid tissue

2006 to 2006 | Grant
University Of Birmingham (Birmingham, GB)
Source: Self-asserted source
Matt Simmonds

Works (50 of 52)

Items per page:
Page 1 of 2

Using PU.1 and Jun dimerization protein 2 transcription factor expression in myelodysplastic syndromes to predict treatment response and leukaemia transformation

Annals of hematology
2019 | Journal article
DOI: 10.1007/s00277-019-03627-9
Source: Self-asserted source
Matt Simmonds

Genetic predictors of long-term graft function in kidney and pancreas transplant patients

Briefings in functional genomics
2017 | Journal article
DOI: 10.1093/bfgp/elw039
Source: Self-asserted source
Matt Simmonds

Caveolin-1 single-nucleotide polymorphism and arterial stiffness in non-dialysis chronic kidney disease

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
2016 | Journal article
DOI: 10.1093/ndt/gfv350
Source: Self-asserted source
Matt Simmonds

Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease

PLoS ONE
2015 | Journal article
DOI: 10.1371/journal.pone.0116160
Source: Self-asserted source
Matt Simmonds

Genetic variation in caveolin-1 correlates with long-term pancreas transplant function

American Journal of Transplantation
2015 | Journal article
DOI: 10.1111/ajt.13104
Source: Self-asserted source
Matt Simmonds

Using genetic variation to predict and extend long-term kidney transplant function

Transplantation
2015 | Journal article
DOI: 10.1097/TP.0000000000000836
Source: Self-asserted source
Matt Simmonds

Identification of Novel Genetic Loci Associated with Thyroid Peroxidase Antibodies and Clinical Thyroid Disease

PLoS Genetics
2014 | Journal article
DOI: 10.1371/journal.pgen.1004123
Source: Self-asserted source
Matt Simmonds

Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe

Journal of Clinical Endocrinology and Metabolism
2014 | Journal article
DOI: 10.1210/jc.2014-1270
Source: Self-asserted source
Matt Simmonds

Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: An association study and meta-analysis

Journal of Clinical Endocrinology and Metabolism
2014 | Journal article
DOI: 10.1210/jc.2013-2667
Source: Self-asserted source
Matt Simmonds

Caveolin-1 Single Nucleotide Polymorphism in Antineutrophil Cytoplasmic Antibody Associated Vasculitis

PLoS ONE
2013 | Journal article
DOI: 10.1371/journal.pone.0069022
Source: Self-asserted source
Matt Simmonds

GWAS in autoimmune thyroid disease: Redefining our understanding of pathogenesis

Nature Reviews Endocrinology
2013 | Journal article
DOI: 10.1038/nrendo.2013.56
Source: Self-asserted source
Matt Simmonds

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

Nature
2013 | Journal article
DOI: 10.1038/nature12170
Source: Self-asserted source
Matt Simmonds

Skewing of female X-chromosome inactivation: An epigenetic risk factor for kidney transplantation outcome

Transplantation
2013 | Journal article
DOI: 10.1097/TP.0b013e318282256f
Source: Self-asserted source
Matt Simmonds

Donor ABCB1 variant associates with increased risk for kidney allograft failure

Journal of the American Society of Nephrology
2012 | Journal article
DOI: 10.1681/ASN.2012030260
Source: Self-asserted source
Matt Simmonds

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Nature Genetics
2012 | Journal article
DOI: 10.1038/ng.1037
Source: Self-asserted source
Matt Simmonds

Seven newly identified loci for autoimmune thyroid disease

Human Molecular Genetics
2012 | Journal article
DOI: 10.1093/hmg/dds357
Source: Self-asserted source
Matt Simmonds

Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases

PLoS Genetics
2011 | Journal article
DOI: 10.1371/journal.pgen.1002216
Source: Self-asserted source
Matt Simmonds

The search for the genetic contribution to autoimmune thyroid disease: The never ending story?

Briefings in Functional Genomics
2011 | Journal article
DOI: 10.1093/bfgp/elq036
Source: Self-asserted source
Matt Simmonds

Association of Caveolin-1 gene polymorphism with kidney transplant fibrosis and allograft failure

JAMA - Journal of the American Medical Association
2010 | Journal article
DOI: 10.1001/jama.2010.356
Source: Self-asserted source
Matt Simmonds

Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3

Clinical Endocrinology
2010 | Journal article
DOI: 10.1111/j.1365-2265.2010.03843.x
Source: Self-asserted source
Matt Simmonds

Association of FcGRIIa with Graves' disease: A potential role for dysregulated autoantibody clearance in disease onset/progression

Clinical Endocrinology
2010 | Journal article
DOI: 10.1111/j.1365-2265.2010.03780.x
Source: Self-asserted source
Matt Simmonds

Confirmation of association of chromosome 5q31-33 with United Kingdom caucasian graves' disease

Thyroid
2010 | Journal article
DOI: 10.1089/thy.2009.0375
Source: Self-asserted source
Matt Simmonds

Evaluation of Five Interleukin Genes for Association with End-Stage Renal Disease in White Europeans

American Journal of Nephrology
2010 | Journal article
DOI: 10.1159/000314943
Source: Self-asserted source
Matt Simmonds

Follow-up of potential novel graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study

European Journal of Human Genetics
2010 | Journal article
DOI: 10.1038/ejhg.2010.55
Source: Self-asserted source
Matt Simmonds

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

Nature
2010 | Journal article
DOI: 10.1038/nature08979
Source: Self-asserted source
Matt Simmonds

Prevalence and Relative Risk of Other Autoimmune Diseases in Subjects with Autoimmune Thyroid Disease

American Journal of Medicine
2010 | Journal article
DOI: 10.1016/j.amjmed.2009.06.030
Source: Self-asserted source
Matt Simmonds

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for graves' disease in three European caucasian cohorts

PLoS ONE
2010 | Journal article
DOI: 10.1371/journal.pone.0015512
Source: Self-asserted source
Matt Simmonds

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease

Human Molecular Genetics
2009 | Journal article
DOI: 10.1093/hmg/ddp087
Source: Self-asserted source
Matt Simmonds

CD226 Gly307Ser association with multiple autoimmune diseases

Genes and Immunity
2009 | Journal article
DOI: 10.1038/gene.2008.82
Source: Self-asserted source
Matt Simmonds

Genome-wide association study identifies eight loci associated with blood pressure

Nature Genetics
2009 | Journal article
DOI: 10.1038/ng.361
Source: Self-asserted source
Matt Simmonds

Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves' disease

Genes and Immunity
2008 | Journal article
DOI: 10.1038/gene.2008.26
Source: Self-asserted source
Matt Simmonds

Genetic developments in autoimmune thyroid disease: An evolutionary process

Clinical Endocrinology
2008 | Journal article
DOI: 10.1111/j.1365-2265.2007.03075.x
Source: Self-asserted source
Matt Simmonds

Phenotypic differences in alpha 1 antitrypsin-deficient sibling pairs may relate to genetic variation

COPD: Journal of Chronic Obstructive Pulmonary Disease
2008 | Journal article
DOI: 10.1080/15412550802522320
Source: Self-asserted source
Matt Simmonds

The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency

Respiratory Research
2008 | Journal article
DOI: 10.1186/1465-9921-9-52
Source: Self-asserted source
Matt Simmonds

A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect

Human Molecular Genetics
2007 | Journal article
DOI: 10.1093/hmg/ddm165
Source: Self-asserted source
Matt Simmonds

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

Nature Genetics
2007 | Journal article
DOI: 10.1038/ng.2007.17
Source: Self-asserted source
Matt Simmonds

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

Nature
2007 | Journal article
DOI: 10.1038/nature06406
Source: Self-asserted source
Matt Simmonds

Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy

Clinical Endocrinology
2007 | Journal article
DOI: 10.1111/j.1365-2265.2007.02942.x
Source: Self-asserted source
Matt Simmonds

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

Nature Genetics
2007 | Journal article
DOI: 10.1038/ng2068
Source: Self-asserted source
Matt Simmonds

Tag SNP screening of the PDCD1 gene for association with Graves' disease

Clinical Endocrinology
2007 | Journal article
DOI: 10.1111/j.1365-2265.2007.02848.x
Source: Self-asserted source
Matt Simmonds

The HLA region and autoimmune disease: Associations and mechanisms of action

Current Genomics
2007 | Journal article
Source: Self-asserted source
Matt Simmonds

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position β74

Clinical Endocrinology
2006 | Journal article
DOI: 10.1111/j.1365-2265.2006.02586.x
Source: Self-asserted source
Matt Simmonds

Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of graves' disease

Journal of Clinical Endocrinology and Metabolism
2006 | Journal article
DOI: 10.1210/jc.2005-1634
Source: Self-asserted source
Matt Simmonds

Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: No association with Graves' disease

Clinical Endocrinology
2006 | Journal article
DOI: 10.1111/j.1365-2265.2006.02608.x
Source: Self-asserted source
Matt Simmonds

IL-13 and chromosome 5q31-q33: Problems of identifying association within regions of linkage to Graves' disease [2]

Clinical Endocrinology
2005 | Journal article
DOI: 10.1111/j.1365-2265.2005.02385.x
Source: Self-asserted source
Matt Simmonds

Regression mapping of association between the human leukocyte antigen region and Graves disease

American Journal of Human Genetics
2005 | Journal article
DOI: 10.1086/426947
Source: Self-asserted source
Matt Simmonds

The CD40 Kozak SNP: A new susceptibility loci for Graves' disease? [2]

Clinical Endocrinology
2005 | Journal article
DOI: 10.1111/j.1365-2265.2005.02305.x
Source: Self-asserted source
Matt Simmonds

A single nucleotide polymorphism in the CD40 gene on chromosome 20q (GD-2) provides no evidence for susceptibility to Graves' disease in UK Caucasians

Clinical Endocrinology
2004 | Journal article
DOI: 10.1111/j.1365-2265.2004.02099.x
Source: Self-asserted source
Matt Simmonds

A systematic approach to the assesment of known TNF-α polymorphisms in Graves' disease

Genes and Immunity
2004 | Journal article
DOI: 10.1038/sj.gene.6364066
Source: Self-asserted source
Matt Simmonds

Genetic insights into disease mechanisms of autoimmunity

British Medical Bulletin
2004 | Journal article
DOI: 10.1093/bmb/ldh032
Source: Self-asserted source
Matt Simmonds
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