Publications by authors named "Timothy G Barrett"

43Publications

Empowering youth sport environments: Implications for daily moderate-to-vigorous physical activity and adiposity.

J Sport Health Sci 2017 Dec 31;6(4):423-433. Epub 2016 Mar 31.

School of Clinical and Experimental Medicine, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

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December 2017

Treatment adherence and BMI reduction are key predictors of HbA1c 1 year after diagnosis of childhood type 2 diabetes in the United Kingdom.

Pediatr Diabetes 2018 12 11;19(8):1393-1399. Epub 2018 Oct 11.

NIHR Biomedical Research Centre: Nutrition, Diet and Lifestyle Theme, School of Oral and Dental Sciences, University of Bristol, Bristol, UK.

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December 2018

Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model.

Dis Model Mech 2017 12 19;10(12):1411-1420. Epub 2017 Dec 19.

The University of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Cambridge, CB2 0QQ, UK

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December 2017

Refining genotype-phenotype correlation in Alström syndrome through study of primary human fibroblasts.

Mol Genet Genomic Med 2017 Jul 15;5(4):390-404. Epub 2017 May 15.

Wellcome Trust-MRC Institute of Metabolic ScienceUniversity of CambridgeCambridgeUK.

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July 2017

Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty.

J Clin Endocrinol Metab 2016 06 22;101(6):2545-53. Epub 2016 Mar 22.

Institutes of Metabolism and Systems Research (J.I., A.E.T., S.S., D.M.O., C.H.L.S., W.A.) and Cancer and Genomic Sciences (T.G.B.), University of Birmingham, Birmingham B15 2TT, United Kingdom; Centres for Endocrinology, Diabetes and Metabolism (J.I., A.E.T., R.P.D., T.G.B., C.H.L.S., J.M.W.K., W.A.) and Rare Diseases and Personalised Medicine (T.G.B.), Birmingham Health Partners, Birmingham B15 2TH, United Kingdom; Departments of Paediatric Endocrinology and Diabetes (J.I., R.P.D., T.G.B., J.M.W.K.) and Paediatric Dermatology (C.M.), Birmingham Children's Hospital National Health Service Foundation Trust, Birmingham B4 6NH, United Kingdom; MRC-Holland bv (R.V.), 1057-DN Amsterdam, The Netherlands; Department of Paediatric Endocrinology (R.A.), Great Ormond St Hospital for Children, London WC1N 3JH, United Kingdom; and Benioff Children's Hospital (C.H.L.S.), University of California San Francisco, Oakland, California 94609.

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June 2016

A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.

Endocr Res 2015 20;40(3):146-50. Epub 2014 Oct 20.

Department of Medical Genetics, Bahcesehir University School of Medicine , Istanbul , Turkey .

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April 2016

One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism.

J Clin Res Pediatr Endocrinol 2014 Sep;6(3):169-73

Bahçeşehir University Faculty of Medicine, Department of Medical Genetics, İstanbul, Turkey. E-ma-il:

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September 2014

Novel truncating thyroglobulin gene mutations associated with congenital hypothyroidism.

Endocrine 2014 Mar 15;45(2):206-12. Epub 2013 Aug 15.

Department of Medical Genetics, Bahcesehir University School of Medicine, Istanbul, Turkey,

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March 2014

Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing.

J Med Genet 2013 Sep 28;50(9):635-9. Epub 2013 Jun 28.

Centre for Rare Diseases and Personalised Medicine, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.

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September 2013

Clinical utility gene card for: Alström Syndrome - update 2013.

Eur J Hum Genet 2013 Nov 24;21(11). Epub 2013 Apr 24.

The Jackson Laboratory, Bar Harbor, ME, USA.

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November 2013

Vacuolar-type H+-ATPase V1A subunit is a molecular partner of Wolfram syndrome 1 (WFS1) protein, which regulates its expression and stability.

Hum Mol Genet 2013 Jan 3;22(2):203-17. Epub 2012 Oct 3.

Section of Medical and Molecular Genetics, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

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January 2013

Premature adrenarche: novel lessons from early onset androgen excess.

Eur J Endocrinol 2011 Aug 26;165(2):189-207. Epub 2011 May 26.

School of Clinical and Experimental Medicine, Centre for Endocrinology, Diabetes and Metabolism, University of Birmingham, Birmingham B15 2TT, UK.

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August 2011

Clinical utility gene card for: Alström syndrome.

Eur J Hum Genet 2011 Oct 27;19(10). Epub 2011 Apr 27.

The Jackson Laboratory, Bar Harbor, ME, USA.

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October 2011

Hearing impairment in genotyped Wolfram syndrome patients.

Ann Otol Rhinol Laryngol 2008 Jul;117(7):494-500

Department of Otorhinolaryngology, Radboud University Nijmegen Medical Center, Nijmegen, the Netherlands.

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July 2008

Sodium-potassium ATPase 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress.

Hum Mol Genet 2008 Jan 18;17(2):190-200. Epub 2007 Oct 18.

Section of Medical and Molecular Genetics, The Medical School, University of Birmingham, Birmingham B15 2TT, UK.

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January 2008

Rising incidence of type 2 diabetes in children in the U.K.

Diabetes Care 2007 May 26;30(5):1097-101. Epub 2007 Jan 26.

Research Division, Royal College of Paediatrics and Child Health, London, UK.

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May 2007

The Birmingham Registry for Twin and Heritability Studies (BiRTHS).

Twin Res Hum Genet 2006 Dec;9(6):907-12

Unit of Genetic Epidemiology, Department of Public Health and Epidemiology, University of Birmingham, Birmingham, UK.

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December 2006

The emergence of type 2 diabetes in childhood.

Ann Clin Biochem 2004 Jan;41(Pt 1):10-6

Diabetes Homecare Unit, Birmingham Children's Hospital, Birmingham B4 6NH, UK.

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January 2004

[Report of a Brazilian patient with Wolfram Syndrome].

J Pediatr (Rio J) 2002 Nov-Dec;78(6):529-32

Genética Clínica, Fundação Faculdade Federal de Ciências Médicas de Porto Alegre, RS.

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February 2004

Wolfram syndrome.

Rev Endocr Metab Disord 2003 Mar;4(1):53-9

Medical and Molecular Genetics, The Medical School, University of Birmingham, Edgbaston, Birmingham B15 2TG, UK.

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March 2003