J. Hewitt

P. Schofield, J. Kwok, K. Kirkby, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Loss of epigenetic silencing of the DUX4 transcription factor gene in facioscapulohumeral muscular dystrophy.

J. Hewitt, 2015, Human molecular genetics.

Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis

R. Lyle, M. Ehrlich, G. Gilfillan, 2012, European Journal of Human Genetics.

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei

M. Ehrlich, U. Bengtsson, Jennifer T. Stocksdale, 2010, European Journal of Human Genetics.

Mutation of Large, which encodes a putative glycosyltransferase, in an animal model of muscular dystrophy.

J. Hewitt, P. Grewal, 2002, Biochimica et biophysica acta.

Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders.

H. Lassmann, H. Hoeger, J. Hewitt, 2002, Human molecular genetics.

A search for genes in the facioscapulohumeral muscular dystrophy region.

R. Frants, J. Hewitt, J. V. van Deutekom, 1996, Biochemical Society transactions.

Post-translational modification of {alpha}-dystroglycan is not critical for lymphocytic choriomeningitis virus receptor function in vivo.

A. Oxenius, J. Hewitt, M. Imperiali, 2008, The Journal of general virology.

Identification of the autoantigen SART-1 as a candidate gene for the development of atopy.

I. Hall, A. Wheatley, J. Hewitt, 2002, Human molecular genetics.

SF4 and SFRS14, two related putative splicing factors on human chromosome 19p13.11.

J. Hewitt, Natalie D Sampson, 2003, Gene.

Evolution of DUX gene macrosatellites in placental mammals

Leopoldo Iannuzzi, J. Hewitt, L. Iannuzzi, 2012, Chromosoma.

Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element.

H. Ding, R. Frants, J. Hewitt, 1999, Gene.

Abnormal glycosylation of dystroglycan in human genetic disease.

J. Hewitt, 2009, Biochimica et biophysica acta.

Dystroglycan glycosylation and muscular dystrophy

J. Hewitt, Christopher J Moore, 2009, Glycoconjugate Journal.

Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies.

J. Hewitt, P. Grewal, C. Browning, 2005, Glycobiology.

The FSHD‐linked locus D4F104S1 (p13E‐11) ON 4q35 has a homologue on 10qter

C. Wijmenga, R. Vossen, E. Bakker, 1995, Muscle & nerve. Supplement.

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

C. Wijmenga, R. Frants, J. Hewitt, 1994, Genomics.

Intron loss in the SART1 genes of Fugu rubripes and Tetraodon nigroviridis.

J E Hewitt, J. Hewitt, D. Bolland, 2001, Gene.

A family history of DUX4 : Phylogenetic analysis of DUXA, B, C and Duxbl reveals the ancestral DUX gene

J. Hewitt, A. Leidenroth, 2011 .

A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patients

Susan C. Brown, J. Hewitt, C. Sewry, 2015, Neuromuscular Disorders.

Glycoproteomic characterization of recombinant mouse α-dystroglycan.

P. Hitchen, A. Dell, H. Morris, 2012, Glycobiology.

Defects in Glycosylation Impair Satellite Stem Cell Function and Niche Composition in the Muscles of the Dystrophic Largemyd Mouse

Susan C. Brown, F. Muntoni, J. Hewitt, 2012, Stem cells.

Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse

J. Hewitt, P. Grewal, R. Bittner, 2001, Nature Genetics.

A rapid PCR method for genotyping the Largemyd mouse, a model of glycosylation-deficient congenital muscular dystrophy

J. Hewitt, P. Grewal, C. Browning, 2005, Neuromuscular Disorders.

Glycosylation defects: a new mechanism for muscular dystrophy?

J. Hewitt, P. Grewal, P. K. Grewal, 2003, Human molecular genetics.

Molecular genetics of facioscapulohumeral muscular dystrophy

C. Wijmenga, R. Frants, J. Hewitt, 1993, Neuromuscular Disorders.

Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements.

C. Wijmenga, J. Farnham, P. Harper, 1993, Human molecular genetics.

Kuo, Cheng-Liang and Lam, Chi Man and Hewitt, Jane E. and Scotting, Paul J. (2013) Formation of the embryonic organizer is restricted by the competitive influences of Fgf signaling and the SoxB1 transcription

J. Hewitt, P. Scotting, Chi Man Lam, 2017 .

Formation of the Embryonic Organizer Is Restricted by the Competitive Influences of Fgf Signaling and the SoxB1 Transcription Factors

J. Hewitt, P. Scotting, C. Kuo, 2013, PloS one.

Genetic Analysis of Glucokinase and the Chromosome 20 Diabetes Susceptibility Locus in Families with Type 2 Diabetes

D. Johnston, R. Williamson, J. Hewitt, 1994, Diabetic medicine : a journal of the British Diabetic Association.

An alternatively spliced transcript, p65 delta 2, of the gene encoding the p65 subunit of the transcription factor NF-kappa B.

R. Lyle, J. Hewitt, P. Sharpe, 1994, Gene.

LARGE enzyme activity deciphered: a new therapeutic target for muscular dystrophies

J. Hewitt, 2012, Genome Medicine.

The mysterious role of LARGE in muscular dystrophies

J. Hewitt, 2012 .

A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)

L. Sandkuijl, E. Bakker, R. Frants, 1999, Journal of medical genetics.

MS screening strategies: investigating the glycomes of knockout and myodystrophic mice and leukodystrophic human brains.

Raphael Schiffmann, Mark Sutton-Smith, Anne Dell, 2002, Biochemical Society symposium.