M. Fraser

发表

Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases

J. Ragoussis, A. Monaco, C. Wise, 2006, Human mutation.

Multiple sclerosis in sibling pairs: an analysis of 250 families

D. Clayton, S. Sawcer, A. Compston, 2001, Journal of neurology, neurosurgery, and psychiatry.

The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen.

P. Goodfellow, D. Clayton, S. Sawcer, 1998, Brain : a journal of neurology.

Age-adjusted recurrence risks for relatives of patients with multiple sclerosis.

D. Clayton, D. Compston, N. Robertson, 1996, Brain : a journal of neurology.

Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study.

A. Monaco, C. Dobson-Stone, L. Lonie, 2004, The Journal of bone and joint surgery. British volume.

Hereditary multiple exostoses: a qualitative study exploring families’ and patients’ perceptions of disease impact and self-expressed needs

D. Porter, M. Fraser, 2000 .

The frequency, longitudinal course, clinical associations, and causes of emotional distress during primary treatment of cerebral glioma.

A. Carson, S. McNamara, R. Grant, 2013, Neuro-oncology.

Screening for major depressive disorder in adults with cerebral glioma: an initial validation of 3 self-report instruments.

A. Carson, S. McNamara, R. Grant, 2013, Neuro-oncology.

Clinical concordance in sibling pairs with multiple sclerosis

D. Clayton, N. Robertson, D. Clayton, 1996, Neurology.

Transcript specific regulation of expression influences susceptibility to multiple sclerosis

M. Ban, S. Sawcer, A. Compston, 2019, European Journal of Human Genetics.

Frequency, clinical associations, and longitudinal course of major depressive disorder in adults with cerebral glioma.

A. Carson, S. McNamara, R. Grant, 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Screening for major depressive disorder in adults with glioma using the PHQ-9: a comparison of patient versus proxy reports

A. Carson, S. McNamara, R. Grant, 2013, Journal of Neuro-Oncology.

Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses

Carol Dobson-Stone, Maria Fraser, Lorraine Southam, 2000, European Journal of Human Genetics.

Multiple sclerosis in south Cambridgeshire: incidence and prevalence based on a district register.

D. Compston, N. Robertson, J. Deans, 1996, Journal of epidemiology and community health.

Multiple sclerosis in the north Cambridgeshire districts of East Anglia.

D. Compston, N. Robertson, J. Deans, 1995, Journal of neurology, neurosurgery, and psychiatry.

Multiple sclerosis in the Cambridge health district of east Anglia.

N. Wood, D. Compston, C. Mumford, 1992, Journal of neurology, neurosurgery, and psychiatry.