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Elite endurance athletes and the ACE I allele : the role of genes in athletic performance

Human genetics, 1998-07, Vol.103 (1), p.48-50

1998

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Molecular medicine: an introductory text

Trent, R.J

3rd ed., 2005

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Regional Specificity of Brain Atrophy in Huntington's Disease

Experimental neurology, 1998-12, Vol.154 (2), p.663-672

1998

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Molecular Medicine: Genomics to Personalized Healthcare

Trent, R. J

4th ed., 2012

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Genetically confirmed clinical Huntington’s disease with no observable cell loss

Journal of neurology, neurosurgery and psychiatry, 2003-07, Vol.74 (7), p.968-970

2003

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The Impact of the Austronesian Expansion: Evidence from mtDNA and Y Chromosome Diversity in the Admiralty Islands of Melanesia

Molecular biology and evolution, 2008-07, Vol.25 (7), p.1362-1374

2008

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Warfarin for non-rheumatic atrial fibrillation: five year experience in a district general hospital

Heart (British Cardiac Society), 2004-11, Vol.90 (11), p.1259-1262

2004

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Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease

Journal of clinical pathology, 2005-05, Vol.58 (5), p.479-485

2005

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Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy

Circulation research, 1997-03, Vol.80 (3), p.427-434

1997

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Gene therapy in sport

British journal of sports medicine, 2006-01, Vol.40 (1), p.4-5

2006

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Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion

Journal of medical genetics, 1996-02, Vol.33 (2), p.107-112

1996

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Frequency of cytochrome P450 3A4 variant genotype in transplant population and lack of association with cyclosporin clearance

European journal of clinical pharmacology, 2000-08, Vol.56 (5), p.395-398

2000

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EGFR mutant-specific immunohistochemistry has high specificity and sensitivity for detecting targeted activating EGFR mutations in lung adenocarcinoma

Journal of clinical pathology, 2013-09, Vol.66 (9), p.744-748

2013

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Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene

Journal of medical genetics, 1998-03, Vol.35 (3), p.205-210

1998

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Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

American journal of medical genetics, 2003-06, Vol.119A (3), p.279-282

2003

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Troponin I, laboratory issues, and clinical outcomes in a district general hospital: crossover study with “traditional” markers of myocardial infarction in a total of 1990 patients

Journal of clinical pathology, 2004-10, Vol.57 (10), p.1027-1032

2004

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Aortic distensibility and stiffness index measured by magnetic resonance imaging in patients with Marfan's syndrome

British Heart Journal, 1995-03, Vol.73 (3), p.265-269

1995

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Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy

Journal of medical genetics, 1997-05, Vol.34 (5), p.426-429

1997

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Polymorphisms in the CAG repeat - a source of error in Huntington disease DNA testing

Clinical genetics, 2000-12, Vol.58 (6), p.469-472

2000

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Aortic complications of Marfan's syndrome

The Lancet (British edition), 1998-11, Vol.352 (9142), p.1722-1723

1998

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Dobutamine magnetic resonance imaging as a predictor of myocardial functional recovery after revascularisation

Heart (British Cardiac Society), 2000-01, Vol.83 (1), p.40-46

2000

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Gene therapy: applications and progress towards the clinic

Internal medicine journal, 2004-11, Vol.34 (11), p.621-625

2004

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Risk stratification after acute myocardial infarction by Doppler stroke distance measurement

Heart (British Cardiac Society), 1999-08, Vol.82 (2), p.187-191

1999

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Frequency of cytochrome P 450 3A4 variant genotype in transplant population and lack of association with cyclosporin clearance

European journal of clinical pharmacology, 2000-08, Vol.56 (5), p.395-398

2000

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Cystic fibrosis genotypes and alcoholic pancreatitis

Journal of gastroenterology and hepatology, 1998-05, Vol.13 (5), p.496-499

1998

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Elite endurance athletes and the ACE I allele : the role of genes in athletic performance

Molecular medicine: an introductory text

Regional Specificity of Brain Atrophy in Huntington's Disease

Molecular Medicine: Genomics to Personalized Healthcare

Genetically confirmed clinical Huntington’s disease with no observable cell loss

The Impact of the Austronesian Expansion: Evidence from mtDNA and Y Chromosome Diversity in the Admiralty Islands of Melanesia

Warfarin for non-rheumatic atrial fibrillation: five year experience in a district general hospital

Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease

Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy

Gene therapy in sport

Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion

Frequency of cytochrome P450 3A4 variant genotype in transplant population and lack of association with cyclosporin clearance

EGFR mutant-specific immunohistochemistry has high specificity and sensitivity for detecting targeted activating EGFR mutations in lung adenocarcinoma

Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

Troponin I, laboratory issues, and clinical outcomes in a district general hospital: crossover study with “traditional” markers of myocardial infarction in a total of 1990 patients

Aortic distensibility and stiffness index measured by magnetic resonance imaging in patients with Marfan's syndrome

Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy

Polymorphisms in the CAG repeat - a source of error in Huntington disease DNA testing

Aortic complications of Marfan's syndrome

Dobutamine magnetic resonance imaging as a predictor of myocardial functional recovery after revascularisation

Gene therapy: applications and progress towards the clinic

Risk stratification after acute myocardial infarction by Doppler stroke distance measurement

Frequency of cytochrome P 450 3A4 variant genotype in transplant population and lack of association with cyclosporin clearance

Cystic fibrosis genotypes and alcoholic pancreatitis

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