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A randomized trial of a strategy for increasing high-density lipoprotein cholesterol levels: effects on progression of coronary heart disease and clinical events

Annals of internal medicine, 2005-01, Vol.142 (2), p.95

2005

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Validating and assessing the sensitivity of the Health Assessment Questionnaire-Disability Index-derived Short Form-6D in patients with early aggressive rheumatoid arthritis

Journal of rheumatology, 2009-06, Vol.36 (6), p.1150-1157

2009

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Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson’s disease cohort

Journal of neurology, neurosurgery and psychiatry, 2006-05, Vol.77 (5), p.665-667

2006

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Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease

Journal of neurology, 2007-07, Vol.254 (7), p.846-848

2007

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A genome screen for linkage in Australian sibling-pairs with multiple sclerosis

Genes and immunity, 2002-12, Vol.3 (8), p.464-469

2002

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Novel Olig1‐coding variants and susceptibility to multiple sclerosis

Journal of neurology, neurosurgery and psychiatry, 2006-11, Vol.77 (11), p.1296-1297

2006

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A High-Density Screen for Linkage in Multiple Sclerosis

American journal of human genetics, 2005-09, Vol.77 (3), p.454-467

2005

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Crohn’s associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis

Journal of neurology, neurosurgery and psychiatry, 2003-08, Vol.74 (8), p.1157-1157

2003

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A genome wide linkage disequilibrium screen in Parkinson's disease

Journal of neurology, 2005-05, Vol.252 (5), p.597-602

2005

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Evidence for a Type 1 diabetes-specific mechanism for the insulin gene-associated IDDM2 locus rather than a general influence on autoimmunity

Diabetic medicine, 2004-03, Vol.21 (3), p.267-270

2004

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A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility

Brain (London, England : 1878), 2002-06, Vol.125 (Pt 6), p.1337-1347

2002

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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

Human molecular genetics, 2004-09, Vol.13 (17), p.1943-1949

2004

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CD24 Ala/Val polymorphism and multiple sclerosis

Journal of neuroimmunology, 2006-06, Vol.175 (1), p.200-202

2006

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No evidence of a significant role for CTLA-4 in multiple sclerosis

Journal of neuroimmunology, 2006-02, Vol.171 (1), p.193-197

2006

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Cytochrome P450 2D6 variants and their association with breast cancer survival

Cancer research (Chicago, Ill.), 2009-01, Vol.69 (2_Supplement), p.3089

2009

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Feasibility and Construct Validity of PROMIS and “Legacy” Instruments in an Academic Scleroderma Clinic

Value in health, 2012-01, Vol.15 (1), p.128-134

2012

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Four single nucleotide polymorphisms from the vitamin D receptor gene in UK multiple sclerosis

Journal of neurology, 2004-06, Vol.251 (6), p.753-754

2004

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SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis

Neuroscience letters, 2006-02, Vol.394 (2), p.92-96

2006

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Novel Olig 1-coding variants and susceptibility to multiple sclerosis

Journal of neurology, neurosurgery and psychiatry, 2006-11, Vol.77 (11), p.1296-1297

2006

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No alterations in α-synuclein gene dosage observed in sporadic Parkinson's disease

Movement disorders, 2006-05, Vol.21 (5), p.731-732

2006

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Ultraconserved regions in multiple sclerosis

European journal of human genetics : EJHG, 2005-09, Vol.13 (9), p.998-999, Article 998

2005

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Refining the analysis of a whole genome linkage disequilibrium association map: the United Kingdom results

Journal of neuroimmunology, 2003-10, Vol.143 (1), p.53-59

2003

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From association to cause: fine mapping of the TNRC9gene region, a novel susceptibility locus identified in the first genome-wide association study for breast cancer

Breast cancer research : BCR, 2008-05, Vol.10 (S2), Article P49

2008

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Glycoprotein IIb/IIIa receptor inhibitor-thrombolytic combination therapy for acute myocardial infarction

Current cardiology reports, 2002-07, Vol.4 (4), p.313-319

2002

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From association to cause: fine mapping of the TNRC9 gene region, a novel susceptibility locus identified in the first genome-wide association study for breast cancer

Breast cancer research : BCR, 2008, Vol.10 Suppl 2 (Suppl 2), p.P49-P49

2008

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A randomized trial of a strategy for increasing high-density lipoprotein cholesterol levels: effects on progression of coronary heart disease and clinical events

Validating and assessing the sensitivity of the Health Assessment Questionnaire-Disability Index-derived Short Form-6D in patients with early aggressive rheumatoid arthritis

Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson’s disease cohort

Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease

A genome screen for linkage in Australian sibling-pairs with multiple sclerosis

Novel Olig1‐coding variants and susceptibility to multiple sclerosis

A High-Density Screen for Linkage in Multiple Sclerosis

Crohn’s associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis

A genome wide linkage disequilibrium screen in Parkinson's disease

Evidence for a Type 1 diabetes-specific mechanism for the insulin gene-associated IDDM2 locus rather than a general influence on autoimmunity

A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

CD24 Ala/Val polymorphism and multiple sclerosis

No evidence of a significant role for CTLA-4 in multiple sclerosis

Cytochrome P450 2D6 variants and their association with breast cancer survival

Feasibility and Construct Validity of PROMIS and “Legacy” Instruments in an Academic Scleroderma Clinic

Four single nucleotide polymorphisms from the vitamin D receptor gene in UK multiple sclerosis

SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis

Novel Olig 1-coding variants and susceptibility to multiple sclerosis

No alterations in α-synuclein gene dosage observed in sporadic Parkinson's disease

Ultraconserved regions in multiple sclerosis

Refining the analysis of a whole genome linkage disequilibrium association map: the United Kingdom results

From association to cause: fine mapping of the TNRC9gene region, a novel susceptibility locus identified in the first genome-wide association study for breast cancer

Glycoprotein IIb/IIIa receptor inhibitor-thrombolytic combination therapy for acute myocardial infarction

From association to cause: fine mapping of the TNRC9 gene region, a novel susceptibility locus identified in the first genome-wide association study for breast cancer

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