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Validation of variants in SLC28A3 and UGT1A6 as genetic markers predictive of anthracycline-induced cardiotoxicity in children

Pediatric blood & cancer, 2013-08, Vol.60 (8), p.1375-1381

2013

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Enhanced immune response to MMP3 stimulation in microglia expressing mutant huntingtin

Neuroscience, 2016-06, Vol.325, p.74-88

2016

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The emerging era of pharmacogenomics: current successes, future potential, and challenges

Clinical genetics, 2014-07, Vol.86 (1), p.21-28

2014

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Developing a comprehensive, effective patient-friendly website to enhance decision making in predictive testing for Huntington disease

Genetics in medicine, 2013-06, Vol.15 (6), p.466-472

2013

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Mutations in ABCA8 underlie reduced plasma high density cholesterol levels in humans

Atherosclerosis, 2015-07, Vol.241 (1), p.e23-e24

2015

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Physicochemical, biological, functional and toxicological characterization of the European follow-on glatiramer acetate product as compared with Copaxone

eNeurologicalSci, 2018-09, Vol.12, p.19-30

2018

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A true mentor and pioneer in medical genetics : legacy

South African medical journal, 2016-06, Vol.106 (sup-1), p.7-9

Hayden, M.R.

2016

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Glutamate receptor abnormalities in the YAC128 transgenic mouse model of Huntington’s disease

Neuroscience, 2007-06, Vol.147 (2), p.354-372

2007

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Plasma apolipoprotein AV levels in mice are positively associated with plasma triglyceride levels

Journal of lipid research, 2009-05, Vol.50 (5), p.880-884

2009

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Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract

Nature genetics, 1996-08, Vol.13 (4), p.442-449

1996

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Phosphate Metabolism in Cardiorenal Metabolic Disease

Cardiorenal medicine, 2011-01, Vol.1 (4), p.261-270

2011

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Evidence-based genetic counselling implications for Huntington disease intermediate allele predictive test results

Clinical genetics, 2014-04, Vol.85 (4), p.303-311

2014

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Personalized gene silencing therapeutics for Huntington disease

Clinical genetics, 2014-07, Vol.86 (1), p.29-36

2014

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Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin

The pharmacogenomics journal, 2012-06, Vol.12 (3), p.233-237

2012

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DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence

Human molecular genetics, 1994-12, Vol.3 (12), p.2103-2114

1994

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Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent

Human molecular genetics, 1993-10, Vol.2 (10), p.1535-1540

1993

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Magnetic resonance spectroscopy biomarkers in premanifest and early Huntington disease

Neurology, 2010-11, Vol.75 (19), p.1702

2010

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Variations on a Gene: Rare and Common Variants in ABCA1 and Their Impact on HDL Cholesterol Levels and Atherosclerosis

Annual review of nutrition, 2006-01, Vol.26 (1), p.105-129

2006

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Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles)

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-01, Vol.153B (1), p.314-320

2010

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role of free fatty acids, pancreatic lipase and Ca²⁺ signalling in injury of isolated acinar cells and pancreatitis model in lipoprotein lipase-deficient mice

Acta Physiologica, 2009, Vol.195 (1), p.13-28

2009

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Higher frequency of genetic variants conferring increased risk for ADRs for commonly used drugs treating cancer, AIDS and tuberculosis in persons of African descent

The pharmacogenomics journal, 2014-04, Vol.14 (2), p.160-170

2014

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A novel microdeletion affecting the CETP gene raises HDL-associated cholesterol levels

Clinical genetics, 2016-04, Vol.89 (4), p.495-500

2016

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Two novel mutations in apolipoprotein C3 underlie atheroprotective lipid profiles in families

Clinical genetics, 2014-05, Vol.85 (5), p.433-440

2014

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Use of genetic technologies to compare medicines

Clinical genetics, 2014-11, Vol.86 (5), p.441-446

2014

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Erratum

Trends in cardiovascular medicine, 2010-04, Vol.20 (3), p.108

2010

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Validation of variants in SLC28A3 and UGT1A6 as genetic markers predictive of anthracycline-induced cardiotoxicity in children

Enhanced immune response to MMP3 stimulation in microglia expressing mutant huntingtin

The emerging era of pharmacogenomics: current successes, future potential, and challenges

Developing a comprehensive, effective patient-friendly website to enhance decision making in predictive testing for Huntington disease

Mutations in ABCA8 underlie reduced plasma high density cholesterol levels in humans

Physicochemical, biological, functional and toxicological characterization of the European follow-on glatiramer acetate product as compared with Copaxone

A true mentor and pioneer in medical genetics : legacy

Glutamate receptor abnormalities in the YAC128 transgenic mouse model of Huntington’s disease

Plasma apolipoprotein AV levels in mice are positively associated with plasma triglyceride levels

Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract

Phosphate Metabolism in Cardiorenal Metabolic Disease

Evidence-based genetic counselling implications for Huntington disease intermediate allele predictive test results

Personalized gene silencing therapeutics for Huntington disease

Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin

DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence

Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent

Magnetic resonance spectroscopy biomarkers in premanifest and early Huntington disease

Variations on a Gene: Rare and Common Variants in ABCA1 and Their Impact on HDL Cholesterol Levels and Atherosclerosis

Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles)

role of free fatty acids, pancreatic lipase and Ca²⁺ signalling in injury of isolated acinar cells and pancreatitis model in lipoprotein lipase-deficient mice

Higher frequency of genetic variants conferring increased risk for ADRs for commonly used drugs treating cancer, AIDS and tuberculosis in persons of African descent

A novel microdeletion affecting the CETP gene raises HDL-associated cholesterol levels

Two novel mutations in apolipoprotein C3 underlie atheroprotective lipid profiles in families

Use of genetic technologies to compare medicines

Erratum

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