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Nutritional ecogenetics : Homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid

American journal of human genetics, 1996, Vol.58 (1), p.17-20

MOTULSKY, A. G

1996

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Hereditary hemochromatosis: gene discovery and its implications for population-based screening

JAMA : the journal of the American Medical Association, 1998-07, Vol.280 (2), p.172

1998

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Preventing coronary heart disease: B vitamins and homocysteine

Circulation (New York, N.Y.), 1998-02, Vol.97 (5), p.421-424

1998

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A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

JAMA : the journal of the American Medical Association, 1995-10, Vol.274 (13), p.1049

1995

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Genetically determined apo B levels and peak LDL density predict angiographic response to intensive lipid‐lowering therapy

Journal of internal medicine, 2006-04, Vol.259 (4), p.401-409

2006

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Jewish diseases and origins

Nature genetics, 1995-02, Vol.9 (2), p.99-101

Motulsky, Arno G

1995

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Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype

Nature genetics, 1999-05, Vol.22 (1), p.90-93

1999

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Pleiotropic genetic effects on LDL size, plasma triglyceride, and HDL cholesterol in families

Arteriosclerosis, thrombosis, and vascular biology, 1999-10, Vol.19 (10), p.2456-2464

1999

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Cardiovascular disease mortality in familial forms of hypertriglyceridemia : A 20-year prospective study

Circulation (New York, N.Y.), 2000-06, Vol.101 (24), p.2777-2782

2000

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Visual Pigment Gene Structure and Expression in Human Retinae

Human molecular genetics, 1997-07, Vol.6 (7), p.981-990

1997

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Screening for Genetic Diseases

The New England journal of medicine, 1997-05, Vol.336 (18), p.1314-1316

Motulsky, Arno G

1997

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The glutathione S-transferase μ polymorphism as a marker for susceptibility to lung carcinoma

Cancer research (Chicago, Ill.), 1993-05, Vol.53 (10), p.2313-2318

1993

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Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon

American journal of human genetics, 1988-09, Vol.43 (3), p.230-238

1988

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The advent of the 'unpatients'

Nature medicine, 1996-06, Vol.2 (6), p.622-624

1996

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Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia

Arteriosclerosis, thrombosis, and vascular biology, 2003-07, Vol.23 (7), p.1289-1294

2003

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Severity of color vision defects: electroretinographic (ERG), molecular and behavioral studies

Vision research (Oxford), 1998-11, Vol.38 (21), p.3377-3385

1998

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Analysis of red/green color discrimination in subjects with a single X-linked photopigment gene

Vision research (Oxford), 1999-02, Vol.39 (4), p.707-719

1999

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The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes

American journal of human genetics, 1988-01, Vol.42 (1), p.113-124

1988

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Genotype-phenotype relationships in human red/green color-vision defects : molecular and psychophysical studies

American journal of human genetics, 1992-10, Vol.51 (4), p.687-700

1992

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Predictive genetic diagnosis

American journal of human genetics, 1994-10, Vol.55 (4), p.603-605

MOTULSKY, A. G

1994

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Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency

American journal of human genetics, 1992-08, Vol.51 (2), p.291-298

1992

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Molecular Patterns of X Chromosome-Linked Color Vision Genes among 134 Men of European Ancestry

Proceedings of the National Academy of Sciences - PNAS, 1989-02, Vol.86 (3), p.983-987

1989

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Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesterase

Analytical biochemistry, 1989-08, Vol.180 (2), p.242-247

1989

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Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex

Arteriosclerosis, thrombosis, and vascular biology, 1998-02, Vol.18 (2), p.215-226

1998

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Selective Expression of Human X Chromosome-Linked Green Opsin Genes

Proceedings of the National Academy of Sciences - PNAS, 1992-10, Vol.89 (20), p.9710-9714

1992

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Nutritional ecogenetics : Homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid

Hereditary hemochromatosis: gene discovery and its implications for population-based screening

Preventing coronary heart disease: B vitamins and homocysteine

A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

Genetically determined apo B levels and peak LDL density predict angiographic response to intensive lipid‐lowering therapy

Jewish diseases and origins

Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype

Pleiotropic genetic effects on LDL size, plasma triglyceride, and HDL cholesterol in families

Cardiovascular disease mortality in familial forms of hypertriglyceridemia : A 20-year prospective study

Visual Pigment Gene Structure and Expression in Human Retinae

Screening for Genetic Diseases

The glutathione S-transferase μ polymorphism as a marker for susceptibility to lung carcinoma

Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon

The advent of the 'unpatients'

Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia

Severity of color vision defects: electroretinographic (ERG), molecular and behavioral studies

Analysis of red/green color discrimination in subjects with a single X-linked photopigment gene

The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes

Genotype-phenotype relationships in human red/green color-vision defects : molecular and psychophysical studies

Predictive genetic diagnosis

Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency

Molecular Patterns of X Chromosome-Linked Color Vision Genes among 134 Men of European Ancestry

Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesterase

Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex

Selective Expression of Human X Chromosome-Linked Green Opsin Genes

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