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Ethnicity, plasma phospholipid fatty acid composition and inflammatory/endothelial activation biomarkers in the Multi-Ethnic Study of Atherosclerosis (MESA)

European journal of clinical nutrition, 2012-05, Vol.66 (5), p.600-605

2012

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Obesity modifies the association between plasma phospholipid polyunsaturated fatty acids and markers of inflammation: the Multi-Ethnic Study of Atherosclerosis

International Journal of Obesity, 2012-06, Vol.36 (6), p.797-804

2012

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High prevalence of a mutation in the cystathionine β-synthase gene

American journal of human genetics, 1996-12, Vol.59 (6), p.1262-1267

1996

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Circulating cellular adhesion molecules and risk of diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA)

Diabetic medicine, 2016-07, Vol.33 (7), p.985-991

2016

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Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases

Atherosclerosis, 1999-03, Vol.143 (1), p.163-170

1999

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C677T and A1298C Polymorphisms of the Methylenetetrahydrofolate Reductase Gene: Incidence and Effect of Combined Genotypes on Plasma Fasting and Post-Methionine Load Homocysteine in Vascular Disease

Clinical chemistry (Baltimore, Md.), 2001-04, Vol.47 (4), p.661-666

2001

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Influence of 699C→T and 1080C→T polymorphisms of the cystathionine β-synthase gene on plasma homocysteine levels

Clinical genetics, 2000-12, Vol.58 (6), p.455-459

2000

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Deletion polymorphism of the angiotensin I converting enzyme gene is a potent risk factor for coronary artery ectasia

Heart (British Cardiac Society), 2003-02, Vol.89 (2), p.213-214

2003

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Endothelial nitric oxide gene polymorphism (Glu298Asp) is not associated with coronary artery disease in Turkish population

Thrombosis and haemostasis, 2002-02, Vol.87 (2), p.347

2002

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Cystatin C Is an Independent Predictor of Fasting and Post-Methionine Load Total Homocysteine Concentrations among Stable Renal Transplant Recipients

Clinical chemistry (Baltimore, Md.), 2001-07, Vol.47 (7), p.1263-1268

2001

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Molecular and biochemical approaches in the identification of heterozygotes for homocystinuria

Atherosclerosis, 1996-04, Vol.122 (1), p.69-77

1996

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Polygenic influence on plasma homocysteine: association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels

Atherosclerosis, 2000-03, Vol.149 (1), p.131-137

2000

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Amplification refractory mutation system to identify mutations in cystathionine beta-synthase deficiency

Clinical chemistry (Baltimore, Md.), 1995-12, Vol.41 (12 Pt 1), p.1775

1995

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Simple and rapid method for extraction of DNA from fresh and cryopreserved clotted human blood

Clinical chemistry (Baltimore, Md.), 1996-04, Vol.42 (4), p.647-648

1996

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MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis

JAMA : the journal of the American Medical Association, 2002-10, Vol.288 (16), p.2023

2002

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Relation between Plasma Homocysteine Concentration, the 844ins68 Variant of the Cystathionine β-Synthase Gene, and Pyridoxal-5′-Phosphate Concentration

Molecular genetics and metabolism, 1999-08, Vol.67 (4), p.352-356

1999

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Determination of a T/G polymorphism at nucleotide 3206 of the apolipoprotein C III gene by amplification refractory mutation system

Clinical chemistry (Baltimore, Md.), 1994-12, Vol.40 (12), p.2235

1994

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Enzymic measurement of total bile acids adapted to the Cobas Fara centrifugal analyzer

Clinical chemistry (Baltimore, Md.), 1989-07, Vol.35 (7), p.1538

1989

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Polygenic influence on plasma homocysteine : association of two prevalent mutations, the 844ins68 of cystathionine β-synthase and A2756G of methionine synthase, with lowered plasma homocysteine levels

Atherosclerosis, 2000-03, Vol.149 (1), p.131-137

2000

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Short-term variability in the measurement of plasma homocysteine, fasting and post-methionine loading

Clinical biochemistry, 2001-02, Vol.34 (1), p.49-52

2001

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Nephelometric assay of apolipoprotein A-I with a centrifugal analyzer

Clinical chemistry (Baltimore, Md.), 1986-11, Vol.32 (11), p.2090

1986

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Electrophoresis on cellulose acetate and chromatography on DEAE-sephadex A-50 compared in the estimation of creatine kinase isoenzymes

Clinical chemistry (Baltimore, Md.), 1975-03, Vol.21 (3), p.381

1975

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Prevalence of nonclassical congenital adrenal hyperplasia among women self-referred for electrolytic treatment of hirsutism

American journal of medical genetics, 1992-01, Vol.42 (2), p.197-200

1992

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Immunonephelometry of apolipoprotein B with a centrifugal analyzer

Clinical chemistry (Baltimore, Md.), 1987-10, Vol.33 (10), p.1882

1987

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Ethnicity, plasma phospholipid fatty acid composition and inflammatory/endothelial activation biomarkers in the Multi-Ethnic Study of Atherosclerosis (MESA)

Obesity modifies the association between plasma phospholipid polyunsaturated fatty acids and markers of inflammation: the Multi-Ethnic Study of Atherosclerosis

High prevalence of a mutation in the cystathionine β-synthase gene

Circulating cellular adhesion molecules and risk of diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA)

Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases

C677T and A1298C Polymorphisms of the Methylenetetrahydrofolate Reductase Gene: Incidence and Effect of Combined Genotypes on Plasma Fasting and Post-Methionine Load Homocysteine in Vascular Disease

Influence of 699C→T and 1080C→T polymorphisms of the cystathionine β-synthase gene on plasma homocysteine levels

Deletion polymorphism of the angiotensin I converting enzyme gene is a potent risk factor for coronary artery ectasia

Endothelial nitric oxide gene polymorphism (Glu298Asp) is not associated with coronary artery disease in Turkish population

Cystatin C Is an Independent Predictor of Fasting and Post-Methionine Load Total Homocysteine Concentrations among Stable Renal Transplant Recipients

Molecular and biochemical approaches in the identification of heterozygotes for homocystinuria

Polygenic influence on plasma homocysteine: association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels

Amplification refractory mutation system to identify mutations in cystathionine beta-synthase deficiency

Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias

Simple and rapid method for extraction of DNA from fresh and cryopreserved clotted human blood

MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis

Relation between Plasma Homocysteine Concentration, the 844ins68 Variant of the Cystathionine β-Synthase Gene, and Pyridoxal-5′-Phosphate Concentration

Determination of a T/G polymorphism at nucleotide 3206 of the apolipoprotein C III gene by amplification refractory mutation system

Enzymic measurement of total bile acids adapted to the Cobas Fara centrifugal analyzer

Polygenic influence on plasma homocysteine : association of two prevalent mutations, the 844ins68 of cystathionine β-synthase and A2756G of methionine synthase, with lowered plasma homocysteine levels

Short-term variability in the measurement of plasma homocysteine, fasting and post-methionine loading

Nephelometric assay of apolipoprotein A-I with a centrifugal analyzer

Electrophoresis on cellulose acetate and chromatography on DEAE-sephadex A-50 compared in the estimation of creatine kinase isoenzymes

Prevalence of nonclassical congenital adrenal hyperplasia among women self-referred for electrolytic treatment of hirsutism

Immunonephelometry of apolipoprotein B with a centrifugal analyzer

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