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GENETICALLY ELEVATED LOW-DENSITY LIPOPROTEIN CHOLESTEROL IS ASSOCIATED WITH AORTIC VALVE CALCIFICATION AND INCIDENT AORTIC STENOSIS: A MENDELIAN RANDOMIZATION STUDY

Canadian journal of cardiology, 2014-10, Vol.30 (10), p.S257-S257

2014

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381 HERITABILITY PATTERNS IN HAND OSTEOARTHRITIS: THE GHOST STUDY

Osteoarthritis and cartilage, 2010, Vol.18, p.S167-S168

2010

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Coincident linkage of fasting plasma insulin and blood pressure to chromosome 7q in hypertensive Hispanic families

Circulation (New York, N.Y.), 2001-09, Vol.104 (11), p.1255-1260

2001

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Associations of pentraxin 3 with cardiovascular disease: the Multi‐Ethnic Study of Atherosclerosis

Journal of thrombosis and haemostasis, 2014-06, Vol.12 (6), p.999-1005

2014

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Association of plasma lipids and apolipoproteins with the insulin response element in the apoC-III promoter region in familial combined hyperlipidemia

Journal of lipid research, 1999-06, Vol.40 (6), p.1036-1044

1999

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P4469Transcriptome-wide gene expression analysis identifies novel associations with blood pressure

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism

Diabetologia, 2012-02, Vol.55 (2), p.331-339

2012

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Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner

The pharmacogenomics journal, 2016-06, Vol.16 (3), p.301-301

2016

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Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q

Nature (London), 1994-09, Vol.371 (6493), p.161-164

1994

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Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

Nature (London), 1991-11, Vol.354 (6349), p.155-159

1991

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HLA class II haplotype associations with inflammatory bowel disease in Jewish (Ashkenazi) and non-Jewish Caucasian populations

Human immunology, 2000-03, Vol.61 (3), p.326-333

2000

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X Chromosome-Linked and Mitochondrial Gene Control of Leber Hereditary Optic Neuropathy: Evidence from Segregation Analysis for Dependence on X Chromosome Inactivation

Proceedings of the National Academy of Sciences - PNAS, 1991-09, Vol.88 (18), p.8198-8202

1991

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An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29

Genes and immunity, 2008-03, Vol.9 (2), p.161-167

2008

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Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A

International Journal of Obesity, 2000-11, Vol.24 (11), p.1381-1391

2000

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Insulin sensitivity, body fat distribution, and family diabetes history: the IRAS family study

Obesity (Silver Spring, Md.), 2004-05, Vol.12 (5), p.831-839

2004

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Families with Familial Combined Hyperlipidemia and Families Enriched for Coronary Artery Disease Share Genetic Determinants for the Atherogenic Lipoprotein Phenotype

American journal of human genetics, 1998-08, Vol.63 (2), p.577-585

1998

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Intestinal permeability in patients with Crohn's disease and their healthy relatives

Gastroenterology (New York, N.Y. 1943), 1989-10, Vol.97 (4), p.927-931

1989

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Wolfram syndrome: a mitochondrial-mediated disorder?

The Lancet (British edition), 1993-09, Vol.342 (8871), p.598-600

1993

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Calpain-10: A Genetic Determinant of Both Diabetes and Atherosclerosis

Journal of investigative medicine, 2004-01, Vol.52 (1_suppl_part_3), p.152-152

2004

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BRCA testing uptake and participation in ovarian cancer prevention in women at risk for an inherited ovarian cancer susceptibility

Genetics in medicine, 2000-01, Vol.2 (1), p.86

2000

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Linkage of blood pressure to a locus on chromosome 4 in dutch dyslipidemic famiilies

Atherosclerosis, 2000-07, Vol.151 (1), p.90-90

2000

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Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in familial combined hyperlipidemia

Journal of lipid research, 1999-11, Vol.41 (2)

1999

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A familial risk profile for osteoporosis

Genetics in medicine, 2000-07, Vol.2 (4), p.222-225

2000

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Genetic and metabolic influences on LDL subclasses

Atherosclerosis, 1994-09, Vol.109 (1), p.351-351

1994

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Evidence for Linkage of the Apolipoprotein A-II Locus to Plasma Apolipoprotein A-II and Free Fatty Acid Levels in Mice and Humans

Proceedings of the National Academy of Sciences - PNAS, 1993-11, Vol.90 (22), p.10886-10890

1993

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GENETICALLY ELEVATED LOW-DENSITY LIPOPROTEIN CHOLESTEROL IS ASSOCIATED WITH AORTIC VALVE CALCIFICATION AND INCIDENT AORTIC STENOSIS: A MENDELIAN RANDOMIZATION STUDY

381 HERITABILITY PATTERNS IN HAND OSTEOARTHRITIS: THE GHOST STUDY

Coincident linkage of fasting plasma insulin and blood pressure to chromosome 7q in hypertensive Hispanic families

Associations of pentraxin 3 with cardiovascular disease: the Multi‐Ethnic Study of Atherosclerosis

Association of plasma lipids and apolipoproteins with the insulin response element in the apoC-III promoter region in familial combined hyperlipidemia

P4469Transcriptome-wide gene expression analysis identifies novel associations with blood pressure

Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism

Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q

Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

HLA class II haplotype associations with inflammatory bowel disease in Jewish (Ashkenazi) and non-Jewish Caucasian populations

X Chromosome-Linked and Mitochondrial Gene Control of Leber Hereditary Optic Neuropathy: Evidence from Segregation Analysis for Dependence on X Chromosome Inactivation

An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A

Insulin sensitivity, body fat distribution, and family diabetes history: the IRAS family study

Families with Familial Combined Hyperlipidemia and Families Enriched for Coronary Artery Disease Share Genetic Determinants for the Atherogenic Lipoprotein Phenotype

Intestinal permeability in patients with Crohn's disease and their healthy relatives

Wolfram syndrome: a mitochondrial-mediated disorder?

Calpain-10: A Genetic Determinant of Both Diabetes and Atherosclerosis

BRCA testing uptake and participation in ovarian cancer prevention in women at risk for an inherited ovarian cancer susceptibility

Linkage of blood pressure to a locus on chromosome 4 in dutch dyslipidemic famiilies

Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in familial combined hyperlipidemia

A familial risk profile for osteoporosis

Genetic and metabolic influences on LDL subclasses

Evidence for Linkage of the Apolipoprotein A-II Locus to Plasma Apolipoprotein A-II and Free Fatty Acid Levels in Mice and Humans

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