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Transcription factor 7-like 2 polymorphisms and type 2 diabetes, glucose homeostasis traits and gene expression in US participants of European and African descent

Diabetologia, 2007-08, Vol.50 (8), p.1621-1630

2007

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A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians

Diabetes (New York, N.Y.), 1999-05, Vol.48 (5), p.1175

1999

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Quantitative trait linkage analysis of lipid-related traits in familial type 2 diabetes: Evidence for linkage of triglyceride levels to chromosome 19q

Diabetes (New York, N.Y.), 2002-02, Vol.51 (2), p.528-535

2002

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Genetic variants associated with protein C levels

Journal of thrombosis and haemostasis, 2013-04, Vol.11 (4), p.715-723

2013

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Genome scan of venous thrombosis in a pedigree with protein C deficiency

Journal of thrombosis and haemostasis, 2004-06, Vol.2 (6), p.868-873

2004

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Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C‐deficient family

Journal of thrombosis and haemostasis, 2004-02, Vol.2 (2), p.242-247

2004

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Type 2 Diabetes Susceptibility Genes on Chromosome 1q21–24

Annals of human genetics, 2008-03, Vol.72 (2), p.163-169

2008

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Is there a link between African iron overload and the described mutations of the hereditary haemochromatosis gene?

British journal of haematology, 1998-09, Vol.102 (5), p.1176-1178

1998

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Evaluation of apolipoprotein A-II as a positional candidate gene for familial Type II diabetes, altered lipid concentrations, and insulin resistance

Diabetologia, 2002-07, Vol.45 (7), p.1026-1033

2002

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Iron overload in Africa: Interaction between a gene and dietary iron content

The New England journal of medicine, 1992-01, Vol.326 (2), p.95-100

1992

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Evidence of Genetic Transmission in African Iron Overload

Blood, 1998-02, Vol.91 (3), p.1076-1082

1998

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Complex segregation analysis of autism

American journal of human genetics, 1991-11, Vol.49 (5), p.932-938

1991

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HLA-linked rheumatoid arthritis

American journal of human genetics, 1994-10, Vol.55 (4), p.738-746

1994

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Heritability of pancreatic β-cell function among nondiabetic members of caucasian familial type 2 diabetic kindreds

The journal of clinical endocrinology and metabolism, 1999-04, Vol.84 (4), p.1398-1403

1999

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A genome search for genetic determinants of markers of protein C activation

Journal of thrombosis and haemostasis, 2006-03, Vol.4 (3), p.706-708

2006

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Genetic Basis of Familial Dyslipidemia and Hypertension: 15-Year Results From Utah

American journal of hypertension, 1993-11, Vol.6 (11-Pt-2), p.319S-327S

1993

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Characterization of the human prostaglandin H synthase 1 gene (PTGS1): exclusion by genetic linkage analysis as a second modifier gene in familial thrombosis

Blood coagulation & fibrinolysis, 2002-09, Vol.13 (6), p.519-531

2002

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A Gene for High Urinary Kallikrein May Protect Against Hypertension in Utah Kindreds

Hypertension (Dallas, Tex. 1979), 1989-01, Vol.13 (1), p.3-8

1989

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GENETIC HERITABILITY AND COMMON ENVIRONMENTAL COMPONENTS OF RESTING AND STRESSED BLOOD PRESSURES, LIPIDS, AND BODY MASS INDEX IN UTAH PEDIGREES AND TWINS

American journal of epidemiology, 1989-03, Vol.129 (3), p.625-638

1989

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Intermediate inheritance of Tourette syndrome, assuming assortative mating

American journal of human genetics, 1995-09, Vol.57 (3), p.682-689

1995

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Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred

Thrombosis and haemostasis, 2001-01, Vol.85 (1), p.82

2001

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Genome scan of clot lysis time and its association with thrombosis in a protein C‐deficient kindred

Journal of thrombosis and haemostasis, 2011-07, Vol.9 (7), p.1383-1390

2011

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An Unknown Genetic Defect Increases Venous Thrombosis Risk, through Interaction with Protein C Deficiency

American journal of human genetics, 1998-08, Vol.63 (2), p.569-576

1998

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Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides

Human genetics, 2005-09, Vol.117 (5), p.444-451

2005

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Hypertension and sodium-lithium countertransport in Utah pedigrees: evidence for major-locus inheritance

American journal of human genetics, 1988-07, Vol.43 (1), p.14-22

1988

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Transcription factor 7-like 2 polymorphisms and type 2 diabetes, glucose homeostasis traits and gene expression in US participants of European and African descent

A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians

Quantitative trait linkage analysis of lipid-related traits in familial type 2 diabetes: Evidence for linkage of triglyceride levels to chromosome 19q

Genetic variants associated with protein C levels

Genome scan of venous thrombosis in a pedigree with protein C deficiency

Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C‐deficient family

Type 2 Diabetes Susceptibility Genes on Chromosome 1q21–24

Is there a link between African iron overload and the described mutations of the hereditary haemochromatosis gene?

Evaluation of apolipoprotein A-II as a positional candidate gene for familial Type II diabetes, altered lipid concentrations, and insulin resistance

Iron overload in Africa: Interaction between a gene and dietary iron content

Evidence of Genetic Transmission in African Iron Overload

Complex segregation analysis of autism

HLA-linked rheumatoid arthritis

Heritability of pancreatic β-cell function among nondiabetic members of caucasian familial type 2 diabetic kindreds

A genome search for genetic determinants of markers of protein C activation

Genetic Basis of Familial Dyslipidemia and Hypertension: 15-Year Results From Utah

Characterization of the human prostaglandin H synthase 1 gene (PTGS1): exclusion by genetic linkage analysis as a second modifier gene in familial thrombosis

A Gene for High Urinary Kallikrein May Protect Against Hypertension in Utah Kindreds

GENETIC HERITABILITY AND COMMON ENVIRONMENTAL COMPONENTS OF RESTING AND STRESSED BLOOD PRESSURES, LIPIDS, AND BODY MASS INDEX IN UTAH PEDIGREES AND TWINS

Intermediate inheritance of Tourette syndrome, assuming assortative mating

Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred

Genome scan of clot lysis time and its association with thrombosis in a protein C‐deficient kindred

An Unknown Genetic Defect Increases Venous Thrombosis Risk, through Interaction with Protein C Deficiency

Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides

Hypertension and sodium-lithium countertransport in Utah pedigrees: evidence for major-locus inheritance

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