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Influence of CYP2C9 and VKORC1 1173C/T Genotype on the Risk of Hemorrhagic Complications in African‐American and European‐American Patients on Warfarin

Clinical pharmacology and therapeutics, 2008-02, Vol.83 (2), p.312-321

2008

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Influence of CYP2C9 and VKORC1 on warfarin response during initiation of therapy

Blood cells, molecules, & diseases, 2009-07, Vol.43 (1), p.119-128

2009

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DMPK-associated myotonic dystrophy and CTG repeats in Alabama African Americans

Clinical genetics, 2007-11, Vol.72 (5), p.448-453

2007

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Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease

The American journal of clinical nutrition, 1994-04, Vol.59 (4), p.940-948

1994

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A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study

Clinical genetics, 2007-06, Vol.71 (6), p.518-529

2007

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Racial differences in the prevalence of Factor V Leiden mutation among patients on chronic warfarin therapy

Blood cells, molecules, & diseases, 2006-09, Vol.37 (2), p.100-106

2006

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Fibromyalgia in 300 adult index patients with primary immunodeficiency

Clinical and experimental rheumatology, 2017-05, Vol.35 Suppl 105 (3), p.68

2017

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Vibrio vulnificus Infection in a Hemodialysis Patient Receiving Intravenous Iron Therapy

Clinical infectious diseases, 2003-09, Vol.37 (5), p.e63-e67

2003

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Genetic association of 11β-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks

Hypertension (Dallas, Tex. 1979), 1996-09, Vol.28 (3), p.478-482

1996

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Variability of the pancreatic islet beta cell/liver (GLUT 2) glucose transporter gene in NIDDM patients

Diabetologia, 1994-04, Vol.37 (4), p.420-427

1994

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Associations of MHC genes with levels of caries-inducing organisms and caries severity in African-American women

Human immunology, 1999-10, Vol.60 (10), p.984-989

1999

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Glucokinase gene in gestational diabetes mellitus : population association study and molecular scanning

Diabetologia, 1994, Vol.37 (1), p.104-110

1994

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Relationships of serum free thyroxine and erythrocyte measures in euthyroid HFE C282Y homozygotes and control subjects: the HEIRS Study

International journal of laboratory hematology, 2010-06, Vol.32 (3), p.282-287

2010

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Toxicity of methotrexate in rheumatoid arthritis

Journal of rheumatology, 1987-02, Vol.14 (1), p.74

1987

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Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics

Academic medicine, 2000-08, Vol.75 (8), p.850-852

2000

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Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative

American journal of medical genetics, 2000-12, Vol.96 (6), p.823-830

2000

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Restriction fragment length polymorphism analysis of HLA-DR, DQ, DP and C4 alleles in Caucasians with systemic lupus erythematosus

Journal of rheumatology, 1991-01, Vol.18 (1), p.14

1991

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Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls

American journal of medical genetics, 2001-05, Vol.105 (4), p.332-342

2001

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Genes within and flanking the major histocompatibility region are risk factors for diabetes, insulin resistance, hypertension, and microalbuminuria in African-American women

Transplantation proceedings, 1997-12, Vol.29 (8), p.3710-3712

1997

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A positive association between maternal serum zinc concentration and birth weight

The American journal of clinical nutrition, 1990-04, Vol.51 (4), p.678-684

1990

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Influence of CYP2C9 Genotype on Warfarin Dose Among African–Americans and European–Americans

Personalized medicine, 2007-05, Vol.4 (2), p.157-169

2007

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Increased prevalence of mitral valve prolapse in IDDM

Diabetes care, 1996-06, Vol.19 (6), p.672

1996

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SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family

American journal of medical genetics, 1995-02, Vol.60 (1), p.12-18

1995

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Genes within the major histocompatibility complex predict NIDDM in African-American women in Alabama

Diabetes care, 1994-12, Vol.17 (12), p.1491

1994

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Concordance of 21-hydroxylase gene ratio, human leukocyte antigen haplotyping and adrenal testing results in a family with late-onset adrenal hyperplasia

Journal of reproductive medicine, 1993-08, Vol.38 (8), p.615

1993

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Influence of CYP2C9 and VKORC1 1173C/T Genotype on the Risk of Hemorrhagic Complications in African‐American and European‐American Patients on Warfarin

Influence of CYP2C9 and VKORC1 on warfarin response during initiation of therapy

DMPK-associated myotonic dystrophy and CTG repeats in Alabama African Americans

Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease

A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study

Racial differences in the prevalence of Factor V Leiden mutation among patients on chronic warfarin therapy

Fibromyalgia in 300 adult index patients with primary immunodeficiency

Vibrio vulnificus Infection in a Hemodialysis Patient Receiving Intravenous Iron Therapy

Genetic association of 11β-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks

Variability of the pancreatic islet beta cell/liver (GLUT 2) glucose transporter gene in NIDDM patients

Associations of MHC genes with levels of caries-inducing organisms and caries severity in African-American women

Glucokinase gene in gestational diabetes mellitus : population association study and molecular scanning

Relationships of serum free thyroxine and erythrocyte measures in euthyroid HFE C282Y homozygotes and control subjects: the HEIRS Study

Toxicity of methotrexate in rheumatoid arthritis

Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics

Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative

Restriction fragment length polymorphism analysis of HLA-DR, DQ, DP and C4 alleles in Caucasians with systemic lupus erythematosus

Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls

Genes within and flanking the major histocompatibility region are risk factors for diabetes, insulin resistance, hypertension, and microalbuminuria in African-American women

A positive association between maternal serum zinc concentration and birth weight

Influence of CYP2C9 Genotype on Warfarin Dose Among African–Americans and European–Americans

Increased prevalence of mitral valve prolapse in IDDM

SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family

Genes within the major histocompatibility complex predict NIDDM in African-American women in Alabama

Concordance of 21-hydroxylase gene ratio, human leukocyte antigen haplotyping and adrenal testing results in a family with late-onset adrenal hyperplasia

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