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A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin

American journal of human genetics, 2016-05, Vol.98 (5), p.869-882

2016

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Pharmacy Student Perceptions of a Virtual Pharmacogenomics Activity

Healthcare (Basel), 2022-02, Vol.10 (2), p.286

2022

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Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Proceedings of the National Academy of Sciences - PNAS, 2013-01, Vol.110 (2), p.588-593

2013

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Efficacy of personal pharmacogenomic testing as an educational tool in the pharmacy curriculum: A nonblinded, randomized controlled trial

Clinical and translational science, 2021-11, Vol.14 (6), p.2532-2543

2021

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Gene Expression Profiling of Transporters in the Solute Carrier and ATP-Binding Cassette Superfamilies in Human Eye Substructures

Molecular pharmaceutics, 2013-02, Vol.10 (2), p.650-663

2013

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Organic Anion Transporter 2 (SLC22A7) Is a Facilitative Transporter of cGMP

Molecular pharmacology, 2008-04, Vol.73 (4), p.1151-1158

2008

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Interprofessional Pharmacokinetics Simulation: Pharmacy and Nursing Students' Perceptions

Pharmacy, 2018-07, Vol.6 (3), p.70

2018

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The Impact of African Ancestry on Prostate Cancer Disparities in the Era of Precision Medicine

Genes, 2020-12, Vol.11 (12), p.1471

2020

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Genome‐wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21‐q22

International journal of cancer, 2011-11, Vol.129 (10), p.2400-2407

2011

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Racial disparities and treatment trends among young-onset colorectal cancer patients: An analysis of a hospital cancer registry

Cancer epidemiology, 2021-06, Vol.72, p.101911, Article 101911

2021

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A Genetics-Focused Lens on Social Constructs in Pharmacy Education

American journal of pharmaceutical education, 2023-09, Vol.87 (9), p.100077-100077, Article 100077

2023

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Revisiting HER2 in Prostate Cancer from an Inclusive Perspective: From Biomarkers to Omics

Cancers, 2024-09, Vol.16 (19), p.3262

2024

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The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population

The American journal of clinical nutrition, 2018-12, Vol.108 (6), p.1334-1341

2018

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Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

Genetics (Austin), 2014-07, Vol.197 (3), p.1039-1044

2014

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The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation

Human molecular genetics, 2017-12, Vol.26 (24), p.4975-4988

2017

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Reduced Renal Clearance of Cefotaxime in Asians with a Low-Frequency Polymorphism of OAT3 (SLC22A8)

Journal of pharmaceutical sciences, 2013-09, Vol.102 (9), p.3451-3457

2013

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ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available

Genetic epidemiology, 2019-02, Vol.43 (1), p.102-111

2019

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Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults

The Journal of nutrition, 2015-07, Vol.145 (7), p.1386-1393

2015

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8q24 risk alleles and prostate cancer in African-Barbadian men

The Prostate, 2014-12, Vol.74 (16), p.1579-1588

2014

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Racial Disparities in the Association Between Variants on 8q24 and Prostate Cancer: A Systematic Review and Meta‐Analysis

The oncologist (Dayton, Ohio), 2012-03, Vol.17 (3), p.312-320

2012

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SLCO1B1 variants and urine arsenic metabolites in the Strong Heart Family Study

Toxicological sciences, 2013-11, Vol.136 (1), p.19-25

2013

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Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis

European journal of human genetics : EJHG, 2013-04, Vol.21 (4), p.437-443

2013

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Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data

BMC proceedings, 2016, Vol.10 (Suppl 7), p.147-152, Article 52

2016

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False-positive rates in two-point parametric linkage analysis

BMC proceedings, 2014-06, Vol.8 (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo), p.S110-S110, Article S110

2014

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Abstract C050: Deleterious coding variants in African American Hereditary Prostate Cancer Study (AAHPC) families

Cancer epidemiology, biomarkers & prevention, 2020-06, Vol.29 (6_Supplement_1), p.C050-C050

2020

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A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin

Pharmacy Student Perceptions of a Virtual Pharmacogenomics Activity

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Efficacy of personal pharmacogenomic testing as an educational tool in the pharmacy curriculum: A nonblinded, randomized controlled trial

Gene Expression Profiling of Transporters in the Solute Carrier and ATP-Binding Cassette Superfamilies in Human Eye Substructures

Organic Anion Transporter 2 (SLC22A7) Is a Facilitative Transporter of cGMP

Interprofessional Pharmacokinetics Simulation: Pharmacy and Nursing Students' Perceptions

The Impact of African Ancestry on Prostate Cancer Disparities in the Era of Precision Medicine

Genome‐wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21‐q22

Racial disparities and treatment trends among young-onset colorectal cancer patients: An analysis of a hospital cancer registry

A Genetics-Focused Lens on Social Constructs in Pharmacy Education

Revisiting HER2 in Prostate Cancer from an Inclusive Perspective: From Biomarkers to Omics

The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation

Reduced Renal Clearance of Cefotaxime in Asians with a Low-Frequency Polymorphism of OAT3 (SLC22A8)

ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available

Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults

8q24 risk alleles and prostate cancer in African-Barbadian men

Racial Disparities in the Association Between Variants on 8q24 and Prostate Cancer: A Systematic Review and Meta‐Analysis

SLCO1B1 variants and urine arsenic metabolites in the Strong Heart Family Study

Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis

Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data

False-positive rates in two-point parametric linkage analysis

Abstract C050: Deleterious coding variants in African American Hereditary Prostate Cancer Study (AAHPC) families

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