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Association of vitamin D binding protein (VDBP) polymorphisms and serum 25(OH)D concentrations in a sample of young Canadian adults of different ancestry

The Journal of steroid biochemistry and molecular biology, 2011-11, Vol.127 (3), p.405-412

2011

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The causal effect of vitamin D binding protein (DBP) levels on calcemic and cardiometabolic diseases: a Mendelian randomization study

PLoS medicine, 2014-10, Vol.11 (10), p.e1001751

2014

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Calcium-Sensing Receptor (CASR) Mutations in Hypercalcemic States: Studies from a Single Endocrine Clinic Over Three Years

The journal of clinical endocrinology and metabolism, 2010-04, Vol.95 (4), p.1819-1829

2010

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Common variants of the vitamin D binding protein gene and adverse health outcomes

Critical reviews in clinical laboratory sciences, 2013-01, Vol.50 (1), p.1-22

2013

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Common genetic variants of the vitamin D binding protein (DBP) predict differences in response of serum 25-hydroxyvitamin D [25(OH)D] to vitamin D supplementation

Clinical biochemistry, 2009-07, Vol.42 (10), p.1174-1177

2009

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Codon Arg15 Mutations of the AP2S1 Gene: Common Occurrence in Familial Hypocalciuric Hypercalcemia Cases Negative for Calcium-Sensing Receptor (CASR) Mutations

The journal of clinical endocrinology and metabolism, 2014-07, Vol.99 (7), p.E1311-E1315

2014

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In Healthy Adults, Biological Activity of Vitamin D, as Assessed by Serum PTH, Is Largely Independent of DBP Concentrations

Journal of bone and mineral research, 2014-02, Vol.29 (2), p.494-499

2014

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Novel homozygous inactivating mutation of the calcium-sensing receptor gene ( CASR ) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet

Bone (New York, N.Y.), 2014-07, Vol.64, p.102-107

2014

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Phase II Trial Evaluating the Palliative Benefit of Second-Line Zoledronic Acid in Breast Cancer Patients With Either a Skeletal-Related Event or Progressive Bone Metastases Despite First-Line Bisphosphonate Therapy

Journal of clinical oncology, 2006-10, Vol.24 (30), p.4895-4900

2006

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Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused by AP2S1 Mutation

The journal of clinical endocrinology and metabolism, 2015-07, Vol.100 (7), p.2515-2518

2015

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Increased Prevalence of the GCM2 Polymorphism, Y282D, in Primary Hyperparathyroidism: Analysis of Three Italian Cohorts

The journal of clinical endocrinology and metabolism, 2014-12, Vol.99 (12), p.E2794-E2798

2014

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Evaluation of the warfarin-resistance polymorphism, VKORC1 Asp36Tyr, and its effect on dosage algorithms in a genetically heterogeneous anticoagulant clinic

Clinical biochemistry, 2012-04, Vol.45 (6), p.397-401

2012

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Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders

European journal of endocrinology, 2022-03, Vol.186 (3), p.351-366

2022

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Genetic variants in the vitamin D pathway and their association with vitamin D metabolite levels: Detailed studies of an inner-city pediatric population suggest a modest but significant effect in early childhood

The Journal of steroid biochemistry and molecular biology, 2023-10, Vol.233, p.106369-106369, Article 106369

2023

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Mild Infantile Hypercalcemia: Diagnostic Tests and Outcomes

The Journal of pediatrics, 2011-08, Vol.159 (2), p.215-221.e1

2011

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Vitamin D binding protein is a key determinant of 25‐hydroxyvitamin D levels in infants and toddlers

Journal of bone and mineral research, 2013-01, Vol.28 (1), p.213-221

2013

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Whole genome amplification of buccal cell DNA: genotyping concordance before and after multiple displacement amplification

Clinical chemistry and laboratory medicine, 2005-01, Vol.43 (2), p.157-162

2005

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Developing DPYD Genotyping Method for Personalized Fluoropyrimidines Therapy

The journal of applied laboratory medicine, 2024-03, Vol.9 (2), p.295-304

2024

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Calcium-sensing receptor mutations and denaturing high performance liquid chromatography

Journal of molecular endocrinology, 2009-04, Vol.42 (4), p.331-339

2009

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Urinary Vitamin D Binding Protein: A Marker of Kidney Tubular Dysfunction in Patients at Risk for Type 2 Diabetes

Journal of the Endocrine Society, 2024-01, Vol.8 (3), p.bvae014-bvae014

2024

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Transforming growth factor beta-1 (TGFB1) and peak bone mass: association between intragenic polymorphisms and quantitative ultrasound of the heel

BMC musculoskeletal disorders, 2005-06, Vol.6 (1), p.29-29, Article 29

2005

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Characterization of additional vitamin D binding protein variants

The Journal of steroid biochemistry and molecular biology, 2016-05, Vol.159, p.54-59

2016

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Thromboembolism in heart transplantation: role of prothrombin G20210A and factor V Leiden

Transplantation, 2005-09, Vol.80 (5), p.590-594

2005

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Genetic determinants of extracellular magnesium concentration: Analysis of multiple candidate genes, and evidence for association with the estrogen receptor α ( ESR1) locus

Clinica chimica acta, 2009-11, Vol.409 (1), p.28-32

2009

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Genetic variation at the calcium-sensing receptor ( CASR) locus: Implications for clinical molecular diagnostics

Clinical biochemistry, 2007-05, Vol.40 (8), p.551-561

2007

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Association of vitamin D binding protein (VDBP) polymorphisms and serum 25(OH)D concentrations in a sample of young Canadian adults of different ancestry

The causal effect of vitamin D binding protein (DBP) levels on calcemic and cardiometabolic diseases: a Mendelian randomization study

Calcium-Sensing Receptor (CASR) Mutations in Hypercalcemic States: Studies from a Single Endocrine Clinic Over Three Years

Common variants of the vitamin D binding protein gene and adverse health outcomes

Common genetic variants of the vitamin D binding protein (DBP) predict differences in response of serum 25-hydroxyvitamin D [25(OH)D] to vitamin D supplementation

Codon Arg15 Mutations of the AP2S1 Gene: Common Occurrence in Familial Hypocalciuric Hypercalcemia Cases Negative for Calcium-Sensing Receptor (CASR) Mutations

In Healthy Adults, Biological Activity of Vitamin D, as Assessed by Serum PTH, Is Largely Independent of DBP Concentrations

Novel homozygous inactivating mutation of the calcium-sensing receptor gene ( CASR ) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet

Phase II Trial Evaluating the Palliative Benefit of Second-Line Zoledronic Acid in Breast Cancer Patients With Either a Skeletal-Related Event or Progressive Bone Metastases Despite First-Line Bisphosphonate Therapy

Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused by AP2S1 Mutation

Increased Prevalence of the GCM2 Polymorphism, Y282D, in Primary Hyperparathyroidism: Analysis of Three Italian Cohorts

Evaluation of the warfarin-resistance polymorphism, VKORC1 Asp36Tyr, and its effect on dosage algorithms in a genetically heterogeneous anticoagulant clinic

Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders

Genetic variants in the vitamin D pathway and their association with vitamin D metabolite levels: Detailed studies of an inner-city pediatric population suggest a modest but significant effect in early childhood

Mild Infantile Hypercalcemia: Diagnostic Tests and Outcomes

Vitamin D binding protein is a key determinant of 25‐hydroxyvitamin D levels in infants and toddlers

Whole genome amplification of buccal cell DNA: genotyping concordance before and after multiple displacement amplification

Developing DPYD Genotyping Method for Personalized Fluoropyrimidines Therapy

Calcium-sensing receptor mutations and denaturing high performance liquid chromatography

Urinary Vitamin D Binding Protein: A Marker of Kidney Tubular Dysfunction in Patients at Risk for Type 2 Diabetes

Transforming growth factor beta-1 (TGFB1) and peak bone mass: association between intragenic polymorphisms and quantitative ultrasound of the heel

Characterization of additional vitamin D binding protein variants

Thromboembolism in heart transplantation: role of prothrombin G20210A and factor V Leiden

Genetic determinants of extracellular magnesium concentration: Analysis of multiple candidate genes, and evidence for association with the estrogen receptor α ( ESR1) locus

Genetic variation at the calcium-sensing receptor ( CASR) locus: Implications for clinical molecular diagnostics

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