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Demographic, dietary, and biochemical determinants of vitamin D status in inner-city children

The American journal of clinical nutrition, 2012-01, Vol.95 (1), p.137-146

2012

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Association of neural tube defects and folic acid food fortification in Canada

The Lancet (British edition), 2002-12, Vol.360 (9350), p.2047-2048

2002

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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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Can bone markers guide more effective treatment of bone metastases from breast cancer?

Breast cancer research and treatment, 2006-05, Vol.97 (1), p.81-90

2006

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Chemical and biomechanical characterization of hyperhomocysteinemic bone disease in an animal model

BMC musculoskeletal disorders, 2003-02, Vol.4 (1), p.2-2, Article 2

2003

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Population BRCA1 and BRCA2 Mutation Frequencies and Cancer Penetrances: A Kin–Cohort Study in Ontario, Canada

JNCI : Journal of the National Cancer Institute, 2006-12, Vol.98 (23), p.1694-1706

2006

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Vitamin D-Related Genetic Variants, Interactions with Vitamin D Exposure, and Breast Cancer Risk among Caucasian Women in Ontario

Cancer epidemiology, biomarkers & prevention, 2011-08, Vol.20 (8), p.1708-1717

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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Genetic Defect in CYP24A1, the Vitamin D 24-Hydroxylase Gene, in a Patient with Severe Infantile Hypercalcemia

The journal of clinical endocrinology and metabolism, 2012-02, Vol.97 (2), p.E268-E274

2012

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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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Serum voriconazole level variability in patients with hematological malignancies receiving voriconazole therapy

The Canadian journal of infectious diseases & medical microbiology, 2014-09, Vol.25 (5), p.271-276

2014

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Metabolic syndrome features and risk of neural tube defects

BMC pregnancy and childbirth, 2007-09, Vol.7 (1), p.21-21, Article 21

2007

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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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Neonatal Hyperparathyroidism with a Heterozygous Calcium-Sensing Receptor (CASR) R185Q Mutation: Clinical Benefit from Cinacalcet

The journal of clinical endocrinology and metabolism, 2011-04, Vol.96 (4), p.E707-E712

2011

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Sporadic and MEN1‐Related Primary Hyperparathyroidism: Differences in Clinical Expression and Severity

Journal of bone and mineral research, 2009-08, Vol.24 (8), p.1404-1410

2009

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Vitamin B-12 and neural tube defects: the Canadian experience

The American journal of clinical nutrition, 2009-02, Vol.89 (2), p.697S-701S

2009

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Type 2 diabetes mellitus and inflammation: Prospects for biomarkers of risk and nutritional intervention

Diabetes, metabolic syndrome and obesity, 2010-05, Vol.3, p.173-186

2010

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Effect of vitamin D–binding protein genotype on the development of asthma in children

Annals of allergy, asthma, & immunology, 2014-06, Vol.112 (6), p.519-524

2014

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Primary Hyperparathyroidism and the Presence of Kidney Stones Are Associated with Different Haplotypes of the Calcium-Sensing Receptor

The journal of clinical endocrinology and metabolism, 2007-01, Vol.92 (1), p.277-283

2007

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Diagnosis of Parathyroid Tumors in Familial Isolated Hyperparathyroidism with HRPT2 Mutation: Implications for Cancer Surveillance

The journal of clinical endocrinology and metabolism, 2006-08, Vol.91 (8), p.2827-2832

2006

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Evidence that vitamin D3 increases serum 25-hydroxyvitamin D more efficiently than does vitamin D2

The American journal of clinical nutrition, 1998-10, Vol.68 (4), p.854-858

1998

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Blood Ionized Calcium Is Associated with Clustered Polymorphisms in the Carboxyl-Terminal Tail of the Calcium-Sensing Receptor

The journal of clinical endocrinology and metabolism, 2004-11, Vol.89 (11), p.5634-5638

2004

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Genetics University of Toronto Thrombophilia Study in Women (GUTTSI): genetic and other risk factors for venous thromboembolism in women

Trials, 2001-01, Vol.2 (3), Article 141

2001

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Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)

American journal of medical genetics. Part A, 2012-03, Vol.158A (3), p.553-558

2012

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Neonatal hyperparathyroidism and pamidronate therapy in an extremely premature infant

Pediatrics (Evanston), 2007-11, Vol.120 (5), p.e1350-e1354

2007

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Demographic, dietary, and biochemical determinants of vitamin D status in inner-city children

Association of neural tube defects and folic acid food fortification in Canada

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

Can bone markers guide more effective treatment of bone metastases from breast cancer?

Chemical and biomechanical characterization of hyperhomocysteinemic bone disease in an animal model

Population BRCA1 and BRCA2 Mutation Frequencies and Cancer Penetrances: A Kin–Cohort Study in Ontario, Canada

Vitamin D-Related Genetic Variants, Interactions with Vitamin D Exposure, and Breast Cancer Risk among Caucasian Women in Ontario

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

Genetic Defect in CYP24A1, the Vitamin D 24-Hydroxylase Gene, in a Patient with Severe Infantile Hypercalcemia

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

Serum voriconazole level variability in patients with hematological malignancies receiving voriconazole therapy

Metabolic syndrome features and risk of neural tube defects

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

Neonatal Hyperparathyroidism with a Heterozygous Calcium-Sensing Receptor (CASR) R185Q Mutation: Clinical Benefit from Cinacalcet

Sporadic and MEN1‐Related Primary Hyperparathyroidism: Differences in Clinical Expression and Severity

Vitamin B-12 and neural tube defects: the Canadian experience

Type 2 diabetes mellitus and inflammation: Prospects for biomarkers of risk and nutritional intervention

Effect of vitamin D–binding protein genotype on the development of asthma in children

Primary Hyperparathyroidism and the Presence of Kidney Stones Are Associated with Different Haplotypes of the Calcium-Sensing Receptor

Diagnosis of Parathyroid Tumors in Familial Isolated Hyperparathyroidism with HRPT2 Mutation: Implications for Cancer Surveillance

Evidence that vitamin D3 increases serum 25-hydroxyvitamin D more efficiently than does vitamin D2

Blood Ionized Calcium Is Associated with Clustered Polymorphisms in the Carboxyl-Terminal Tail of the Calcium-Sensing Receptor

Genetics University of Toronto Thrombophilia Study in Women (GUTTSI): genetic and other risk factors for venous thromboembolism in women

Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)

Neonatal hyperparathyroidism and pamidronate therapy in an extremely premature infant

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