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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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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 B₁₂ and the Risk of Neural Tube Defects in a Folic-Acid-Fortified Population

Epidemiology (Cambridge, Mass.), 2007-05, Vol.18 (3), p.362-366

2007

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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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Greater maternal weight and the ongoing risk of neural tube defects after folic acid flour fortification

Obstetrics and gynecology (New York. 1953), 2005-02, Vol.105 (2), p.261-265

2005

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A phase II trial evaluating the palliative benefit of second-line oral ibandronate in breast cancer patients with either a skeletal related event (SRE) or progressive bone metastases (BM) despite standard bisphosphonate (BP) therapy

Breast cancer research and treatment, 2008-03, Vol.108 (1), p.79-85

2008

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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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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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Polymorphisms at the regulatory regions of the CASR gene influence stone risk in primary hyperparathyroidism

European journal of endocrinology, 2011-03, Vol.164 (3), p.421-427

2011

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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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Inherited disorders of renal magnesium handling

Journal of the American Society of Nephrology, 2000-10, Vol.11 (10), p.1937-1947

2000

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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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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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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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Stage Dependence, Cell-Origin Independence, and Prognostic Capacity of Serum Glycan Fucosylation, β1–4 Branching, β1–6 Branching, and α2–6 Sialylation in Cancer

Journal of proteome research, 2018-01, Vol.17 (1), p.543-558

2018

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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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Serum 25-Hydroxyvitamin D Concentrations Fluctuate Seasonally in Young Adults of Diverse Ancestry Living in Toronto

The Journal of nutrition, 2010-12, Vol.140 (12), p.2213-2220

2010

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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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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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G protein-coupled receptor mutations and human genetic disease

Methods in molecular biology (Clifton, N.J.), 2014-01, Vol.1175, p.153

2014

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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

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

Vitamin B₁₂ and the Risk of Neural Tube Defects in a Folic-Acid-Fortified Population

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

Greater maternal weight and the ongoing risk of neural tube defects after folic acid flour fortification

A phase II trial evaluating the palliative benefit of second-line oral ibandronate in breast cancer patients with either a skeletal related event (SRE) or progressive bone metastases (BM) despite standard bisphosphonate (BP) therapy

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

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

Polymorphisms at the regulatory regions of the CASR gene influence stone risk in primary hyperparathyroidism

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

Inherited disorders of renal magnesium handling

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

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

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

Stage Dependence, Cell-Origin Independence, and Prognostic Capacity of Serum Glycan Fucosylation, β1–4 Branching, β1–6 Branching, and α2–6 Sialylation in Cancer

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

Serum 25-Hydroxyvitamin D Concentrations Fluctuate Seasonally in Young Adults of Diverse Ancestry Living in Toronto

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

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

G protein-coupled receptor mutations and human genetic disease

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