Association of vitamin D binding protein (VDBP) polymorphisms and serum 25(OH)D concentrations in a sample of young Canadian adults of different ancestry von Gozdzik, Agnes, Zhu, Justin, Wong, Betty Y.-L., Fu, Lei, Cole, David E.C., Parra, Esteban J.

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The causal effect of vitamin D binding protein (DBP) levels on calcemic and cardiometabolic diseases: a Mendelian randomization study von Leong, Aaron, Rehman, Waheed, Dastani, Zari, Greenwood, Celia, Timpson, Nicholas, Langsetmo, Lisa, Berger, Claudie, Fu, Lei, Wong, Betty Y L, Malik, Suneil, Malik, Rainer, Hanley, David A, Cole, David E C, Goltzman, David, Richards, J Brent

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Calcium-Sensing Receptor (CASR) Mutations in Hypercalcemic States: Studies from a Single Endocrine Clinic Over Three Years von Guarnieri, Vito, Canaff, Lucie, Yun, Francisco H. J, Scillitani, Alfredo, Battista, Claudia, Muscarella, Lucia A, Wong, Betty Y. L, Notarangelo, Angelantonio, D'Agruma, Leonardo, Sacco, Michele, Cole, David E. C, Hendy, Geoffrey N

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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 von Fu, Lei, Yun, Francisco, Oczak, Marko, Wong, Betty Y.L., Vieth, Reinhold, Cole, David E.C.

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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 von Hendy, Geoffrey N, Canaff, Lucie, Newfield, Ron S, Tripto-Shkolnik, Liana, Wong, Betty Y. L, Lee, Bonnie S. P, Cole, David E. C

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In Healthy Adults, Biological Activity of Vitamin D, as Assessed by Serum PTH, Is Largely Independent of DBP Concentrations von Dastani, Zari, Berger, Claudie, Langsetmo, Lisa, Fu, Lei, Wong, Betty YL, Malik, Suneil, Goltzman, David, Cole, David E, Richards, J Brent

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Novel homozygous inactivating mutation of the calcium-sensing receptor gene ( CASR ) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet von Atay, Zeynep, Bereket, Abdullah, Haliloglu, Belma, Abali, Saygin, Ozdogan, Tutku, Altuncu, Emel, Canaff, Lucie, Vilaça, Tatiane, Wong, Betty Y.L, Cole, David E.C, Hendy, Geoffrey N, Turan, Serap

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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 Despit... von CLEMONS, Mark J, DRANITSARIS, George, OOI, Wei S, YOGENDRAN, Geetha, SUKOVIC, Tatjana, WONG, Betty Y. L, VERMA, Sunil, PRITCHARD, Kathleen I, TRUDEAU, Maureen, COLE, David E. C

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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 von Tenhola, Sirpa, Hendy, Geoffrey N, Valta, Helena, Canaff, Lucie, Lee, Bonnie S. P, Wong, Betty Y. L, Välimäki, Matti J, Cole, David E. C, Mäkitie, Outi

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Increased Prevalence of the GCM2 Polymorphism, Y282D, in Primary Hyperparathyroidism: Analysis of Three Italian Cohorts von D'Agruma, Leonardo, Coco, Michela, Guarnieri, Vito, Battista, Claudia, Canaff, Lucie, Salcuni, Antonio S, Corbetta, Sabrina, Cetani, Filomena, Minisola, Salvatore, Chiodini, Iacopo, Eller-Vainicher, Cristina, Spada, Anna, Marcocci, Claudio, Guglielmi, Giuseppe, Zini, Michele, Clemente, Rosanna, Wong, Betty Y. L, de Martino, Danilo, Scillitani, Alfredo, Hendy, Geoffrey N, Cole, David E. C

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Evaluation of the warfarin-resistance polymorphism, VKORC1 Asp36Tyr, and its effect on dosage algorithms in a genetically heterogeneous anticoagulant clinic von Shuen, Andrew Y., Wong, Betty Y.L., Fu, Lei, Selby, Rita, Cole, David E.C.

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Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders von Canaff, Lucie, Guarnieri, Vito, Kim, Yoojung, Wong, Betty Y L, Nolin-Lapalme, Alexis, Cole, David E C, Minisola, Salvatore, Eller-Vainicher, Cristina, Cetani, Filomena, Repaci, Andrea, Turchetti, Daniela, Corbetta, Sabrina, Scillitani, Alfredo, Goltzman, David

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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 signif... von Fu, Lei, Wong, Betty Y.L., Li, Zhenyu, Horst, Ronald L., Williams, Rashida, Lee, Bonnie, Miller, Jessica, Carpenter, Thomas O., Cole, David E.C.

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Mild Infantile Hypercalcemia: Diagnostic Tests and Outcomes von Koltin, Dror, MD, Rachmiel, Marianna, MD, Wong, Betty Y.L., MD, Cole, David E.C., MD, Harvey, Elizabeth, MD, Sochett, Etienne, MD

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Vitamin D binding protein is a key determinant of 25‐hydroxyvitamin D levels in infants and toddlers von Carpenter, Thomas O, Zhang, Jane H, Parra, Esteban, Ellis, Bruce K, Simpson, Christine, Lee, William M, Balko, Jody, Fu, Lei, Wong, Betty Y‐L, Cole, David EC

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Whole genome amplification of buccal cell DNA: genotyping concordance before and after multiple displacement amplification von Thompson, Miles D., Bowen, Raffick A. R., Wong, Betty Y. L., Antal, Joan, Liu, Zhanqin, Yu, Helen, Siminovitch, Katherine, Kreiger, Nancy, Rohan, Tom E., Cole, David E. C.

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Developing DPYD Genotyping Method for Personalized Fluoropyrimidines Therapy von Wong, Betty Y L, Li, Zhenyu, Raphael, Michael Jonathon, De Angelis, Carlo, Hwang, David M, Fu, Lei

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Calcium-sensing receptor mutations and denaturing high performance liquid chromatography von Cole, David E C, Yun, Francisco H J, Wong, Betty Y L, Shuen, Andrew Y, Booth, Ronald A, Scillitani, Alfredo, Pidasheva, Svetlana, Zhou, Xiang, Canaff, Lucie, Hendy, Geoffrey N

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Urinary Vitamin D Binding Protein: A Marker of Kidney Tubular Dysfunction in Patients at Risk for Type 2 Diabetes von Semnani-Azad, Zhila, Wang, Windy Z N, Cole, David E C, Johnston, Luke W, Wong, Betty Y L, Fu, Lei, Retnakaran, Ravi, Harris, Stewart B, Hanley, Anthony J

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Transforming growth factor beta-1 (TGFB1) and peak bone mass: association between intragenic polymorphisms and quantitative ultrasound of the heel von Tzakas, Peter, Wong, Betty Y L, Logan, Alexander G, Rubin, Laurence A, Cole, David E C

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