Cobalamin deficiency in elderly patients

per Ray, Joel G., Cole, David E.C.
Publicat 2005

Vitamin B(12) and homocysteine

per Ray, Joel G., Cole, David E.C.
Publicat 2005

Ruling in a Suspect: The Role of AP2S1 Mutations in Familial Hypocalciuric Hypercalcemia Type 3

per Hendy, Geoffrey N., Cole, David E. C.
Publicat 2013

Maternal ethnicity and risk of neural tube defects: a population-based study

per Ray, Joel G., Vermeulen, Marian J., Meier, Chris, Cole, David E.C., Wyatt, Philip R.
Publicat 2004

Predictors of 25-Hydroxyvitamin D Concentration Measured at Multiple Time Points in a Multiethnic Population

per Knight, Julia A, Wong, Jody, Cole, David E C, Lee, Tim K, Parra, Esteban J
Publicat a Am J Epidemiol (2017)

Topiramate Treatment May Interfere With Urinary Cortisol Measurement By Radioimmunoassay (RIA) – A Case Report

per Chan, Pak Cheung R., Silverberg, Jay, Cole, David E. C., Lem-Ragosnig, Bonny, Recknagel, Frank
Publicat a EJIFCC (2005)

Low wintertime vitamin D levels in a sample of healthy young adults of diverse ancestry living in the Toronto area: associations with vitamin D intake and skin pigmentation

per Gozdzik, Agnes, Barta, Jodi Lynn, Wu, Hongyu, Wagner, Dennis, Cole, David E, Vieth, Reinhold, Whiting, Susan, Parra, Esteban J
Publicat 2008

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

per Malik, Suneil, Fu, Lei, Juras, David James, Karmali, Mohamed, Wong, Betty Y. L., Gozdzik, Agnes, Cole, David E. C.
Publicat 2013

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

per Dauber, Andrew, Nguyen, Thutrang T., Sochett, Etienne, Cole, David E. C., Horst, Ronald, Abrams, Steven A., Carpenter, Thomas O., Hirschhorn, Joel N.
Publicat 2012

Relationship of Total and Free 25-Hydroxyvitamin D to Biomarkers and Metabolic Indices in Healthy Children

per Simpson, Christine A, Zhang, Jane H, Vanderschueren, Dirk, Fu, Lei, Pennestri, Teresita C, Bouillon, Roger, Cole, David E C, Carpenter, Thomas O
Publicat a J Clin Endocrinol Metab (2019)

25-OHD response to vitamin D supplementation in children: effect of dose but not GC haplotype

per Simpson, Christine A., Zhang, Jane H., Vanderschueren, Dirk, Fu, Lei, Pennestri, Teresita C., Bouillon, Roger, Cole, David E.C., Carpenter, Thomas O.
Publicat a Eur J Endocrinol (2021)

Vitamin D Binding Protein is a key determinant of 25-hydroxyvitamin D levels in infants and toddlers

per 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 E. C.
Publicat 2013

Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family

per Guarnieri, Vito, Seaberg, Raewyn M., Kelly, Catherine, Jean Davidson, M., Raphael, Simon, Shuen, Andrew Y., Baorda, Filomena, Palumbo, Orazio, Scillitani, Alfredo, Hendy, Geoffrey N., Cole, David E. C.
Publicat a BMC Med Genet (2017)

Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family

per Guarnieri, Vito, Seaberg, Raewyn M., Kelly, Catherine, Jean Davidson, M., Raphael, Simon, Shuen, Andrew Y., Baorda, Filomena, Palumbo, Orazio, Scillitani, Alfredo, Hendy, Geoffrey N., Cole, David E.C.
Publicat a BMC Med Genet (2017)

Haplotypes in the Dystrophin DNA Segment Point to a Mosaic Origin of Modern Human Diversity

per Ziętkiewicz, Ewa, Yotova, Vania, Gehl, Dominik, Wambach, Tina, Arrieta, Isabel, Batzer, Mark, Cole, David E. C., Hechtman, Peter, Kaplan, Feige, Modiano, David, Moisan, Jean-Paul, Michalski, Roman, Labuda, Damian
Publicat 2003

Traditional foods and 25(OH)D concentrations in a subarctic First Nations community

per Mansuri, Sudaba, Badawi, Alaa, Kayaniyil, Sheena, Cole, David E., Harris, Stewart B., Mamakeesick, Mary, Wolever, Thomas, Gittelsohn, Joel, Maguire, Jonathon L., Connelly, Philip W., Zinman, Bernard, Hanley, Anthony J.
Publicat a Int J Circumpolar Health (2016)

Vitamin D in adult health and disease: a review and guideline statement from Osteoporosis Canada

per Hanley, David A., Cranney, Ann, Jones, Glenville, Whiting, Susan J., Leslie, William D., Cole, David E.C., Atkinson, Stephanie A., Josse, Robert G., Feldman, Sidney, Kline, Gregory A., Rosen, Cheryl
Publicat 2010

Association of Directly Measured Plasma Free 25(OH)D With Insulin Sensitivity and Secretion: The IRAS Family Study

per Lee, C. Christine, Young, Kendra A., Norris, Jill M., Rotter, Jerome I., Liu, Yeheng, Lorenzo, Carlos, Wagenknecht, Lynne E., Cole, David E., Haffner, Steven M., Chen, Yii-Der I., Hanley, Anthony J.
Publicat a J Clin Endocrinol Metab (2017)

MEN1 gene mutation with parathyroid carcinoma: first report of a familial case

per Cinque, Luigia, Sparaneo, Angelo, Salcuni, Antonio S, de Martino, Danilo, Battista, Claudia, Logoluso, Francesco, Palumbo, Orazio, Cocchi, Roberto, Maiello, Evaristo, Graziano, Paolo, Hendy, Geoffrey N, Cole, David E C, Scillitani, Alfredo, Guarnieri, Vito
Publicat a Endocr Connect (2017)

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

per Ferdosi, Shadi, Rehder, Douglas S., Maranian, Paul, Castle, Erik P., Ho, Thai H., Pass, Harvey I., Cramer, Daniel W., Anderson, Karen S., Fu, Lei, Cole, David E. C., Le, Tao, Wu, Xifeng, Borges, Chad R.
Publicat a J Proteome Res (2017)