Sarah Dyack, MD
Division of Medical Genetics, Associate Professor
Related information
- CV [PDF - 179 KB]
Email: sarah.dyack@iwk.nshealth.ca
Phone: 902-470-8754
Fax: 902-470-8709
Mailing Address:
Division of Medical Genetics
IWK Health Centre
PO Box 9700
5850-5980 University Ave.
Halifax, NS B3K 6R8
Research Topics:IWK Health Centre
PO Box 9700
5850-5980 University Ave.
Halifax, NS B3K 6R8
- New born screening
- New gene discovery
- Cardiomyopathy
- Microdeletion 22q11
- Syndromes
Education
- BA/BSc (Dalhousie University)
- MD (Dalhousie University)
- FRCPC Pediatrics (University of Alberta)
- FCCMG Clinical Genetics (University of Toronto)
Selected publications
- Urinary biomarker investigation in children with Fabry disease using tandem mass spectrometry.
Auray-Blais C, Blais CM, Ramaswami U, Boutin M, Germain DP, Dyack S, Bodamer O, Pintos-Morell G, Clarke JT, Bichet DG, Warnock DG, Echevarria L, West ML, Lavoie P.
Clin Chim Acta. 2015 Jan 1;438:195-204. doi: 10.1016/j.cca.2014.08.002. Epub 2014 Aug 19. - Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.
Guo DC, Regalado E, Casteel DE, Santos-Cortez RL, Gong L, Kim JJ, Dyack S, Horne SG, Chang G, Jondeau G, Boileau C, Coselli JS, Li Z, Leal SM, Shendure J, Rieder MJ, Bamshad MJ, Nickerson DA; GenTAC Registry Consortium; National Heart, Lung, and Blood Institute Grand Opportunity Exome Sequencing Project, Kim C, Milewicz DM.
Am J Hum Genet. 2013 Aug 8;93(2):398-404. doi: 10.1016/j.ajhg.2013.06.019. Epub 2013 Aug 1. - Incidence of medium-chain acyl-CoA dehydrogenase deficiency in Canada using the Canadian Paediatric Surveillance Program: Role of newborn screening.
Prasad C, Speechley KN, Dyack S, Rupar CA, Chakraborty P, Kronick JB.
Paediatr Child Health. 2012 Apr;17(4):185-9. - Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man.
Tuschl K, Clayton PT, Gospe SM Jr, Gulab S, Ibrahim S, Singhi P, Aulakh R, Ribeiro RT, Barsottini OG, Zaki MS, Del Rosario ML, Dyack S, Price V, Rideout A, Gordon K, Wevers RA, Chong WK, Mills PB.
Am J Hum Genet. 2012 Mar 9;90(3):457-66. doi: 10.1016/j.ajhg.2012.01.018. Epub 2012 Feb 16.