Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

55 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Primary care providers' lived experiences of genetics in practice.
Harding B, Webber C, Ruhland L, Dalgarno N, Armour CM, Birtwhistle R, Brown G, Carroll JC, Flavin M, Phillips S, MacKenzie JJ. Harding B, et al. Among authors: mackenzie jj. J Community Genet. 2019 Jan;10(1):85-93. doi: 10.1007/s12687-018-0364-6. Epub 2018 Apr 26. J Community Genet. 2019. PMID: 29700759 Free PMC article.
Parents' Understanding of Genetics and Heritability.
Harding B, Egan R, Kannu P, MacKenzie JJ. Harding B, et al. Among authors: mackenzie jj. J Genet Couns. 2017 Jun;26(3):541-547. doi: 10.1007/s10897-016-0021-3. Epub 2016 Oct 17. J Genet Couns. 2017. PMID: 27747461
Bridging the gap in genetics: a progressive model for primary to specialist care.
Harding B, Webber C, Rühland L, Dalgarno N, Armour C, Birtwhistle R, Brown G, Carroll JC, Flavin M, Phillips SP, MacKenzie JJ. Harding B, et al. Among authors: mackenzie jj. BMC Med Educ. 2019 Jun 11;19(1):195. doi: 10.1186/s12909-019-1622-y. BMC Med Educ. 2019. PMID: 31185964 Free PMC article.
Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in Canada.
Lamoureux MF, Tingley K, Kronick JB, Potter BK, Chan AK, Coyle D, Dodds L, Dyack S, Feigenbaum A, Geraghty M, Gillis J, Rockman-Greenberg C, Khan A, Little J, MacKenzie J, Maranda B, Mhanni A, Mitchell JJ, Mitchell G, Laberge AM, Potter M, Prasad C, Siriwardena K, Speechley KN, Stockler S, Trakadis Y, Turner L, Van Karnebeek C, Wilson K, Chakraborty P; Canadian Inherited Metabolic Diseases Research Network. Lamoureux MF, et al. Among authors: mackenzie j. JIMD Rep. 2015;21:15-22. doi: 10.1007/8904_2014_347. Epub 2015 Feb 26. JIMD Rep. 2015. PMID: 25716610 Free PMC article.
Achieving the "triple aim" for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework.
Potter BK, Chakraborty P, Kronick JB, Wilson K, Coyle D, Feigenbaum A, Geraghty MT, Karaceper MD, Little J, Mhanni A, Mitchell JJ, Siriwardena K, Wilson BJ, Syrowatka A; Canadian Inherited Metabolic Diseases Research Network. Potter BK, et al. Genet Med. 2013 Jun;15(6):415-22. doi: 10.1038/gim.2012.153. Epub 2012 Dec 6. Genet Med. 2013. PMID: 23222662 Free PMC article. Review.
Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007-2014).
Gannavarapu S, Prasad C, DiRaimo J, Napier M, Goobie S, Potter M, Chakraborty P, Karaceper M, Munoz T, Schulze A, MacKenzie J, Li L, Geraghty MT, Al-Dirbashi OY, Rupar CA. Gannavarapu S, et al. Mol Genet Metab. 2015 Nov;116(3):146-51. doi: 10.1016/j.ymgme.2015.08.010. Epub 2015 Aug 31. Mol Genet Metab. 2015. PMID: 26361991
Student Reflections on the Queen's Accelerated Route to Medical School Programme.
MacKenzie JJ, Stockley D, Hastings-Truelove A, Nowlan Suart T, Katsoulas E, Kawaja M, Reznick R, Sanfilippo A. MacKenzie JJ, et al. J Med Educ Curric Dev. 2019 Mar 28;6:2382120519836789. doi: 10.1177/2382120519836789. eCollection 2019 Jan-Dec. J Med Educ Curric Dev. 2019. PMID: 30944887 Free PMC article.
55 results