Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2005 1
2006 1
2007 2
2008 2
2009 3
2010 1
2011 2
2012 3
2013 1
2015 1
2016 3
2017 3
2018 4
2019 5
2020 6
2021 3
2022 2
Text availability
Article attribute
Article type
Publication date

Search Results

35 results
Results by year
Filters applied: . Clear all
Page 1
Otitis Media: Rapid Evidence Review.
Gaddey HL, Wright MT, Nelson TN. Gaddey HL, et al. Among authors: nelson tn. Am Fam Physician. 2019 Sep 15;100(6):350-356. Am Fam Physician. 2019. PMID: 31524361 Free article. Review.
Renpenning syndrome in a female.
Cho RY, Peñaherrera MS, Du Souich C, Huang L, Mwenifumbo J, Nelson TN, Elliott AM, Adam S; CAUSES Study, Eydoux P, Yang GX, Chijiwa C, Van Allen MI, Friedman JM, Robinson WP, Lehman A. Cho RY, et al. Among authors: nelson tn. Am J Med Genet A. 2020 Mar;182(3):498-503. doi: 10.1002/ajmg.a.61451. Epub 2019 Dec 16. Am J Med Genet A. 2020. PMID: 31840929
CCMG practice guideline: laboratory guidelines for next-generation sequencing.
Hume S, Nelson TN, Speevak M, McCready E, Agatep R, Feilotter H, Parboosingh J, Stavropoulos DJ, Taylor S, Stockley TL; Canadian College of Medical Geneticists (CCMG). Hume S, et al. Among authors: nelson tn. J Med Genet. 2019 Dec;56(12):792-800. doi: 10.1136/jmedgenet-2019-106152. Epub 2019 Jul 12. J Med Genet. 2019. PMID: 31300550 Free PMC article.
Alpha-1-antitrypsin molecular testing in Canada: A seven year, multi-centre comparison.
Mattman A, Gilfix BM, Chen SX, DeMarco ML, Kyle BD, Parker ML, Agbor TA, Jung B, Selvarajah S, Barakauskas VE, Vaags AK, Estey MP, Nelson TN, Speevak MD. Mattman A, et al. Among authors: nelson tn. Clin Biochem. 2020 Jul;81:27-33. doi: 10.1016/j.clinbiochem.2020.05.001. Epub 2020 May 6. Clin Biochem. 2020. PMID: 32387440
CCMG statement on direct-to-consumer genetic testing.
CCMG Ethics and Public Policy Committee, Nelson TN, Armstrong L, Richer J, Evans J, Lauzon J, McGillivray B, Bruyere H, Dougan S. CCMG Ethics and Public Policy Committee, et al. Among authors: nelson tn. Clin Genet. 2012 Jan;81(1):1-3. doi: 10.1111/j.1399-0004.2011.01789.x. Epub 2011 Nov 10. Clin Genet. 2012. PMID: 21943145 No abstract available.
De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome.
Sleven H, Welsh SJ, Yu J, Churchill MEA, Wright CF, Henderson A, Horvath R, Rankin J, Vogt J, Magee A, McConnell V, Green A, King MD, Cox H, Armstrong L, Lehman A, Nelson TN; Deciphering Developmental Disorders study; CAUSES study, Williams J, Clouston P, Hagman J, Németh AH. Sleven H, et al. Among authors: nelson tn. Am J Hum Genet. 2017 Jan 5;100(1):138-150. doi: 10.1016/j.ajhg.2016.11.020. Epub 2016 Dec 23. Am J Hum Genet. 2017. PMID: 28017370 Free PMC article.
Alpha1-antitrypsin deficiency: a clinical-genetic overview.
Abboud RT, Nelson TN, Jung B, Mattman A. Abboud RT, et al. Among authors: nelson tn. Appl Clin Genet. 2011 Mar 31;4:55-65. doi: 10.2147/TACG.S10604. Print 2011. Appl Clin Genet. 2011. PMID: 23776367 Free PMC article.
35 results