Dougan SD - Search Results

1

Ultrasonographic Fetal Nuchal Translucency Measurements and Cytogenetic Outcomes.

Bellai-Dussault K, Dougan SD, Fell DB, Little J, Meng L, Okun N, Walker MC, Armour CM, Potter BK. Bellai-Dussault K, et al. Among authors: dougan sd. JAMA Netw Open. 2024 Mar 4;7(3):e243689. doi: 10.1001/jamanetworkopen.2024.3689. JAMA Netw Open. 2024. PMID: 38530313 Free PMC article.

2

Newborn Bilirubin Screening for Preventing Severe Hyperbilirubinemia and Bilirubin Encephalopathy: A Rapid Review.

Bhardwaj K, Locke T, Biringer A, Booth A, Darling EK, Dougan S, Harrison J, Hill S, Johnson A, Makin S, Potter B, Lacaze-Masmonteil T, Little J. Bhardwaj K, et al. Curr Pediatr Rev. 2017;13(1):67-90. doi: 10.2174/1573396313666170110144345. Curr Pediatr Rev. 2017. PMID: 28071585 Review.

3

Enhanced First Trimester Screening for Trisomy 21 with Contingent Cell-Free Fetal DNA: A Comparative Performance and Cost Analysis.

Huang T, Meschino WS, Teitelbaum M, Dougan S, Okun N. Huang T, et al. J Obstet Gynaecol Can. 2017 Sep;39(9):742-749. doi: 10.1016/j.jogc.2017.01.025. Epub 2017 Jun 16. J Obstet Gynaecol Can. 2017. PMID: 28624447

4

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.

Armour CM, Dougan SD, Brock JA, Chari R, Chodirker BN, DeBie I, Evans JA, Gibson WT, Kolomietz E, Nelson TN, Tihy F, Thomas MA, Stavropoulos DJ; On-Behalf-Of the Canadian College of Medical Geneticists. Armour CM, et al. Among authors: dougan sd. J Med Genet. 2018 Apr;55(4):215-221. doi: 10.1136/jmedgenet-2017-105013. Epub 2018 Mar 1. J Med Genet. 2018. PMID: 29496978 Free PMC article.

5

Trends in the use of prenatal testing services for fetal aneuploidy in Ontario: a descriptive study.

Huang T, Dougan S, Walker M, Armour CM, Okun N. Huang T, et al. CMAJ Open. 2018 Oct 5;6(4):E436-E444. doi: 10.9778/cmajo.20180046. Print 2018 Oct-Dec. CMAJ Open. 2018. PMID: 30291139 Free PMC article.

6

Comparing Maternal Serum Screening Markers Among IVF and Spontaneous Conceptions in Ontario Through Registry Data.

Lanes A, Dougan S, Fell DB, Huang T, Sprague A, Johnson M, Leader A, Potter B, Okun N, Walker M. Lanes A, et al. J Obstet Gynaecol Can. 2018 Dec;40(12):1608-1617. doi: 10.1016/j.jogc.2018.02.024. Epub 2018 Oct 26. J Obstet Gynaecol Can. 2018. PMID: 30539731

7

A 2-year review of publicly funded cell-free DNA screening in Ontario: utilization and adherence to funding criteria.

Bellai-Dussault K, Meng L, Huang T, Reszel J, Walker M, Lanes A, Okun N, Armour C, Dougan S. Bellai-Dussault K, et al. Prenat Diagn. 2020 Jan;40(2):164-172. doi: 10.1002/pd.5563. Epub 2019 Nov 21. Prenat Diagn. 2020. PMID: 31525278

8

Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions in Average-Risk Pregnancies: A Cost-Effectiveness Analysis.

Xie X, Wang M, Goh ES, Ungar WJ, Little J, Carroll JC, Okun N, Huang T, Rousseau F, Dougan SD, Tu HA, Higgins C, Holubowich C, Sikich N, Dhalla IA, Ng V. Xie X, et al. Among authors: dougan sd. J Obstet Gynaecol Can. 2020 Jun;42(6):740-749.e12. doi: 10.1016/j.jogc.2019.12.007. Epub 2020 Jan 31. J Obstet Gynaecol Can. 2020. PMID: 32008974

9

Application of exome sequencing for prenatal diagnosis: a rapid scoping review.

Pratt M, Garritty C, Thuku M, Esmaeilisaraji L, Hamel C, Hartley T, Millar K, Skidmore B, Dougan S, Armour CM. Pratt M, et al. Genet Med. 2020 Dec;22(12):1925-1934. doi: 10.1038/s41436-020-0918-y. Epub 2020 Aug 4. Genet Med. 2020. PMID: 32747765 Free article. Review.

10

Gastroschisis in Ontario, Canada: 2012-2018.

Bourque DK, Meng L, Dougan S, Momoli F, Riddell C, Walker M, Armour CM. Bourque DK, et al. Birth Defects Res. 2021 Aug 15;113(14):1044-1051. doi: 10.1002/bdr2.1896. Epub 2021 Apr 19. Birth Defects Res. 2021. PMID: 33871183

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