Sylvie Langlois

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 14

Top Topics

Liquid Chromatography

Clinical Practice

Top Venues

Prenatal diagnosis

JMIR research protocols

Genetics in medicine : official journal of the American College of Medical Genetics

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use". Prenatal diagnosis (2024)
Sunu Kim, Carly Pistawka, Sylvie Langlois, Horacio Osiovich, Alice Virani, Vanessa Kitchin, null null, Alison M Elliott
Genetic counselling considerations with genetic/genomic testing in Neonatal and Pediatric Intensive Care Units: A scoping review. Clinical genetics (2023)
Lisa Hui, Sylvie Langlois
Prenatal screening and diagnosis of sex chromosome conditions: The new normal? Prenatal diagnosis 43 (2) (2023)
Lisa Hui, Sylvie Langlois
Prenatal screening and diagnosis of sex chromosome conditions: The new normal? Prenatal diagnosis 43 (2) (2023)
Lisa Hui, Sylvie Langlois
Prenatal screening and diagnosis of sex chromosome conditions: The new normal. Prenatal diagnosis (2023)
Lisa Hui, Sylvie Langlois
Prenatal screening and diagnosis of sex chromosome conditions: The new normal? Prenatal diagnosis (2023)
Lisa Hui, Sylvie Langlois
Prenatal screening and diagnosis of sex chromosome conditions: The new normal? Prenatal diagnosis 43 (2) (2023)
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use. Prenatal diagnosis (2023)
Melissa Cornthwaite, Kelly Turner, Linlea Armstrong, Cornelius F Boerkoel, Caitlin Chang, Anna Lehman, Sarah M Nikkel, Millan S Patel, Margot Van Allen, Sylvie Langlois
Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: Need for greater adherence to published guidelines. Prenatal diagnosis 42 (12) (2022)
Elizabeth L Digby, Jessica Liauw, Janis Dionne, Sylvie Langlois, Sarah M Nikkel
Etiologies and outcomes of prenatally diagnosed hyperechogenic kidneys. Prenatal diagnosis 41 (4) (2021)
Lieve Christiaens, Lyn S Chitty, Sylvie Langlois
Current controversies in prenatal diagnosis: Expanded NIPT that includes conditions other than trisomies 13, 18, and 21 should be offered. Prenatal diagnosis 41 (10) (2021)
My Linh Thibodeau, Sylvie Langlois
Correspondence on "The prevalence of genetic diagnoses in fetuses with severe congenital heart defects" by Nisselrooij et al. Genetics in medicine : official journal of the American College of Medical Genetics 23 (1) (2020)
Samira Abbasgholizadeh Rahimi, Patrick Michel Archambault, Vardit Ravitsky, Marie-Ève Lemoine, Sylvie Langlois, Jean-Claude Forest, Anik M C Giguere, Francois Rousseau, James G Dolan, France Légaré
An Analytical Mobile App for Shared Decision Making About Prenatal Screening: Protocol for a Mixed Methods Study. JMIR research protocols 8 (10) (2019)
Sylvie Langlois, JoAnn Johnson, François Audibert, Jean Gekas, Jean-Claude Forest, André Caron, Keli Harrington, Melanie Pastuck, Hasna Meddour, Amélie Tétu, Julian Little, François Rousseau
Comparison of first-tier cell-free DNA screening for common aneuploidies with conventional publically funded screening. Prenatal diagnosis 37 (12) (2017)