Sylvie Langlois

14PUBLICATIONS
31CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsPsychosocial aspects of childbirth and perinatal mental healthFoetal development and medicineNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (14)

|Mar 13, 2026
Clinical outcomes after nondiagnostic prenatal exome sequencing: Need for balancing reassurance and residual risks in genetic counseling.

Sophie Albert, Anne Swenerton, Kirsten M Niles

|Mar 07, 2026
Validation of PREM-PS, a patient-reported experience instrument, in a randomized controlled trial of pregnant women undergoing prenatal screening.

Alix Dubeau, Meryeme El Balqui, Denis Talbot

|Jul 05, 2025
Prenatal Cell-Free DNA Screening With Fetal Enrichment Enables Sampling From 8 Weeks of Gestational Age.

Seyedeh Saideh Daryabari, Sylvie Giroux, André Caron

|Mar 10, 2025
Navigating the Challenges of Exome Sequencing in Structurally Normal Fetuses.

Sylvie Langlois, Lyn S Chitty

|Sep 14, 2024
Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use".

Neeta L Vora, Sylvie Langlois, Lyn S Chitty

|Nov 22, 2023
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use.

Neeta L Vora, Sylvie Langlois, Lyn S Chitty

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Frequent Collaborators

4 joint publications

Lyn S Chitty

3 joint publications

Jean-Claude Forest

3 joint publications

François Rousseau

2 joint publications

Emmanuel Bujold