Lauren MacNeil

Years Active: 2019-2021
Publications (10 Years): 3

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

Publications

Janet R Zhou, Ross Ridsdale, Lauren MacNeil, Margaret Lilley, Stephanie C Hoang, Susan Christian, Pamela Blumenschein, Vanessa Wolan, Aisha Bruce, Gurpreet Singh, Nicola Wright, Jillian S Parboosingh, Ryan E Lamont, Iveta Sosova
The Alberta Newborn Screening Approach for Sickle Cell Disease: The Advantages of Molecular Testing. International journal of neonatal screening 7 (4) (2021)
Maian Roifman, Kirsten M Niles, Lauren MacNeil, Susan Blaser, Abdul Noor, Ruth Godoy, Tim van Mieghem, Greg Ryan, Gareth Seaward, Neal Sondheimer, Saadet Mercimek-Andrews, Andreas Schulze, Stacy Hewson, Adi Ovadia, David Chitayat, Eric K Morgen, Carlo Hojilla, Elena Kolomietz, Nicholas Watkins, Johannes Häberle, Patrick Shannon
Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency. Clinical genetics 98 (6) (2020)
Areej Mahjoub, Zuzana Cihlarova, Martine Tétreault, Lauren MacNeil, Neal Sondheimer, Keith W Caldecott, Hana Hanzlikova, Grace Yoon, null null
Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxia. Neurology. Genetics 5 (5) (2019)

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