Author

Nicole M. Roslin

Hospital for Sick ChildrenORCID 0000-0002-4609-8299Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Nicole M. Roslin1 paper

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andrew D. PatersoniD· 1 shared Bhooma ThiruvahindrapuramiD· 1 shared Brett TrostiD· 1 shared Care4Rare Canada· 1 shared Casper Shyr· 1 shared Cheryl Y. GregoryiD· 1 shared Christian R. MarshalliD· 1 shared Christie L. BurtoniD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andrew D. PatersonORCID

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2 papers

Recent·Most cited

Gene copy number variation in pediatric mental illness in a general population

Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, Edward J. Higginbotham, John Wei, Sabah Shaikh, Nicole M. Roslin, Jeffrey R. MacDonald, Giovanna Pellecchia, Thomas Nalpathamkalam, Sylvia Lamoureux, Roozbeh Manshaei, Jennifer Howe, Brett Trost, Bhooma Thiruvahindrapuram, , Stephen W. Scherer

The paper investigates the association between gene copy number variation and mental health traits in children, finding links to ADHD, OCD, and cognitive biomarkers.

medRxiv · Sep 12, 2022 · PreprintGenetic & Genomic Medicine

Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region

Xin Ye, Nicole M. Roslin, Andrew D. Paterson, Care4Rare Canada, Christopher J. Lyons, Victor D. Pegado, Phillip A. Richmond, Casper Shyr, Oriol Fornés, Xiaohua Han, Michelle Higginson, Colin J. Ross, Deborah Eileen Giaschi, Cheryl Y. Gregory, Millan S. Patel, Wyeth W. Wasserman

This study identifies a 4bp non-coding deletion in the FOXG1 locus at 14q12 as a candidate for isolated strabismus, showing its potential role in regulating FOXG1 expression.

Journal of Medical Genetics · Nov 30, 2020Peer-reviewedGenetic & Genomic Medicine