Nicole M. Roslin

686 Bay Street
Toronto, ON, Canada

Last Updated: 09/26/2026

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Found 20 publications

Population-based characterisation of child and adolescent oral bacterial microbiomes.

Population-based characterisation of child and adolescent oral bacterial microbiomes.

Journal: Microbiome
Published: February 19, 2026

Genetic Linkage for Bipolar Disorder to the Distal Region of Chromosome 19q: A Large Family Whole Genome Sequencing Study.

Genetic Linkage for Bipolar Disorder to the Distal Region of Chromosome 19q: A Large Family Whole Genome Sequencing Study.

Journal: Bipolar disorders
Published: November 26, 2024

Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication.

Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication.

Journal: JCI insight
Published: December 21, 2023

Gene copy number variation and pediatric mental health/neurodevelopment in a general population.

Gene copy number variation and pediatric mental health/neurodevelopment in a general population.

Journal: Human molecular genetics
Published: March 09, 2023

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Journal: medRxiv : the preprint server for health sciences
Published: February 13, 2023

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Journal: Nature genetics
Published: January 25, 2023

Trans-ancestry meta-analysis of genome wide association studies of inhibitory control.

Trans-ancestry meta-analysis of genome wide association studies of inhibitory control.

Journal: Molecular psychiatry
Published: October 12, 2022

Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses.

Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses.

Journal: European journal of human genetics : EJHG
Published: April 21, 2022

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Journal: Human genetics
Published: May 24, 2021

CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiency.

CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiency.

Journal: Ophthalmic genetics
Published: July 22, 2020

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

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

Journal: Journal of medical genetics
Published: June 02, 2020

Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss.

Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss.

Journal: BMC medical genetics
Published: October 13, 2018
Showing 1-12 of 20

Last Updated: 09/26/2026