Michelle T. Siu

Toronto, ON M5G0A4, Canada

Last Updated: 09/26/2026

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Found 12 publications

Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.

Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.

Journal: American journal of human genetics

Published: January 20, 2021

DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental Disorders.

DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental Disorders.

Journal: Journal of autism and developmental disorders

Published: November 09, 2020

Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation.

Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation.

Journal: Journal of neurodevelopmental disorders

Published: November 18, 2019

New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndrome.

New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndrome.

Journal: BMC medical genomics

Published: April 25, 2019

Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.

Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.

Journal: Clinical epigenetics

Published: August 23, 2018

Epigenetics of Autism Spectrum Disorder.

Epigenetics of Autism Spectrum Disorder.

Journal: Advances in experimental medicine and biology

Published: May 20, 2017

CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.

CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.

Journal: American journal of human genetics

Published: December 22, 2016

Genome-wide characteristics of de novo mutations in autism.

Genome-wide characteristics of de novo mutations in autism.

Journal: NPJ genomic medicine

Published: August 16, 2016

NSD1 mutations generate a genome-wide DNA methylation signature.

NSD1 mutations generate a genome-wide DNA methylation signature.

Journal: Nature communications

Published: June 03, 2015

A pilot study examining the unmet needs of cancer survivors living with polypathology.

A pilot study examining the unmet needs of cancer survivors living with polypathology.

Journal: Current oncology (Toronto, Ont.)

Published: June 06, 2013

A role for glutathione, independent of oxidative stress, in the developmental toxicity of methanol.

A role for glutathione, independent of oxidative stress, in the developmental toxicity of methanol.

Journal: Toxicology and applied pharmacology

Published: May 03, 2013

Methanol teratogenicity in mutant mice with deficient catalase activity and transgenic mice expressing human catalase.

Methanol teratogenicity in mutant mice with deficient catalase activity and transgenic mice expressing human catalase.

Journal: Reproductive toxicology (Elmsford, N.Y.)

Published: March 19, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026