Roumiana Alexandrova
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 12 publications
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism.
Journal: Nature
Published: December 10, 2024
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder.
Journal: medRxiv : the preprint server for health sciences
Published: August 07, 2024
Chromosome X-wide common variant association study in autism spectrum disorder.
Journal: American journal of human genetics
Published: August 05, 2024
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neurons.
Journal: BMC medical genomics
Published: June 07, 2022
Expanding the search for genetic biomarkers of Parkinson's disease into the living brain.
Journal: Neurobiology of disease
Published: January 29, 2020
Prevalence of Anxiety and Depression and Their Impact on the Quality of Life of Cancer Patients Treated with Palliative Antineoplasic Therapy - Results of the PALINT Trial.
Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti
Published: June 21, 2019
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.
Journal: Stem cell reports
Published: February 14, 2019
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.
Journal: Stem cell reports
Published: June 11, 2018
A homozygous mutation in the stem II domain of RNU4ATAC causes typical Roifman syndrome.
Journal: NPJ genomic medicine
Published: March 15, 2017
Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network.
Journal: Oncotarget
Published: April 07, 2016
Largen: a molecular regulator of mammalian cell size control.
Journal: Molecular cell
Published: March 11, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026