Kristina Calli
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 11 publications
Uncovering the complexity of structural variants in four individuals with autism spectrum disorder.
Journal: Genome
Published: December 12, 2024
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant.
Journal: Genes
Published: October 31, 2023
Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Journal: Cell
Published: May 05, 2022
Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous POLR2A Variant.
Journal: Genes
Published: January 27, 2022
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder.
Journal: NPJ genomic medicine
Published: May 21, 2021
Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Journal: Clinical genetics
Published: February 26, 2019
Blood Mitochondrial DNA Content in HIV-Exposed Uninfected Children with Autism Spectrum Disorder.
Journal: Viruses
Published: November 23, 2017
Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
Journal: European journal of medical genetics
Published: February 28, 2013
Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.
Journal: Clinical genetics
Published: February 29, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026