Evica Separovic-Rajcan

Vancouver, BC V6H3N1, Canada

Last Updated: 09/26/2026

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Found 30 publications

Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected Siblings.

Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected Siblings.

Journal: Genes
Published: May 29, 2021

Genomic imbalances in the placenta are associated with poor fetal growth.

Genomic imbalances in the placenta are associated with poor fetal growth.

Journal: Molecular medicine (Cambridge, Mass.)
Published: July 02, 2020

A genome-wide DNA methylation signature for SETD1B-related syndrome.

A genome-wide DNA methylation signature for SETD1B-related syndrome.

Journal: Clinical epigenetics
Published: July 15, 2019

Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency.

Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency.

Journal: Journal of clinical immunology
Published: March 13, 2019

Next generation sequencing in recurrent pregnancy loss-approaches and outcomes.

Next generation sequencing in recurrent pregnancy loss-approaches and outcomes.

Journal: European journal of medical genetics
Published: January 18, 2019

The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review.

The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review.

Journal: Frontiers in genetics
Published: April 10, 2018

Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication.

Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication.

Journal: European journal of medical genetics
Published: January 04, 2018

Whole exome sequencing of families with 1q21.1 microdeletion or microduplication.

Whole exome sequencing of families with 1q21.1 microdeletion or microduplication.

Journal: American journal of medical genetics. Part A
Published: December 02, 2016

Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.

Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.

Journal: JCI insight
Published: October 05, 2016

Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication.

Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication.

Journal: BMC medical genetics
Published: May 03, 2016

Whole exome sequencing in recurrent early pregnancy loss.

Whole exome sequencing in recurrent early pregnancy loss.

Journal: Molecular human reproduction
Published: December 11, 2015

Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb.

Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb.

Journal: Human mutation
Published: October 21, 2015
Showing 1-12 of 30

Last Updated: 09/26/2026