1. DNA methylation signatures in mendelian developmental disorders as a diagnostic bridge between genotype and phenotype. (15th March 2019) Authors: Sadikovic, Bekim; Aref-Eshghi, Erfan; Levy, Michael A; Rodenhiser, David Journal: Epigenomics Issue: Volume 11:Number 5(2019) Page Start: 563 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Functional annotation of genomic variation: DNA methylation episignatures in neurodevelopmental Mendelian disorders. (9th July 2020) Authors: Sadikovic, Bekim; Levy, Michael A; Aref-Eshghi, Erfan Journal: Human molecular genetics Issue: Volume 29:Number R1(2020) Page Start: R27 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Validation and clinical performance of a combined nuclear‐mitochondrial next‐generation sequencing and copy number variant analysis panel in a Canadian population. Issue 2 (10th December 2020) Authors: Levy, Michael A; Kerkhof, Jennifer; Belmonte, Frances R.; Kaufman, Brett A.; Bhai, Pratibha; Brady, Lauren; Bursztyn, Lulu L.C.D.; Tarnopolsky, Mark; Rupar, Tony; Sadikovic, Bekim Journal: American journal of medical genetics Issue: Volume 185:Issue 2(2021) Page Start: 486 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗