Vasilios Zachariadis

De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations

Margot R.F. Reijnders, Vasilios Zachariadis, Brooke Latour et al. · The American Journal of Human Genetics · 2016 · 106 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +11

A Highly Scalable Method for Joint Whole-Genome Sequencing and Gene-Expression Profiling of Single Cells

Vasilios Zachariadis, Huaitao Cheng, Nathanael Andrews et al. · Molecular Cell · 2020 · 91 citations · Full text

Gene-expression Profiling, Genetics, Complex Cell Mixtures +25

Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation

Daniel Nilsson, Maria Pettersson, Peter Gustavsson et al. · Human Mutation · 2016 · 78 citations · Full text

Cytogenetics, Genetics, Genomic Mechanism +16

DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia

Jessica Nordlund, Christofer Bäcklin, Vasilios Zachariadis et al. · Clinical Epigenetics · 2015 · 77 citations · Full text

Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes

B. Malmgren, Kristofer Andersson, Karin Lindahl et al. · Oral Diseases · 2016 · 59 citations