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 · 109 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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 · 96 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia

Jessica Nordlund, Christofer Bäcklin, Vasilios Zachariadis et al. · Clinical Epigenetics · 2015 · 81 citations · Full text

Medicine, Molecular Biology, Oncology +17

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 · 80 citations

Life Sciences, Genetics, Molecular Genetics +17

Spinal Cord Injury Induces Permanent Reprogramming of Microglia into a Disease-Associated State Which Contributes to Functional Recovery

Ramil Hakim, Vasilios Zachariadis, Sreenivasa Raghavan Sankavaram et al. · Journal of Neuroscience · 2021 · 63 citations · Full text

Medicine, Neurobiology, Neuroscience +16