Savvas Kinalis

Copenhagen, 2100, Denmark

Last Updated: 09/26/2026

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Found 14 publications

A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data.

A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data.

Journal: Cancers

Published: November 02, 2021

Interpretable Autoencoders Trained on Single Cell Sequencing Data Can Transfer Directly to Data from Unseen Tissues.

Interpretable Autoencoders Trained on Single Cell Sequencing Data Can Transfer Directly to Data from Unseen Tissues.

Journal: Cells

Published: October 27, 2021

A catalog of curated breast cancer genes.

A catalog of curated breast cancer genes.

Journal: Breast cancer research and treatment

Published: August 09, 2021

Genomic profiling of newly diagnosed glioblastoma patients and its potential for clinical utility - a prospective, translational study.

Genomic profiling of newly diagnosed glioblastoma patients and its potential for clinical utility - a prospective, translational study.

Journal: Molecular oncology

Published: April 17, 2020

High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer.

High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer.

Journal: NPJ genomic medicine

Published: February 04, 2019

Deconvolution of autoencoders to learn biological regulatory modules from single cell mRNA sequencing data.

Deconvolution of autoencoders to learn biological regulatory modules from single cell mRNA sequencing data.

Journal: BMC bioinformatics

Published: February 04, 2019

The Number of Signaling Pathways Altered by Driver Mutations in Chronic Lymphocytic Leukemia Impacts Disease Outcome.

The Number of Signaling Pathways Altered by Driver Mutations in Chronic Lymphocytic Leukemia Impacts Disease Outcome.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research

Published: December 19, 2018

A Gain-of-Function p53-Mutant Oncogene Promotes Cell Fate Plasticity and Myeloid Leukemia through the Pluripotency Factor FOXH1.

A Gain-of-Function p53-Mutant Oncogene Promotes Cell Fate Plasticity and Myeloid Leukemia through the Pluripotency Factor FOXH1.

Journal: Cancer discovery

Published: November 27, 2018

BloodSpot: a database of healthy and malignant haematopoiesis updated with purified and single cell mRNA sequencing profiles.

BloodSpot: a database of healthy and malignant haematopoiesis updated with purified and single cell mRNA sequencing profiles.

Journal: Nucleic acids research

Published: September 15, 2018

Circulating tumor DNA as a marker of treatment response in BRAF V600E mutated non-melanoma solid tumors.

Circulating tumor DNA as a marker of treatment response in BRAF V600E mutated non-melanoma solid tumors.

Journal: Oncotarget

Published: June 04, 2018

Deep targeted sequencing of TP53 in chronic lymphocytic leukemia: clinical impact at diagnosis and at time of treatment.

Deep targeted sequencing of TP53 in chronic lymphocytic leukemia: clinical impact at diagnosis and at time of treatment.

Journal: Haematologica

Published: April 17, 2018

Molecular subtyping of breast cancer improves identification of both high and low risk patients.

Molecular subtyping of breast cancer improves identification of both high and low risk patients.

Journal: Acta oncologica (Stockholm, Sweden)

Published: November 23, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026