Matteo Floris - Publications

Correction: Position statement from the Italian Society of Human Genetics (SIGU) on the implementation of germline pharmacogenetic testing.

Journal: European journal of human genetics : EJHG

Published: May 13, 2026

Identification of a large DPYD gene deletion undetected by standard genotyping in a patient with severe capecitabine-related toxicity: a case report.

Journal: Frontiers in pharmacology

Published: April 27, 2026

Rethinking Onconephrology: A Nephro-Nutritional Integrated Approach in Patients with Chronic Kidney Disease and Urological Malignancies.

Journal: Nutrients

Published: April 08, 2026

Hemoadsorption Combined with Hemodialysis (HAHD): a Consensus Statement from an International Expert Panel.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: March 03, 2026

Steroid-Resistant Focal Segmental Glomerulosclerosis with Alport-like Glomerular Basement Membrane Lesions Due to a MYO1E Mutation: A Pediatric Case Report.

Journal: International journal of molecular sciences

Published: February 15, 2026

Toward multimodal integration of colorectal cancer and chronic kidney disease: transcriptomic modeling as a framework for the SIRIO study "Spatial radiomics and transcriptomics to the discovery of the cross-link between colon cancer and chronic kidney disease".

Journal: Radiology and oncology

Published: February 05, 2026

Sex-Related Differences in Circular RNA Expression in Multiple Sclerosis: A Pilot Study.

Journal: Journal of molecular neuroscience : MN

Published: January 23, 2026

FlowCLOc, a New Tool for Selecting the Most Appropriate Antibodies in Flow Cytometry.

Journal: International journal of molecular sciences

Published: January 08, 2026

Personalized Hemodialysis Approaches in Frail Older Individuals.

Journal: Geriatrics (Basel, Switzerland)

Published: December 31, 2025

Slow continuous ultrafiltration and prolonged intermittent renal replacement therapy: Tailoring renal replacement therapy in intensive care unit.

Journal: World journal of nephrology

Published: December 28, 2025

Whole-Exome Sequencing Identifies Novel Genetic Variants Associated with Unexplained Neurodevelopmental Disorders in Children.

Journal: International journal of molecular sciences

Published: December 27, 2025

Pharmacogenetic testing in Italy: results of a nationwide survey by the Joint Working Group for the pharmacogenetics implementation in Italy.

Journal: European journal of human genetics : EJHG

Published: December 20, 2025