RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data. - Tomasz Stokowy; Mateusz Garbulowski; Torunn Fiskerstrand; Rita Holdhus; Kornel Labun; Pawel Sztromwasser; Christian Gilissen; Alexander Hoischen; Gunnar Houge; Kjell Petersen; Inge Jonassen; Vidar M. Steen (Bioinform., 2016)

Consensus Approach for Detection of Cancer Somatic Mutations. - Katarzyna Sieradzka; Kinga Leszczorz; Mateusz Garbulowski; Andrzej Polanski (ICMMI, 2017)

R.ROSETTA: an interpretable machine learning framework. - Mateusz Garbulowski; Klev Diamanti; Karolina Smolinska; Nicholas Baltzer; Patricia Stoll; Susanne Bornelöv; Aleksander Øhrn; Lars Feuk; Jan Komorowski (BMC Bioinform., 2021)

Patterns in big data bioinformatics: Understanding complex diseases with interpretable machine learning. - Mateusz Garbulowski (2021)