NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing. - Lennart F. Johansson; Hendrik A. de Weerd; Eddy N. de Boer; Freerk van Dijk; Gerard J. te Meerman; Rolf Sijmons; Birgit Sikkema-Raddatz; Morris A. Swertz (BMC Bioinform., 2018)

The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research. - David Salgado; Irina M. Armean; Michael Baudis; Sergi Beltran; Salvador Capella-Gutiérrez; Denise Carvalho-Silva; Victoria Dominguez Del Angel; Joaquín Dopazo; Laura I. Furlong; Bo Gao; Leyla Jael García Castro; Dietlind Gerloff; et al. (F1000Research, 2020)

Ten quick tips for building FAIR workflows. - Casper de Visser; Lennart F. Johansson; Purva Kulkarni; Hailiang Mei; Pieter B. T. Neerincx; K. Joeri van der Velde; Peter Horvatovich; Alain J. van Gool; Morris A. Swertz; Peter A. C. 't Hoen; Anna Niehues (PLoS Comput. Biol., 2023)

Comparing Sequence-Based and Literature-Based Pathogenicity Scoring Methods for Human Variants. - Luc Mottin; Nona Naderi; Anaïs Mottaz; Pierre-André Michel; Lennart F. Johansson; Morris A. Swertz; Andrew Stubbs; Emilie Pasche; Julien Gobeill; Patrick Ruch (MIE, 2024)