BTKbase, mutation database for X-linked agammaglobulinemia (XLA). - Mauno Vihinen; Oliver Brandau; Lars J. Brandén; Sau-Ping Kwan; Ilkka Lappalainen; Tracy Lester; Jeroen G. Noordzij; Hans D. Ochs; Juha Ollila; Sandy M. Pienaar; Pentti Riikonen; Bratin K. Saha; et al. (Nucleic Acids Res., 1998)

A System for Information Management in BioMedical Studies - SIMBioMS. - Maria Krestyaninova; Andris Zarins; Juris Viksna; Natalja Kurbatova; Peteris Rucevskis; Sudeshna Guha Neogi; Mike Gostev; Teemu Perheentupa; Juha Knuuttila; Amy Barrett; Ilkka Lappalainen; Johan Rung; et al. (Bioinform., 2009)

dbVar and DGVa: public archives for genomic structural variation. - Ilkka Lappalainen; John Lopez; Lisa Skipper; Timothy Hefferon; J. Dylan Spalding; John Garner; Chao Chen; Michael Maguire; Matthew Corbett; George Zhou; Justin E. Paschall; Victor Ananiev; et al. (Nucleic Acids Res., 2013)

Orchestrating differential data access for translational research: a pilot implementation. - Marco Brandizi; Olga Melnichuk; Raffael Bild; Florian Kohlmayer; Benedicto Rodriguez-Castro; Helmut Spengler; Klaus A. Kuhn; Wolfgang Kuchinke; Christian Ohmann; Timo Mustonen; Mikael Linden; Tommi H. Nyrönen; et al. (BMC Medical Informatics Decis. Mak., 2017)

Common ELIXIR Service for Researcher Authentication and Authorisation. - Mikael Linden; Michal Procházka; Ilkka Lappalainen; Dominik Bucik; Pavel Vyskocil; Martin Kuba; Sami Silén; Peter Belmann; Alexander Sczyrba; Steven J. Newhouse; Ludek Matyska; Tommi H. Nyrönen (F1000Research, 2018)

Annotation and curation of human genomic variations: an ELIXIR Implementation Study. - Alessia David; Valérie Barbié; Marcella Attimonelli; Roberto Preste; Enni Makkonen; Heidi Marjonen; Mats R. K. Lindstedt; Kati Kristiansson; Sarah E. Hunt; Fiona Cunningham; Ilkka Lappalainen; Michael J. E. Sternberg (F1000Research, 2020)