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

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

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

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

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

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