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ORCIDIlkka Lappalainen
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2020 – today
- 2020
[i2]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:
Annotation and curation of human genomic variations: an ELIXIR Implementation Study. F1000Research 9: 1207 (2020)
2010 – 2019
- 2018
- [i1]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:
Common ELIXIR Service for Researcher Authentication and Authorisation. F1000Research 7: 1199 (2018) - 2017
- [j4]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, Ilkka Lappalainen, Alvis Brazma, Ugis Sarkans:
Orchestrating differential data access for translational research: a pilot implementation. BMC Medical Informatics Decis. Mak. 17(1): 30:1-30:14 (2017) - 2013
- [j3]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, Paul Flicek, Deanna M. Church:
dbVar and DGVa: public archives for genomic structural variation. Nucleic Acids Res. 41(Database-Issue): 936-941 (2013)
2000 – 2009
- 2009
- [j2]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, Karlis Podnieks, Ugis Sarkans, Mark I. McCarthy, Alvis Brazma:
A System for Information Management in BioMedical Studies - SIMBioMS. Bioinform. 25(20): 2768-2769 (2009)
1990 – 1999
- 1998
- [j1]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, C. I. Edvard Smith:
BTKbase, mutation database for X-linked agammaglobulinemia (XLA). Nucleic Acids Res. 26(1): 242-247 (1998)
Coauthor Index
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