Ilkka Lappalainen
Ilkka Lappalainen
CSC - IT Center for Science
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Cited by
Cited by
The European Genome-phenome Archive of human data consented for biomedical research
I Lappalainen, J Almeida-King, V Kumanduri, A Senf, JD Spalding, ...
Nature genetics 47 (7), 692-695, 2015
DbVar and DGVa: public archives for genomic structural variation
I Lappalainen, J Lopez, L Skipper, T Hefferon, JD Spalding, J Garner, ...
Nucleic acids research 41 (D1), D936-D941, 2012
Structure-function analysis of PrsA reveals roles for the parvulin-like and flanking N-and C-terminal domains in protein folding and secretion in Bacillus subtilis
M Vitikainen, I Lappalainen, R Seppala, H Antelmann, H Boer, S Taira, ...
Journal of Biological Chemistry 279 (18), 19302-19314, 2004
4 Primary immunodeficiency mutation databases
M Vihinen, FX Arredondo-Vega, JL Casanova, A Etzioni, S Giliani, ...
Academic Press 43, 103-188, 2001
The metal dependence of Bacillus subtilis phytase
J Kerovuo, I Lappalainen, T Reinikainen
Biochemical and Biophysical Research Communications 268 (2), 365-369, 2000
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, O Brandau, LJ Brandén, SP Kwan, I Lappalainen, T Lester, ...
Nucleic acids research 26 (1), 242-247, 1998
Leveraging European infrastructures to access 1 million human genomes by 2022
G Saunders, M Baudis, R Becker, S Beltran, C Béroud, E Birney, ...
Nature Reviews Genetics 20 (11), 693-701, 2019
Public data archives for genomic structural variation
DM Church, I Lappalainen, TP Sneddon, J Hinton, M Maguire, J Lopez, ...
Nature genetics 42 (10), 813-814, 2010
Federated discovery and sharing of genomic data using Beacons
M Fiume, M Cupak, S Keenan, J Rambla, S de la Torre, SOM Dyke, ...
Nature biotechnology 37 (3), 220-224, 2019
Sequence specificity in CpG mutation hotspots
J Ollila, I Lappalainen, M Vihinen
FEBS letters 396 (2-3), 119-122, 1996
Genome wide analysis of pathogenic SH2 domain mutations
I Lappalainen, J Thusberg, B Shen, M Vihinen
Proteins: Structure, Function, and Bioinformatics 72 (2), 779-792, 2008
Pattern of somatic androgen receptor gene mutations in patients with hormone-refractory prostate cancer
ER Hyytinen, K Haapala, J Thompson, I Lappalainen, M Roiha, I Rantala, ...
Laboratory investigation 82 (11), 1591-1598, 2002
Plasticity within the obligatory folding nucleus of an immunoglobulin-like domain
I Lappalainen, MG Hurley, J Clarke
Journal of molecular biology 375 (2), 547-559, 2008
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, BH Belohradsky, RN Haire, E Holinski-Feder, SP Kwan, ...
Nucleic acids research 25 (1), 166-171, 1997
A system for information management in biomedical studies—SIMBioMS
M Krestyaninova, A Zarins, J Viksna, N Kurbatova, P Rucevskis, SG Neogi, ...
Bioinformatics 25 (20), 2768-2769, 2009
Six X-linked agammaglobulinemia-causing missense mutations in the Src homology 2 domain of Bruton’s tyrosine kinase: phosphotyrosine-binding and circular dichroism analysis
PT Mattsson, I Lappalainen, CM Bäckesjö, E Brockmann, S Laurén, ...
The Journal of Immunology 164 (8), 4170-4177, 2000
Using Model Proteins to Quantify the Effects of Pathogenic Mutations in Ig-like Proteins*♦
LG Randles, I Lappalainen, SB Fowler, B Moore, SJ Hamill, J Clarke
Journal of biological chemistry 281 (34), 24216-24226, 2006
Registered access: a ‘Triple-A’approach
SOM Dyke, E Kirby, M Shabani, A Thorogood, K Kato, BM Knoppers
European Journal of Human Genetics 24 (12), 1676-1680, 2016
Registered access: authorizing data access
SOM Dyke, M Linden, I Lappalainen, JR De Argila, K Carey, D Lloyd, ...
European Journal of Human Genetics 26 (12), 1721-1731, 2018
Common ELIXIR service for researcher authentication and authorisation
M Linden, M Procházka, I Lappalainen, D Bucik, P Vyskocil, M Kuba, ...
F1000Research 7, 2018
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