Publications (628)

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Gameful Experience Questionnaire (GAMEFULQUEST): an instrument for measuring the perceived gamefulness of system use
(2019)
User Modeling and User-Adapted Interaction
Johan Högberg, Juho Hamari, Erik Wästlund
Gender diversity and firm value: Evidence from UK financial institutions
(2019)
International Journal of Accounting and Information Management
Peter Agyemang-Mintah, Hannu Schadewitz
Gene-environment correlations in parental emotional warmth and intolerance: genome-wide analysis over two generations of the Young Finns Study
(2019)
Journal of Child Psychology and Psychiatry
Henrik Dobewall, Kateryna Savelieva, Ilkka Seppälä, Ariel Knafo‐Noam, Christian Hakulinen, Marko Elovainio,
Liisa Keltikangas‐Järvinen, Laura Pulkki‐Råback, Olli T. Raitakari, Terho Lehtimäki, Mirka Hintsanen
Genetic and environmental perturbations lead to regulatory decoherence
(2019)
eLife
Amanda Lea, Meena Subramaniam, Arthur Ko, Terho Lehtimäki, Emma Raitoharju, Mika Kähönen, Ilkka Seppälä, Nina Mononen, Olli T Raitakari, Mika Ala-Korpela, Päivi Pajukanta, Noah Zaitlen, Julien F Ayroles
Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy
(2019)
ESC Heart Failure
Jääskeläinen P, Vangipurapu J, Raivo J, Kuulasmaa T, Heliö T, Aalto-Setälä K, Kaartinen M, Ilveskoski E, Vanninen S, Hämäläinen L, Melin J, Kokkonen J, Nieminen MS, Laakso M, Kuusisto J, Kervinen H, Mustonen J, Juvonen J, Niemi M, Uusimaa P, Junttila J, Kotila M, Pietilä M, Jyrkilä H, Mähönen I, Vartia P; The FinHCM Study Group
Genetic Contribution to the Divergence in Type 1 Diabetes Risk Between Children From the General Population and Children From Affected Families
(2019)
Diabetes
Hippich M, Beyerlein A, Hagopian WA, Krischer JP, Vehik K, Knoop J, Winker C, Toppari J, Lernmark A, Rewers MJ, Steck AK, She JX, Akolkar B, Robertson CC, Onengut-Gumuscu S, Rich SS, Bonifacio E, Ziegler AG
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
(2019)
Nature Genetics
Sakornsakolpat P, Prokopenko D, Lamontagne M, Reeve NF, Guyatt AL, Jackson VE, Shrine N, Qiao DD, Bartz TM, Kim DK, Lee MK, Latourelle JC, Li XN, Morrow JD, Obeidat M, Wyss AB, Bakke P, Barr RG, Beaty TH, Belinsky SA, Brusselle GG, Crapo JD, de Jong K, DeMeo DL, Fingerlin TE, Gharib SA, Gulsvik A, Hall IP, Hokanson JE, Kim WJ, Lomas DA, London SJ, Meyers DA, O'Connor GT, Rennard SI, Schwartz DA, Sliwinski P, Sparrow D, Strachan DP, Tal-Singer R, Tesfaigzi Y, Vestbo J, Vonk JM, Yim JJ, Zhou XB, Bosse Y, Manichaikul A, Lahousse L, Silverman EK, Boezen HM, Wain LV, Tobin MD, Hobbs BD, Cho; SpiroMeta Consortium & International COPD Genetics Consortium
Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008
(2019)
British Journal of Haematology
Sofie G. Højfeldt, Benjamin O. Wolthers, Morten Tulstrup, Jonas Abrahamsson, Ramneek Gupta, Arja Harila-Saari, Mats Heyman, Louise T. Henriksen, Òlafur G. Jónsson, Päivi M. Lähteenmäki, Bendik Lund, Kaie Pruunsild, Goda Vaitkeviciene, Kjeld Schmiegelow, Birgitte K. Albertsen; on behalf of the Nordic Society of Paediatric Haematology Oncology (NOPHO) group
Genetic risk factors for schizophrenia associate with sleep spindle activity in healthy adolescents
(2019)
Journal of Sleep Research
Merikanto I, Utge S, Lahti J, Kuula L, Makkonen T, Lahti-Pulkkinen M, Heinonen K, Raikkonen K, Andersson S, Strandberg T, Pesonen AK
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