Schiöth, Helgi B
< Back to all Authors17 January 2017
Ciuculete, Diana M, Boström, Adrian E, Voisin, Sarah ORCID: 0000-0002-4074-7083, Philipps, H, Titova, Olga E, Bandstein, Marcus, Nikontovic, L, Williams, Michael, Mwinyi, Jessica and Schiöth, Helgi B
(2017)
A methylome-wide mQTL analysis reveals associations of methylation sites with GAD1 and HDAC3 SNPs and a general psychiatric risk score.
Translational Psychiatry, 7.
ISSN 2158-3188
July 2018
Ciuculete, Diana M, Boström, Adrian E, Tuunainen, Anna-Kaisa ORCID: 0000-0003-4907-4433, Sohrabi, Farah
ORCID: 0000-0001-8575-639X, Kular, Lara, Jagodic, Maja, Voisin, Sarah
ORCID: 0000-0002-4074-7083, Mwinyi, J and Schiöth, Helgi B
(2018)
Changes in methylation within the STK32B promoter are associated with an increased risk for generalized anxiety disorder in adolescents.
Journal of psychiatric research, 102.
pp. 44-51.
ISSN 0022-3956
22 August 2018
Cedernaes, Jonathan ORCID: 0000-0002-9052-8372, Schönke, Milena
ORCID: 0000-0003-2030-6958, Westholm, Jakub Orzechowski
ORCID: 0000-0002-6849-6220, Mi, Jia, Chibalin, Alexander V, Voisin, Sarah
ORCID: 0000-0002-4074-7083, Osler, Megan, Vogel, Heike, Hörnaeus, Katarina, Dickson, Suzanne L, Lind, Sara Bergstrom, Bergquist, Jonas, Schiöth, Helgi B, Zierath, Juleen R and Benedict, Christian
(2018)
Acute sleep loss results in tissue-specific alterations in genome-wide DNA methylation state and metabolic fuel utilization in humans.
Science Advances, 4 (8).
ISSN 2375-2548
19 December 2019
Ciuculete, Diana M, Voisin, Sarah ORCID: 0000-0002-4074-7083, Kular, Lara, Welihinda, Nipuni, Jonsson, Jörgen, Jagodic, Maja, Mwinyi, J and Schiöth, Helgi B
(2019)
Longitudinal DNA methylation changes at MET may alter HGF/c-MET signalling in adolescents at risk for depression.
Epigenetics.
ISSN 1559-2294
2 July 2020
Ciuculete, Diana M, Voisin, Sarah ORCID: 0000-0002-4074-7083, Kular, Lara, Jonsson, Jörgen, Rask-Andersen, Mathias, Mwinyi, J and Schiöth, Helgi B
(2020)
meQTL and ncRNA functional analyses of 102 GWAS-SNPs associated with depression implicate HACE1 and SHANK2 genes.
Clinical Epigenetics, 12.
ISSN 1868-7075