Mwinyi, J

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Number of items: 7.

24 February 2015

Nilsson, EK, Ernst, B, Voisin, Sarah ORCID: 0000-0002-4074-7083, Almén, MS, Benedict, C, Mwinyi, J, Fredriksson, R, Schultes, B and Schiöth, HB (2015) Roux-En Y Gastric Bypass Surgery Induces Genome-Wide Promoter-Specific Changes in DNA Methylation in Whole Blood of Obese Patients. PLOS ONE, 10 (2). ISSN 1932-6203

22 April 2016

Boström, Adrian E, Mwinyi, J, Voisin, Sarah ORCID: 0000-0002-4074-7083, Wu, W, Schultes, B, Zhang, K and Schiöth, HB (2016) Longitudinal genome-wide methylation study of Roux-en-Y gastric bypass patients reveals novel CpG sites associated with essential hypertension. BMC Medical Genomics, 9. ISSN 1755-8794

September 2016

Bandstein, M, Voisin, Sarah ORCID: 0000-0002-4074-7083, Nilsson, EK, Schultes, B, Ernst, B, Thurnheer, M, Benedict, C, Mwinyi, J and Schiöth, HB (2016) A Genetic Risk Score Is Associated with Weight Loss Following Roux-en Y Gastric Bypass Surgery. Obesity Surgery, 26 (9). 2183 - 2189. ISSN 0960-8923

17 January 2017

Ciuculete, D, Boström, Adrian E, Voisin, Sarah ORCID: 0000-0002-4074-7083, Philipps, H, Titova, O, Bandstein, M, Nikontovic, L, Williams, M, Mwinyi, J 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

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