Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Buil Demur A"'
Autor:
Francesco Bettella, Andrew A Brown, Olav B Smeland, Yunpeng Wang, Aree Witoelar, Alfonso A Buil Demur, Wesley K Thompson, Verena Zuber, Anders M Dale, Srdjan Djurovic, Ole A Andreassen
Publikováno v:
PLoS ONE, Vol 13, Iss 9, p e0202812 (2018)
The genome-wide association study of the Psychiatric Genomics Consortium identified over one hundred schizophrenia susceptibility loci. The number of non-coding variants discovered suggests that gene regulation could mediate the effect of these varia
Externí odkaz:
https://doaj.org/article/5201fd31959a463c87afed3fc832b37f
Autor:
Martin Tesli, John Shorter, Andreas Jangmo, Joëlle Pasman, Ole Andreassen, Patrick Sullivan, Thomas Werge, Yi Lu, Alfonso Buil Demur
Publikováno v:
European Neuropsychopharmacology. 63:e32
Autor:
Bettella, Francesco, Brown, AA, Smeland, Olav Bjerkehagen, Wang, Yunpeng, Witoelar, Aree, Buil Demur, AA, Thompson, WK, Zuber, Verena, Dale, AM, Djurovic, Srdjan, Andreassen, Ole Andreas
Publikováno v:
Bettella, Francesco Brown, AA Smeland, Olav Bjerkehagen Wang, Yunpeng Witoelar, Aree Buil Demur, AA Thompson, WK Zuber, Verena Dale, AM Djurovic, Srdjan Andreassen, Ole Andreas . Cross-tissue eQTL enrichment of associations in schizophrenia.. PLoS ONE. 2018, 13(9)
PLoS ONE
PLoS ONE
Autor:
Graham Johnson, Timothy E. Reddy, Chunyu Liu, Lingyun Song, Paola Giusti-Rodríguez, Craig A. Stockmeier, Melanie E. Garrett, Panos Roussos, Alfonso Buil Demur, Patrick F. Sullivan, Allison E. Ashley-Koch, Julien Bryois, Vahram Haroutunian, Pamela Sklar, Kevin P. White, Gregory E. Crawford, Gregory A. Wray, Alexias Safi, John F. Fullard, Schahram Akbarian
Schizophrenia genome-wide association (GWA) studies have identified over 150 regions of the genome that are associated with disease risk, yet there is little evidence that coding mutations contribute to this disorder. To explore the mechanism of non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a2c80e1d13331cef89ef0a574b3412
https://doi.org/10.1101/141986
https://doi.org/10.1101/141986
Autor:
Dungu KHS; Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital, Copenhagen, Denmark. kia.hee.schultz.dungu@regionh.dk.; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark. kia.hee.schultz.dungu@regionh.dk., Hagen CM; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark., Bækvad-Hansen M; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark., Yakimov V; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark., Buil Demur A; Mental Health Centre Sct. Hans, Capital Region of Denmark, Institute of Biological Psychiatry, Copenhagen University Hospital, Copenhagen, Denmark., Carlsen EM; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.; Department of Neonatology, Copenhagen University Hospital, Copenhagen, Denmark., Vissing NH; Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital, Copenhagen, Denmark., Brink Henriksen T; Department of Paediatrics & Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.; Department of Clincal Medicine, Aarhus University, Aarhus, Denmark., Mogensen TH; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.; Department of Biomedicine, Aarhus University, Aarhus, Denmark., Hougaard DM; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark., Nygaard U; Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital, Copenhagen, Denmark.; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark., Bybjerg-Grauholm J; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
Publikováno v:
Communications medicine [Commun Med (Lond)] 2024 Dec 18; Vol. 4 (1), pp. 268. Date of Electronic Publication: 2024 Dec 18.