Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Eva Lindholm"'
Autor:
Eva Lindholm Carlström, Jonatan Halvardson, Mitra Etemadikhah, Lennart Wetterberg, Karl-Henrik Gustavson, Lars Feuk
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-9 (2019)
Abstract Background Non-syndromic intellectual disability is genetically heterogeneous with dominant, recessive and complex forms of inheritance. We have performed detailed genetic studies in a large multi-generational Swedish family, including sever
Externí odkaz:
https://doaj.org/article/7722400c1fef40928b252530b1a420ea
Publikováno v:
PLoS ONE, Vol 5, Iss 9, p e13079 (2010)
The human QKI gene, called quaking homolog, KH domain RNA binding (mouse), is a candidate gene for schizophrenia encoding an RNA-binding protein. This gene was shown to be essential for myelination in oligodendrocytes. QKI is also highly expressed in
Externí odkaz:
https://doaj.org/article/5731ee0d823345e5a308daa7c60dc01a
Autor:
Torabi Moghadam, Behrooz, Etemadikhah, Mitra, Rajkowska, Grazyna, Stockmeier, Craig, Grabherr, Manfred, Komorowski, Jan, Feuk, Lars, Carlström, Eva Lindholm
Publikováno v:
In Journal of Psychiatric Research July 2019 114:41-47
Autor:
Mitra Etemadikhah, Grazyna Rajkowska, Craig A. Stockmeier, Lars Feuk, Adnan Niazi, Eva Lindholm Carlström, Bo Nilsson, Jonatan Halvardson, Stefan Enroth
Publikováno v:
Genes
Volume 12
Issue 8
Genes, Vol 12, Iss 1242, p 1242 (2021)
Volume 12
Issue 8
Genes, Vol 12, Iss 1242, p 1242 (2021)
Schizophrenia is a genetically complex neuropsychiatric disorder with largely unresolved mechanisms of pathology. Identification of genes and pathways associated with schizophrenia is important for understanding the development, progression and treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bebb20a80bd0557d44878dc5ba7e11f2
https://pubmed.ncbi.nlm.nih.gov/34440415
https://pubmed.ncbi.nlm.nih.gov/34440415
Autor:
Jonatan Halvardson, Lars Feuk, Mitra Etemadikhah, Eva Lindholm Carlström, Lennart Wetterberg, Karl-Henrik Gustavson
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-9 (2019)
BMC Medical Genomics
BMC Medical Genomics
Background Non-syndromic intellectual disability is genetically heterogeneous with dominant, recessive and complex forms of inheritance. We have performed detailed genetic studies in a large multi-generational Swedish family, including several member
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f2276309d4c765ee3bbe158fbf4cc79
http://link.springer.com/article/10.1186/s12920-019-0606-4
http://link.springer.com/article/10.1186/s12920-019-0606-4
Autor:
Jan Komorowski, Craig A. Stockmeier, Manfred Grabherr, Lars Feuk, Grazyna Rajkowska, Eva Lindholm Carlström, Mitra Etemadikhah, Behrooz Torabi Moghadam
Publikováno v:
J Psychiatr Res
Schizophrenia is a common mental disorder with high heritability. It is genetically complex and to date more than a hundred risk loci have been identified. Association of environmental factors and schizophrenia has also been reported, while epigeneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc163dcbed9a7fce4095563720480c4
https://doi.org/10.1016/j.jpsychires.2019.04.001
https://doi.org/10.1016/j.jpsychires.2019.04.001
Akademický článek
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Autor:
Jan Mulder, Eva Lindholm Carlström, Mathias Uhlén, Nicholas Mitsios, Anna Månberg, David Just, Lars Feuk, Peter Nilsson, Grazyna Rajkowska, Craig A. Stockmeier, Janet L. Cunningham
Publikováno v:
Translational Psychiatry, Vol 10, Iss 1, Pp 1-12 (2020)
Translational Psychiatry
Translational Psychiatry
In recent years, studies have shown higher prevalence of autoantibodies in patients with schizophrenia compared to healthy individuals. This study applies an untargeted and a targeted affinity proteomics approach to explore and characterize the autoa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef48286d3993ef01518e389ee77e0a5b
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-428314
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-428314
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
CarlstrĂśm, Eva Lindholm, Jonatan Halvardson, Etemadikhah, Mitra, Wetterberg, Lennart, Karl-Henrik Gustavson, Feuk, Lars
Additional file 1: Figure S1. The figure shows the karyotype of two individuals from the family. The karyotype on the left shows the chromosomes for an affected individual (individual 3) and the karyotype to the right shows the chromosomes for the un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa0e99728b2cbee66d5a3e52443060ac