Zobrazeno 1 - 10
of 346
pro vyhledávání: '"Lars Oreland"'
The objective was two-fold: to examine possible associations between dopamine-related genetic polymorphisms and (1) substance dependence; and (2) self-reported psychiatric disturbances, behavioral problems, and personality. Genotyping of single nucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21231da02e2b55d11b89c73fb72ea984
https://hdl.handle.net/10037/24255
https://hdl.handle.net/10037/24255
Publikováno v:
Journal of Neural Transmission
Since the pioneering finding of Caspi and co-workers in 2002 that exposure to childhood maltreatment predicted later antisocial behaviour (ASB) in male carriers of the low-activity MAOA-uVNTR allele, frequent replication studies have been published.
Publikováno v:
Personality and Individual Differences. 118:71-76
The objective was to outline results from our scientific studies on the associations among childhood behavior, adult personality, and biochemical factors in smoking habits. The studies consisted of ...
Autor:
C. Robert Cloninger, Kent W. Nilsson, Lars Oreland, Erika Comasco, Simone Toffoletto, Gianvito Lagravinese, Jaanus Harro
Publikováno v:
Journal of Neural Transmission
Genetic and environmental interactive influences on predisposition to develop alcohol use disorder (AUD) account for the high heterogeneity among AUD patients and make research on the risk and resiliency factors complicated. Several attempts have bee
Autor:
Erika Comasco, Tommy Lewander, Nikolaos Venizelos, Lena Flyckt, Lars Bjerkenstedt, Erik Söderman, Lars Oreland, Dimitrios Andreou, Ingrid Agartz, Erik G. Jönsson, Simone Toffoletto, Lars Terenius, Jessica Johansson, Ravi Vumma
Publikováno v:
Neuropsychobiology. 74:96-103
Schizophrenia involves neural catecholaminergic dysregulation. Tyrosine is the precursor of catecholamines, and its major transporter, according to studies on fibroblasts, in the brain is the L-type amino acid transporter 1 (LAT1). The present study
Autor:
Erik G. Jönsson, Tomas Moberg, Johan Königsson, Jari Tiihonen, Peter Nordström, Lars Oreland, Jussi Jokinen, Marie Åsberg
Publikováno v:
Psychiatry research. 260
Low platelet monoamine oxidase B (MAO-B) activity, proxy of low central serotonergic functions, has been shown to correlate with criminal behavior in adolescents that come from an unfavorable psychosocial environment but not in adolescents from good
Autor:
Adrian Andrzej Chrobak, Dena Sadeghi Bahmani, Erika Comasco, Erik G. Jönsson, Erik Söderman, Janusz K. Rybakowski, Hiroaki Jitsuiki, R. Michael Bagby, Dominika Dudek, Mohammad Ahmadpanah, Satz Mengensatzproduktion, Lena Flyckt, Masahiro Takamura, Lars Oreland, Dimitrios Andreou, Anjali Janardhanan, Daniela S.S. Lobo, Tetsuya Yamamoto, Livia Voneschen, Kazuo Awai, Marzieh Nazaribadie, Mohammad Haghighi, Akiko Kurata, Lars Terenius, Anjana Sadanand, Jens Gaab, Yoko Kaichi, Ewa Dopierala, Marcin Siwek, Anna Tereszko, Druckerei Stückle, Mehran Shayganfard, Osamu Yamamoto, Julia Jiménez, Edith Holsboer-Trachsler, Daniel Oschwald, Serge Brand, Yuji Akiyama, Simone Toffoletto, Tatsuji Tamura, Arambakkam Janardhanam Vanisree, Andrea H. Meyer, Urs M. Nater, Hafez Bajoghli, Lena C. Quilty, Victoria S. Marshe, Ewa Ferensztajn-Rochowiak, Ingrid Agartz, Shigeru Toki, Yasumasa Okamoto, Peter Krummenacher, Jan Jaracz, Daniel J. Müller, N. Yokota, Jessica Johansson, Ravi Vumma, Kate L. Harkness, Flávio Kapczinski, Lars Bjerkenstedt, Tommy Lewander, Leila Jahangard, Shigeto Yamawaki, Michał Michalak, Nikolaos Venizelos, Go Okada
Publikováno v:
Neuropsychobiology. 74(2)
Publikováno v:
BMC Musculoskeletal Disorders, Vol 18, Iss 1, Pp 1-7 (2017)
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders
Background The COMT (Catechol-O-Methyl Transferase) gene may influence a person’s vulnerability to develop long-term pain and some COMT single nucleotide polymorphisms (SNPs) may associate with patterns of acute or chronic pain. Many patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cba7c7e2703e54f85e2b363e30201f4
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-344219
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-344219
Autor:
Britt af Klinteberg, Roman A. Koposov, Elena L. Grigorenko, Johan Isaksson, Vladislav Ruchkin, Lars Oreland
Publikováno v:
European Archives of Psychiatry and Clinical Neuroscience. 266:771-773
Early onset of conduct disorder (CD) with callous-unemotional traits has been linked to low levels of dopamine β-hydroxylase (DβH), an enzyme involved in dopamine turnover. The C1021T polymorphism in the DβH gene is a major quantitative-trait locu
Publikováno v:
European Neuropsychopharmacology. 23:1300-1306
Both the serotonin transporter linked promoter region (5-HTTLPR) and the brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms have been shown to interact with unfavourable environment in relation to depression symptoms and to depression di