Zobrazeno 1 - 10
of 108
pro vyhledávání: '"V. Golimbet"'
Publikováno v:
European Psychiatry, Vol 67, Pp S293-S293 (2024)
Introduction Negative symptoms (NS) are an important clinical characteristic of schizophrenia. In recent years, clinical research on NS has focused on their clinical heterogeneity. Based on two-factor analysis, it has been proposed to divide NS into
Externí odkaz:
https://doaj.org/article/b9458db432574ff29303e4093311b34f
Publikováno v:
European Psychiatry, Vol 67, Pp S337-S338 (2024)
Introduction ASCL1 (Achaete-scute homolog 1) is a neuron-specific transcription factor involved in CNS maturation in the mammalian brain. It has been shown to be associated with schizophrenia (SZ), Parkinson’s disease, and the development of brain
Externí odkaz:
https://doaj.org/article/9ab899584b6847b68cb2d61b59c4b7c4
Publikováno v:
European Psychiatry, Vol 67, Pp S293-S294 (2024)
Introduction Understanding the relations between genetic (G) and environmental (E) factors in the development of schizophrenia is important for psychosis prevention. These relations may vary from G x E correlations to G x E interactions and independe
Externí odkaz:
https://doaj.org/article/ee0c88929aee4430a4d374b2810fea58
Autor:
V. Mikhailova, N. Kondratyev, M. Alfimova, V. Kaleda, T. Lezheiko, M. Ublinsky, V. Ushakov, I. Lebedeva, A. Galiakberova, A. Artyuhov, E. Dashinimaev, V. Golimbet
Publikováno v:
European Psychiatry, Vol 67, Pp S764-S765 (2024)
Introduction The main finding of a large-scale collaborative study (Rees et al. Nat Neurosci 2020;23(2) 179-184), which focused on de novo mutations in schizophrenia, was the discovery of an enrichment of these mutations in the SLC6A1 gene. This gene
Externí odkaz:
https://doaj.org/article/615aaa95103341d99968e46981f38849
Publikováno v:
European Psychiatry, Vol 67, Pp S588-S588 (2024)
Introduction Schizophrenia (SZ) is a common psychiatric neurodevelopmental disorder with a complex genetic architecture. Genomic association studies indicate the involvement of transcription factors in the pathogenesis of SZ. A recent GWAS showed a s
Externí odkaz:
https://doaj.org/article/e9dcbbad658442f88367992a6a06d8fd
Publikováno v:
European Psychiatry, Vol 66, Pp S890-S890 (2023)
Introduction Schizotypy is conceptualized to be on the continuum of the risk for psychosis. However, previous studies that used the dimensional approach to schizotypy failed to confirm the expected relations between schizotypal traits and polygenic r
Externí odkaz:
https://doaj.org/article/fd0d1cb056954218bebaa3fab0bdec38
Autor:
V. Mikhailova, M. Alfimova, T. Lezheiko, N. Kondratyev, V. Kaleda, A. Galiakberova, E. Dashinimaev, V. Golimbet
Publikováno v:
European Psychiatry, Vol 66, Pp S890-S891 (2023)
Introduction Schizophrenia is a severe mental disorder mainly caused by genetic risk factors. Many studies have demonstrated that both multiple genetic variants and rare mutations are associated with schizophrenia risk. The next step is to study the
Externí odkaz:
https://doaj.org/article/fb8ee019d9d6428e9f730d0b5f31e1ed
Publikováno v:
European Psychiatry, Vol 66, Pp S890-S890 (2023)
Introduction Schizophrenia (SZ) is an inherited mental illness that affects 1% of the world’s population. Schizophrenia is a common functional psychosis with some unifying features that appears to have a universal distribution. Much of the research
Externí odkaz:
https://doaj.org/article/c916d247e2fe4b40bc575f0d24b6479f
Publikováno v:
European Psychiatry, Vol 66, Pp S495-S495 (2023)
Introduction A large body of evidence shows that both genetic and environmental factors play an important role in the etiology of schizophrenia. There is also growing evidence of an interaction between these factors. Objectives To investigate the inf
Externí odkaz:
https://doaj.org/article/a9292724b810463d96897b59d62aeb6e
Autor:
A. Kibitov, A. Rakitko, E. Kasyanov, D. Yermakovich, G. Rukavishnikov, V. Ilinsky, V. Golimbet, A. Shmukler, N. Neznanov, G. Mazo
Publikováno v:
European Psychiatry, Vol 65, Pp S327-S327 (2022)
Introduction Depression is a chronic, recurrent mental disorder with a moderate level of genetic impact. Modern GWAS of depression require extra-large sample sizes and new effective, clinically sensitive, objective and simple to fill online phenotypi
Externí odkaz:
https://doaj.org/article/24bdc02260784f65b130082205d280ed