Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Sourena Soheili‐Nezhad"'
Autor:
Jitse S. Amelink, Merel C. Postema, Xiang-Zhen Kong, Dick Schijven, Amaia Carrión-Castillo, Sourena Soheili-Nezhad, Zhiqiang Sha, Barbara Molz, Marc Joliot, Simon E. Fisher, Clyde Francks
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-13 (2024)
Abstract Language is supported by a distributed network of brain regions with a particular contribution from the left hemisphere. A multi-level understanding of this network requires studying its genetic architecture. We used resting-state imaging da
Externí odkaz:
https://doaj.org/article/17c544a269d24efe8f55349c3b7073bc
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)
Abstract Handedness is a manifestation of brain hemispheric specialization. Left-handedness occurs at increased rates in neurodevelopmental disorders. Genome-wide association studies have identified common genetic effects on handedness or brain asymm
Externí odkaz:
https://doaj.org/article/fed3b20726024c7586856c91f8c0f000
Autor:
Christienne G. Damatac, Sourena Soheili-Nezhad, Guilherme Blazquez Freches, Marcel P. Zwiers, Sanne de Bruijn, Seyma Ikde, Christel M. Portengen, Amy C. Abelmann, Janneke T. Dammers, Daan van Rooij, Sophie E.A. Akkermans, Jilly Naaijen, Barbara Franke, Jan K. Buitelaar, Christian F. Beckmann, Emma Sprooten
Publikováno v:
NeuroImage: Clinical, Vol 35, Iss , Pp 103057- (2022)
Background: Variation in the longitudinal course of childhood attention deficit/hyperactivity disorder (ADHD) coincides with neurodevelopmental maturation of brain structure and function. Prior work has attempted to determine how alterations in white
Externí odkaz:
https://doaj.org/article/3e4db9bb51eb43dfa28bacaaa1087b80
Autor:
Anne E. M. Leenders, Christienne G. Damatac, Sourena Soheili‐Nezhad, Roselyne J. M. Chauvin, Maarten J. J. Mennes, Marcel P. Zwiers, Daan vanRooij, Sophie E. A. Akkermans, Jilly Naaijen, Barbara Franke, Jan K. Buitelaar, Christian F. Beckmann, Emma Sprooten
Publikováno v:
JCPP Advances, Vol 1, Iss 3, Pp n/a-n/a (2021)
Abstract Background Attention‐deficit hyperactivity disorder (ADHD) is associated with white matter (WM) microstructure. Our objective was to investigate how WM microstructure is longitudinally related to symptom remission in adolescents and young
Externí odkaz:
https://doaj.org/article/2556e5ee80764f83842fbbd1c648b26c
Autor:
Renata Basso Cupertino, Sourena Soheili-Nezhad, Eugenio Horacio Grevet, Cibele Edom Bandeira, Felipe Almeida Picon, Maria Eduarda de Araujo Tavares, Jilly Naaijen, Daan van Rooij, Sophie Akkermans, Eduardo Schneider Vitola, Marcel P Zwiers, Diego Luiz Rovaris, Pieter J. Hoekstra, Vitor Breda, Jaap Oosterlaan, Catharina A Hartman, Christian F Beckmann, Jan K Buitelaar, Barbara Franke, Claiton Henrique Dotto Bau, Emma Sprooten
Publikováno v:
NeuroImage: Clinical, Vol 28, Iss , Pp 102403- (2020)
Attention-Deficit/Hyperactivity Disorder (ADHD) has been associated with altered brain anatomy in neuroimaging studies. However, small and heterogeneous study samples, and the use of region-of-interest and tissue-specific analyses have limited the co
Externí odkaz:
https://doaj.org/article/eae6488a72ea4d8e8122e84e48ee57fb
Autor:
Sourena Soheili-Nezhad, Alireza Sedghi, Ferdinand Schweser, Amir Eslami Shahr Babaki, Neda Jahanshad, Paul M. Thompson, Christian F. Beckmann, Emma Sprooten, Mansoureh Toghae
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
It remains unknown whether migraine headache has a progressive component in its pathophysiology. Quantitative MRI may provide valuable insight into abnormal changes in the migraine interictum and assist in identifying disrupted brain networks. We car
Externí odkaz:
https://doaj.org/article/9b5ae473e0cb42228c1d22fb80746b6c
IntroductionHuman brain structure and function, as measured using magnetic resonance imaging (MRI), is heritable. The genetic associations are highly polygenic and pleiotropic, complicating translation of genetic association studies to concrete biolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae5e7d1d1fca23a5ebae70d66793176d
https://doi.org/10.1101/2022.07.13.499912
https://doi.org/10.1101/2022.07.13.499912
Autor:
Tim van der Es, Emma Sprooten, Sourena Soheili-Nezhad, Christienne G Damatac, Barbara Franke, Jan Buitelaar, Nina Roth Mota
Genome-wide association studies (GWAS) indicate neuropsychiatric disorders to be highly polygenic. Polygenicity refers to the additive influence of multiple genes on variation in a disorder. GWAS have identified many single-nucleotide polymorphisms (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c70e19898d1107f73f4b3100b0edb392
https://doi.org/10.1101/2022.06.16.22276110
https://doi.org/10.1101/2022.06.16.22276110
Autor:
Emma Sprooten, Anne E. M. Leenders, Maarten Mennes, Marcel P. Zwiers, Sourena Soheili-Nezhad, Christienne G. Damatac, Christian F. Beckmann, Jilly Naaijen, Sophie E.A. Akkermans, Jan K. Buitelaar, Daan van Rooij, Roselyne Chauvin, Barbara Franke
Publikováno v:
JCPP Advances, 1, 3
JCPP Advances, 1
JCPP Advances, Vol 1, Iss 3, Pp n/a-n/a (2021)
JCPP Advances, 1
JCPP Advances, Vol 1, Iss 3, Pp n/a-n/a (2021)
Contains fulltext : 251409.pdf (Publisher’s version ) (Open Access) BACKGROUND: Attention-deficit hyperactivity disorder (ADHD) is associated with white matter (WM) microstructure. Our objective was to investigate how WM microstructure is longitudi
Autor:
Guilherme Blazquez Freches, Christienne G. Damatac, Sourena Soheili-Nezhad, Amy C. Abelmann, Sanne de Bruijn, Sophie E.A. Akkermans, Jilly Naaijen, Emma Sprooten, Seyma Ikde, Jan K. Buitelaar, Christel M. Portengen, Janneke Dammers, Christian F. Beckmann, Barbara Franke, Marcel P. Zwiers, Daan van Rooij
BackgroundVariation in the longitudinal course of childhood attention deficit/hyperactivity disorder (ADHD) coincides with neurodevelopmental maturation of brain structure and function. Prior work has attempted to determine how alterations in white m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d5a75eb375b84f363c471f6d4ce2e82
https://doi.org/10.1101/2021.11.19.469248
https://doi.org/10.1101/2021.11.19.469248