Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ann Nordgren"'
Autor:
Charlotte Willfors, Jacqueline Borg, Johan Lundin Kleberg, Astrid Hallman, Marcus Van Der Poll, Karl Lundin Remnélius, Hanna Björlin Avdic, Sven Bölte, Ann Nordgren
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Williams syndrome (WS) is associated with atypical social communication and cognition reminiscent of the behaviours observed in autism. Nonetheless, WS also differs significantly from autism, such as regarding social motivation, which is typ
Externí odkaz:
https://doaj.org/article/f7701274778a49d6b4125a7340040fab
Autor:
Johan Lundin Kleberg, Astrid E. Z. Hallman, Martyna A. Galazka, Deborah M. Riby, Sven Bölte, Charlotte Willfors, Christine Fawcett, Ann Nordgren
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Typically developing humans automatically synchronize their arousal levels, resulting in pupillary contagion, or spontaneous adaptation of pupil size to that of others. This phenomenon emerges in infancy and is believed to facilitate social
Externí odkaz:
https://doaj.org/article/2a1cbbb3a4dc43df9ba1cfac7b420c7d
Autor:
Hanna Björlin Avdic, Claes Strannegård, Hedvig Engberg, Charlotte Willfors, Ida Nordgren, Louise Frisén, Angelica Lindén Hirschberg, Mona Guath, Ann Nordgren, Johan Lundin Kleberg
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Turner syndrome is a genetic condition caused by a complete or partial loss of one of the X chromosomes. Previous studies indicate that Turner syndrome is associated with challenges in social skills, but the underlying mechanisms remain larg
Externí odkaz:
https://doaj.org/article/3a471176cc094b27a8ceb37afa52cfed
Autor:
Hannes Runheim, Maria Pettersson, Anna Hammarsjö, Ann Nordgren, Martin Henriksson, Anna Lindstrand, Lars-Åke Levin, Maria Johansson Soller
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Whole genome sequencing (WGS) has the potential to be a comprehensive genetic test, especially relevant for individuals with neurodevelopmental disorders, syndromes and congenital malformations. However, the cost consequences of using whole
Externí odkaz:
https://doaj.org/article/ed547b24e60847ae8691c1c9643cc7ce
Autor:
Johan Lundin Kleberg, Charlotte Willfors, Hanna Björlin Avdic, Deborah Riby, Martyna A. Galazka, Mona Guath, Ann Nordgren, Claes Strannegård
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Williams syndrome (WS) is a rare genetic condition characterized by high social interest and approach motivation as well as intellectual disability and anxiety. Despite the fact that social stimuli are believed to have an increased intrinsic
Externí odkaz:
https://doaj.org/article/78f9795ba295482dababef0c7b2f4e75
Autor:
Ruth Godoy, M. Baktashian, Wolfgang Hofmeister, Li Yan, Anna Lindstrand, Long Guo, Anna Hammarsjö, Zheng Wang, Phillip T Newton, Patrick Shannon, Raquel Vaz, Jafar Nasiri, Naomichi Matsumoto, David Chitayat, Kalpana Gowrishankar, Fulya Taylan, Andrei S. Chagin, Gen Nishimura, Shiro Ikegawa, Maryam Sedghi, Giedre Grigelioniene, Noriko Miyake, K. Neethukrishna, Katta M. Girisha, Maria Pettersson, Ann Nordgren
Publikováno v:
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
The skeletal ciliopathies are a heterogeneous group of disorders with a significant clinical and genetic variability and the main clinical features are thoracic hypoplasia and short tubular bones. To date, 25 genes have been identified in association