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Charlotte Willfors

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Citations 277
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Recent Articles
1.
Willfors C, Borg J, Kleberg J, Hallman A, Van Der Poll M, Lundin Remnelius K, et al.
Sci Rep . 2024 Jul; 14(1):17583. PMID: 39080307
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,...
2.
Kleberg J, Hallman A, Galazka M, Riby D, Bolte S, Willfors C, et al.
Sci Rep . 2023 Oct; 13(1):18397. PMID: 37884631
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...
3.
Bjorlin Avdic H, Strannegard C, Engberg H, Willfors C, Nordgren I, Frisen L, et al.
Sci Rep . 2023 Sep; 13(1):15858. PMID: 37739980
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...
4.
Bjorlin Avdic H, Kleberg J, Van Der Poll M, Frisen L, Hutley M, Sarjanen M, et al.
Cogn Neuropsychiatry . 2023 May; 28(3):207-225. PMID: 37165648
Introduction: The behavioural phenotype in Turner syndrome (TS) is associated with an uneven cognitive profile and social and executive difficulties. Still, studies in adult populations of TS are scarce, and...
5.
Kleberg J, Willfors C, Bjorlin Avdic H, Riby D, Galazka M, Guath M, et al.
Sci Rep . 2023 Jan; 13(1):164. PMID: 36599864
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...
6.
Guath M, Willfors C, Bjorlin Avdic H, Nordgren A, Kleberg J
J Int Neuropsychol Soc . 2022 May; 29(3):306-315. PMID: 35545874
Objective: Major depressive disorder (MDD) is associated with impaired reward processing and reward learning. The literature is inconclusive regarding whether these impairments persist after remission. The current study examined reward...
7.
Kleberg J, Riby D, Fawcett C, Bjorlin Avdic H, Frick M, Brocki K, et al.
J Autism Dev Disord . 2022 Apr; 53(7):2786-2797. PMID: 35445369
Williams syndrome (WS) is a rare genetic condition associated with high sociability, intellectual disability, and social cognitive challenges. Attention to others' eyes is crucial for social understanding. Orienting to, and...
8.
Willfors C, Riby D, Van Der Poll M, Ekholm K, Avdic Bjorlin H, Kleberg J, et al.
Orphanet J Rare Dis . 2021 Nov; 16(1):472. PMID: 34743752
Background: Individuals with Williams syndrome (WS) have an elevated risk for anxiety disorders throughout the life span, making it a research priority to identify the individual factors associated with anxiety....
9.
Becker M, Mastropasqua F, Reising J, Maier S, Ho M, Rabkina I, et al.
Transl Psychiatry . 2020 Sep; 10(1):312. PMID: 32929080
CASK-related disorders are genetically defined neurodevelopmental syndromes. There is limited information about the effects of CASK mutations in human neurons. Therefore, we sought to delineate CASK-mutation consequences and neuronal effects...
10.
Austin C, Curtin P, Curtin A, Gennings C, Arora M, Tammimies K, et al.
Transl Psychiatry . 2019 Sep; 9(1):238. PMID: 31551411
Attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) are neurodevelopmental conditions of overlapping etiologies and phenotypes. For ASD, we recently reported altered elemental metabolic patterns in the form...