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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Williams syndrome
Rachel Royston, Jane Waite, Patricia Howlin
Current Opinion in Psychiatry (2018) Vol. 32, Iss. 2, pp. 60-66
Open Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

Cognitive strengths in neurodevelopmental disorders, conditions and differences: A critical review
Katherine Maw, Geoff Beattie, Edwin J. Burns
Neuropsychologia (2024) Vol. 197, pp. 108850-108850
Open Access | Times Cited: 6
Clinical phenotypes study of 231 children with Williams syndrome in China: A single‐center retrospective study
Fang-Fang Li, Weijun Chen, Dan Yao, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 12
Open Access | Times Cited: 25
Pragmatic Profiles of Adults with Fragile X Syndrome and Williams Syndrome
Eliseo Díez-Itza, Aitana Viejo, Maite Fernández-Urquiza
Brain Sciences (2022) Vol. 12, Iss. 3, pp. 385-385
Open Access | Times Cited: 19
Heritability of social behavioral phenotypes and preliminary associations with autism spectrum disorder risk genes in rhesus macaques: A whole exome sequencing study
Chris Gunter, R. Alan Harris, Zsofia Kovacs‐Balint, et al.
Autism Research (2022) Vol. 15, Iss. 3, pp. 447-463
Open Access | Times Cited: 18
Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders
Jianrong Zhou, Ying Zheng, Guiying Liang, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 15
Cannabinoid signaling modulation through JZL184 restores key phenotypes of a mouse model for Williams–Beuren syndrome
Alba Navarro-Romero, Lorena Galera-López, Paula Ortiz‐Romero, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 14
Anxiety, concerns and emotion regulation in individuals with Williams syndrome and Down syndrome during the COVID-19 outbreak: a global study
Vassilis Sideropoulos, Nayla Sokhn, Olympia Palikara, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 4
Anxiety during transition from primary to secondary schools in neurodivergent children
Vassilis Sideropoulos, Olympia Palikara, Elizabeth Burchell, et al.
JCPP Advances (2024)
Open Access | Times Cited: 1
Upregulated 5-HT1A receptor-mediated currents in the prefrontal cortex layer 5 neurons in the 15q11–13 duplication mouse model of autism
Fumihito Saitow, Toru Takumi, Hidenori Suzuki
Molecular Brain (2020) Vol. 13, Iss. 1
Open Access | Times Cited: 9
The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes
Rachel Royston, Chris Oliver, Patricia Howlin, et al.
Journal of Autism and Developmental Disorders (2019) Vol. 50, Iss. 3, pp. 893-903
Open Access | Times Cited: 9
Quality of life of Brazilian families who have children with Williams syndrome
Rafaela Catelan Martins Pereira, Aline Apis, Thamires Rosa Dos Santos, et al.
Journal of Intellectual Disabilities (2022) Vol. 27, Iss. 3, pp. 794-807
Closed Access | Times Cited: 5
Psychiatric and behavioral manifestations of Williams syndrome
Robyn P. Thom
Current Opinion in Psychiatry (2023) Vol. 37, Iss. 2, pp. 65-70
Closed Access | Times Cited: 2
Epigenetic aging in Williams syndrome
Kenji Okazaki, Ryo Kimura, Ikuo Otsuka, et al.
Journal of Child Psychology and Psychiatry (2022) Vol. 63, Iss. 12, pp. 1553-1562
Closed Access | Times Cited: 4
Williams syndrome: on the role of intellectual abilities in anxiety
Charlotte Willfors, Deborah M. Riby, Marcus van der Poll, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 5
Nationwide questionnaire data of 229 Williams-Beuren syndrome patients using WhatsApp tool
Lucas Vieira Lacerda Pires, Rogério Lemos Ribeiro, Adriana Sousa, et al.
Arquivos de Neuro-Psiquiatria (2021) Vol. 79, Iss. 11, pp. 950-956
Open Access | Times Cited: 4
Pragmatic skills in people with Williams syndrome: the perception of families
Esther Moraleda Sepúlveda, Patricia López-Resa
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Patients with Genetic Syndromes
Tamar Katz, Christine Finn, Joan M. Stoler
Elsevier eBooks (2024), pp. 711-723
Closed Access
Symptoms of autism in Williams syndrome: a transdiagnostic approach
Charlotte Willfors, Jacqueline Borg, Johan Lundin Kleberg, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
Early Cognitive and Language Development Characteristics of Children with Williams Syndrome in China
Dan Yao, Yan Zeng, Fangfang Li, et al.
Research Square (Research Square) (2024)
Closed Access
Overuse of familiar phrases by individuals with Williams syndrome masks differences in language processing
Ioana Sederias, Ariane Krakovitch, Vesna Stojanovik, et al.
Journal of Child Language (2024), pp. 1-15
Closed Access
News insights into social cognition in Williams syndrome from a comprehensive assessment and a virtual reality task
Niccolò Butti, Elisabetta Ferrari, Viola Oldrati, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
Fluorescence in situ hybridization (FISH) as an irreplaceable diagnostic tool for Williams-Beuren syndrome in developing countries: a literature review
Bianca Soares Carlotto, Desirée Deconte, Bruna Lixinski Diniz, et al.
Revista Paulista de Pediatria (2023) Vol. 42
Open Access | Times Cited: 1
Williams Syndrome With Rare Ureteric Abnormality
Jaffar M. Khan, Khaleel I. Al‐Obaidy, Rong Fan
Cureus (2021)
Open Access | Times Cited: 1
Pragmatic Skills in People With Williams Syndrome: the Perception of Families
Esther Moraleda Sepúlveda, Patricia López-Resa
Research Square (Research Square) (2023)
Open Access
Multisensory Texture Perception in Individuals with Williams Syndrome
Caroline Cheam, Koviljka Barisnikov, Édouard Gentaz, et al.
Children (2023) Vol. 10, Iss. 9, pp. 1494-1494
Open Access
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