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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:

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Afsheen Yousaf, Regina Waltes, Denise Haslinger, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 20

Showing 20 citing articles:

Genetic contributions to autism spectrum disorder
Alexandra Havdahl, Maria Niarchou, Anna Starnawska, et al.
Psychological Medicine (2021) Vol. 51, Iss. 13, pp. 2260-2273
Open Access | Times Cited: 61
Dimensional and transdiagnostic phenotypes in psychiatric genome-wide association studies
Monika A. Waszczuk, Katherine Jonas, Marina A. Bornovalova, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 12, pp. 4943-4953
Open Access | Times Cited: 21
The Neurogenetics of Functional Connectivity Alterations in Autism: Insights From Subtyping in 657 Individuals
Javier Rasero, Antonio Jiménez-Marín, Ibai Díez, et al.
Biological Psychiatry (2023) Vol. 94, Iss. 10, pp. 804-813
Open Access | Times Cited: 18
Neuroprotective Effects of Quercetin in Pediatric Neurological Diseases
Lourdes Álvarez‐Arellano, Marcela Salazar–García, Juan Carlos Corona
Molecules (2020) Vol. 25, Iss. 23, pp. 5597-5597
Open Access | Times Cited: 33
Deep Phenotyping of the Broader Autism Phenotype in Epilepsy: A Transdiagnostic Marker of Epilepsy and Autism Spectrum Disorder
Annie Richard, Ingrid E. Scheffer, Sarah J. Wilson
Annals of the Child Neurology Society (2025)
Open Access
CHAS infers cell type-specific signatures in bulk brain histone acetylation studies of neurological and psychiatric disorders
Kitty B. Murphy, Yuqian Ye, Maria Tsalenchuk, et al.
Cell Reports Methods (2025), pp. 101032-101032
Open Access
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
Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population
Taylor R. Thomas, Tanner Koomar, Lucas G. Casten, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 18
Risk and protective factors for mental disorders with onset in childhood/adolescence: An umbrella review of published meta-analyses of observational longitudinal studies
Marco Solmi, Elena Dragioti, Celso Arango, et al.
Neuroscience & Biobehavioral Reviews (2020) Vol. 120, pp. 565-573
Open Access | Times Cited: 26
Von den tiefgreifenden Entwicklungsstörungen in ICD-10 zur Autismus-Spektrum-Störung in ICD-11
Christine M. Freitag
Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie (2020) Vol. 49, Iss. 6, pp. 437-441
Closed Access | Times Cited: 9
Associations between the pupil light reflex and the broader autism phenotype in children and adults
Sapir Soker-Elimaliah, Aviva Lehrfield, Samuel R. Scarano, et al.
Frontiers in Human Neuroscience (2023) Vol. 16
Open Access | Times Cited: 3
CHAS, a deconvolution tool, infers cell type-specific signatures in bulk brain histone acetylation studies of brain disorders
Kitty B. Murphy, Yuqian Ye, Maria Tsalenchuk, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 7
A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
Ron Nudel, Richard Zetterberg, Nicoline Hemager, et al.
Behavioral and Brain Functions (2022) Vol. 18, Iss. 1
Open Access | Times Cited: 4
The STAR collaborative nonsuicidal self-injury study: methods and sample description of the face-to-face sample
Jennifer Spohrs, Anna Michélsen, Birgit Abler, et al.
Child and Adolescent Psychiatry and Mental Health (2024) Vol. 18, Iss. 1
Open Access
Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population
Taylor R. Thomas, Tanner Koomar, Lucas G. Casten, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 2
Genes involved in cholesterol cascades are linked to brain connectivity in one third of autistic patients
Javier Rasero, Antonio Jiménez-Marín, Ibai Díez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 1
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder
Nele Cosemans, Jarymke Maljaars, Annick Vogels, et al.
Neurogenetics (2021) Vol. 22, Iss. 3, pp. 207-213
Closed Access | Times Cited: 1
Applications of Polygenic Risk Scores in Psychiatric Genetics.
Qiao Mao, Zhimin Lan, Ping Liu, et al.
PubMed (2023) Vol. 12, Iss. 4, pp. 19-21
Closed Access
Autism excitation-inhibition imbalance linked to brain hyperconnectivity: An analysis based on 657 autistic subjects
Javier Rasero, Antonio Jiménez-Marín, Ibai Díez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
東北メディカル・メガバンク計画における大規模ゲノム・オミックス解析と疾患発症リスク予測
梅影 創, 清水 厚志
日本生物学的精神医学会誌 (2021) Vol. 32, Iss. 2, pp. 68-74
Closed Access
Gut and neurodevelopment: The role of gut microbiota dysbiosis in attention-deficit hyperactivity disorder and autism spectrum disorder
Caspar Bundgaard‐Nielsen
(2021)
Open Access
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