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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:

Association of Genetic Risks With Autism Spectrum Disorder and Early Neurodevelopmental Delays Among Children Without Intellectual Disability
Nagahide Takahashi, Taeko Harada, Tomoko Nishimura, et al.
JAMA Network Open (2020) Vol. 3, Iss. 2, pp. e1921644-e1921644
Open Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

The contributions of rare inherited and polygenic risk to ASD in multiplex families
Matilde Cirnigliaro, Timothy S. Chang, Stephanie A. Arteaga, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 31
Open Access | Times Cited: 50
Early Motor Signs in Autism Spectrum Disorder
Annio Posar, Paola Visconti
Children (2022) Vol. 9, Iss. 2, pp. 294-294
Open Access | Times Cited: 39
Cord blood lipid correlation network profiles are associated with subsequent attention-deficit/hyperactivity disorder and autism spectrum disorder symptoms at 2 years: a prospective birth cohort study
Kristina Vacy, Sarah Thomson, Archer Moore, et al.
EBioMedicine (2024) Vol. 100, pp. 104949-104949
Open Access | Times Cited: 10
Can the “female protective effect” liability threshold model explain sex differences in autism spectrum disorder?
Joseph Dougherty, Natasha Marrus, Susan E. Maloney, et al.
Neuron (2022) Vol. 110, Iss. 20, pp. 3243-3262
Open Access | Times Cited: 31
Association of intellectual disability with overall and type-specific cardiovascular diseases: a population-based cohort study in Denmark
Hui Wang, Priscilla Ming Yi Lee, Jun Zhang, et al.
BMC Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 16
Heterogeneity and Polygenicity in Psychiatric Disorders: A Genome-Wide Perspective
Frank R. Wendt, Gita A. Pathak, Daniel S. Tylee, et al.
Chronic Stress (2020) Vol. 4
Open Access | Times Cited: 49
Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders
Veronica B. Searles Quick, Belinda Wang, Matthew W. State
Neuropsychopharmacology (2020) Vol. 46, Iss. 1, pp. 55-69
Open Access | Times Cited: 39
The association between screen time and genetic risks for neurodevelopmental disorders in children
Nagahide Takahashi, Kenji J. Tsuchiya, Akemi Okumura, et al.
Psychiatry Research (2023) Vol. 327, pp. 115395-115395
Open Access | Times Cited: 13
Autism common variants associated with white matter alterations at birth: cross-sectional fixel-based analyses of 221 European term-born neonates from the developing human connectome project
Hai Le, Alexandra F. Bonthrone, Alena Uus, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
Autism spectrum disorder common variants associated with regional lobe volume variations at birth: cross-sectional study in 273 European term neonates in developing human connectome project
Hai Le, Daphna Fenchel, Konstantina Dimitrakopoulou, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
Classifying developmental delays with EEG: A comparative study of machine learning and deep learning approaches
Muhammad Usman, Wenyi Lin, Yi‐Chung Lin, et al.
Journal of Applied Biomedicine (2025) Vol. 45, Iss. 2, pp. 229-246
Closed Access
Systematic Review and Meta-Analysis: Phenotypic Correlates of the Autism Polygenic Score
Melanie M. de Wit, M. MORGAN, Ilan Libedinsky, et al.
JAACAP Open (2025)
Open Access
Peripheral biomarkers of attention-deficit hyperactivity disorder: Current status and future perspective
Nagahide Takahashi, Kanako Ishizuka, Toshiya Inada
Journal of Psychiatric Research (2021) Vol. 137, pp. 465-470
Closed Access | Times Cited: 23
Early manifestations of genetic risk for neurodevelopmental disorders
Ragna Bugge Askeland, Laurie J. Hannigan, Helga Ask, et al.
Journal of Child Psychology and Psychiatry (2021) Vol. 63, Iss. 7, pp. 810-819
Open Access | Times Cited: 21
Developmental milestones in early childhood and genetic liability to neurodevelopmental disorders
Laurie J. Hannigan, Ragna Bugge Askeland, Helga Ask, et al.
Psychological Medicine (2021) Vol. 53, Iss. 5, pp. 1750-1758
Open Access | Times Cited: 20
Autismo no Brasil: uma revisão sobre estudos em neurogenética
Victor Gustavo Oliveira Evangelho, Fabrício da Mota Ramalho Costa, Helena Carla Castro, et al.
Revista Neurociências (2021) Vol. 29, pp. 1-20
Open Access | Times Cited: 15
Elevated risk of attention deficit hyperactivity disorder (ADHD) in Japanese children with higher genetic susceptibility to ADHD with a birth weight under 2000 g
Md. Shafiur Rahman, Nagahide Takahashi, Toshiki Iwabuchi, et al.
BMC Medicine (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 13
The Need for a Motor Assessment Tool for Children with Autism—An Opinion Article
Hasan Wael Battah, Meir Lotan, Danny S. Moran
Diagnostics (2023) Vol. 13, Iss. 12, pp. 2095-2095
Open Access | Times Cited: 5
Genetic and Environmental Effects on the Early Motor Development as a Function of Parental Educational Attainment
Yahua Zi, C.E.M. van Beijsterveldt, Meike Bartels, et al.
Medicine & Science in Sports & Exercise (2023)
Open Access | Times Cited: 4
A Systematic Review and Meta-Analysis: Research Using the Autism Polygenic Score
Melanie M. de Wit, M. MORGAN, Ilan Libedinsky, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
AUTISMO E SEUS IMPACTOS NO DESENVOLVIMENTO NEUROPSICOMOTOR
Luana Tavares Neves, Laissa Giongo Spillari, Talma Reis Leal Fernandes, et al.
Revista Foco (2024) Vol. 17, Iss. 5, pp. e4937-e4937
Open Access | Times Cited: 1
Autism spectrum disorder common variants associated with regional lobe volume variations at birth: cross-sectional study in 273 European term neonates in developing Human Connectome Project
Hai Le, Daphna Fenchel, Konstantina Dimitrakopoulou, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
MUCOPOLYSACARIDOSIS TYPE IIIB MISDIAGNOSED AS AN AUTISTIC SPECTRUM DISORDER: A CASE REPORT AND LITERATURE REVIEW
Alan Tibério Dalpiaz Irigonhê, Angélica Malman Thomazine Moreira, Daniel Almeida do Valle, et al.
Revista Paulista de Pediatria (2020) Vol. 39
Open Access | Times Cited: 8
The Contributions of Rare Inherited and Polygenic Risk to ASD in Multiplex Families
Timothy S. Chang, Matilde Cirnigliaro, Stephanie A. Arteaga, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 4
Erwachsene interprofessionell versorgen – Autismus-Spektrum-Störung
Simon Stiehl, Markus Witzmann, Matthias Prommersberger, et al.
ergopraxis (2024) Vol. 17, Iss. 03, pp. 18-24
Closed Access
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