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:

Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
Bregje W.M. van Bon, Bradley P. Coe, Raphael Bernier, et al.
Molecular Psychiatry (2015) Vol. 21, Iss. 1, pp. 126-132
Open Access | Times Cited: 161

Showing 1-25 of 161 citing articles:

Autism spectrum disorder
Catherine Lord, Traolach Brugha, Tony Charman, et al.
Nature Reviews Disease Primers (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 1135

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Holly A.F. Stessman, Bo Xiong, Bradley P. Coe, et al.
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 515-526
Open Access | Times Cited: 511

De novo genic mutations among a Chinese autism spectrum disorder cohort
Tianyun Wang, Hui Guo, Bo Xiong, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 331

The neuroanatomy of autism – a developmental perspective
Alex P. A. Donovan, M. Albert Basson
Journal of Anatomy (2016) Vol. 230, Iss. 1, pp. 4-15
Open Access | Times Cited: 214

Inhibition of DYRK1A and GSK3B induces human β-cell proliferation
Weijun Shen, Brandon L. Taylor, Qihui Jin, et al.
Nature Communications (2015) Vol. 6, Iss. 1
Open Access | Times Cited: 185

A Short Review on the Current Understanding of Autism Spectrum Disorders
Hye Ran Park, Jae Meen Lee, Hyo Eun Moon, et al.
Experimental Neurobiology (2016) Vol. 25, Iss. 1, pp. 1-13
Open Access | Times Cited: 183

Optical genome mapping enables constitutional chromosomal aberration detection
Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1409-1422
Open Access | Times Cited: 168

Role of phosphodiesterases in the pathophysiology of neurodevelopmental disorders
Sébastien Delhaye, Barbara Bardoni
Molecular Psychiatry (2021) Vol. 26, Iss. 9, pp. 4570-4582
Open Access | Times Cited: 125

High-throughput functional analysis of autism genes in zebrafish identifies convergence in dopaminergic and neuroimmune pathways
Hellen Weinschutz Mendes, Uma Neelakantan, Yunqing Liu, et al.
Cell Reports (2023) Vol. 42, Iss. 3, pp. 112243-112243
Open Access | Times Cited: 44

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Madeleine R. Geisheker, Gabriel Heymann, Tianyun Wang, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 8, pp. 1043-1051
Open Access | Times Cited: 164

DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome
Arnaud Duchon, Yann Hérault
Frontiers in Behavioral Neuroscience (2016) Vol. 10
Open Access | Times Cited: 161

Toward a conceptual framework for early brain and behavior development in autism
Joseph Piven, J T Elison, Mark J. Zylka
Molecular Psychiatry (2017) Vol. 22, Iss. 10, pp. 1385-1394
Open Access | Times Cited: 150

DYRK1A and cognition: A lifelong relationship
María L. Arbonés, Aurore Thomazeau, Akiko Nakano-Kobayashi, et al.
Pharmacology & Therapeutics (2018) Vol. 194, pp. 199-221
Open Access | Times Cited: 150

Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders
Holly A.F. Stessman, Marjolein H. Willemsen, Michaela Fencková, et al.
The American Journal of Human Genetics (2016) Vol. 98, Iss. 3, pp. 541-552
Open Access | Times Cited: 149

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model
Hui Guo, Tianyun Wang, Huidan Wu, et al.
Molecular Autism (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 144

Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
Anke Van Dijck, Anneke T. Vulto‐van Silfhout, Elisa Cappuyns, et al.
Biological Psychiatry (2018) Vol. 85, Iss. 4, pp. 287-297
Open Access | Times Cited: 133

Neocortical neurogenesis and the etiology of autism spectrum disorder
Alan Packer
Neuroscience & Biobehavioral Reviews (2016) Vol. 64, pp. 185-195
Closed Access | Times Cited: 127

Zebrafish knockout of Down syndrome gene, DYRK1A, shows social impairments relevant to autism
Oc-Hee Kim, Hyun-Ju Cho, Enna Han, et al.
Molecular Autism (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 114

A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons
Yu‐Chih Lin, Jeannine A. Frei, Michaela B. C. Kilander, et al.
Frontiers in Cellular Neuroscience (2016) Vol. 10
Open Access | Times Cited: 96

Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders
Jinchen Li, Lin Wang, Hui Guo, et al.
Molecular Psychiatry (2017) Vol. 22, Iss. 9, pp. 1282-1290
Closed Access | Times Cited: 96

Genetic control of postnatal human brain growth
Laura I. van Dyck, Eric M. Morrow
Current Opinion in Neurology (2016) Vol. 30, Iss. 1, pp. 114-124
Open Access | Times Cited: 94

The Promise of Multi-Omics and Clinical Data Integration to Identify and Target Personalized Healthcare Approaches in Autism Spectrum Disorders
Roger Higdon, Rachel K. Earl, Larissa Stanberry, et al.
OMICS A Journal of Integrative Biology (2015) Vol. 19, Iss. 4, pp. 197-208
Open Access | Times Cited: 93

Autism and developmental disability caused by KCNQ3 gain‐of‐function variants
Tristan T. Sands, Francesco Miceli, Gaëtan Lesca, et al.
Annals of Neurology (2019) Vol. 86, Iss. 2, pp. 181-192
Open Access | Times Cited: 90

Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience
Helen Rankin Willsey, Cameron R. T. Exner, Yuxiao Xu, et al.
Neuron (2021) Vol. 109, Iss. 5, pp. 788-804.e8
Open Access | Times Cited: 82

The DYRK Family of Kinases in Cancer: Molecular Functions and Therapeutic Opportunities
Jacopo Boni, Carlota Rubio-Pérez, Núria López-Bigas, et al.
Cancers (2020) Vol. 12, Iss. 8, pp. 2106-2106
Open Access | Times Cited: 74

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