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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:

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

Showing 1-25 of 149 citing articles:

Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice
Gil Sharon, Nikki Jamie Cruz, Dae‐Wook Kang, et al.
Cell (2019) Vol. 177, Iss. 6, pp. 1600-1618.e17
Open Access | Times Cited: 905
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
Autism genetics: opportunities and challenges for clinical translation
Jacob Vorstman, Jeremy Parr, Daniel Moreno‐De‐Luca, et al.
Nature Reviews Genetics (2017) Vol. 18, Iss. 6, pp. 362-376
Open Access | Times Cited: 411
Transposable elements in human genetic disease
Lindsay M. Payer, Kathleen H. Burns
Nature Reviews Genetics (2019) Vol. 20, Iss. 12, pp. 760-772
Closed Access | Times Cited: 285
Insights into genetics, human biology and disease gleaned from family based genomic studies
Jennifer E. Posey, Anne O’Donnell‐Luria, Jessica X. Chong, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 4, pp. 798-812
Open Access | Times Cited: 186
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 165
Recurrent evolution of vertebrate transcription factors by transposase capture
Rachel Cosby, Julius Judd, Ruiling Zhang, et al.
Science (2021) Vol. 371, Iss. 6531
Open Access | Times Cited: 132
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
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications
Amy B. Wilfert, Arvis Sulovari, Tychele N. Turner, et al.
Genome Medicine (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 131
Our Conflict with Transposable Elements and Its Implications for Human Disease
Kathleen H. Burns
Annual Review of Pathology Mechanisms of Disease (2020) Vol. 15, Iss. 1, pp. 51-70
Open Access | Times Cited: 100
Severe childhood speech disorder
Michael S. Hildebrand, Victoria E. Jackson, Thomas Scerri, et al.
Neurology (2020) Vol. 94, Iss. 20
Open Access | Times Cited: 91
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients
Elouan Chérot, Boris Keren, Christèle Dubourg, et al.
Clinical Genetics (2017) Vol. 93, Iss. 3, pp. 567-576
Open Access | Times Cited: 88
Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes
Kensuke Matsumura, Kaoru Seiriki, Shota Okada, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 80
The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease
Miriam S. Reuter, Rajiv Chaturvedi, Eriskay Liston, et al.
Genetics in Medicine (2020) Vol. 22, Iss. 6, pp. 1015-1024
Open Access | Times Cited: 73
Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing
Ange‐Line Bruel, Sophie Nambot, Virginie Quéré, et al.
European Journal of Human Genetics (2019) Vol. 27, Iss. 10, pp. 1519-1531
Open Access | Times Cited: 58
Evolution of pogo, a separate superfamily of IS630-Tc1-mariner transposons, revealing recurrent domestication events in vertebrates
Bo Gao, Yali Wang, Mohamed Diaby, et al.
Mobile DNA (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 57
Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
Reut Suliman-Lavie, Ben Title, Yahel Cohen, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 51
Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes
Eirene Markenscoff-Papadimitriou, Fadya Binyameen, Sean Whalen, et al.
Cell Reports (2021) Vol. 37, Iss. 10, pp. 110089-110089
Open Access | Times Cited: 49
Understanding autism spectrum disorders with animal models: applications, insights, and perspectives
Li Zhu, Yuanxiang Zhu, Lijun Gu, et al.
动物学研究 (2021) Vol. 42, Iss. 6, pp. 800-823
Open Access | Times Cited: 42
New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing
Lucia Pia Bruno, Gabriella Doddato, Floriana Valentino, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 24, pp. 13439-13439
Open Access | Times Cited: 41
Whole exome/genome sequencing in cyclic vomiting syndrome reveals multiple candidate genes, suggesting a model of elevated intracellular cations and mitochondrial dysfunction
Omri Bar, Laurie Ebenau, Kellee Weiner, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 16
Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders
Michaela Fencková, Laura E.R. Blok, Lenke Asztalos, et al.
Biological Psychiatry (2019) Vol. 86, Iss. 4, pp. 294-305
Open Access | Times Cited: 52
Bayesian approach to determining penetrance of pathogenic SDH variants
Diana E. Benn, Ying Zhu, Katrina Andrews, et al.
Journal of Medical Genetics (2018) Vol. 55, Iss. 11, pp. 729-734
Open Access | Times Cited: 51
Short-term transcriptome and microRNAs responses to exposure to different air pollutants in two population studies
Almudena Espín-Pérez, Julian Krauskopf, Marc Chadeau‐Hyam, et al.
Environmental Pollution (2018) Vol. 242, pp. 182-190
Open Access | Times Cited: 49
Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome)
Nurit Assia Batzir, Jennifer E. Posey, Xiaofei Song, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 1, pp. 38-52
Open Access | Times Cited: 48
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