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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:

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
Michael E. Talkowski, Jill A. Rosenfeld, Ian Blumenthal, et al.
Cell (2012) Vol. 149, Iss. 3, pp. 525-537
Open Access | Times Cited: 572

Showing 26-50 of 572 citing articles:

CHD8 haploinsufficiency results in autistic-like phenotypes in mice
Yuta Katayama, Masaaki Nishiyama, Hirotaka Shoji, et al.
Nature (2016) Vol. 537, Iss. 7622, pp. 675-679
Closed Access | Times Cited: 298
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Claire Redin, Harrison Brand, Ryan L. Collins, et al.
Nature Genetics (2016) Vol. 49, Iss. 1, pp. 36-45
Open Access | Times Cited: 292
The WAVE Regulatory Complex Links Diverse Receptors to the Actin Cytoskeleton
Baoyu Chen, Klaus Brinkmann, Zhucheng Chen, et al.
Cell (2014) Vol. 156, Iss. 1-2, pp. 195-207
Open Access | Times Cited: 282
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M. Werling, Harrison Brand, Joon‐Yong An, et al.
Nature Genetics (2018) Vol. 50, Iss. 5, pp. 727-736
Open Access | Times Cited: 279
The Emerging Picture of Autism Spectrum Disorder: Genetics and Pathology
Jason Chen, Olga Peñagarikano, T. Grant Belgard, et al.
Annual Review of Pathology Mechanisms of Disease (2015) Vol. 10, Iss. 1, pp. 111-144
Closed Access | Times Cited: 250
Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity
James Gilbert, Heng‐Ye Man
Frontiers in Cellular Neuroscience (2017) Vol. 11
Open Access | Times Cited: 240
CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in cerebral organoids derived from iPS cells
Ping Wang, Ryan Mokhtari, Erika Pedrosa, et al.
Molecular Autism (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 239
Synergistic effects of common schizophrenia risk variants
Nadine Schrode, Seok‐Man Ho, Kazuhiko Yamamuro, et al.
Nature Genetics (2019) Vol. 51, Iss. 10, pp. 1475-1485
Open Access | Times Cited: 226
A cross-disorder dosage sensitivity map of the human genome
Ryan L. Collins, Joseph Glessner, Eleonora Porcu, et al.
Cell (2022) Vol. 185, Iss. 16, pp. 3041-3055.e25
Open Access | Times Cited: 224
Genome-wide characteristics of de novo mutations in autism
Ryan K. C. Yuen, Daniele Merico, Hongzhi Cao, et al.
npj Genomic Medicine (2016) Vol. 1, Iss. 1
Open Access | Times Cited: 218
GRIN2Bencephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
Konrad Platzer, Hongjie Yuan, Hannah M. Schutz, et al.
Journal of Medical Genetics (2017) Vol. 54, Iss. 7, pp. 460-470
Open Access | Times Cited: 218
Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling
Omer Durak, Fan Gao, Yea Jin Kaeser‐Woo, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1477-1488
Open Access | Times Cited: 214
Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits
Randall J. Platt, Yang Zhou, Ian M. Slaymaker, et al.
Cell Reports (2017) Vol. 19, Iss. 2, pp. 335-350
Open Access | Times Cited: 210
Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons
Karina Griesi‐Oliveira, Allan Acab, Arpana Gupta, et al.
Molecular Psychiatry (2014) Vol. 20, Iss. 11, pp. 1350-1365
Open Access | Times Cited: 209
Human GRIN2B variants in neurodevelopmental disorders
Chun Hu, Wenjuan Chen, Scott J. Myers, et al.
Journal of Pharmacological Sciences (2016) Vol. 132, Iss. 2, pp. 115-121
Open Access | Times Cited: 205
Medical comorbidities in children and adolescents with autism spectrum disorders and attention deficit hyperactivity disorders: a systematic review
Jet B. Muskens, Fleur P. Velders, Wouter Staal
European Child & Adolescent Psychiatry (2017) Vol. 26, Iss. 9, pp. 1093-1103
Open Access | Times Cited: 204
Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly
Tatsiana Aneichyk, William T. Hendriks, Rachita Yadav, et al.
Cell (2018) Vol. 172, Iss. 5, pp. 897-909.e21
Open Access | Times Cited: 200
Molecular Genetic Contributions to Social Deprivation and Household Income in UK Biobank
W. David Hill, Saskia P. Hagenaars, Riccardo E. Marioni, et al.
Current Biology (2016) Vol. 26, Iss. 22, pp. 3083-3089
Open Access | Times Cited: 181
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome
Ryan L. Collins, Harrison Brand, Claire Redin, et al.
Genome biology (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 175
Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in mice
I-Ting Judy Wang, Megan Allen, Darren Goffin, et al.
Proceedings of the National Academy of Sciences (2012) Vol. 109, Iss. 52, pp. 21516-21521
Open Access | Times Cited: 200
Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample
Michael E. Talkowski, Zehra Ordulu, Vamsee Pillalamarri, et al.
New England Journal of Medicine (2012) Vol. 367, Iss. 23, pp. 2226-2232
Open Access | Times Cited: 192
NMDA receptor subunit mutations in neurodevelopmental disorders
Nail Burnashev, Pierre Szepetowski
Current Opinion in Pharmacology (2014) Vol. 20, pp. 73-82
Closed Access | Times Cited: 184
Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders
Elaine Kenny, Paul Cormican, Sarah Furlong, et al.
Molecular Psychiatry (2013) Vol. 19, Iss. 8, pp. 872-879
Open Access | Times Cited: 182
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders
Zafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.
Human Molecular Genetics (2013) Vol. 22, Iss. 10, pp. 1960-1970
Open Access | Times Cited: 170
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus
Gea Beunders, Els Voorhoeve, Christelle Golzio, et al.
The American Journal of Human Genetics (2013) Vol. 92, Iss. 2, pp. 210-220
Open Access | Times Cited: 169

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