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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:

The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov, Brian J. O’Roak, Stephan Sanders, et al.
Nature (2014) Vol. 515, Iss. 7526, pp. 216-221
Open Access | Times Cited: 2499

Showing 1-25 of 2499 citing articles:

Coming of age: ten years of next-generation sequencing technologies
Sara Goodwin, John D. McPherson, W. Richard McCombie
Nature Reviews Genetics (2016) Vol. 17, Iss. 6, pp. 333-351
Open Access | Times Cited: 3769
10 Years of GWAS Discovery: Biology, Function, and Translation
Peter M. Visscher, Naomi R. Wray, Qian Zhang, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 1, pp. 5-22
Open Access | Times Cited: 3418
Schizophrenia risk from complex variation of complement component 4
Aswin Sekar, Hon‐Cheong So, Heather de Rivera, et al.
Nature (2016) Vol. 530, Iss. 7589, pp. 177-183
Open Access | Times Cited: 2193
Identification of common genetic risk variants for autism spectrum disorder
Jakob Grove, Stephan Ripke, Thomas D. Als, et al.
Nature Genetics (2019) Vol. 51, Iss. 3, pp. 431-444
Open Access | Times Cited: 2068
Predicting Splicing from Primary Sequence with Deep Learning
Kishore Jaganathan, Sofia Kyriazopoulou Panagiotopoulou, Jeremy F. McRae, et al.
Cell (2019) Vol. 176, Iss. 3, pp. 535-548.e24
Open Access | Times Cited: 1968
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, et al.
Cell (2020) Vol. 180, Iss. 3, pp. 568-584.e23
Open Access | Times Cited: 1898
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan Sanders, Xin He, A. Jeremy Willsey, et al.
Neuron (2015) Vol. 87, Iss. 6, pp. 1215-1233
Open Access | Times Cited: 1396
Prevalence and architecture of de novo mutations in developmental disorders

Nature (2017) Vol. 542, Iss. 7642, pp. 433-438
Open Access | Times Cited: 1360
Autism spectrum disorder
Catherine Lord, Traolach Brugha, Tony Charman, et al.
Nature Reviews Disease Primers (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 1151
Gene expression elucidates functional impact of polygenic risk for schizophrenia
Menachem Fromer, Panos Roussos, Solveig K. Sieberts, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1442-1453
Open Access | Times Cited: 1056
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap
Michael J. Gandal, Jillian R. Haney, Neelroop Parikshak, et al.
Science (2018) Vol. 359, Iss. 6376, pp. 693-697
Open Access | Times Cited: 957
Clinical application of whole-exome sequencing across clinical indications
Kyle Retterer, Jane Juusola, Megan T. Cho, et al.
Genetics in Medicine (2015) Vol. 18, Iss. 7, pp. 696-704
Open Access | Times Cited: 918
From the genetic architecture to synaptic plasticity in autism spectrum disorder
Thomas Bourgeron
Nature reviews. Neuroscience (2015) Vol. 16, Iss. 9, pp. 551-563
Closed Access | Times Cited: 891
InterVar: Clinical Interpretation of Genetic Variants by the 2015 ACMG-AMP Guidelines
Quan Li, Kai Wang
The American Journal of Human Genetics (2017) Vol. 100, Iss. 2, pp. 267-280
Open Access | Times Cited: 883
Accurate proteome-wide missense variant effect prediction with AlphaMissense
Jun Cheng, Guido Novati, Joshua Pan, et al.
Science (2023) Vol. 381, Iss. 6664
Open Access | Times Cited: 882
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K. C. Yuen, Daniele Merico, Matt Bookman, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 4, pp. 602-611
Open Access | Times Cited: 824
Advancing the understanding of autism disease mechanisms through genetics
Luis de la Torre-Ubieta, Hyejung Won, Jason L. Stein, et al.
Nature Medicine (2016) Vol. 22, Iss. 4, pp. 345-361
Open Access | Times Cited: 779
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
Sheng Chih Jin, Jason Homsy, Samir Zaidi, et al.
Nature Genetics (2017) Vol. 49, Iss. 11, pp. 1593-1601
Open Access | Times Cited: 765
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
Jason Homsy, Samir Zaidi, Yufeng Shen, et al.
Science (2015) Vol. 350, Iss. 6265, pp. 1262-1266
Open Access | Times Cited: 763
Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism
Neelroop Parikshak, Vivek Swarup, T. Grant Belgard, et al.
Nature (2016) Vol. 540, Iss. 7633, pp. 423-427
Open Access | Times Cited: 660
Inferring the molecular and phenotypic impact of amino acid variants with MutPred2
Vikas Pejaver, Jorge Urresti, Jose Lugo-Martinez, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 612
A spectral approach integrating functional genomic annotations for coding and noncoding variants
Iuliana Ionita‐Laza, K. J. McCallum, Bin Xu, et al.
Nature Genetics (2016) Vol. 48, Iss. 2, pp. 214-220
Open Access | Times Cited: 601
Excess of rare, inherited truncating mutations in autism
Niklas Krumm, Tychele N. Turner, Carl Baker, et al.
Nature Genetics (2015) Vol. 47, Iss. 6, pp. 582-588
Open Access | Times Cited: 597
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
Molecular Autism (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 589
The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting
Peter D. Stenson, Matthew Mort, Edward V. Ball, et al.
Human Genetics (2020) Vol. 139, Iss. 10, pp. 1197-1207
Open Access | Times Cited: 547
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