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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 26-50 of 2499 citing articles:

Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority
Alycia Halladay, Somer Bishop, John N. Constantino, et al.
Molecular Autism (2015) Vol. 6, Iss. 1
Open Access | Times Cited: 518
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K. C. Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
Nature Medicine (2015) Vol. 21, Iss. 2, pp. 185-191
Closed Access | Times Cited: 513
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: 512
Genetics and Genomics of Congenital Heart Disease
Samir Zaidi, Martina Brueckner
Circulation Research (2017) Vol. 120, Iss. 6, pp. 923-940
Open Access | Times Cited: 481
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
Giulio Genovese, Menachem Fromer, Eli A. Stahl, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1433-1441
Open Access | Times Cited: 473
Genetic Causes and Modifiers of Autism Spectrum Disorder
Lauren Rylaarsdam, Alicia Guemez‐Gamboa
Frontiers in Cellular Neuroscience (2019) Vol. 13
Open Access | Times Cited: 460
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Daniel J. Weiner, Emilie M. Wigdor, Stephan Ripke, et al.
Nature Genetics (2017) Vol. 49, Iss. 7, pp. 978-985
Open Access | Times Cited: 456
Gene hunting in autism spectrum disorder: on the path to precision medicine
Daniel H. Geschwind, Matthew W. State
The Lancet Neurology (2015) Vol. 14, Iss. 11, pp. 1109-1120
Open Access | Times Cited: 453
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Tarjinder Singh, Mitja Kurki, David Curtis, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 4, pp. 571-577
Open Access | Times Cited: 447
The serotonin system in autism spectrum disorder: From biomarker to animal models
Christopher L. Muller, Allison M. J. Anacker, Jeremy Veenstra‐VanderWeele
Neuroscience (2015) Vol. 321, pp. 24-41
Open Access | Times Cited: 445
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability
Stefan H. Lelieveld, Margot R.F. Reijnders, Rolph Pfundt, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 9, pp. 1194-1196
Open Access | Times Cited: 443
An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome
Bernard Ng, Charles C. White, Hans‐Ulrich Klein, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 10, pp. 1418-1426
Open Access | Times Cited: 440
Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders
Neelroop Parikshak, Michael J. Gandal, Daniel H. Geschwind
Nature Reviews Genetics (2015) Vol. 16, Iss. 8, pp. 441-458
Open Access | Times Cited: 432
Autism spectrum disorder: neuropathology and animal models
Merina Varghese, Neha U. Keshav, Sarah Jacot-Descombes, et al.
Acta Neuropathologica (2017) Vol. 134, Iss. 4, pp. 537-566
Open Access | Times Cited: 428
Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder
Arjun Krishnan, Ran Zhang, Vicky Yao, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1454-1462
Open Access | Times Cited: 426
New insights into the generation and role of de novo mutations in health and disease
Rocío Acuña‐Hidalgo, Joris A. Veltman, Alexander Hoischen
Genome biology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 422
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
Alejandro Sifrim, Marc‐Phillip Hitz, Anna Wilsdon, et al.
Nature Genetics (2016) Vol. 48, Iss. 9, pp. 1060-1065
Open Access | Times Cited: 420
The PsychENCODE project
Schahram Akbarian, Chunyu Liu, James A. Knowles, et al.
Nature Neuroscience (2015) Vol. 18, Iss. 12, pp. 1707-1712
Open Access | Times Cited: 417
Drug development in the era of precision medicine
Sarah A. Dugger, Adam Platt, David B. Goldstein
Nature Reviews Drug Discovery (2017) Vol. 17, Iss. 3, pp. 183-196
Open Access | Times Cited: 417
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: 415
Genetics and genomics of psychiatric disease
Daniel H. Geschwind, Jonathan Flint
Science (2015) Vol. 349, Iss. 6255, pp. 1489-1494
Open Access | Times Cited: 409
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
Kristiina Tammimies, Christian R. Marshall, Susan Walker, et al.
JAMA (2015) Vol. 314, Iss. 9, pp. 895-895
Closed Access | Times Cited: 406
Predicting the clinical impact of human mutation with deep neural networks
Laksshman Sundaram, Hong Gao, Samskruthi Reddy Padigepati, et al.
Nature Genetics (2018) Vol. 50, Iss. 8, pp. 1161-1170
Open Access | Times Cited: 402
Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
Patrick F. Sullivan, Daniel H. Geschwind
Cell (2019) Vol. 177, Iss. 1, pp. 162-183
Open Access | Times Cited: 401
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F. Hamdan, Candace T. Myers, Patrick Cossette, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 5, pp. 664-685
Open Access | Times Cited: 400

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