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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:

Prevalence and architecture of de novo mutations in developmental disorders

Nature (2017) Vol. 542, Iss. 7642, pp. 433-438
Open Access | Times Cited: 1360

Showing 26-50 of 1360 citing articles:

The sources of adaptive variation
Deborah Charlesworth, Nick Barton, Brian Charlesworth
Proceedings of the Royal Society B Biological Sciences (2017) Vol. 284, Iss. 1855, pp. 20162864-20162864
Open Access | Times Cited: 288
Schizophrenia and the neurodevelopmental continuum:evidence from genomics
Michael J. Owen, Michael O’Donovan
World Psychiatry (2017) Vol. 16, Iss. 3, pp. 227-235
Open Access | Times Cited: 288
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity
Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari, et al.
Nature Genetics (2018) Vol. 51, Iss. 1, pp. 106-116
Open Access | Times Cited: 287
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: 280
Transcriptome and epigenome landscape of human cortical development modeled in organoids
Anahita Amiri, Gianfilippo Coppola, Soraya Scuderi, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 277
Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk
Jian Zhou, Christopher Y. Park, Chandra L. Theesfeld, et al.
Nature Genetics (2019) Vol. 51, Iss. 6, pp. 973-980
Open Access | Times Cited: 273
De novo mutations in regulatory elements in neurodevelopmental disorders
Patrick J. Short, Jeremy F. McRae, Giuseppe Gallone, et al.
Nature (2018) Vol. 555, Iss. 7698, pp. 611-616
Open Access | Times Cited: 271
De novo variants in neurodevelopmental disorders with epilepsy
Henrike Heyne, Tarjinder Singh, Hannah Stamberger, et al.
Nature Genetics (2018) Vol. 50, Iss. 7, pp. 1048-1053
Open Access | Times Cited: 270
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1305-1319
Open Access | Times Cited: 266
A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles
Nancy Y. A. Sey, Benxia Hu, Won Mah, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 4, pp. 583-593
Open Access | Times Cited: 262
Brain organoids for the study of human neurobiology at the interface of in vitro and in vivo
Ilaria Chiaradia, Madeline A. Lancaster
Nature Neuroscience (2020) Vol. 23, Iss. 12, pp. 1496-1508
Closed Access | Times Cited: 256
Why is it so hard to reach agreement on terminology? The case of developmental language disorder (DLD)
Dorothy Bishop
International Journal of Language & Communication Disorders (2017) Vol. 52, Iss. 6, pp. 671-680
Open Access | Times Cited: 238
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1182-1201
Open Access | Times Cited: 238
A map of constrained coding regions in the human genome
James M. Havrilla, Brent S. Pedersen, Ryan M. Layer, et al.
Nature Genetics (2018) Vol. 51, Iss. 1, pp. 88-95
Open Access | Times Cited: 237
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders
Víctor Faúndes, William G. Newman, Laura Bernardini, et al.
The American Journal of Human Genetics (2017) Vol. 102, Iss. 1, pp. 175-187
Open Access | Times Cited: 235
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
Tarjinder Singh, James Walters, Mandy Johnstone, et al.
Nature Genetics (2017) Vol. 49, Iss. 8, pp. 1167-1173
Open Access | Times Cited: 228
Genomic diagnosis for children with intellectual disability and/or developmental delay
Kevin M. Bowling, Michelle L. Thompson, Michelle D. Amaral, et al.
Genome Medicine (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 225
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: 220
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
Vincenzo Salpietro, Christine L. Dixon, Hui Guo, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 201
Paternally inherited cis-regulatory structural variants are associated with autism
William M. Brandler, Danny Antaki, Madhusudan Gujral, et al.
Science (2018) Vol. 360, Iss. 6386, pp. 327-331
Open Access | Times Cited: 199
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants
F. Kyle Satterstrom, Raymond K. Walters, Tarjinder Singh, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 12, pp. 1961-1965
Open Access | Times Cited: 198
Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting
Caroline F. Wright, Ben C. West, Marcus A. Tuke, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 2, pp. 275-286
Open Access | Times Cited: 194
Quantifying the contribution of recessive coding variation to developmental disorders
Hilary C. Martin, Wendy D. Jones, Rebecca E. McIntyre, et al.
Science (2018) Vol. 362, Iss. 6419, pp. 1161-1164
Open Access | Times Cited: 191
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: 188
Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Deidre R. Krupp, Rebecca Barnard, Yannis Duffourd, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 3, pp. 369-390
Open Access | Times Cited: 179

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