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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:

Refining analyses of copy number variation identifies specific genes associated with developmental delay
Bradley P. Coe, Kali Witherspoon, Jill A. Rosenfeld, et al.
Nature Genetics (2014) Vol. 46, Iss. 10, pp. 1063-1071
Open Access | Times Cited: 654

Showing 1-25 of 654 citing articles:

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: 1886
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: 1391
Genetic studies in intellectual disability and related disorders
Lisenka E.L.M. Vissers, Christian Gilissen, Joris A. Veltman
Nature Reviews Genetics (2015) Vol. 17, Iss. 1, pp. 9-18
Closed Access | Times Cited: 714
Mechanisms underlying structural variant formation in genomic disorders
Claudia M.B. Carvalho, James R. Lupski
Nature Reviews Genetics (2016) Vol. 17, Iss. 4, pp. 224-238
Open Access | Times Cited: 641
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
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Joanna Kaplanis, Kaitlin E. Samocha, Laurens Wiel, et al.
Nature (2020) Vol. 586, Iss. 7831, pp. 757-762
Open Access | Times Cited: 499
A genomic mutational constraint map using variation in 76,156 human genomes
Siwei Chen, Laurent C. Francioli, Julia K. Goodrich, et al.
Nature (2023) Vol. 625, Iss. 7993, pp. 92-100
Closed Access | Times Cited: 491
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: 420
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
Elizabeth K. Ruzzo, Laura Pérez‐Cano, Jae-Yoon Jung, et al.
Cell (2019) Vol. 178, Iss. 4, pp. 850-866.e26
Open Access | Times Cited: 396
High-resolution comparative analysis of great ape genomes
Zev Kronenberg, Ian T. Fiddes, David Gordon, et al.
Science (2018) Vol. 360, Iss. 6393
Open Access | Times Cited: 355
De novo genic mutations among a Chinese autism spectrum disorder cohort
Tianyun Wang, Hui Guo, Bo Xiong, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 331
Global diversity, population stratification, and selection of human copy-number variation
Peter H. Sudmant, Swapan Mallick, Bradley J. Nelson, et al.
Science (2015) Vol. 349, Iss. 6253
Open Access | Times Cited: 329
Recurrent de novo mutations implicate novel genes underlying simplex autism risk
Brian J. O’Roak, Holly A.F. Stessman, Evan A. Boyle, et al.
Nature Communications (2014) Vol. 5, Iss. 1
Open Access | Times Cited: 316
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
A genome-wide mutational constraint map quantified from variation in 76,156 human genomes
Siwei Chen, Laurent C. Francioli, Julia K. Goodrich, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 279
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA
Tychele N. Turner, Fereydoun Hormozdiari, Michael H. Duyzend, et al.
The American Journal of Human Genetics (2015) Vol. 98, Iss. 1, pp. 58-74
Open Access | Times Cited: 276
The GABAA Receptor as a Therapeutic Target for Neurodevelopmental Disorders
Sien Braat, R. Frank Kooy
Neuron (2015) Vol. 86, Iss. 5, pp. 1119-1130
Open Access | Times Cited: 269
The discovery of integrated gene networks for autism and related disorders
Fereydoun Hormozdiari, Osnat Penn, Elhanan Borenstein, et al.
Genome Research (2014) Vol. 25, Iss. 1, pp. 142-154
Open Access | Times Cited: 260
A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology
Lisenka E.L.M. Vissers, K.J.M. van Nimwegen, Jolanda Schieving, et al.
Genetics in Medicine (2017) Vol. 19, Iss. 9, pp. 1055-1063
Open Access | Times Cited: 249
Human Structural Variation: Mechanisms of Chromosome Rearrangements
Brooke Weckselblatt, M. Katharine Rudd
Trends in Genetics (2015) Vol. 31, Iss. 10, pp. 587-599
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: 226
Single-cell epigenomics reveals mechanisms of human cortical development
Ryan Ziffra, Chang N. Kim, Jayden M. Ross, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 205-213
Open Access | Times Cited: 222
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
Pamela Feliciano, Xueya Zhou, Irina Astrovskaya, et al.
npj Genomic Medicine (2019) Vol. 4, Iss. 1
Open Access | Times Cited: 214
Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database
Jinchen Li, Tao Cai, Yi Jiang, et al.
Molecular Psychiatry (2015) Vol. 21, Iss. 2, pp. 290-297
Open Access | Times Cited: 213
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects
Kimberley Kendall, Elliott Rees, Valentina Escott‐Price, et al.
Biological Psychiatry (2016) Vol. 82, Iss. 2, pp. 103-110
Open Access | Times Cited: 201
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