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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:

A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
Céline Helsmoortel, Anneke T. Vulto-van Silfhout, Bradley P. Coe, et al.
Nature Genetics (2014) Vol. 46, Iss. 4, pp. 380-384
Open Access | Times Cited: 313

Showing 1-25 of 313 citing articles:

Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P. Goldberg, et al.
Nature (2014) Vol. 515, Iss. 7526, pp. 209-215
Open Access | Times Cited: 2583
Large-scale discovery of novel genetic causes of developmental disorders

Nature (2014) Vol. 519, Iss. 7542, pp. 223-228
Open Access | Times Cited: 1095
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: 711
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: 511
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: 411
Deficient autophagy in microglia impairs synaptic pruning and causes social behavioral defects
HJ Kim, M-H Cho, Won Heum Shim, et al.
Molecular Psychiatry (2016) Vol. 22, Iss. 11, pp. 1576-1584
Open Access | Times Cited: 404
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
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
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
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
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
Genetics and genomics of autism spectrum disorder: embracing complexity
Silvia De Rubeis, Joseph D. Buxbaum
Human Molecular Genetics (2015) Vol. 24, Iss. R1, pp. R24-R31
Open Access | Times Cited: 198
Activity-dependent neuroprotective protein recruits HP1 and CHD4 to control lineage-specifying genes
Veronika Ostapcuk, Fabio Mohn, Sarah H. Carl, et al.
Nature (2018) Vol. 557, Iss. 7707, pp. 739-743
Closed Access | Times Cited: 195
A Short Review on the Current Understanding of Autism Spectrum Disorders
Hye Ran Park, Jae Meen Lee, Hyo Eun Moon, et al.
Experimental Neurobiology (2016) Vol. 25, Iss. 1, pp. 1-13
Open Access | Times Cited: 183
The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders
Micaela Lasser, Jessica Tiber, Laura Anne Lowery
Frontiers in Cellular Neuroscience (2018) Vol. 12
Open Access | Times Cited: 180
Genetics of autism spectrum disorder
Gokul Ramaswami, Daniel H. Geschwind
Handbook of clinical neurology (2018), pp. 321-329
Open Access | Times Cited: 180
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 165
Genomic frontiers in congenital heart disease
Sarah U. Morton, Daniel Quiat, Jonathan G. Seidman, et al.
Nature Reviews Cardiology (2021) Vol. 19, Iss. 1, pp. 26-42
Open Access | Times Cited: 155
Signalling pathways in autism spectrum disorder: mechanisms and therapeutic implications
Chen-Chen Jiang, Lishan Lin, Sen Long, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 126
Taming transposable elements in vertebrates: from epigenetic silencing to domestication
Miguel Vasconcelos Almeida, Grégoire Vernaz, Audrey L. K. Putman, et al.
Trends in Genetics (2022) Vol. 38, Iss. 6, pp. 529-553
Closed Access | Times Cited: 97
Proximity labeling identifies a repertoire of site-specific R-loop modulators
Qingqing Yan, Phillip Wulfridge, J. Kenneth Doherty, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 73
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Madeleine R. Geisheker, Gabriel Heymann, Tianyun Wang, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 8, pp. 1043-1051
Open Access | Times Cited: 164
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
Bregje W.M. van Bon, Bradley P. Coe, Raphael Bernier, et al.
Molecular Psychiatry (2015) Vol. 21, Iss. 1, pp. 126-132
Open Access | Times Cited: 161
Prioritization of neurodevelopmental disease genes by discovery of new mutations
Alexander Hoischen, Niklas Krumm, Evan E. Eichler
Nature Neuroscience (2014) Vol. 17, Iss. 6, pp. 764-772
Open Access | Times Cited: 154
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders
Holly A.F. Stessman, Marjolein H. Willemsen, Michaela Fencková, et al.
The American Journal of Human Genetics (2016) Vol. 98, Iss. 3, pp. 541-552
Open Access | Times Cited: 149
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