Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
Jennifer C. Darnell, Sarah J. Van Driesche, Chaolin Zhang, et al.
Cell (2011) Vol. 146, Iss. 2, pp. 247-261
Open Access | Times Cited: 2034

Showing 1-25 of 2034 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
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: 2489
Ribosome Profiling of Mouse Embryonic Stem Cells Reveals the Complexity and Dynamics of Mammalian Proteomes
Nicholas T. Ingolia, Liana F. Lareau, Jonathan S. Weissman
Cell (2011) Vol. 147, Iss. 4, pp. 789-802
Open Access | Times Cited: 2146
De novo mutations in schizophrenia implicate synaptic networks
Menachem Fromer, Andrew Pocklington, David H. Kavanagh, et al.
Nature (2014) Vol. 506, Iss. 7487, pp. 179-184
Open Access | Times Cited: 1612
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, et al.
Nature Genetics (2018) Vol. 50, Iss. 3, pp. 381-389
Open Access | Times Cited: 1525
De Novo Gene Disruptions in Children on the Autistic Spectrum
Ivan Iossifov, Michael Ronemus, Dan Levy, et al.
Neuron (2012) Vol. 74, Iss. 2, pp. 285-299
Open Access | Times Cited: 1447
A polygenic burden of rare disruptive mutations in schizophrenia
Shaun Purcell, Jennifer L. Moran, Menachem Fromer, et al.
Nature (2014) Vol. 506, Iss. 7487, pp. 185-190
Open Access | Times Cited: 1398
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: 1385
Robust transcriptome-wide discovery of RNA-binding protein binding sites with enhanced CLIP (eCLIP)
Eric L. Van Nostrand, Gabriel A. Pratt, A.A. Shishkin, et al.
Nature Methods (2016) Vol. 13, Iss. 6, pp. 508-514
Open Access | Times Cited: 1333
The human splicing code reveals new insights into the genetic determinants of disease
Hui Xiong, Babak Alipanahi, Leo J. Lee, et al.
Science (2014) Vol. 347, Iss. 6218
Open Access | Times Cited: 1188
Autism spectrum disorder
Catherine Lord, Traolach Brugha, Tony Charman, et al.
Nature Reviews Disease Primers (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 1135
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
Michael J. Gandal, Pan Zhang, Evi Hadjimichael, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 1069
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: 1050
A framework for the interpretation of de novo mutation in human disease
Kaitlin E. Samocha, Elise Robinson, Stephan Sanders, et al.
Nature Genetics (2014) Vol. 46, Iss. 9, pp. 944-950
Open Access | Times Cited: 1037
RNA-binding proteins in human genetic disease
Fátima Gebauer, Thomas Schwarzl, Juan Valcárcel, et al.
Nature Reviews Genetics (2020) Vol. 22, Iss. 3, pp. 185-198
Open Access | Times Cited: 1025
Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
Neelroop Parikshak, Rui Luo, Alice Zhang, et al.
Cell (2013) Vol. 155, Iss. 5, pp. 1008-1021
Open Access | Times Cited: 1020
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Dalila Pinto, Elsa Delaby, Daniele Merico, et al.
The American Journal of Human Genetics (2014) Vol. 94, Iss. 5, pp. 677-694
Open Access | Times Cited: 943
Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders
Sacha B. Nelson, Vera Valakh
Neuron (2015) Vol. 87, Iss. 4, pp. 684-698
Open Access | Times Cited: 941
ERK signalling: a master regulator of cell behaviour, life and fate
Hugo Lavoie, Jessica K. Gagnon, Marc Therrien
Nature Reviews Molecular Cell Biology (2020) Vol. 21, Iss. 10, pp. 607-632
Closed Access | Times Cited: 827
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: 767
Functional 5′ UTR mRNA structures in eukaryotic translation regulation and how to find them
Kathrin Leppek, Rhiju Das, Maria Barna
Nature Reviews Molecular Cell Biology (2017) Vol. 19, Iss. 3, pp. 158-174
Open Access | Times Cited: 744
FMRP targets distinct mRNA sequence elements to regulate protein expression
Manuel Ascano, Neelanjan Mukherjee, Pradeep Bandaru, et al.
Nature (2012) Vol. 492, Iss. 7429, pp. 382-386
Open Access | Times Cited: 681
The Neurology of mTOR
Jonathan O. Lipton, Mustafa Şahin
Neuron (2014) Vol. 84, Iss. 2, pp. 275-291
Open Access | Times Cited: 656
Activity-dependent neuronal signalling and autism spectrum disorder
Daniel H. Ebert, Michael E. Greenberg
Nature (2013) Vol. 493, Iss. 7432, pp. 327-337
Open Access | Times Cited: 616
Fragile X syndrome
Randi J. Hagerman, Elizabeth Berry‐Kravis, Heather C. Hazlett, et al.
Nature Reviews Disease Primers (2017) Vol. 3, Iss. 1
Closed Access | Times Cited: 614
Page 1 - Next Page

Scroll to top