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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:

Increased L1 Retrotransposition in the Neuronal Genome in Schizophrenia
Miki Bundo, Manabu Toyoshima, Yohei Okada, et al.
Neuron (2014) Vol. 81, Iss. 2, pp. 306-313
Open Access | Times Cited: 296

Showing 1-25 of 296 citing articles:

TEtranscripts: a package for including transposable elements in differential expression analysis of RNA-seq datasets
Ying Jin, Oliver H. Tam, Eric Paniagua, et al.
Bioinformatics (2015) Vol. 31, Iss. 22, pp. 3593-3599
Open Access | Times Cited: 581
The role of adult hippocampal neurogenesis in brain health and disease
Tomohisa Toda, Sarah Parylak, Sara B. Linker, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 1, pp. 67-87
Open Access | Times Cited: 573
Restricting retrotransposons: a review
John L. Goodier
Mobile DNA (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 401
Mobile DNA in Health and Disease
Haig H. Kazazian, John V. Moran
New England Journal of Medicine (2017) Vol. 377, Iss. 4, pp. 361-370
Open Access | Times Cited: 393
Retrotransposons as regulators of gene expression
Reyad A. Elbarbary, Bronwyn A. Lucas, Lynne E. Maquat
Science (2016) Vol. 351, Iss. 6274
Open Access | Times Cited: 384
The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology
Eugene J. Gardner, Vincent K. L. Lam, Daniel Harris, et al.
Genome Research (2017) Vol. 27, Iss. 11, pp. 1916-1929
Open Access | Times Cited: 346
A hot L1 retrotransposon evades somatic repression and initiates human colorectal cancer
Emma C. Scott, Eugene J. Gardner, Ashiq Masood, et al.
Genome Research (2016) Vol. 26, Iss. 6, pp. 745-755
Open Access | Times Cited: 267
Mobile DNA elements in the generation of diversity and complexity in the brain
Jennifer A. Erwin, Maria C. Marchetto, Fred H. Gage
Nature reviews. Neuroscience (2014) Vol. 15, Iss. 8, pp. 497-506
Open Access | Times Cited: 245
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network
Michael J. McConnell, John V. Moran, Alexej Abyzov, et al.
Science (2017) Vol. 356, Iss. 6336
Open Access | Times Cited: 242
iPS cell technologies: significance and applications to CNS regeneration and disease
Hideyuki Okano, Shinya Yamanaka
Molecular Brain (2014) Vol. 7, Iss. 1, pp. 22-22
Open Access | Times Cited: 227
Somatic mosaicism and neurodevelopmental disease
Alissa M. D’Gama, Christopher A. Walsh
Nature Neuroscience (2018) Vol. 21, Iss. 11, pp. 1504-1514
Closed Access | Times Cited: 221
Brain changes in a maternal immune activation model of neurodevelopmental brain disorders
Lara Bergdolt, Anna Dunaevsky
Progress in Neurobiology (2018) Vol. 175, pp. 1-19
Open Access | Times Cited: 217
Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights
Itaru Kushima, Branko Aleksić, Masahiro Nakatochi, et al.
Cell Reports (2018) Vol. 24, Iss. 11, pp. 2838-2856
Open Access | Times Cited: 213
Extracellular vesicles and intercellular communication within the nervous system
Valentina Zappulli, Kristina Pagh Friis, Zachary Fitzpatrick, et al.
Journal of Clinical Investigation (2016) Vol. 126, Iss. 4, pp. 1198-1207
Open Access | Times Cited: 212
The impact of transposable elements on mammalian development
José L. García-Pérez, Thomas J. Widmann, Ian R. Adams
Development (2016) Vol. 143, Iss. 22, pp. 4101-4114
Open Access | Times Cited: 196
Revisiting the Relationship between Transposable Elements and the Eukaryotic Stress Response
Vivien Horváth, Miriam Merenciano, Josefa González
Trends in Genetics (2017) Vol. 33, Iss. 11, pp. 832-841
Closed Access | Times Cited: 188
Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons
Elaine Y. Liu, Jenny Russ, Christopher P. Cali, et al.
Cell Reports (2019) Vol. 27, Iss. 5, pp. 1409-1421.e6
Open Access | Times Cited: 185
Losing DNA methylation at repetitive elements and breaking bad
Xena Giada Pappalardo, Viviana Barra
Epigenetics & Chromatin (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 106
Transposable elements as essential elements in the control of gene expression
Alemu Gebrie
Mobile DNA (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 58
L1 Retrotransposons and Somatic Mosaicism in the Brain
Sandra R. Richardson, Santiago Morell, Geoffrey J. Faulkner
Annual Review of Genetics (2014) Vol. 48, Iss. 1, pp. 1-27
Closed Access | Times Cited: 166
Resolving rates of mutation in the brain using single-neuron genomics
Gilad D. Evrony, Eunjung Lee, Peter J. Park, et al.
eLife (2016) Vol. 5
Open Access | Times Cited: 161
Transposable elements in the mammalian embryo: pioneers surviving through stealth and service
Patricia Gerdes, Sandra R. Richardson, Dixie L. Mager, et al.
Genome biology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 153
Human induced pluripotent stem cells for modelling neurodevelopmental disorders
Karthikeyan Ardhanareeswaran, Jessica Mariani, Gianfilippo Coppola, et al.
Nature Reviews Neurology (2017) Vol. 13, Iss. 5, pp. 265-278
Open Access | Times Cited: 146
Stress and the dynamic genome: Steroids, epigenetics, and the transposome
Richard Hunter, Khatuna Gagnidze, Bruce S. McEwen, et al.
Proceedings of the National Academy of Sciences (2014) Vol. 112, Iss. 22, pp. 6828-6833
Open Access | Times Cited: 124
High-resolution copy number variation analysis of schizophrenia in Japan
Itaru Kushima, Branko Aleksić, Masahiro Nakatochi, et al.
Molecular Psychiatry (2016) Vol. 22, Iss. 3, pp. 430-440
Closed Access | Times Cited: 122
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