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:

Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier
Jenny Russ, Elaine Y. Liu, Kathryn Wu, et al.
Acta Neuropathologica (2014) Vol. 129, Iss. 1, pp. 39-52
Open Access | Times Cited: 121

Showing 1-25 of 121 citing articles:

C9orf72-mediated ALS and FTD: multiple pathways to disease
Rubika Balendra, Adrian M. Isaacs
Nature Reviews Neurology (2018) Vol. 14, Iss. 9, pp. 544-558
Open Access | Times Cited: 616
C9orf72 is required for proper macrophage and microglial function in mice
Jacqueline G. O’Rourke, Laurent Bogdanik, Alberto Yáñez, et al.
Science (2016) Vol. 351, Iss. 6279, pp. 1324-1329
Open Access | Times Cited: 505
Gain of Toxicity from ALS/FTD-Linked Repeat Expansions in C9ORF72 Is Alleviated by Antisense Oligonucleotides Targeting GGGGCC-Containing RNAs
Jie Jiang, Qiang Zhu, Tania F. Gendron, et al.
Neuron (2016) Vol. 90, Iss. 3, pp. 535-550
Open Access | Times Cited: 502
Repeat expansion diseases
Henry L. Paulson
Handbook of clinical neurology (2018), pp. 105-123
Open Access | Times Cited: 374
The frontotemporal dementia-motor neuron disease continuum
James R. Burrell, Glenda M. Halliday, Jillian J. Kril, et al.
The Lancet (2016) Vol. 388, Iss. 10047, pp. 919-931
Closed Access | Times Cited: 345
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
Cyril Pottier, Kevin F. Bieniek, Ni Cole A. Finch, et al.
Acta Neuropathologica (2015) Vol. 130, Iss. 1, pp. 77-92
Open Access | Times Cited: 288
C9orf72 BAC Transgenic Mice Display Typical Pathologic Features of ALS/FTD
Jacqueline G. O’Rourke, Laurent Bogdanik, A.K.M. Ghulam Muhammad, et al.
Neuron (2015) Vol. 88, Iss. 5, pp. 892-901
Open Access | Times Cited: 284
Molecular mechanisms underlying nucleotide repeat expansion disorders
Indranil Malik, Chase P. Kelley, Eric T. Wang, et al.
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 9, pp. 589-607
Open Access | Times Cited: 263
Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine
David J. Irwin, Nigel J. Cairns, Murray Grossman, et al.
Acta Neuropathologica (2014) Vol. 129, Iss. 4, pp. 469-491
Open Access | Times Cited: 245
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Katrina Moore, Jennifer Nicholas, Murray Grossman, et al.
The Lancet Neurology (2019) Vol. 19, Iss. 2, pp. 145-156
Open Access | Times Cited: 245
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, et al.
Molecular Psychiatry (2015) Vol. 21, Iss. 8, pp. 1112-1124
Open Access | Times Cited: 225
R Loops and Links to Human Disease
P. Richard, James L. Manley
Journal of Molecular Biology (2016) Vol. 429, Iss. 21, pp. 3168-3180
Open Access | Times Cited: 194
The expanding biology of the C9orf72 nucleotide repeat expansion in neurodegenerative disease
Aaron R. Haeusler, Christopher J. Donnelly, Jeffrey D. Rothstein
Nature reviews. Neuroscience (2016) Vol. 17, Iss. 6, pp. 383-395
Open Access | Times Cited: 183
ALS: A bucket of genes, environment, metabolism and unknown ingredients
Mónica Zufiría, Francisco J. Gil‐Bea, Roberto Fernández‐Torrón, et al.
Progress in Neurobiology (2016) Vol. 142, pp. 104-129
Closed Access | Times Cited: 183
Analysis of short tandem repeat expansions and their methylation state with nanopore sequencing
Pay Gießelmann, Björn Brändl, Etienne Raimondeau, et al.
Nature Biotechnology (2019) Vol. 37, Iss. 12, pp. 1478-1481
Open Access | Times Cited: 166
An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics
Sanjog R. Chintalaphani, Sandy S. Pineda, Ira W. Deveson, et al.
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 128
G-Quadruplexes as pathogenic drivers in neurodegenerative disorders
Ernest Wang, Ravi Thombre, Yajas Shah, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 9, pp. 4816-4830
Open Access | Times Cited: 115
C9ORF72: What It Is, What It Does, and Why It Matters
Julie Smeyers, Elena-Gaia Banchi, Morwena Latouche
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 113
Distribution of dipeptide repeat proteins in cellular models and C9orf72 mutation cases suggests link to transcriptional silencing
Martin H. Schludi, Stephanie May, Friedrich A. Grässer, et al.
Acta Neuropathologica (2015) Vol. 130, Iss. 4, pp. 537-555
Open Access | Times Cited: 175
Familial Amyotrophic Lateral Sclerosis
Khrista Boylan
Neurologic Clinics (2015) Vol. 33, Iss. 4, pp. 807-830
Open Access | Times Cited: 166
There has been an awakening: Emerging mechanisms of C9orf72 mutations in FTD/ALS
Aaron D. Gitler, Hitomi Tsuiji
Brain Research (2016) Vol. 1647, pp. 19-29
Open Access | Times Cited: 148
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients
Zhengrui Xi, Ming Zhang, Amalia C. Bruni, et al.
Acta Neuropathologica (2015) Vol. 129, Iss. 5, pp. 715-727
Open Access | Times Cited: 136
Relationship between C9orf72 repeat size and clinical phenotype
Sara Van Mossevelde, Julie van der Zee, Marc Cruts, et al.
Current Opinion in Genetics & Development (2017) Vol. 44, pp. 117-124
Open Access | Times Cited: 127
RNA metabolism in neurodegenerative disease
Elaine Y. Liu, Christopher P. Cali, Edward B. Lee
Disease Models & Mechanisms (2017) Vol. 10, Iss. 5, pp. 509-518
Open Access | Times Cited: 126
DNA Methylation Clocks and Their Predictive Capacity for Aging Phenotypes and Healthspan
Tessa Bergsma, Ekaterina Rogaeva
Neuroscience Insights (2020) Vol. 15
Open Access | Times Cited: 109
Page 1 - Next Page

Scroll to top