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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:

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

Showing 26-50 of 225 citing articles:

Molecular hallmarks of ageing in amyotrophic lateral sclerosis
Cyril J. Jagaraj, Sina Shadfar, Sara Assar Kashani, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 14
Accurate DNA Methylation Predictor for C9orf72 Repeat Expansion Alleles in the Pathogenic Range
N Ramesh, Alexandria Evans, Kevin Wojta, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access | Times Cited: 1
Blood DNA methylation as a potential biomarker of dementia: A systematic review
Peter Fransquet, Paul Lacaze, Richard Saffery, et al.
Alzheimer s & Dementia (2017) Vol. 14, Iss. 1, pp. 81-103
Open Access | Times Cited: 84
Genotype–phenotype links in frontotemporal lobar degeneration
Sara Van Mossevelde, Sebastiaan Engelborghs, Julie van der Zee, et al.
Nature Reviews Neurology (2018) Vol. 14, Iss. 6, pp. 363-378
Open Access | Times Cited: 80
Genetic testing and genetic counseling for amyotrophic lateral sclerosis: an update for clinicians
Jennifer Roggenbuck, Adam Quick, Stephen J. Kolb
Genetics in Medicine (2016) Vol. 19, Iss. 3, pp. 267-274
Open Access | Times Cited: 74
Role of Genetics and Epigenetics in the Pathogenesis of Alzheimer’s Disease and Frontotemporal Dementia
Chiara Fenoglio, Elio Scarpini, María Serpente, et al.
Journal of Alzheimer s Disease (2018) Vol. 62, Iss. 3, pp. 913-932
Open Access | Times Cited: 74
Repeat-Associated Non-ATG Translation: Molecular Mechanisms and Contribution to Neurological Disease
Lien Nguyen, John D. Cleary, Laura P.W. Ranum
Annual Review of Neuroscience (2019) Vol. 42, Iss. 1, pp. 227-247
Open Access | Times Cited: 73
Mitochondrial DNA Copy Number and D-Loop Region Methylation in Carriers of Amyotrophic Lateral Sclerosis Gene Mutations
Andrea Stoccoro, Lorena Mosca, Vittoria Carnicelli, et al.
Epigenomics (2018) Vol. 10, Iss. 11, pp. 1431-1443
Closed Access | Times Cited: 69
Opening up the DNA methylome of dementia
Raúl Delgado‐Morales, Manel Esteller
Molecular Psychiatry (2017) Vol. 22, Iss. 4, pp. 485-496
Open Access | Times Cited: 67
C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studies
Sarat C. Vatsavayai, Alissa L. Nana, Jennifer S. Yokoyama, et al.
Acta Neuropathologica (2018) Vol. 137, Iss. 1, pp. 1-26
Open Access | Times Cited: 67
Cellular and physiological functions of C9ORF72 and implications for ALS/FTD
Weilun Pang, Fenghua Hu
Journal of Neurochemistry (2020) Vol. 157, Iss. 3, pp. 334-350
Open Access | Times Cited: 67
Molecular Genetics of Neurodegenerative Dementias
Flora I. Hinz, Daniel H. Geschwind
Cold Spring Harbor Perspectives in Biology (2016) Vol. 9, Iss. 4, pp. a023705-a023705
Open Access | Times Cited: 62
Molecular Mechanisms of Neurodegeneration Related to C9orf72 Hexanucleotide Repeat Expansion
Mirjana Babić Leko, Vera Župunski, Jason Kirincich, et al.
Behavioural Neurology (2019) Vol. 2019, pp. 1-18
Open Access | Times Cited: 62
REVIEW: Current understanding of the pathogenesis of Fuchs' endothelial corneal dystrophy.
Gargi Gouranga Nanda, Debasmita Pankaj Alone
PubMed (2019) Vol. 25, pp. 295-310
Closed Access | Times Cited: 60
Mitochondrial Dysfunction, Neurogenesis, and Epigenetics: Putative Implications for Amyotrophic Lateral Sclerosis Neurodegeneration and Treatment
Michele Longoni Calió, Elisandra Henriques, Amanda Siena, et al.
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 56
C9orf72 loss-of-function: a trivial, stand-alone or additive mechanism in C9 ALS/FTD?
Elke Braems, Bart Swinnen, Ludo Van Den Bosch
Acta Neuropathologica (2020) Vol. 140, Iss. 5, pp. 625-643
Open Access | Times Cited: 56
C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy
Christopher P. Cali, Maribel Patiño, Yee Kit Tai, et al.
Acta Neuropathologica (2019) Vol. 138, Iss. 5, pp. 795-811
Open Access | Times Cited: 55
Multifaceted Genes in Amyotrophic Lateral Sclerosis-Frontotemporal Dementia
Ramya Ranganathan, Shaila Haque, Kayesha Coley, et al.
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 55
Unravelling the clinical spectrum and the role of repeat length in C9ORF72 repeat expansions
Emma L. van der Ende, Jazmyne L. Jackson, Adrianna White, et al.
Journal of Neurology Neurosurgery & Psychiatry (2021) Vol. 92, Iss. 5, pp. 502-509
Open Access | Times Cited: 47
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis
Ahmad Al Khleifat, Alfredo Iacoangeli, Joke J.F.A. van Vugt, et al.
npj Genomic Medicine (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 38
DeepRepeat: direct quantification of short tandem repeats on signal data from nanopore sequencing
Fang Li, Qian Liu, Alex Mas Monteys, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 37
The Role of Epigenetics in Neuroinflammatory-Driven Diseases
Sebastiano Giallongo, Lucia Longhitano, Simona Denaro, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 23, pp. 15218-15218
Open Access | Times Cited: 33
Expanding Clinical Spectrum of C9ORF72-Related Disorders and Promising Therapeutic Strategies
Sarah R. Breevoort, Summer Gibson, Karla P. Figueroa, et al.
Neurology Genetics (2022) Vol. 8, Iss. 3
Open Access | Times Cited: 29
Evidence‐based consensus guidelines for ALS genetic testing and counseling
Jennifer Roggenbuck, Breda Eubank, Joshua D. Wright, et al.
Annals of Clinical and Translational Neurology (2023) Vol. 10, Iss. 11, pp. 2074-2091
Open Access | Times Cited: 22
Utility of DNA Methylation as a Biomarker in Aging and Alzheimer’s Disease
Lidija Milicic, Tenielle Porter, Michaël Vacher, et al.
Journal of Alzheimer s Disease Reports (2023) Vol. 7, Iss. 1, pp. 475-503
Open Access | Times Cited: 17

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