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:

Novel STMN2 Variant Linked to Amyotrophic Lateral Sclerosis Risk and Clinical Phenotype
Frances Theunissen, Ryan S. Anderton, Frank Mastaglia, et al.
Frontiers in Aging Neuroscience (2021) Vol. 13
Open Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

A cellular taxonomy of the adult human spinal cord
Archana Yadav, Kaya J.E. Matson, Li Li, et al.
Neuron (2023) Vol. 111, Iss. 3, pp. 328-344.e7
Open Access | Times Cited: 116
Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders
Jonathan Gilley, Oscar Jackson, Menelaos Pipis, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 63
Pharmacotherapy for Amyotrophic Lateral Sclerosis: A Review of Approved and Upcoming Agents
Stephen A. Johnson, Ton Fang, Fabiola De Marchi, et al.
Drugs (2022) Vol. 82, Iss. 13, pp. 1367-1388
Closed Access | Times Cited: 62
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy
Kelsey L. Krus, Amy Strickland, Yurie Yamada, et al.
Cell Reports (2022) Vol. 39, Iss. 13, pp. 111001-111001
Open Access | Times Cited: 60
Loss of mouse Stmn2 function causes motor neuropathy
Irune Guerra San Juan, Leslie A. Nash, Kevin S. Smith, et al.
Neuron (2022) Vol. 110, Iss. 10, pp. 1671-1688.e6
Open Access | Times Cited: 55
Unraveling the Heterogeneity of ALS—A Call to Redefine Patient Stratification for Better Outcomes in Clinical Trials
Laura Tzeplaeff, Alexandra V. Jürs, Camilla Wohnrade, et al.
Cells (2024) Vol. 13, Iss. 5, pp. 452-452
Open Access | Times Cited: 8
The role of structural variations in Alzheimer’s disease and other neurodegenerative diseases
Hui Wang, Li‐San Wang, Gerard D. Schellenberg, et al.
Frontiers in Aging Neuroscience (2023) Vol. 14
Open Access | Times Cited: 18
TDP-43 Proteinopathy Specific Biomarker Development
Isabell Cordts, Annika Wachinger, Carlo Scialò, et al.
Cells (2023) Vol. 12, Iss. 4, pp. 597-597
Open Access | Times Cited: 17
The Stathmin-2 membrane-targeting domain is required for axon protection and regulated degradation by DLK signaling
Emma J. C. Thornburg‐Suresh, Jerianne E. Richardson, Daniel W. Summers
Journal of Biological Chemistry (2023) Vol. 299, Iss. 7, pp. 104861-104861
Open Access | Times Cited: 17
Progress in Amyotrophic Lateral Sclerosis Gene Discovery
Samuel N. Smukowski, Heather Maioli, Caitlin S. Latimer, et al.
Neurology Genetics (2022) Vol. 8, Iss. 3
Open Access | Times Cited: 24
New perspectives on cytoskeletal dysregulation and mitochondrial mislocalization in amyotrophic lateral sclerosis
Frances Theunissen, Phillip K. West, Samuel Brennan, et al.
Translational Neurodegeneration (2021) Vol. 10, Iss. 1
Open Access | Times Cited: 31
Stathmins and Motor Neuron Diseases: Pathophysiology and Therapeutic Targets
Delia Gagliardi, Elisa Pagliari, Megi Meneri, et al.
Biomedicines (2022) Vol. 10, Iss. 3, pp. 711-711
Open Access | Times Cited: 21
Targeting common disease pathomechanisms to treat amyotrophic lateral sclerosis
Kiterie M. E. Faller, Helena Chaytow, Thomas H. Gillingwater
Nature Reviews Neurology (2025) Vol. 21, Iss. 2, pp. 86-102
Closed Access
Updates on Disease Mechanisms and Therapeutics for Amyotrophic Lateral Sclerosis
Lien Nguyen
Cells (2024) Vol. 13, Iss. 11, pp. 888-888
Open Access | Times Cited: 3
Integrated Analysis of Cortex Single-Cell Transcriptome and Serum Proteome Reveals the Novel Biomarkers in Alzheimer’s Disease
Qing-Shan Yu, Wan-Qing Feng, Lanlan Shi, et al.
Brain Sciences (2022) Vol. 12, Iss. 8, pp. 1022-1022
Open Access | Times Cited: 14
Advances in the genetic classification of amyotrophic lateral sclerosis
Johnathan Cooper‐Knock, Calum Harvey, Sai Zhang, et al.
Current Opinion in Neurology (2021) Vol. 34, Iss. 5, pp. 756-764
Open Access | Times Cited: 19
A Cellular Taxonomy of the Adult Human Spinal Cord
Archana Yadav, Kaya J.E. Matson, Li Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 13
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy
Kelsey L. Krus, Amy Strickland, Yurie Yamada, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 9
Gene expression profiles in sporadic ALS fibroblasts define disease subtypes and the metabolic effects of the investigational drug EH301
Jasmine A. Fels, Gabriella Casalena, Csaba Konràd, et al.
Human Molecular Genetics (2022) Vol. 31, Iss. 20, pp. 3458-3477
Open Access | Times Cited: 9
Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis
Wei‐Ming Su, Xiaojing Gu, Qing-Qing Duan, et al.
BMC Medicine (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 9
AtypicalTDP‐43 protein expression in anALSpedigree carrying a p.Y374Xtruncation mutation inTARDBP
Johnathan Cooper‐Knock, Thomas Julian, Emily Feneberg, et al.
Brain Pathology (2022) Vol. 33, Iss. 1
Open Access | Times Cited: 7
Short structural variants as informative genetic markers for ALS disease risk and progression
Frances Theunissen, Loren L. Flynn, Ryan S. Anderton, et al.
BMC Medicine (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 6
Bridging the gap: Short structural variants in the genetics of anorexia nervosa
Natasha Berthold, Julia Pytte, Cynthia M. Bulik, et al.
International Journal of Eating Disorders (2022) Vol. 55, Iss. 6, pp. 747-753
Open Access | Times Cited: 6
Intronic NEFH variant is associated with reduced risk for sporadic ALS and later age of disease onset
Frances Theunissen, Ryan S. Anderton, Frank Mastaglia, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 6
Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders
Jonathan Gilley, Oscar Jackson, Menelaos Pipis, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 8
Page 1 - Next Page

Scroll to top