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:

Depletion of WFS1 compromises mitochondrial function in hiPSC-derived neuronal models of Wolfram syndrome
Malgorzata Zatyka, Tatiana R. Rosenstock, Congxin Sun, et al.
Stem Cell Reports (2023) Vol. 18, Iss. 5, pp. 1090-1106
Open Access | Times Cited: 19

Showing 19 citing articles:

ER calcium depletion as a key driver for impaired ER-to-mitochondria calcium transfer and mitochondrial dysfunction in Wolfram syndrome
Mailis Liiv, Annika Vaarmann, Dzhamilja Safiulina, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 12
The Wolfram-like variant WFS1 E864K destabilizes MAM and compromises autophagy and mitophagy in human and mice
Simone Patergnani, Méghane S. Bataillard, Alberto Danese, et al.
Autophagy (2024) Vol. 20, Iss. 9, pp. 2055-2066
Closed Access | Times Cited: 7
Identification of a pathogenic founder variant in the WFS1 gene that causes Wolfram syndrome in the Druze population
Inbal Halabi, Yardena Tenenbaum‐Rakover, Lena Sagi‐Dain, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
GABA and GLP-1 receptor agonist combination therapy modifies diabetes and Langerhans islet cytoarchitecture in a rat model of Wolfram syndrome
Toomas Jagomäe, Sandra Velling, Tessa Britt Tikva, et al.
Diabetology & Metabolic Syndrome (2025) Vol. 17, Iss. 1
Open Access
SIRTUINS MODULATORS MITIGATE HYPOXIA-INDUCED CELL DEATH DUE TO CHANGES IN HISTONE 3 ACETYLATION, AND MITOCHONDRIAL FUNCTION, DYNAMICS, AND CONTENT
Luiz Silva, Amanda Siena, Jéssica Mayumi Camargo Yuzawa, et al.
Neuropharmacology (2025), pp. 110484-110484
Closed Access
Mitochondria–membranous organelle contacts at a glance
Antigoni Diokmetzidou, Luca Scorrano
Journal of Cell Science (2025) Vol. 138, Iss. 9
Open Access
Comprehensive overview of disease models for Wolfram syndrome: toward effective treatments
Shuntaro Morikawa, Katsuya Tanabe, Naoya Kaneko, et al.
Mammalian Genome (2024) Vol. 35, Iss. 1, pp. 1-12
Closed Access | Times Cited: 3
Wolfram Syndrome 1: A Neuropsychiatric Perspective on a Rare Disease
Valerio Caruso, Accursio Raia, Luciana Rigoli
(2024)
Open Access | Times Cited: 3
Not So Rare: Diseases Based on Mutant Proteins Controlling Endoplasmic Reticulum-Mitochondria Contact (MERC) Tethering
Tadashi Makio, Thomas Simmen
Contact (2024) Vol. 7
Open Access | Times Cited: 3
Extra-nuclear TERT counteracts oxidative stress and promotes progression in papillary thyroid carcinoma
Marina Muzza, Gabriele Pogliaghi, Carla Colombo, et al.
Translational research (2024) Vol. 271, pp. 1-12
Closed Access | Times Cited: 2
Targeting the autophagy-NAD axis protects against cell death in Niemann-Pick type C1 disease models
Tetsushi Kataura, Lucia Sedlackova, Congxin Sun, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 5
Open Access | Times Cited: 2
Tale of mitochondria and mitochondria-associated ER membrane in patient-derived neuronal models of Wolfram syndrome
Laëtitia Aubry, Timothy Barrett, Sovan Sarkar
Neural Regeneration Research (2024) Vol. 20, Iss. 9, pp. 2587-2588
Open Access | Times Cited: 1
Wolfram Syndrome 1: A Neuropsychiatric Perspective on a Rare Disease
Valerio Caruso, Accursio Raia, Luciana Rigoli
Genes (2024) Vol. 15, Iss. 8, pp. 984-984
Open Access | Times Cited: 1
ER Calcium Depletion as a Key Driver for Impaired ER-to-Mitochondria Calcium Transfer and Mitochondrial Dysfunction in Wolfram Syndrome
Mailis Liiv, Annika Vaarmann, Malle Kuum, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
A deep phenotyping study in mouse and iPSC models to understand the role of oligodendroglia in optic neuropathy in Wolfram syndrome
Karan Ahuja, Marjan Vandenabeele, Fatemeharefeh Nami, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Does Recessive Optic Atrophy Due to WFS1 is a Specific Entity?
Christophe Orssaud
(2024)
Closed Access
A deep phenotyping study in mouse and iPSC models to understand the role of oligodendroglia in optic neuropathy in Wolfram syndrome
Karan Ahuja, Marjan Vandenabeele, Fatemeharefeh Nami, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access
Defects of WFS1-mediated peptide hormones secretion contribute to the manifestations of Wolfram syndrome
Suli Li, Linlin Wang, Yunfei Li, et al.
Life Sciences (2024) Vol. 359, pp. 123219-123219
Closed Access
Implementing genomic medicine in clinical practice for adults with undiagnosed rare diseases
Jong Hyeon Ahn, Jihoon G. Yoon, Jaeso Cho, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access
The Wolfram-like variant WFS1E864Kdestabilizes MAM and compromises autophagy and mitophagy in human and mice
Simone Patergnani, Méghane S. Bataillard, Alberto Danese, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Page 1

Scroll to top