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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:

Human iPSC-derived cerebral organoids model features of Leigh syndrome and reveal abnormal corticogenesis
Alejandra I. Romero-Morales, Gabriella L. Robertson, Anuj Rastogi, et al.
Development (2022) Vol. 149, Iss. 20
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome
Gizem Inak, Agnieszka Rybak‐Wolf, Paweł Lisowski, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 100
Variants in Human ATP Synthase Mitochondrial Genes: Biochemical Dysfunctions, Associated Diseases, and Therapies
Valentina Del Dotto, Francesco Musiani, Alessandra Baracca, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2239-2239
Open Access | Times Cited: 10
Linking mitochondria metabolism, developmental timing, and human brain evolution
Pierre Casimir, Ryohei Iwata, Pierre Vanderhaeghen
Current Opinion in Genetics & Development (2024) Vol. 86, pp. 102182-102182
Open Access | Times Cited: 8
Human TSC2 mutant cells exhibit aberrations in early neurodevelopment accompanied by changes in the DNA Methylome
Mary‐Bronwen L. Chalkley, Lindsey N. Guerin, Tenhir Iyer, et al.
Human Molecular Genetics (2025)
Open Access | Times Cited: 1
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
Emanuela Bottani, Costanza Lamperti, Alessandro Prigione, et al.
Pharmaceutics (2020) Vol. 12, Iss. 11, pp. 1083-1083
Open Access | Times Cited: 56
Common molecular mechanisms ofSLC6A1variant-mediated neurodevelopmental disorders in astrocytes and neurons
Felicia Mermer, Sarah Poliquin, Kathryn Rigsby, et al.
Brain (2021) Vol. 144, Iss. 8, pp. 2499-2512
Open Access | Times Cited: 52
Modeling mitochondrial DNA diseases: from base editing to pluripotent stem‐cell‐derived organoids
Isabella Tolle, Valeria Tiranti, Alessandro Prigione
EMBO Reports (2023) Vol. 24, Iss. 4
Open Access | Times Cited: 19
Neural and metabolic dysregulation in PMM2-deficient human in vitro neural models
Silvia Radenkovic, Rohit Budhraja, Teun M. Klein Gunnewiek, et al.
Cell Reports (2024) Vol. 43, Iss. 3, pp. 113883-113883
Open Access | Times Cited: 7
Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humans
Felicia Mermer, Sarah Poliquin, Shuizhen Zhou, et al.
Neurobiology of Disease (2022) Vol. 172, pp. 105810-105810
Open Access | Times Cited: 22
iPSC models of mitochondrial diseases
Sonja Heiduschka, Alessandro Prigione
Neurobiology of Disease (2025), pp. 106822-106822
Open Access
Leptomeningeal Neural Organoid Fusions as Models to Study Meninges-Brain Signaling
Hannah E. Jones, Gabriella L. Robertson, Caroline Bodnya, et al.
Stem Cells and Development (2025)
Closed Access
4-Phenylbutyrate restored γ-aminobutyric acid uptake and reduced seizures in SLC6A1 patient variant-bearing cell and mouse models
Gerald Nwosu, Felicia Mermer, Carson Flamm, et al.
Brain Communications (2022) Vol. 4, Iss. 3
Open Access | Times Cited: 16
Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations
Chao Chen, Min‐Xin Guan
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 9
Mutant huntingtin impairs neurodevelopment in human brain organoids through CHCHD2-mediated neurometabolic failure
Paweł Lisowski, Selene Lickfett, Agnieszka Rybak‐Wolf, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Dynamic properties of mitochondria during human corticogenesis
Tierney Baum, Vivian Gama
Development (2021) Vol. 148, Iss. 4
Open Access | Times Cited: 17
Bacterial muropeptides promote OXPHOS and suppress mitochondrial stress in mammals
Dong Tian, Mingxue Cui, Min Han
Cell Reports (2024) Vol. 43, Iss. 4, pp. 114067-114067
Open Access | Times Cited: 2
Fetal and obstetrics manifestations of mitochondrial diseases
Adelizzi Alessia, Giri Anastasia, Di Donfrancesco Alessia, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
Disease models of Leigh syndrome: From yeast to organoids
Marie‐Thérèse Henke, Alessandro Prigione, Markus Schuelke
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 6, pp. 1292-1321
Open Access | Times Cited: 2
Induced pluripotent stem cells derived from patients carrying mitochondrial mutations exhibit altered bioenergetics and aberrant differentiation potential
Fibi Meshrkey, Kelly M. Scheulin, Christopher M. Littlejohn, et al.
Stem Cell Research & Therapy (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 6
Toward an understanding of glucose metabolism in radial glial biology and brain development
Madeline G. Andrews, Caroline A. Pearson
Life Science Alliance (2023) Vol. 7, Iss. 1, pp. e202302193-e202302193
Open Access | Times Cited: 5
Modeling the function of BAX and BAK in early human brain development using iPSC-derived systems
Piyush Joshi, Caroline Bodnya, Megan L. Rasmussen, et al.
Cell Death and Disease (2020) Vol. 11, Iss. 9
Open Access | Times Cited: 12
Human In Vitro Models of Neuroenergetics and Neurometabolic Disturbances: Current Advances and Clinical Perspectives
Julia Rogal, Laura N. Zamproni, Polyxeni Nikolakopoulou, et al.
Stem Cells Translational Medicine (2024) Vol. 13, Iss. 6, pp. 505-514
Open Access | Times Cited: 1
Human TSC2 Mutant Cells Exhibit Aberrations in Early Neurodevelopment Accompanied by Changes in the DNA Methylome
Mary‐Bronwen L. Chalkley, Lindsey N. Guerin, Tenhir Iyer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Brain organoid as a model to study the role of mitochondria in neurodevelopmental disorders: achievements and weaknesses
Raquel Coronel, Enrique García-Moreno, Emilio Siendones, et al.
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
The power of human stem cell-based systems in the study of neurodevelopmental disorders
Megha Jhanji, Elisa M. York, Sofia B. Lizarraga
Current Opinion in Neurobiology (2024) Vol. 89, pp. 102916-102916
Open Access | Times Cited: 1
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