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:
An overview of inborn errors of metabolism affecting the brain: from neurodevelopment to neurodegenerative disorders
Jean‐Marie Saudubray, Angela Garcia-Cazorla
Dialogues in Clinical Neuroscience (2018) Vol. 20, Iss. 4, pp. 301-325
Open Access | Times Cited: 89
Jean‐Marie Saudubray, Angela Garcia-Cazorla
Dialogues in Clinical Neuroscience (2018) Vol. 20, Iss. 4, pp. 301-325
Open Access | Times Cited: 89
Showing 1-25 of 89 citing articles:
Cell type-specific biotin labeling in vivo resolves regional neuronal and astrocyte proteomic differences in mouse brain
Sruti Rayaprolu, Sara Bitarafan, Juliet V. Santiago, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 58
Sruti Rayaprolu, Sara Bitarafan, Juliet V. Santiago, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 58
The multifaceted role of mitochondria in autism spectrum disorder
Igor Khaliulin, Wajeha Hamoudi, Haitham Amal
Molecular Psychiatry (2024)
Open Access | Times Cited: 8
Igor Khaliulin, Wajeha Hamoudi, Haitham Amal
Molecular Psychiatry (2024)
Open Access | Times Cited: 8
Inborn Errors of Metabolism Associated With Autism Spectrum Disorders: Approaches to Intervention
Tamara Žigman, Danijela Petković Ramadža, Goran Šimić, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 55
Tamara Žigman, Danijela Petković Ramadža, Goran Šimić, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 55
Proposal for a simplified classification of IMD based on a pathophysiological approach: A practical guide for clinicians
Jean‐Marie Saudubray, Fanny Mochel, Foudil Lamari, et al.
Journal of Inherited Metabolic Disease (2019) Vol. 42, Iss. 4, pp. 706-727
Closed Access | Times Cited: 54
Jean‐Marie Saudubray, Fanny Mochel, Foudil Lamari, et al.
Journal of Inherited Metabolic Disease (2019) Vol. 42, Iss. 4, pp. 706-727
Closed Access | Times Cited: 54
Sulfur Metabolism Under Stress
Colin G. Miller, Edward E. Schmidt
Antioxidants and Redox Signaling (2020) Vol. 33, Iss. 16, pp. 1158-1173
Open Access | Times Cited: 43
Colin G. Miller, Edward E. Schmidt
Antioxidants and Redox Signaling (2020) Vol. 33, Iss. 16, pp. 1158-1173
Open Access | Times Cited: 43
Abnormalities of synaptic mitochondria in autism spectrum disorder and related neurodevelopmental disorders
Liliana Rojas-Charry, Leonardo Nardi, Axel Methner, et al.
Journal of Molecular Medicine (2020) Vol. 99, Iss. 2, pp. 161-178
Open Access | Times Cited: 40
Liliana Rojas-Charry, Leonardo Nardi, Axel Methner, et al.
Journal of Molecular Medicine (2020) Vol. 99, Iss. 2, pp. 161-178
Open Access | Times Cited: 40
Targetable Pathways for Alleviating Mitochondrial Dysfunction in Neurodegeneration of Metabolic and Non-Metabolic Diseases
Lauren Millichap, Elisabetta Damiani, Luca Tiano, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 21, pp. 11444-11444
Open Access | Times Cited: 34
Lauren Millichap, Elisabetta Damiani, Luca Tiano, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 21, pp. 11444-11444
Open Access | Times Cited: 34
Nuclear Factor Erythroid-2-Related Factor 2 Signaling in the Neuropathophysiology of Inherited Metabolic Disorders
Bianca Seminotti, Mateus Grings, Paolo Tucci, et al.
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 28
Bianca Seminotti, Mateus Grings, Paolo Tucci, et al.
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 28
Ifosfamide - History, efficacy, toxicity and encephalopathy
Jeffrey R. Idle, Diren Beyoğlu
Pharmacology & Therapeutics (2023) Vol. 243, pp. 108366-108366
Closed Access | Times Cited: 12
Jeffrey R. Idle, Diren Beyoğlu
Pharmacology & Therapeutics (2023) Vol. 243, pp. 108366-108366
Closed Access | Times Cited: 12
Biochemical, Genetic and Clinical Diagnostic Approaches to Autism-Associated Inherited Metabolic Disorders
Udara D. Senarathne, Neluwa-Liyanage R. Indika, Aleksandra Jezela‐Stanek, et al.
Genes (2023) Vol. 14, Iss. 4, pp. 803-803
Open Access | Times Cited: 12
Udara D. Senarathne, Neluwa-Liyanage R. Indika, Aleksandra Jezela‐Stanek, et al.
Genes (2023) Vol. 14, Iss. 4, pp. 803-803
Open Access | Times Cited: 12
Metabolite Biomarkers for Early Ischemic–Hypoxic Encephalopathy: An Experimental Study Using the NeoBase 2 MSMS Kit in a Rat Model
Yulia Shevtsova, Natalia Starodubtseva, Alisa Tokareva, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2035-2035
Open Access | Times Cited: 4
Yulia Shevtsova, Natalia Starodubtseva, Alisa Tokareva, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2035-2035
Open Access | Times Cited: 4
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency
Henry H.C. Lee, Itay Tokatly Latzer, Mariarita Bertoldi, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 3, pp. 476-493
Closed Access | Times Cited: 4
Henry H.C. Lee, Itay Tokatly Latzer, Mariarita Bertoldi, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 3, pp. 476-493
Closed Access | Times Cited: 4
Challenges Faced by Newborns with Inherited Metabolic Disorders and Their Mothers During Antepartum, Intrapartum, and Postpartum Periods
Merve Koç Yekedüz, G. Yagci, İlknur Sürücü Kara, et al.
Fetal and Pediatric Pathology (2025), pp. 1-10
Closed Access
Merve Koç Yekedüz, G. Yagci, İlknur Sürücü Kara, et al.
Fetal and Pediatric Pathology (2025), pp. 1-10
Closed Access
Behandlung von Verhaltensauffälligkeiten bei Menschen mit Intelligenzminderung
Christian Figge
InFo Neurologie + Psychiatrie (2025) Vol. 27, Iss. 1, pp. 36-49
Closed Access
Christian Figge
InFo Neurologie + Psychiatrie (2025) Vol. 27, Iss. 1, pp. 36-49
Closed Access
The Metabolic Evaluation of the Patient with a Developmental Disorder
Arzu Selamioglu
IntechOpen eBooks (2025)
Closed Access
Arzu Selamioglu
IntechOpen eBooks (2025)
Closed Access
Organellar crosstalk as a potential therapeutic target for rare neurodegenerative diseases
Josephine Lam, Chenxu Li, Márcia R. Terluk, et al.
Rare Disease and Orphan Drugs Journal (2025) Vol. 4, Iss. 1
Open Access
Josephine Lam, Chenxu Li, Márcia R. Terluk, et al.
Rare Disease and Orphan Drugs Journal (2025) Vol. 4, Iss. 1
Open Access
Psychosocial Challenges Facing Young People With Inherited Metabolic Disorders and Their Parents: A Systematic Review
Clara Sherlock, Kim Clarke, Norah Jordan
JIMD Reports (2025) Vol. 66, Iss. 2
Open Access
Clara Sherlock, Kim Clarke, Norah Jordan
JIMD Reports (2025) Vol. 66, Iss. 2
Open Access
Disulfidptosis in tumor progression
Senlin Wan, Cong Liang, Chunfeng Wu, et al.
Cell Death Discovery (2025) Vol. 11, Iss. 1
Open Access
Senlin Wan, Cong Liang, Chunfeng Wu, et al.
Cell Death Discovery (2025) Vol. 11, Iss. 1
Open Access
Manganese Mapping Using a Fluorescent Mn2+ Sensor and Nanosynchrotron X-ray Fluorescence Reveals the Role of the Golgi Apparatus as a Manganese Storage Site
Sayani Das, Asunción Carmona, Kaustav Khatua, et al.
Inorganic Chemistry (2019) Vol. 58, Iss. 20, pp. 13724-13732
Open Access | Times Cited: 34
Sayani Das, Asunción Carmona, Kaustav Khatua, et al.
Inorganic Chemistry (2019) Vol. 58, Iss. 20, pp. 13724-13732
Open Access | Times Cited: 34
Aromatic l -amino acid decarboxylase deficiency: a patient-derived neuronal model for precision therapies
Giada Rossignoli, Karolin Krämer, Eleonora Lugarà, et al.
Brain (2021) Vol. 144, Iss. 8, pp. 2443-2456
Open Access | Times Cited: 24
Giada Rossignoli, Karolin Krämer, Eleonora Lugarà, et al.
Brain (2021) Vol. 144, Iss. 8, pp. 2443-2456
Open Access | Times Cited: 24
Childhood neurodevelopmental disorders and maternal hypertensive disorder of pregnancy
K.T. Chen, Tsung Yu, Lin Kang, et al.
Developmental Medicine & Child Neurology (2021) Vol. 63, Iss. 9, pp. 1107-1113
Open Access | Times Cited: 23
K.T. Chen, Tsung Yu, Lin Kang, et al.
Developmental Medicine & Child Neurology (2021) Vol. 63, Iss. 9, pp. 1107-1113
Open Access | Times Cited: 23
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review
Emma N. M. M. von Scheibler, Agnies M. van Eeghen, Tom J. de Koning, et al.
Movement Disorders Clinical Practice (2022) Vol. 10, Iss. 1, pp. 17-31
Open Access | Times Cited: 15
Emma N. M. M. von Scheibler, Agnies M. van Eeghen, Tom J. de Koning, et al.
Movement Disorders Clinical Practice (2022) Vol. 10, Iss. 1, pp. 17-31
Open Access | Times Cited: 15
Microcephaly in Neurometabolic Diseases
Wiktoria Kempińska, Karolina Korta, Magdalena Marchaj, et al.
Children (2022) Vol. 9, Iss. 1, pp. 97-97
Open Access | Times Cited: 13
Wiktoria Kempińska, Karolina Korta, Magdalena Marchaj, et al.
Children (2022) Vol. 9, Iss. 1, pp. 97-97
Open Access | Times Cited: 13
Temporal brain transcriptome analysis reveals key pathological events after germinal matrix hemorrhage in neonatal rats
Juan Song, Gisela Nilsson, Yiran Xu, et al.
Journal of Cerebral Blood Flow & Metabolism (2022) Vol. 42, Iss. 9, pp. 1632-1649
Open Access | Times Cited: 13
Juan Song, Gisela Nilsson, Yiran Xu, et al.
Journal of Cerebral Blood Flow & Metabolism (2022) Vol. 42, Iss. 9, pp. 1632-1649
Open Access | Times Cited: 13
Brain Hypothermia Therapy and Targeted Temperature Management for Acute Encephalopathy in Children: Status and Prospects
George Imataka, Yuji Fujita, Jin Kikuchi, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 6, pp. 2095-2095
Open Access | Times Cited: 7
George Imataka, Yuji Fujita, Jin Kikuchi, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 6, pp. 2095-2095
Open Access | Times Cited: 7
