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:
Lissencephaly: Update on diagnostics and clinical management
Matti Koenig, William B. Dobyns, Nataliya Di Donato
European Journal of Paediatric Neurology (2021) Vol. 35, pp. 147-152
Closed Access | Times Cited: 36
Matti Koenig, William B. Dobyns, Nataliya Di Donato
European Journal of Paediatric Neurology (2021) Vol. 35, pp. 147-152
Closed Access | Times Cited: 36
Showing 1-25 of 36 citing articles:
Dysregulation of mTOR signalling is a converging mechanism in lissencephaly
Ce Zhang, Dan Liang, A. Gulhan Ercan‐Sencicek, et al.
Nature (2025)
Open Access
Ce Zhang, Dan Liang, A. Gulhan Ercan‐Sencicek, et al.
Nature (2025)
Open Access
Hypertension due to ACTH treatment for lissencephaly with a novel PAFAH1B1 variant
N Ida, Yoshifusa Abe, Ryo Karato, et al.
Brain and Development Case Reports (2025) Vol. 3, Iss. 1, pp. 100065-100065
Open Access
N Ida, Yoshifusa Abe, Ryo Karato, et al.
Brain and Development Case Reports (2025) Vol. 3, Iss. 1, pp. 100065-100065
Open Access
A novel missense heterozygous MACF1 variant in a patient with global developmental delay, lissencephaly and drug-resistant epilepsy
E. O. Belyaeva, L. I. Minaycheva, V.M. Sivokha, et al.
Deleted Journal (2025) Vol. 2, Iss. 1
Open Access
E. O. Belyaeva, L. I. Minaycheva, V.M. Sivokha, et al.
Deleted Journal (2025) Vol. 2, Iss. 1
Open Access
A Novel Variant c.149G >A in CDK5 Gene Causing Lissencephaly Type 7
Amita Moirangthem, Anjana Kar, M Bhinde Sagar, et al.
Clinical Genetics (2025)
Closed Access
Amita Moirangthem, Anjana Kar, M Bhinde Sagar, et al.
Clinical Genetics (2025)
Closed Access
GRASPs link Reelin to the Golgi during neocortical development to control neuronal migration and dendritogenesis
Elisa Calvo-Jiménez, Kirsten Stam, Angélique Jossi, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access
Elisa Calvo-Jiménez, Kirsten Stam, Angélique Jossi, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access
Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly
Eyyüp Üçtepe, Barbara Vona, Fatma Nisa Esen, et al.
European Journal of Human Genetics (2023) Vol. 32, Iss. 1, pp. 52-60
Open Access | Times Cited: 9
Eyyüp Üçtepe, Barbara Vona, Fatma Nisa Esen, et al.
European Journal of Human Genetics (2023) Vol. 32, Iss. 1, pp. 52-60
Open Access | Times Cited: 9
14‐3‐3 Family of Proteins: Biological Implications, Molecular Interactions, and Potential Intervention in Cancer, Virus and Neurodegeneration Disorders
Zheng Yao Low, Ashley Jia Wen Yip, Alvin Man Lung Chan, et al.
Journal of Cellular Biochemistry (2024) Vol. 125, Iss. 7
Open Access | Times Cited: 3
Zheng Yao Low, Ashley Jia Wen Yip, Alvin Man Lung Chan, et al.
Journal of Cellular Biochemistry (2024) Vol. 125, Iss. 7
Open Access | Times Cited: 3
Congenital Brain Malformations: An Integrated Diagnostic Approach
Bimal P. Chaudhari, Mai‐Lan Ho
Seminars in Pediatric Neurology (2022) Vol. 42, pp. 100973-100973
Closed Access | Times Cited: 15
Bimal P. Chaudhari, Mai‐Lan Ho
Seminars in Pediatric Neurology (2022) Vol. 42, pp. 100973-100973
Closed Access | Times Cited: 15
Diagnostic work‐up in malformations of cortical development
Ellen Rijckmans, Katrien Stouffs, Anna Jansen
Developmental Medicine & Child Neurology (2024) Vol. 66, Iss. 8, pp. 974-989
Open Access | Times Cited: 2
Ellen Rijckmans, Katrien Stouffs, Anna Jansen
Developmental Medicine & Child Neurology (2024) Vol. 66, Iss. 8, pp. 974-989
Open Access | Times Cited: 2
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
Radha Procopio, Francesco Fortunato, Monica Gagliardi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5505-5505
Open Access | Times Cited: 2
Radha Procopio, Francesco Fortunato, Monica Gagliardi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5505-5505
Open Access | Times Cited: 2
Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy
Bin Mao, Na Lin, Danhua Guo, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 6
Bin Mao, Na Lin, Danhua Guo, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 6
Brain organoids: Establishment and application
Hao Chen, Xin Jin, Tie Li, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 9
Hao Chen, Xin Jin, Tie Li, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 9
Aquatic Freshwater Vertebrate Models of Epilepsy Pathology: Past Discoveries and Future Directions for Therapeutic Discovery
Rachel E. Williams, K Mruk
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 15, pp. 8608-8608
Open Access | Times Cited: 3
Rachel E. Williams, K Mruk
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 15, pp. 8608-8608
Open Access | Times Cited: 3
Cerebral organoids expressing mutant actin genes reveal cellular mechanism underlying microcephaly
Indra Niehaus, Michaela Wilsch‐Bräuninger, Felipe Mora‐Bermúdez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Indra Niehaus, Michaela Wilsch‐Bräuninger, Felipe Mora‐Bermúdez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Multi-Omics Approach Reveals Genes and Pathways Affected in Miller-Dieker Syndrome
Gowthami Mahendran, Kurtis Breger, Phillip J. McCown, et al.
Molecular Neurobiology (2024)
Open Access
Gowthami Mahendran, Kurtis Breger, Phillip J. McCown, et al.
Molecular Neurobiology (2024)
Open Access
Heterozygous Inversion on Chromosome 17 involving PAFAH1B1 Detected by Whole Genome Sequencing in a Patient Suffering from Pachygyria
Jun Chen, Xiaoping Li, George Luo, et al.
European Journal of Medical Genetics (2024), pp. 104991-104991
Open Access
Jun Chen, Xiaoping Li, George Luo, et al.
European Journal of Medical Genetics (2024), pp. 104991-104991
Open Access
ACLASP1variant suggests a phenotypic relation with lissencephaly in humans
Rawan Alsafeh, Amal Alhashem, A. Y.A. M. Elsayed, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Rawan Alsafeh, Amal Alhashem, A. Y.A. M. Elsayed, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Prenatal Imaging of Supratentorial Fetal Brain Malformation
Sheng‐Che Hung, Hisham Dahmoush, Han-Jui Lee, et al.
Magnetic Resonance Imaging Clinics of North America (2024) Vol. 32, Iss. 3, pp. 395-412
Closed Access
Sheng‐Che Hung, Hisham Dahmoush, Han-Jui Lee, et al.
Magnetic Resonance Imaging Clinics of North America (2024) Vol. 32, Iss. 3, pp. 395-412
Closed Access
Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration)
Laura Sciuto, Valeria Fichera, Antonio Zanghì, et al.
Journal of Pediatric Neurology (2024) Vol. 22, Iss. 05, pp. 332-340
Closed Access
Laura Sciuto, Valeria Fichera, Antonio Zanghì, et al.
Journal of Pediatric Neurology (2024) Vol. 22, Iss. 05, pp. 332-340
Closed Access
Lissencephaly
Qasim Mehmood, Hafiz Muhammad Iqbal, Saira Naz, et al.
(2024), pp. 181-191
Closed Access
Qasim Mehmood, Hafiz Muhammad Iqbal, Saira Naz, et al.
(2024), pp. 181-191
Closed Access
Síndrome de Miller-Dieker: reporte de dos casos
José Cruz Mendoza Torres, Nelson Ramón Coiscou Domínguez
Revista de la Facultad de Medicina (2024) Vol. 67, Iss. 2, pp. 19-25
Closed Access
José Cruz Mendoza Torres, Nelson Ramón Coiscou Domínguez
Revista de la Facultad de Medicina (2024) Vol. 67, Iss. 2, pp. 19-25
Closed Access
6-MONTH-OLD INFANT WITH LISSENCEPHALY TYPE I ASSOCIATED WITH MILLER DIEKER SYNDROME: A CASE REPORT
Dewi Asih, Audrina Ernes
Ibnu Sina Jurnal Kedokteran dan Kesehatan-Fakultas Kedokteran Universitas Islam Sumatera Utara (2024) Vol. 23, Iss. 2, pp. 252-257
Open Access
Dewi Asih, Audrina Ernes
Ibnu Sina Jurnal Kedokteran dan Kesehatan-Fakultas Kedokteran Universitas Islam Sumatera Utara (2024) Vol. 23, Iss. 2, pp. 252-257
Open Access
Multiplex Consanguineous Family Highlights CLASP1 as a Candidate Gene for Lissencephaly
Rawan Alsafh, Amal Alhashem, Aly Elsyed, et al.
Neurology Genetics (2024) Vol. 10, Iss. 4
Closed Access
Rawan Alsafh, Amal Alhashem, Aly Elsyed, et al.
Neurology Genetics (2024) Vol. 10, Iss. 4
Closed Access
Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly Patients
Sofia M. Schuetz, Christiane R. Proepper, Lisa-Maria Schwarz, et al.
Neuropediatrics (2024)
Closed Access
Sofia M. Schuetz, Christiane R. Proepper, Lisa-Maria Schwarz, et al.
Neuropediatrics (2024)
Closed Access
Congenital Brain Lesions
Sajjad G. Al‐Badri, Mahmood S. Bilal, Ameer M. Aynona, et al.
(2024), pp. 3-30
Closed Access
Sajjad G. Al‐Badri, Mahmood S. Bilal, Ameer M. Aynona, et al.
(2024), pp. 3-30
Closed Access
