The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
Assembly of functionally integrated human forebrain spheroids
Open accessAbstract
The development of the nervous system involves a coordinated succession of events including the migration of GABAergic (γ-aminobutyric-acid-releasing) neurons from ventral to dorsal forebrain and their integration into cortical circuits. However, these interregional interactions have not yet been modelled with human cells. Here we generate three-dimensional spheroids from human pluripotent stem cells that resemble either the dorsal or ventral forebrain and contain cortical glutamatergic or GABAergic neurons. These subdomain-specific forebrain spheroids can be assembled in vitro to recapitulate the saltatory migration of interneurons observed in the fetal forebrain. Using this system, we find that in Timothy syndrome-a neurodevelopmental disorder that is caused by mutations in the Ca V 1.2 calcium channel-interneurons display abnormal migratory saltations. We also show that after migration, interneurons functionally integrate with glutamatergic neurons to form a microphysiological system. We anticipate that this approach will be useful for studying neural development and disease, and for deriving spheroids that resemble other brain regions to assemble circuits in vitro.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“With their 3D structures and cell components resembling the human brain, these organoids can replicate the complex brain microenvironment better than 2D in vitro models (15–17, 19)”
From Understanding monocyte-driven neuroinflammation in Alzheimer’s disease using human cortical organoid microphysiological systems (2025) · cites this paper as [19]
Experimental — accuracy not yet measuredIn the citing paper
“The ‘extrinsic’ organoid model whereby patterning is influenced by externally added molecules rather than relying on intrinsic self-organization shows promise with regard to better reproducibility5,6,25.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [6]
In the citing paper
“These findings were further supported by another report documenting interneuron migration following fusion of dorsal and ventral brain organoids26, and both studies demonstrated disruption of migration by antagonism of C-X-C chemokine receptor type 4 (CXCR4), which has an important role in interneuron migration6,26.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [6]
In the citing paper
“In the dorsal-ventral fused model mentioned earlier6, cells that migrated from the subpallial spheroid to the cortical spheroid expressed cortical interneuron markers, and whole-cell voltage-clamp recordings demonstrated that these interneuron-like cells can receive excitatory inputs from cells in the dorsal cortical organoids; conversely, the cells in the dorsal cortical organoids can receive”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [6]
In the citing paper
“The organoid-derived interneurons migrated in a manner similar to that of their in vivo counterparts.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [6]
In the citing paper
“The cells that had migrated into the cortical spheroids also fired action potentials at twice the rate of cells in unfused subpallial spheres or non-migrated cells in the fused organoid, suggesting maturation of membrane properties.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [6]
In the citing paper
“For example, the fusion of human cortical spheroids and human subpallial spheroids was used to model the migration of interneurons from the subpallium to the cortex6.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [6]
In the citing paper
“This revealed a cell-autonomous migration defect in Timothy syndrome-derived interneurons.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [6]
In the citing paper
“Brain organoid models have been shown to recapitulate cell proliferation effects in microcephaly (Thomas et al., 2017) and have been used to study neural migration defects in Timothy syndrome, a rare ASD form caused by mutations in the Cav1.2 calcium channel gene (Birey et al., 2017).”
From Getting to the cores of autism (2019) · cites this paper as Birey et al., 2017
In the citing paper
“We have previously developed an approach to model complex cellular interactions during human brain development by specifying region-specific spheroids or organoids and then fusing them in vitro to generate three-dimensional (3D) assembloids”
From Generation of Functional Human 3D Cortico-Motor Assembloids (2020) · cites this paper as Birey et al., 2017
In the citing paper
“We previously described the generation of 3D spheroids resembling the cerebral cortex (human cortical spheroids [hCS]) (Birey et al., 2017; Paşca et al., 2015; Sloan et al., 2017, 2018), which contain deep and superficial glutamatergic neurons.”
From Generation of Functional Human 3D Cortico-Motor Assembloids (2020) · cites this paper as Birey et al., 2017
In the citing paper
“We verified expression of cortico-spinal-associated markers in hCS, including FEZF2, BCL11B (CTIP2), and SOX5, using single-cell profiling of hCS (Birey et al., 2017) and found a population of cells co-expressing these genes in the glutamatergic neuron cluster but not in a subpallial-derived GABAergic cluster”
From Generation of Functional Human 3D Cortico-Motor Assembloids (2020) · cites this paper as Birey et al., 2017
In the citing paper
“We previously showed the potential of using region-specific spheroids as a modular approach to study human interneuron migration and identify disease phenotypes (Birey et al., 2017).”
From Generation of Functional Human 3D Cortico-Motor Assembloids (2020) · cites this paper as Birey et al., 2017
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
(2008) · Journal of Machine Learning Research · Cited by 33,051
Differential expression analysis for sequence count data
Anders, S., & Huber, W. (2010) · Genome Biology · doi:10.1186/gb-2010-11-10-r106 · Cited by 15,581
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
Biological insights from 108 schizophrenia-associated genetic loci
Schizophrenia Working Group of the Psychiatric Genomics Consortium (2014) · Nature · doi:10.1038/nature13595 · Cited by 7,577
Highly parallel genome-wide expression profiling of individual cells using nanoliter droplets.
Macosko, E. Z., Basu, A., Satija, R., Nemesh, J., Shekhar, K., Goldman, M., Tirosh, I., Bialas, A. R., Kamitaki, N., Martersteck, E. M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.05.002 · Cited by 7,110
Spatial reconstruction of single-cell gene expression data
Satija, R., Farrell, J. A., Gennert, D., Schier, A. F., & Regev, A. (2015) · Nature Biotechnology · doi:10.1038/nbt.3192 · Cited by 7,055
Cerebral organoids model human brain development and microcephaly
Lancaster, M. A., Renner, M., Martin, C.-A., Wenzel, D., Bicknell, L. S., Hurles, M. E., Homfray, T., Penninger, J. M., Jackson, A. P., & Knoblich, J. A. (2013) · Nature · doi:10.1038/nature12517 · Cited by 5,372
Meijer, L., Nelson, D. J., Riazanski, V., Gabdoulkhakova, A. G., Héry-Arnaud, G., Berre, R. L., Loaëc, N., Oumata, N., Galons, H., Nowak, E., et al. (2016) · Journal of Innate Immunity · doi:10.1159/000444256 · Cited by 5,008
(2013) · The Lancet · doi:10.1016/s0140-6736(12)62129-1 · Cited by 3,010
Model of autism: increased ratio of excitation/inhibition in key neural systems
Rubenstein, J. L. R., & Merzenich, M. M. (2003) · Genes, Brain and Behavior · doi:10.1034/j.1601-183x.2003.00037.x · Cited by 2,768
Flagged first, then by citations
Cited by
Sorted by citations
Items 501–600 of 999
Acharya, P., Joshi, P., Shrestha, S., Choi, N. Y., Jeong, S., & Lee, M. (2024) · Biofabrication · doi:10.1088/1758-5090/ad1b1e · Cited by 28
Song, L., Tsai, A., Yuan, X., Bejoy, J., Sart, S., Ma, T., & Li, Y. (2017) · Tissue Engineering Part A · doi:10.1089/ten.tea.2017.0403 · Cited by 25
Gonzalez‐Fernandez, T., Tenorio, A. J., & Leach, J. K. (2020) · 3D Printing and Additive Manufacturing · doi:10.1089/3dp.2019.0129 · Cited by 26
Brighi, C., Cordella, F., Chiriatti, L., Soloperto, A., & Angelantonio, S. D. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00655 · Cited by 25
Transcriptome sequencing and molecular markers discovery in the gonads of Portunus sanguinolentus
Zhang, Y., Miao, G., Wu, Q., Lin, F., You, C., Wang, S., Aweya, J. J., & Ma, H. (2018) · Scientific Data · doi:10.1038/sdata.2018.131 · Cited by 24
Jia, S., Liu, J., Chu, Y., Liu, Q., Mai, L., & Fan, W. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1038539 · Cited by 23
The Use of Patient-Derived Induced Pluripotent Stem Cells for Alzheimer’s Disease Modeling
Lee, C., Willerth, S. M., & Nygaard, H. B. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101804 · Cited by 24
Adhya, D., Chennell, G., Crowe, J. A., Valencia-Alarcón, E. P., Seyforth, J., Hosny, N. A., Yasvoina, M. V., Forster, R., Baron‐Cohen, S., Vernon, A. C., et al. (2021) · Molecular Autism · doi:10.1186/s13229-021-00413-1 · Cited by 25
Three dimensional bioelectronic interfaces to small-scale biological systems
Park, Y., Chung, T. S., & Rogers, J. A. (2021) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2021.07.023 · Cited by 27
Brain Organoids: Studying Human Brain Development and Diseases in a Dish
Xu, J., & Wen, Z. (2021) · Stem Cells International · doi:10.1155/2021/5902824 · Cited by 25
Screening Platforms for Genetic Epilepsies—Zebrafish, iPSC-Derived Neurons, and Organoids
Shcheglovitov, A., & Peterson, R. T. (2021) · Neurotherapeutics · doi:10.1007/s13311-021-01115-5 · Cited by 23
Bhattacharya, A., Choi, W. W. Y., Muffat, J., & Li, Y. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167386 · Cited by 24
Cell Aggregate Assembly through Microengineering for Functional Tissue Emergence
Eke, G., Vaysse, L., Yao, X., Escudero, M., Carrière, A., Trévisiol, E., Christophe Vieu, A., Dani, C., Casteilla, L., & Malaquin, L. (2022) · Cells · doi:10.3390/cells11091394 · Cited by 27
Buttermore, E. D., Chamberlain, S. J., Cody, J. D., Costain, G., Dang, L. T., DeWoody, J. A., DeWoody, Y., Dies, K. A., Eichler, E. E., Girirajan, S., et al. (2022) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2022.07.003 · Cited by 25
Modeling Autism Spectrum Disorders with Induced Pluripotent Stem Cell-Derived Brain Organoids
Santos, J. L. D. S., Araújo, C. D. A., Rocha, C. A. G., Costa‐Ferro, Z. S. M., & Souza, B. S. D. F. (2023) · Biomolecules · doi:10.3390/biom13020260 · Cited by 29
Clair, D. S., & Johnstone, M. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0037 · Cited by 24
Three-dimensional in vitro tissue culture models of brain organoids
Gong, J., Meng, T., Yang, J., Hu, N., Zhao, H., & Tian, T. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113619 · Cited by 23
Applications of multiphoton microscopy in imaging cerebral and retinal organoids
Lacin, M. E., & Yıldırım, M. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1360482 · Cited by 23
Organoid-based personalized medicine: from tumor outcome prediction to autologous transplantation
Soto-Gamez, A., Gunawan, J. P., Barazzuol, L., Pringle, S. A., & Coppes, R. P. (2024) · Stem Cells · doi:10.1093/stmcls/sxae023 · Cited by 26
Central nervous system vascularization in human embryos and neural organoids
Boutom, S., Silva, T. P., Palecek, S. P., Shusta, E. V., Fernandes, T. G., & Ashton, R. S. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.115068 · Cited by 26
Brain Organoids and Assembloids—From Disease Modeling to Drug Discovery
Ajongbolo, A. O., & Langhans, S. A. (2025) · Cells · doi:10.3390/cells14110842 · Cited by 25
Preconfigured neuronal firing sequences in human brain organoids
van der Molen, T., Spaeth, A., Chini, M., Hernandez, S., Kaurala, G. A., Schweiger, H. E., Duncan, C., McKenna, S., Geng, J., Lim, M., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02111-0 · Cited by 39
An On‐Chip Method for Long‐Term Growth and Real‐Time Imaging of Brain Organoids
Karzbrun, E., Tshuva, R. Y., & Reiner, O. (2018) · Current Protocols in Cell Biology · doi:10.1002/cpcb.62 · Cited by 23
WWOX-Related Neurodevelopmental Disorders: Models and Future Perspectives
Steinberg, D. J., & Aqeilan, R. I. (2021) · Cells · doi:10.3390/cells10113082 · Cited by 22
A matter of space and time: Emerging roles of disease-associated proteins in neural development
Panagiotakos, G., & Pașca, S. P. (2021) · Neuron · doi:10.1016/j.neuron.2021.10.035 · Cited by 25
Self-citationZhang, W., Li, J., Zhou, J., Rastogi, A., & Ma, S. (2022) · Trends in biotechnology · doi:10.1016/j.tibtech.2022.03.003 · Cited by 23
Mass spectrometry imaging as an emerging tool for studying metabolism in human brain organoids
Cappuccio, G., Khalil, S. M., Osenberg, S., Li, F., & Maletić‐Savatić, M. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1181965 · Cited by 24
Pavon, N., Diep, K., Yang, F., Sebastian, R., Martinez-Martin, B., Ranjan, R., Sun, Y., & Pak, C. (2024) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100689 · Cited by 24
Engineering Human Brain Organoids: From Basic Research to Tissue Regeneration
Jeong, H., Jiménez-Pérez, Z. E., Mukhambetiyar, K., Seo, M., Choi, J.-W., & Park, T. (2020) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-020-00250-y · Cited by 23
Reality check for organoids in neuroscience
Marx, V. (2020) · Nature Methods · doi:10.1038/s41592-020-0964-z · Cited by 24
An integrated transcriptomic cell atlas of human neural organoidsPreprint
He, Z., Dony, L., Fleck, J. S., Szałata, A., Li, K. X., Slišković, I., Lin, H., Santel, M., Atamian, A., Quadrato, G., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.05.561097 · Cited by 23
Self-citationThe Impact of Oxygen Availability and Multilineage Communication on Organoid Maturation
Wörsdörfer, P., & Ergün, S. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8195 · Cited by 23
Boylin, K., Aquino, G. V., Purdon, M., Abedi, K., Kasendra, M. J., & Barrile, R. (2024) · Biofabrication · doi:10.1088/1758-5090/ad4c08 · Cited by 21
Organoid intelligence for developmental neurotoxicity testing
Din, D. A. E., Shin, J., Lysinger, A., Roos, M. J., Johnson, E. C., Shafer, T. J., Härtung, T., & Smirnova, L. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1480845 · Cited by 25
Mohamed, N., Larroquette, F., Beitel, L. K., Fon, E. A., & Durcan, T. M. (2019) · Journal of Parkinson s Disease · doi:10.3233/jpd-181515 · Cited by 23
Generation of cerebral cortical GABAergic interneurons from pluripotent stem cells
Fitzgerald, M., Sotuyo, N. P., Tischfield, D. J., & Anderson, S. A. (2020) · Stem Cells · doi:10.1002/stem.3252 · Cited by 20
Methadone Suppresses Neuronal Function and Maturation in Human Cortical Organoids
Wu, W., Yao, H., Dwivedi, I., Negraes, P. D., Zhao, H. W., Wang, J., Trujillo, C. A., Muotri, A. R., & Haddad, G. G. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.593248 · Cited by 22
An in vitro model of neuronal ensembles
Rabadán, M. A., Cruz, E. D. D. L., Rao, S. B., Chen, Y., Gong, C., Crabtree, G. W., Xu, B., Markx, S., Gogos, J. A., Yuste, R., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31073-1 · Cited by 22
Cerebral Organoids and Antisense Oligonucleotide Therapeutics: Challenges and Opportunities
Lange, J., Zhou, H., & McTague, A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.941528 · Cited by 22
Ma, C., Seong, H., Li, X., Yu, X., Xu, S., & Li, Y. (2022) · Stem Cells International · doi:10.1155/2022/2150680 · Cited by 25
Arthur, P., Muok, L., Nathani, A., Zeng, E. Z., Sun, L. J., Li, Y., & Singh, M. S. (2022) · Cells · doi:10.3390/cells11213429 · Cited by 24
A Cross-Sectional Study of the Neuropsychiatric Phenotype of CACNA1C-Related Disorder
Levy, R. J., Timothy, K. W., Underwood, J. F. G., Hall, J., Bernstein, J. A., & Pașca, S. P. (2022) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2022.10.013 · Cited by 20
Self-citationChen, H., Wu, X., Sun, R., Lu, H., Lin, R., Gao, X., Li, G., Feng, Z., Zhu, R., Yao, Y., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2172668 · Cited by 23
Chai, Y. C., To, S. K., Simorgh, S., Zaunz, S., Zhu, Y., Ahuja, K., Lemaitre, A., Ramezankhani, R., van der Veer, B. K., Wierda, K. D. B., et al. (2023) · Advanced Science · doi:10.1002/advs.202304421 · Cited by 23
Generation of human region-specific brain organoids with medullary spinal trigeminal nuclei
Pang, W., Zhu, J., Yang, K., Zhu, X., Zhou, W., Jiang, L., Zhuang, X., Liu, Y., Wei, J., Lu, X., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.08.004 · Cited by 21
Organoids for Modeling Genetic Diseases
Pérez-Lanzón, M., Kroemer, G., & Maiuri, M. C. (2018) · International review of cytology · doi:10.1016/bs.ircmb.2017.12.006 · Cited by 24
Oxidative DNA Damage Signalling in Neural Stem Cells in Alzheimer’s Disease
Kieroń, M., Żekanowski, C., Falk, A., & Wężyk, M. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/2149812 · Cited by 22
Cerebral Organoids—Challenges to Establish a Brain Prototype
Валерьевич, Е. А., Lebedeva, O. S., Bogomiakova, M. E., Lagarkova, M. A., & Bogomazova, A. N. (2021) · Cells · doi:10.3390/cells10071790 · Cited by 23
The road to synthetic multicellularity
Solé, R., Ollé-Vila, A., Vidiella, B., Duran-Nebreda, S., & Conde-Pueyo, N. (2018) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2017.11.007 · Cited by 19
Walsh, R. M., Crabtree, G. W., Kalpana, K., Jubierre, L., Koo, S. Y., Ciceri, G., Gogos, J. A., Kruglikov, I., & Studer, L. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.017 · Cited by 24
Modeling cell-cell interactions in the brain using cerebral organoids
Oliveira, B., Yahya, A. Ç., & Novarino, G. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146458 · Cited by 20
Expanding the boundaries of synthetic development
Martyn, I., & Gartner, Z. J. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.01.017 · Cited by 19
Methodologies for Generating Brain Organoids to Model Viral Pathogenesis in the CNS
Hopkins, H. K., Traverse, E. M., & Barr, K. L. (2021) · Pathogens · doi:10.3390/pathogens10111510 · Cited by 21
Engineering Brain Organoids: Toward Mature Neural Circuitry with an Intact Cytoarchitecture
Jang, H., Kim, S. H., Koh, Y., & Yoon, K. (2022) · International Journal of Stem Cells · doi:10.15283/ijsc22004 · Cited by 22
Aly, K. A., Moutaoufik, M. T., Zilocchi, M., Phanse, S., & Babu, M. (2022) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2022.102211 · Cited by 21
Koch, L., Deiwick, A., Soriano, J., & Chichkov, B. N. (2023) · International Journal of Bioprinting · doi:10.18063/ijb.v9i2.672 · Cited by 21
McCaughey‐Chapman, A., & Connor, B. (2023) · Journal of Neuroscience Research · doi:10.1002/jnr.25173 · Cited by 21
Modeling Human Brain Tumors and the Microenvironment Using Induced Pluripotent Stem Cells
Khamis, Z. I., Sarker, D. B., Xue, Y., Al-Akkary, N., James, V. D., Zeng, C., Li, Y., & Sang, Q. A. (2023) · Cancers · doi:10.3390/cancers15041253 · Cited by 22
Park, Y., Hernandez, S., Hernandez, C. O., Schweiger, H. E., Li, H., Voitiuk, K., Dechiraju, H., Hawthorne, N., Muzzy, E. M., Selberg, J. A., et al. (2024) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100686 · Cited by 25
Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids
Bombieri, C., Corsi, A., Trabetti, E., Ruggiero, A., Marchetto, G., Vattemi, G. N. A., Valenti, M. T., Zipeto, D., & Romanelli, M. G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021014 · Cited by 23
Rylaarsdam, L. E., Rakotomamonjy, J., Pope, E. G., & Guemez‐Gamboa, A. (2024) · Nature Communications · doi:10.1038/s41467-024-44989-7 · Cited by 23
Engineering human midbrain organoid microphysiological systems to model prenatal PFOS exposure
Tian, C., Cai, H., Ao, Z., Gu, L., Li, X., Niu, V. C., Bondesson, M., Gu, M., Mackie, K., & Guo, F. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.174478 · Cited by 22
Mojares, E., Nadal, C., Hayler, D., Kanso, H., Chrysanthou, A., Neri-Cruz, C. E., & Gautrot, J. E. (2024) · Advanced Materials · doi:10.1002/adma.202406333 · Cited by 20
Zhang, S., Moy, W., Zhang, H., Leites, C., McGowan, H., Shi, J., Sanders, A. R., Pang, Z. P., Gejman, P. V., & Duan, J. (2018) · Stem Cell Research · doi:10.1016/j.scr.2018.03.014 · Cited by 21
Stem cells: A path towards improved epilepsy therapies
Lybrand, Z. R., Goswami, S., & Hsieh, J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107781 · Cited by 22
Next-Generation Human Cerebral Organoids as Powerful Tools To Advance NeuroHIV Research
Premeaux, T. A., Mediouni, S., Léda, A. R., O’Brien, R. L. F., Valente, S. T., Fine, H. A., Nixon, D. F., & Ndhlovu, L. C. (2021) · mBio · doi:10.1128/mbio.00680-21 · Cited by 22
Microfabricated disk technology: Rapid scale up in midbrain organoid generation
Mohamed, N., Lépine, P., Lacalle‐Aurioles, M., Sirois, J., Mathur, M., Reintsch, W., Beitel, L. K., Fon, E. A., & Durcan, T. M. (2021) · Methods · doi:10.1016/j.ymeth.2021.07.008 · Cited by 23
Uzquiano, A., Kedaigle, A. J., Pigoni, M., Paulsen, B. D. S., Adiconis, X., Kim, K., Faits, T., Nagaraja, S., Antón-Bolaños, N., Gerhardinger, C., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.17.484798 · Cited by 21
Assembloid model to study loop circuits of the human nervous systemPreprint
Miura, Y., Kim, J., Jurjuţ, O. F., Kelley, K. W., Yang, X., Chen, X., Thete, M. V., Revah, O., Cui, B., Pachitariu, M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.13.617729 · Cited by 23
Self-citationOrganoids: Principle, application and perspective
Liu, K., Fang, X., Aazmi, A., Wang, Q., Gong, X., Chen, Z., Qin, M., Pu, C., Zhao, Y., Qiu, X., et al. (2024) · The Innovation Life · doi:10.59717/j.xinn-life.2024.100088 · Cited by 21
Deciphering the physiopathology of neurodevelopmental disorders using brain organoids
Dionne, O., Sabatié, S., & Laurent, B. (2024) · Brain · doi:10.1093/brain/awae281 · Cited by 22
Harnessing Intelligence from Brain Cells In Vitro
Kagan, B. J., Habibollahi, F., Watmuff, B., Azadi, S. A., Doensen, F., Loeffler, A., Byun, S. H., Servais, B., Desouza, C., Abu-Bonsrah, K. D., et al. (2025) · The Neuroscientist · doi:10.1177/10738584251321438 · Cited by 20
Organoids – the future of pre-clinical development of AAV gene therapy for CNS disorders
Kaiser, V., & Gonzalez-Cordero, A. (2025) · Gene Therapy · doi:10.1038/s41434-025-00527-8 · Cited by 19
From Organoids to Assembloids: Experimental Approaches to Study Human Neuropsychiatric Disorders
Levy, R. J., & Pașca, S. P. (2025) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-112723-023232 · Cited by 24
Self-citationDevelopment of GABAergic Interneurons in the Human Cerebral Cortex
Marín, Ó. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70136 · Cited by 22
New developments and applications of human organoids
Andersson-Rolf, A., & Clevers, H. C. (2026) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-026-00974-0 · Cited by 25
Yan, Y., Bejoy, J., Marzano, M., & Li, Y. (2019) · Cells · doi:10.3390/cells8030242 · Cited by 21
Toward the formation of neural circuits in human brain organoids
Seto, Y., & Eiraku, M. (2019) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2019.07.010 · Cited by 20
Horigane, S., Ozawa, Y., Zhang, J., Todoroki, H., Pan, M., Haijima, A., Yanagawa, Y., Ueda, S., Nakamura, S., Kakeyama, M., et al. (2020) · FEBS Open Bio · doi:10.1002/2211-5463.12924 · Cited by 19
Zourray, C., Kurian, M. A., Barral, S., & Lignani, G. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.839366 · Cited by 20
Neural Organoids, a Versatile Model for Neuroscience
Lee, J., & Sun, W. (2022) · Molecules and Cells · doi:10.14348/molcells.2022.2019 · Cited by 22
What Makes Organoids Good Models of Human Neurogenesis?
Yang, Q., Hong, Y., Zhao, T., Song, H., & Ming, G. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.872794 · Cited by 26
Wu, W., Yao, H., Negraes, P. D., Wang, J., Trujillo, C. A., de Souza, J. S., Muotri, A. R., & Haddad, G. G. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105882 · Cited by 19
Jalilian, E., & Shin, S. (2023) · Scientific Reports · doi:10.1038/s41598-023-35077-9 · Cited by 19
Generation of iPSC-derived human forebrain organoids assembling bilateral eye primordia
Gabriel, E., Albanna, W., Pasquini, G., Ramani, A., Josipović, N., Mariappan, A., Riparbelli, M. G., Callaini, G., Karch, C. M. M., Goureau, O., et al. (2023) · Nature Protocols · doi:10.1038/s41596-023-00814-x · Cited by 21
Guidelines for Manufacturing and Application of Organoids: Brain
Kwak, T., Park, S.-H., Lee, S., Shin, Y., Yoon, K., Cho, S., Park, J., Yang, S.-H., Cho, H., Im, H., et al. (2024) · International Journal of Stem Cells · doi:10.15283/ijsc24056 · Cited by 20
Brain organoids: A new tool for modelling of neurodevelopmental disorders
Aili, Y., Maimaitiming, N., Wang, Z., & Wang, Y. (2024) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.18560 · Cited by 24
A novel recombinant cccDNA-based mouse model with long term maintenance of rcccDNA and antigenemia
Wu, M., Wang, C., Shi, B., Fang, Z., Qin, B., Zhou, X., Zhang, X., & Yuan, Z. (2020) · Antiviral Research · doi:10.1016/j.antiviral.2020.104826 · Cited by 19
APOE4 impacts cortical neurodevelopment and alters network formation in human brain organoids
Meyer-Acosta, K. K., Díaz‐Guerra, E., Varma, P., Aruk, A., Mirsadeghi, S., Perez, A. M., Rafati, Y., Hosseini, A., Nieto‐Estévez, V., Giugliano, M., et al. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102537 · Cited by 19
Bone organoid construction and evolution
Hong, Y., Li, R., Sheng, S., Zhou, F., Bai, L., & Su, J. (2025) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2025.06.011 · Cited by 20
Use of standard U-bottom and V-bottom well plates to generate neuroepithelial embryoid bodies
Buentello, D. C., Koch, L. S., Santiago, G. T., Álvarez, M. M., & Broersen, K. (2022) · PLoS ONE · doi:10.1371/journal.pone.0262062 · Cited by 18
Microfabrication methods for 3D spheroids formation and their application in biomedical engineering
Ahn, S., Kim, D., Cho, K., & Koh, W. (2023) · Korean Journal of Chemical Engineering · doi:10.1007/s11814-022-1327-5 · Cited by 22
Baker, M. R., Lee, A. S., & Rajadhyaksha, A. M. (2023) · Channels · doi:10.1080/19336950.2023.2176984 · Cited by 21
Villanueva, R. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1178494 · Cited by 20
Host circuit engagement of human cortical organoids transplanted in rodents
Kelley, K. W., Revah, O., Gore, F., Kaganovsky, K., Chen, X., Deisseroth, K. A., & Pașca, S. P. (2024) · Nature Protocols · doi:10.1038/s41596-024-01029-4 · Cited by 17
Self-citationConcise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric Diseases
Adegbola, A. A., Bury, L. A. D., Fu, C. S., Zhang, M., & Wynshaw-Boris, A. J. (2017) · Stem Cells Translational Medicine · doi:10.1002/sctm.17-0150 · Cited by 21
Prytkova, I., & Brennand, K. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00360 · Cited by 20
iPSC modeling of rare pediatric disorders
Freel, B. A., Sheets, J. N., & Francis, K. R. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108533 · Cited by 20
Brain Organoids: Tiny Mirrors of Human Neurodevelopment and Neurological Disorders
Yadav, A., Seth, B., & Chaturvedi, R. K. (2020) · The Neuroscientist · doi:10.1177/1073858420943192 · Cited by 19
Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates
Brady, M. V., & Vaccarino, F. M. (2021) · Cells · doi:10.3390/cells10040914 · Cited by 22
Metadata
- Authors
- Birey, F., Andersen, J., Makinson, C. D., Islam, S., Wei, W., Huber, N., Fan, H. C., Metzler, K. R. C., Panagiotakos, G., Thom, N., O’Rourke, N. A., Steinmetz, L. M., Bernstein, J. A., Hallmayer, J., Huguenard, J. R., & Paşca, S. P.
- Affiliations
- Stanford Medicine (US)
- University of California, San Francisco (US)
- ORCID
- Venue
- Nature
- Published
- 2017-04-26
- Volume
- 545
- Issue
- 7652
- Pages
- 54-59
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5805137
- OpenAlex
- W2609473806
- Cited by
- 1,365
- References
- 58
- Citations by year
- 2026: 148 · 2025: 169 · 2024: 164 · 2023: 135 · 2022: 161 · 2021: 165 · 2020: 168 · 2019: 135 · 2018: 84 · 2017: 34
- FWCI
- 48.69
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Mental Health (R33MH100717, R01MH107800, R01MH100900)
- National Human Genome Research Institute (P01HG000205)
- National Institute of Neurological Disorders and Stroke (R01NS090911, R01NS034774)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- human pluripotent stem cells, GABAergic interneurons, interneuron migration, Timothy syndrome, Cav1.2 calcium channel, glutamatergic neurons, brain organoids, neural development
- MeSH terms
- Autistic Disorder, Cell Line, Cell Movement, Cells, Cultured, Female, Humans, Interneurons, Long QT Syndrome, Male, Models, Biological, Neurons, Synapses, Syndactyly, Prosencephalon, Glutamic Acid, Spheroids, Cellular, Pluripotent Stem Cells, Neurogenesis, GABAergic Neurons
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review