The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Cell diversity and network dynamics in photosensitive human brain organoids
Open accessAbstract
In vitro models of the developing brain such as three-dimensional brain organoids offer an unprecedented opportunity to study aspects of human brain development and disease. However, the cells generated within organoids and the extent to which they recapitulate the regional complexity, cellular diversity and circuit functionality of the brain remain undefined. Here we analyse gene expression in over 80,000 individual cells isolated from 31 human brain organoids. We find that organoids can generate a broad diversity of cells, which are related to endogenous classes, including cells from the cerebral cortex and the retina. Organoids could be developed over extended periods (more than 9 months), allowing for the establishment of relatively mature features, including the formation of dendritic spines and spontaneously active neuronal networks. Finally, neuronal activity within organoids could be controlled using light stimulation of photosensitive cells, which may offer a way to probe the functionality of human neuronal circuits using physiological sensory stimuli.
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
“Although such regional diversity is appealing, it also leads to a relatively variable outcome and the differentiation of some cells into non-ectodermal cell types28,29.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Apart from growth factor cues, other modulators — such as scaffold support provided by the extracellular matrix — are important features of current protocols2,5,28.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
The cited source says what the claim attributes to it.
In the citing paper
“hiPSC-derived astrocytes, which can be generated with a fast protocol in 2D layers104 or integrated in 3D systems such as spheroids and organoids105–108”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [107]
In the citing paper
“Some protocols build on the principles of spontaneous neural induction by using medium that is free of neural induction signalling molecules2,27. This promotes the generation of diverse brain regions and cell populations2,28,29.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“One important issue is that organoids derived from the same cell line under the same conditions can often produce tissues with different regional identities and spatial and cellular heterogeneity28,29.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“A recent paper used droplet-based single-cell mRNA sequencing to analyse gene expression in 80,000 cells from 31 brain organoids after 3 and 6 months in vitro28. Using principal component analysis, 10 distinct populations of cells (clusters) were identified in 6-month old organoids.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“As one might expect, 6-month-old organoids presented a greater diversity of cell types than 3-month-old organoids, as well as enrichment of genes associated with neuronal and glial maturation.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Recently, it was demonstrated that photosensitive cells in retinal-like regions of brain organoids can respond to light28.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Also, the authors observed that some cell types were only produced by a subset of organoids and that organoids grown in the same bioreactor tended to be similar in terms of their ability to make cells of each cluster, suggesting that batch effects and local microenvironments are important in patterning and possibly that organoids secrete signalling factors that influence sister organoids.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“In addition to these findings, electrophysiological studies have demonstrated functional synapses in several brain organoid models25,28, and electron microscopy has confirmed the presence of structurally defined synaptic junctions28.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Several reports suggest that long-term organoid culture can improve the correlation between the molecular signatures of organoid and endogenous cells28,52.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“For example, a large number of cells were assigned to a mesodermal lineage, emphasizing the variability inherent in the protocol.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“These initial reports identified striking parallels among organoid development, human primary tissue and in vivo organogenesis”
From The organoid cell atlas (2021) · cites this paper as [10]
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
DAVID: Database for Annotation, Visualization, and Integrated Discovery
Dennis, G., Sherman, B. T., Hosack, D. A., Yang, J., Gao, W., Lane, H. C., & Lempicki, R. A. (2003) · Genome Biology · doi:10.1186/gb-2003-4-5-p3 · Cited by 9,327
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
Self-citationSpatial 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
Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875 · cited 1×
“Cluster c9 (17,103 cells) contained progenitors of neuroepithelial origin, including cells with an oligodendrocyte-precursor-like identity 20,26 .”
BackgroundCahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Zhang, Y., Sloan, S. A., Clarke, L. E., Caneda, C., Plaza, C. A., Blumenthal, P. D., Vogel, H., Steinberg, G. K., Edwards, M. S. B., Li, G., et al. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.013 · Cited by 2,295
Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure
Qian, X., Nguyen, H. N., Song, M. M., Hadiono, C., Ogden, S. C., Hammack, C., Yao, B., Hamersky, G. R., Jacob, F., Zhong, C., et al. (2016) · Cell · doi:10.1016/j.cell.2016.04.032 · Cited by 2,127
Generation of cerebral organoids from human pluripotent stem cells
Lancaster, M. A., & Knoblich, J. A. (2014) · Nature Protocols · doi:10.1038/nprot.2014.158 · Cited by 1,823
Cited by
Sorted by citations
Items 101–200 of 997
Pereira, J. D., DuBreuil, D. M., Devlin, A., Held, A., Sapir, Y., Berezovski, E., Hawrot, J., Dorfman, K., Chander, V., & Wainger, B. J. (2021) · Nature Communications · doi:10.1038/s41467-021-24776-4 · Cited by 159
Rotenone exerts developmental neurotoxicity in a human brain spheroid model
Pamies, D., Block, K., Lau, P., Gribaldo, L., Pardo, C. A., Barreras, P., Smirnova, L., Wiersma, D., Zhao, L., Harris, G., et al. (2018) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2018.02.003 · Cited by 155
Andrews, M. G., Subramanian, L., & Kriegstein, A. R. (2020) · eLife · doi:10.7554/elife.58737 · Cited by 148
Human iPSC‐derived microglia: A growing toolset to study the brain's innate immune cells
Hasselmann, J., & Blurton‐Jones, M. (2020) · Glia · doi:10.1002/glia.23781 · Cited by 145
Inak, G., Rybak‐Wolf, A., Lisowski, P., Pentimalli, T. M., Jüttner, R., Glažar, P., Uppal, K., Bottani, E., Brunetti, D., Secker, C., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22117-z · Cited by 151
Modelling human brain development and disease with organoids
Birtele, M., Lancaster, M. A., & Quadrato, G. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00804-1 · Cited by 177
Self-citationZhang, W., Ma, L., Yang, M., Shao, Q., Xu, J., Lu, Z., Zhao, Z., Chen, R., Chai, Y., & Chen, J. (2020) · Genes & Development · doi:10.1101/gad.332494.119 · Cited by 143
Stem Cells, Genome Editing, and the Path to Translational Medicine
Soldner, F., & Jaenisch, R. (2018) · Cell · doi:10.1016/j.cell.2018.09.010 · Cited by 144
Applications of Human Brain Organoids to Clinical Problems
Chen, H.-C. I., Song, H., & Ming, G. (2018) · Developmental Dynamics · doi:10.1002/dvdy.24662 · Cited by 147
Short term changes in the proteome of human cerebral organoids induced by 5-MeO-DMT
Dakic, V., Minardi Nascimento, J., Costa Sartore, R., Maciel, R. D. M., de Araujo, D. B., Ribeiro, S., Martins-de-Souza, D., & Rehen, S. K. (2017) · Scientific Reports · doi:10.1038/s41598-017-12779-5 · Cited by 134
Biomaterials‐Based Approaches to Tumor Spheroid and Organoid Modeling
Thakuri, P. S., Liu, C., Luker, G. D., & Tavana, H. (2017) · Advanced Healthcare Materials · doi:10.1002/adhm.201700980 · Cited by 142
Brain Organoids and the Study of Neurodevelopment
Trujillo, C. A., & Muotri, A. R. (2018) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.09.005 · Cited by 139
The Ethics of Cerebral Organoid Research: Being Conscious of Consciousness
Sawai, T., Sakaguchi, H., Thomas, E. S., Takahashi, J. B., & Fujita, M. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.08.003 · Cited by 140
Shifting Developmental Trajectories During Critical Periods of Brain Formation
Dehorter, N., & del Pino, I. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00283 · Cited by 143
Human organoids-on-chips for biomedical research and applications
Wang, H., Ning, X., Zhao, F. H., Zhao, H., & Li, D. (2024) · Theranostics · doi:10.7150/thno.90492 · Cited by 148
Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy
Suzuki, N., Nishiyama, A., Warita, H., & Aoki, M. (2022) · Journal of Human Genetics · doi:10.1038/s10038-022-01055-8 · Cited by 148
Sakaguchi, H., Ozaki, Y., Ashida, T., Matsubara, T., Oishi, N., Kihara, S., & Takahashi, J. B. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.05.029 · Cited by 134
Mechanisms of radial glia progenitor cell lineage progression
Beattie, R., & Hippenmeyer, S. (2017) · FEBS Letters · doi:10.1002/1873-3468.12906 · Cited by 136
Buchsbaum, I. Y., & Cappello, S. (2019) · Development · doi:10.1242/dev.163766 · Cited by 132
Resolving organoid brain region identities by mapping single-cell genomic data to reference atlases
Fleck, J. S., Sanchís-Calleja, F., He, Z., Santel, M., Boyle, M. J., Camp, J. G., & Treutlein, B. (2021) · Cell Stem Cell · doi:10.1016/j.stem.2021.02.015 · Cited by 118
Three-dimensional modeling of human neurodegeneration: brain organoids coming of age
Grenier, K., Kao, J., & Diamandis, P. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0500-7 · Cited by 131
Revolutionizing Neurocare: Biomimetic Nanodelivery Via Cell Membranes
Liao, J., Gong, L., Xu, Q., Wang, J., Yang, Y., Zhang, S., Dong, J., Lin, K., Liang, Z., Sun, Y., et al. (2024) · Advanced Materials · doi:10.1002/adma.202402445 · Cited by 126
Transplantation of Human Brain Organoids: Revisiting the Science and Ethics of Brain Chimeras
Chen, H. I., Wolf, J. A., Blue, R., Song, M. M., Moreno, J. D., Ming, G., & Song, H. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.09.002 · Cited by 131
Microglia-like Cells Promote Neuronal Functions in Cerebral Organoids
Fagerlund, I., Dougalis, A., Shakirzyanova, A., Gómez‐Budia, M., Pelkonen, A., Konttinen, H., Ohtonen, S., Fazaludeen, M. F., Koskuvi, M., Kuusisto, J., et al. (2021) · Cells · doi:10.3390/cells11010124 · Cited by 127
Sawada, T., Chater, T. E., Sasagawa, Y., Yoshimura, M., Fujimori-Tonou, N., Tanaka, K. Y., Benjamin, K. J., Paquola, A. C. M., Erwin, J. A., Goda, Y., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0844-z · Cited by 127
Advancing models of neural development with biomaterials
Roth, J. G., Huang, M. S., Li, T. L., Feig, V. R., Jiang, Y., Cui, B., Greely, H. T., Bao, Z., Pașca, S. P., & Heilshorn, S. C. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00496-y · Cited by 122
Papamichail, L., Koch, L. S., Veerman, D., Broersen, K., & van der Meer, A. D. (2025) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2025.1515340 · Cited by 120
In vivo modeling of human neuron dynamics and Down syndrome
Real, R., Peter, M., Trabalza, A., Khan, S., Smith, M. A., Dopp, J., Barnes, S. J., Momoh, A., Strano, A., Volpi, E., et al. (2018) · Science · doi:10.1126/science.aau1810 · Cited by 120
Glial cell diversity and methamphetamine-induced neuroinflammation in human cerebral organoids
Dang, J. W., Tiwari, S. K., Agrawal, K., Hui, H., Qin, Y., & Rana, T. M. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0676-x · Cited by 124
Organoids are not organs: Sources of variation and misinformation in organoid biology
Jensen, K. B., & Little, M. H. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2023.05.009 · Cited by 127
Reproducible generation of human midbrain organoids for in vitro modeling of Parkinson’s disease
Nickels, S., Modamio, J., Mendes-Pinheiro, B., Monzel, A. S., Betsou, F., & Schwamborn, J. C. (2020) · Stem Cell Research · doi:10.1016/j.scr.2020.101870 · Cited by 129
Logan, S., Arzua, T., Canfield, S. G., Seminary, E. R., Sison, S. L., Ebert, A. D., & Bai, X. (2019) · Comprehensive physiology · doi:10.1002/cphy.c180025 · Cited by 143
da Silva, B., Mathew, R. K., Polson, E. S., Williams, J. M., & Wurdak, H. (2018) · SLAS DISCOVERY · doi:10.1177/2472555218764623 · Cited by 117
Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids
Zafeiriou, M.-P., Bao, G., Hudson, J. E., Halder, R., Blenkle, A., Schreiber, M.-K., Fischer, A., Schild, D., & Zimmermann, W. (2020) · Nature Communications · doi:10.1038/s41467-020-17521-w · Cited by 118
Brain Organoids: Human Neurodevelopment in a DishPreprint
Benito-Kwiecinski, S. K., & Lancaster, M. A. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a035709 · Cited by 118
DIALOGUE maps multicellular programs in tissue from single-cell or spatial transcriptomics data
Jerby‐Arnon, L., & Regev, A. (2022) · Nature Biotechnology · doi:10.1038/s41587-022-01288-0 · Cited by 119
Electrophysiological Analysis of Brain Organoids: Current Approaches and Advancements
Passaro, A. P., & Stice, S. L. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.622137 · Cited by 120
3D Brain Organoids: Studying Brain Development and Disease Outside the Embryo
Velasco, S., Paulsen, B. D. S., & Arlotta, P. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050154 · Cited by 111
Self-citationModeling and Targeting Alzheimer’s Disease With Organoids
Papaspyropoulos, A., Tsolaki, M., Foroglou, N., & Pantazaki, Α. A. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00396 · Cited by 107
Polymer Hydrogels to Guide Organotypic and Organoid Cultures
Magno, V., Meinhardt, A., & Werner, C. (2020) · Advanced Functional Materials · doi:10.1002/adfm.202000097 · Cited by 110
Mullane, K., & Williams, M. J. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.113945 · Cited by 109
Wilson, M. N., Thunemann, M., Liu, X., Lu, Y., Puppo, F., Adams, J. W., Kim, J., Ramezani, M., Pizzo, D. P., Djurovic, S., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35536-3 · Cited by 110
Three‐Dimensional Models of the Human Brain Development and Diseases
Jorfi, M., D’Avanzo, C., Kim, D. Y., & Irimia, D. (2017) · Advanced Healthcare Materials · doi:10.1002/adhm.201700723 · Cited by 106
Upgrading the Physiological Relevance of Human Brain Organoids
Dosso, A. D., Urenda, J., Nguyen, T. N., & Quadrato, G. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.029 · Cited by 106
Self-citation3D Electrodes for Bioelectronics
Cho, Y. H., Park, Y., Kim, S., & Park, J. (2021) · Advanced Materials · doi:10.1002/adma.202005805 · Cited by 110
Barák, M., Fedorová, V., Pospíšilová, V., Raška, J., Vochyánová, S., Sedmík, J., Hříbková, H., Klímová, H., Váňová, T., & Bohačiaková, D. (2022) · Stem Cell Reviews and Reports · doi:10.1007/s12015-021-10254-3 · Cited by 102
Tissue morphology influences the temporal program of human brain organoid development
Chiaradia, I., Imaz-Rosshandler, I., Nilges, B. S., Boulanger, J., Pellegrini, L., Das, R., Kashikar, N. D., & Lancaster, M. A. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.09.003 · Cited by 106
Mapping the Ethical Issues of Brain Organoid Research and Application
Sawai, T., Hayashi, Y., Niikawa, T., Shepherd, J., Thomas, E., Lee, T.-L., Erler, A., Watanabe, M., & Sakaguchi, H. (2021) · AJOB Neuroscience · doi:10.1080/21507740.2021.1896603 · Cited by 104
Applications of brain organoids in neurodevelopment and neurological diseases
Sun, N., Meng, X., Liu, Y., Song, D., Jiang, C., & Cai, J. (2021) · Journal of Biomedical Science · doi:10.1186/s12929-021-00728-4 · Cited by 103
Effects of 3D culturing conditions on the transcriptomic profile of stem-cell-derived neurons
Tekin, H., Simmons, S., Cummings, B. B., Gao, L. A., Adiconis, X., Hession, C. C., Ghoshal, A., Dionne, D. A., Choudhury, S., Yesilyurt, V., et al. (2018) · Nature Biomedical Engineering · doi:10.1038/s41551-018-0219-9 · Cited by 97
Cell diversity in the human cerebral cortex: from the embryo to brain organoids
Arlotta, P., & Pașca, S. P. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.03.001 · Cited by 99
Self-citationAdvanced 3D imaging and organoid bioprinting for biomedical research and therapeutic applications
Maharjan, S., Ma, C., Singh, B., Kang, H., Orive, G., Yao, J., & Zhang, Y. S. (2024) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2024.115237 · Cited by 107
Testicular organoids: a new model to study the testicular microenvironment in vitro?
Alves-Lopes, J. P., & Stukenborg, J. (2017) · Human Reproduction Update · doi:10.1093/humupd/dmx036 · Cited by 102
Wang, Y., Chiola, S., Yang, G., Russell, C., Armstrong, C. J., Wu, Y., Spampanato, J. G., Tarboton, P., Ullah, H. M. A., Edgar, N. U., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33364-z · Cited by 104
Present and future of modeling human brain development in 3D organoids
Quadrato, G., & Arlotta, P. (2017) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2017.11.010 · Cited by 100
Self-citationArzua, T., Yan, Y., Jiang, C., Logan, S., Allison, R. L., Wells, C. W., Kumar, S. N., Schäfer, R., & Bai, X. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-01029-4 · Cited by 99
Biologically inspired approaches to enhance human organoid complexity
Holloway, E. M., Capeling, M. M., & Spence, J. R. (2019) · Development · doi:10.1242/dev.166173 · Cited by 99
Heinzelmann, E., Piraino, F., Costa, M., Roch, A., Norkin, M. N., Garnier, V., Homicskó, K., & Brandenberg, N. (2024) · Current Research in Toxicology · doi:10.1016/j.crtox.2024.100197 · Cited by 109
Pavoni, S., Jarray, R., Nassor, F., Guyot, A.-C., Cottin, S., Rontard, J., Mikol, J., Mabondzo, A., Deslys, J.-P., & Yates, F. (2018) · PLOS ONE · doi:10.1371/journal.pone.0209150 · Cited by 97
High-throughput single-cell transcriptomics on organoids
Brazovskaja, A., Treutlein, B., & Camp, J. G. (2018) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2018.11.002 · Cited by 95
Human cerebral organoids and consciousness: a double-edged sword
Lavazza, A. (2020) · Bioethics News · doi:10.1007/s40592-020-00116-y · Cited by 96
Modelling viral encephalitis caused by herpes simplex virus 1 infection in cerebral organoids
Rybak‐Wolf, A., Wyler, E., Pentimalli, T. M., Legnini, I., Oliveras, A., Glažar, P., Loewa, A., Kim, S. J., Kaufer, B. B., Woehler, A., et al. (2023) · Nature Microbiology · doi:10.1038/s41564-023-01405-y · Cited by 100
3d organ-on-a-chip: the convergence of microphysiological systems and organoids
Baptista, L. S., Porrini, C., Kronemberger, G. S., Kelly, D. J., & Perrault, C. M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1043117 · Cited by 90
“The subsequent articles showed a diversity of cell types related to the human cerebral cortex (Quadrato et al., 2017; Velasco et al., 2019) with a correlation of genetic variability according to donor cells (Velasco et al.”
BackgroundVilla, C. E., Cheroni, C., Dotter, C. P., López-Tóbon, A., Oliveira, B., Sacco, R., Yahya, A. Ç., Morandell, J., Gabriele, M., Tavakoli, M. R., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110615 · Cited by 92
Véjux, A., Abed-Vieillard, D., Hajji, K., Zarrouk, A., Mackrill, J. J., Ghosh, S., Nury, T., Yammine, A., Zaibi, M. S., Mihoubi, W., et al. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.113648 · Cited by 92
Past, Present, and Future of Brain Organoid Technology.
Koo, B., Choi, B., Park, H., & Yoon, K. (2019) · Europe PMC (PubMed Central) · doi:10.14348/molcells.2019.0162 · Cited by 93
Multiscale 3D phenotyping of human cerebral organoids
Albanese, A., Swaney, J., Yun, D. H., Evans, N. B., Antonucci, J. M., Velasco, S., Sohn, C. H., Arlotta, P., Gehrke, L., & Chung, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-78130-7 · Cited by 92
Self-citationSalaris, F., & Rosa, A. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146393 · Cited by 88
Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities
Nascimento, J. M., Saia-Cereda, V. M., Sartore, R., da Costa, R. M., Schitine, C., Freitas, H. R., Murgu, M., Reis, R. A. D. M., Rehen, S. K., & Martins‐de‐Souza, D. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00303 · Cited by 92
Zheng, F., Xiao, Y., Liu, H., Fan, Y., & Dao, M. (2021) · Advanced Biology · doi:10.1002/adbi.202000024 · Cited by 96
Rosebrock, D., Arora, S., Mutukula, N., Volkman, R., Gralinska, E., Balaskas, A., Aragonés Hernández, A., Buschow, R., Brändl, B., Müller, F.-J., et al. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-00929-5 · Cited by 89
The Application of Brain Organoids: From Neuronal Development to Neurological Diseases
Shou, Y., Liang, F., Xu, S., & Li, X. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.579659 · Cited by 87
Birtele, M., Dosso, A. D., Xu, T., Nguyen, T. N., Wilkinson, B., Hosseini, N., Nguyen, S. C., Urenda, J., Knight, G. T., Rojas, C., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01477-3 · Cited by 101
Self-citationInnovations in 3D Tissue Models of Human Brain Physiology and Diseases
Lovett, M. L., Nieland, T. J. F., Dingle, Y. L., & Kaplan, D. L. (2020) · Advanced Functional Materials · doi:10.1002/adfm.201909146 · Cited by 87
Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly
Wang, L., Li, Z., Sievert, D., Smith, D. E. C., Mendes, M. I. S., Chen, D. Y., Stanley, V., Ghosh, S. G., Wang, Y., Kara, M., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17454-4 · Cited by 85
Advancing Drug Discovery for Neurological Disorders Using iPSC-Derived Neural Organoids
Costamagna, G., Comi, G. P., & Corti, S. P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052659 · Cited by 91
Organoids: An intermediate modeling platform in precision oncology
Jin, M., Han, R.-R., Qiu, G., Ju, X.-C., Lou, G., & Jin, W. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.11.021 · Cited by 90
Microfluidics for Neuronal Cell and Circuit Engineering
Habibey, R., Arias, J. E. R., Striebel, J., & Busskamp, V. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00212 · Cited by 88
Tan, H. Y., Cho, H., & Lee, L. P. (2020) · Nature Biomedical Engineering · doi:10.1038/s41551-020-00643-3 · Cited by 87
A mesh microelectrode array for non-invasive electrophysiology within neural organoids
McDonald, M., Sebinger, D., Brauns, L., González-Cano, L., Menuchin-Lasowski, Y., Mierzejewski, M., Psathaki, O. E., Stumpf, A., Wickham, J., Rauen, T., et al. (2023) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2023.115223 · Cited by 83
Shared and derived features of cellular diversity in the human cerebral cortex
Miller, D. J., Bhaduri, A., Šestan, N., & Kriegstein, A. R. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.12.005 · Cited by 79
Bioprinting Neural Systems to Model Central Nervous System Diseases
Qiu, B., Bessler, N., Figler, K. P., Buchholz, M., Rios, A. C., Malda, J., Levato, R., & Caiazzo, M. (2020) · Advanced Functional Materials · doi:10.1002/adfm.201910250 · Cited by 83
Mechanisms of dietary flavonoid action in neuronal function and neuroinflammation
Jaeger, B. N., Parylak, S., & Gage, F. H. (2017) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2017.11.003 · Cited by 83
Epigenetics and cerebral organoids: promising directions in autism spectrum disorders
Forsberg, S. L., Ilieva, M. S., & Michel, T. M. (2018) · Translational Psychiatry · doi:10.1038/s41398-017-0062-x · Cited by 82
Organoid Models for Infectious Disease
Blutt, S. E., & Estes, M. K. (2021) · Annual Review of Medicine · doi:10.1146/annurev-med-042320-023055 · Cited by 81
Limitations of human brain organoids to study neurodegenerative diseases: a manual to survive
Urrestizala-Arenaza, N., Cerchio, S., Cavaliere, F., & Magliaro, C. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1419526 · Cited by 80
Single-cell genomics to guide human stem cell and tissue engineering
Camp, J. G., Wollny, D., & Treutlein, B. (2018) · Nature Methods · doi:10.1038/s41592-018-0113-0 · Cited by 83
Fowler, J. L., Ang, L. T., & Loh, K. M. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.368 · Cited by 87
Hernández, D., Rooney, L. A., Daniszewski, M., Gulluyan, L. M., Liang, H. H., Cook, A. L., Hewitt, A. W., & Pébay, A. (2021) · Stem Cell Reviews and Reports · doi:10.1007/s12015-021-10147-5 · Cited by 79
Human Brain Organoids and Consciousness
Niikawa, T., Hayashi, Y., Shepherd, J., & Sawai, T. (2022) · Neuroethics · doi:10.1007/s12152-022-09483-1 · Cited by 79
Chen, C., Rengarajan, V., Kjar, A., & Huang, Y. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2020.10.003 · Cited by 77
A reproducible scaffold-free 3D organoid model to study neoplastic progression in breast cancer
Djomehri, S. I., Burman, B., González, M. E., Takayama, S., & Kleer, C. G. (2018) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-018-0498-7 · Cited by 79
Robust production of uniform human cerebral organoids from pluripotent stem cells
Sivitilli, A., Gosio, J., Ghoshal, B., Evstratova, A., Trcka, D., Ghiasi, P., Hernández, J. J., Beaulieu, J., Wrana, J. L., & Attisano, L. (2020) · Life Science Alliance · doi:10.26508/lsa.202000707 · Cited by 85
CNS organoids: an innovative tool for neurological disease modeling and drug neurotoxicity screening
Chhibber, T., Bagchi, S., Lahooti, B., Verma, A., Al-Ahmad, A. J., Paul, M. K., Pendyala, G., & Jayant, R. D. (2019) · Drug Discovery Today · doi:10.1016/j.drudis.2019.11.010 · Cited by 78
Brain Transcriptome Databases: A User's Guide
Keil, J. M., Qalieh, A., & Kwan, K. Y. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1930-17.2018 · Cited by 79
Neural Lineage Differentiation From Pluripotent Stem Cells to Mimic Human Brain Tissues
Hong, Y. J., & Tae, J. (2019) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2019.00400 · Cited by 78
Culotta, L., & Penzes, P. (2020) · Molecular Autism · doi:10.1186/s13229-020-00339-0 · Cited by 83
Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics
Nguyen, T., Lehr, A. W., & Roche, K. W. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00033 · Cited by 79
Self-citationEmerging Bioelectronics for Brain Organoid Electrophysiology
Tasnim, K., & Jia Liu, B. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167165 · Cited by 82
Tristan, C. A., Ormanoglu, P., Slamecka, J., Malley, C., Chu, P.-H., Jovanovic, V. M., Gedik, Y., Jethmalani, Y., Bonney, C., Barnaeva, E., et al. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.11.004 · Cited by 80
Metadata
- Authors
- Quadrato, G., Nguyen, T., Macosko, E. Z., Sherwood, J. L., Min Yang, S., Berger, D. R., Maria, N., Scholvin, J., Goldman, M., Kinney, J. P., Boyden, E. S., Lichtman, J. W., Williams, Z. M., McCarroll, S. A., & Arlotta, P.
- Affiliations
- Broad Institute (US)
- Harvard University (US)
- Leaflabs (United States) (US)
- McGovern Institute for Brain Research (US)
- Corresponding author
- Quadrato, Giorgia
- Arlotta, Paola
- ORCID
- Venue
- Nature
- Published
- 2017-04-26
- Volume
- 545
- Issue
- 7652
- Pages
- 48-53
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5659341
- OpenAlex
- W2609844460
- Cited by
- 1,321
- References
- 45
- Citations by year
- 2026: 118 · 2025: 131 · 2024: 167 · 2023: 131 · 2022: 162 · 2021: 168 · 2020: 178 · 2019: 137 · 2018: 91 · 2017: 35
- FWCI
- 51.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-sa)
- Funders
- National Institute of Mental Health (P50MH094271)
- National Institute of Neurological Disorders and Stroke (DP1NS087724, R01NS073124)
- 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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Keywords
- human brain organoids, cellular diversity, neuronal network dynamics, spontaneous neuronal activity, photostimulation, dendritic spines, cortical development, retinal development, single-cell gene expression, pluripotent stem cell differentiation, interneuron migration, synaptogenesis
- MeSH terms
- Brain, Cell Line, Cell Separation, Cerebral Cortex, Dendrites, Humans, Light, Nerve Net, Neural Pathways, Organ Specificity, Organoids, Retina, Time Factors, Sequence Analysis, RNA, Photoreceptor Cells, Vertebrate, Gene Expression Profiling, Pluripotent Stem Cells, Neurogenesis, Single-Cell Analysis, Transcriptome, In Vitro Techniques
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