The DOI matches its Crossref record; 57 of the 57 references it cites were found in a registry or an index.
Cerebral organoids model human brain development and microcephaly
Open accessAbstract
The complexity of the human brain has made it difficult to study many brain disorders in model organisms, highlighting the need for an in vitro model of human brain development. Here we have developed a human pluripotent stem cell-derived three-dimensional organoid culture system, termed cerebral organoids, that develop various discrete, although interdependent, brain regions. These include a cerebral cortex containing progenitor populations that organize and produce mature cortical neuron subtypes. Furthermore, cerebral organoids are shown to recapitulate features of human cortical development, namely characteristic progenitor zone organization with abundant outer radial glial stem cells. Finally, we use RNA interference and patient-specific induced pluripotent stem cells to model microcephaly, a disorder that has been difficult to recapitulate in mice. We demonstrate premature neuronal differentiation in patient organoids, a defect that could help to explain the disease phenotype. Together, these data show that three-dimensional organoids can recapitulate development and disease even in this most complex human tissue.
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 [15]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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 [106]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The differentiation protocol was further optimized by integrating established principles of neuronal development to ensure reproducibility and high neuronal purity (Lancaster et al. 2013;Lancaster and Knoblich 2014a;Lancaster and Knoblich 2014b).”
From TMEM55B downregulation promotes neurodegeneration in Alzheimer’s disease models (2026) · cites this paper as Lancaster et al. 2013
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Promising disease models of the liver65,66, pancreas67,68, central nervous system35,69,70, skin71, lung72,73, intestine72–76, musculoskeletal system77 and heart78–81 have been developed, but their equivalence or superiority over their animal models needs to be demonstrated.”
From Human disease models in drug development (2023) · cites this paper as [35]
The cited source says what the claim attributes to it.
In the citing paper
“These 3D “organoids” are often found to have instructive morphogenetic cues resulting in self organization similarly found in vivo [53,54].”
From Utility of iPSC-Derived Cells for Disease Modeling, Drug Development, and Cell Therapy (2022) · cites this paper as [53]
The cited source says what the claim attributes to it.
In the citing paper
“Human brain organoids are 3D cultures derived from human pluripotent stem cells and recapitulate native brain cellular components, cytoarchitecture, and exhibit neural activity.22–24”
From Tubular human brain organoids to model microglia-mediated neuroinflammation (2021) · cites this paper as [22]
The cited source says what the claim attributes to it.
In the citing paper
“Organoid development followed the expected temporal changes (Lancaster et al., 2013; Velasco et al., 2019; Watanabe et al., 2017; Yoon et al., 2019; Figures 1B–1D; Figure S1A).”
From ELAVL4, splicing, and glutamatergic dysfunction precede neuron loss in MAPT mutation cerebral organoids (2021) · cites this paper as Lancaster et al., 2013
The cited source says what the claim attributes to it.
In the citing paper
“Although organoids have been used to investigate disease-associated genes9–11, they are limited by phenotypic variability and low throughput.”
From Single-cell brain organoid screening identifies developmental defects in autism (2023) · cites this paper as [9]
The cited source says what the claim attributes to it.
In the citing paper
“Brain organoids recapitulate early brain development and generate diverse cell types found in vivo9.”
From Single-cell brain organoid screening identifies developmental defects in autism (2023) · cites this paper as [9]
In the citing paper
“Consistent with a more mature phenotype, APOE3Ch organoids stained prominently with Reelin, a marker of more mature neurons (Figures 4A–D; Lancaster et al., 2013; Di Lullo and Kriegstein, 2017).”
From APOE3 Christchurch modulates β-catenin/Wnt signaling in iPS cell-derived cerebral organoids from Alzheimer’s cases (2024) · cites this paper as Lancaster et al., 2013
In the citing paper
“The production of radial glial cells, intermediate progenitors, and deep- and superficial-layer neurons in an ordered temporal fashion has been reported by studies using all of the protocols currently in use2,3,5,25.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [2]
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 [2]
In the citing paper
“Both of these protocols generated organoids containing a dorsalized neuroepithelium that reproduced certain aspects of cortical development, both structurally and in terms of cell behaviour.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [2]
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 [2]
In the citing paper
“Bioreactors designed to improve oxygen diffusion and nutrient distribution have been used to produce larger and more viable structures that can grow for longer periods2,5 (BOX 1).”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [2]
In the citing paper
“Cerebral organoids grown from these cells contained fewer proliferating progenitor cells and showed premature neural differentiation compared to wild-type counterparts.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [2]
In the citing paper
“Interestingly, the developmental timing of cortical neurogenesis appears to be conserved in vitro and has been demonstrated with both suspension and adherent differentiation methods2,3,5,39.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [2]
In the citing paper
“Intriguingly, UBA1 is widely expressed in the human body, but loss-of-function mutations are linked to neurodegenerative diseases110.”
From CRISPR-based functional genomics for neurological disease (2020) · cites this paper as [110]
In the citing paper
“Cerebral or other unguided neural organoids develop from embryonic stem (ES) cells or induced pluripotent stem (iPS) cells into a three-dimensional neuroepithelium that self-patterns, regionalizes and, ultimately, forms neurons of the different brain regions1–3.”
From Inferring and perturbing cell fate regulomes in human brain organoids (2023) · cites this paper as [2]
In the citing paper
“Self-organizing neural organoids grown from pluripotent stem cells1–3 combined with single-cell genomic technologies provide opportunities to examine gene regulatory networks underlying human brain development.”
From Inferring and perturbing cell fate regulomes in human brain organoids (2023) · cites this paper as [2]
In the citing paper
“Brain organoids have been used to successfully model microcephaly2, periventricular heterotopia10, autism11 and other neurodevelopmental disorders12,13 that may have differential effects on the various human brain regions.”
From Inferring and perturbing cell fate regulomes in human brain organoids (2023) · cites this paper as [2]
In the citing paper
“IPSC models of rare microcephaly syndromes have been shown to undergo loss of neuronal progenitor cells and premature neural differentiation (Lancaster et al., 2013).”
From Getting to the cores of autism (2019) · cites this paper as Lancaster et al., 2013
In the citing paper
“Three-dimensional brain organoids derived from human pluripotent stem cells (hPSCs) have shown significant advantages in modeling neurological disorders including autism, microcephaly and Parkinson’s disease.528–530”
From Amyloid β-based therapy for Alzheimer’s disease: Challenges, successes and future (2023) · cites this paper as [528]
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
Takahashi, K., & Yamanaka, S. (2006) · Cell · doi:10.1016/j.cell.2006.07.024 · Cited by 26,673
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
Sato, T., Vries, R. G., Snippert, H. J., van de Wetering, M., Barker, N., Stange, D. E., van Es, J. H., Abo, A., Kujala, P., Peters, P. J., et al. (2009) · Nature · doi:10.1038/nature07935 · Cited by 7,204
Generation of germline-competent induced pluripotent stem cells
Okita, K., Ichisaka, T., & Yamanaka, S. (2007) · Nature · doi:10.1038/nature05934 · Cited by 4,438
Organoid Models and Applications in Biomedical Research
Xinaris, C., Brizi, V., & Remuzzi, G. (2015) · The Nephron journals/Nephron journals · doi:10.1159/000433566 · Cited by 3,519
The cell biology of neurogenesis
Götz, M., & Huttner, W. B. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1739 · Cited by 2,130
A ROCK inhibitor permits survival of dissociated human embryonic stem cells
Watanabe, K., Ueno, M., Kamiya, D., Nishiyama, A., Matsumura, M., Wataya, T., Takahashi, J. B., Nishikawa, S., Nishikawa, S.-I., Muguruma, K., et al. (2007) · Nature Biotechnology · doi:10.1038/nbt1310 · Cited by 2,055
Self-organizing optic-cup morphogenesis in three-dimensional culture
Eiraku, M., Takata, N., Ishibashi, H., Kawada, M., Sakakura, E., Okuda, S., Sekiguchi, K., Adachi, T., & Sasai, Y. (2011) · Nature · doi:10.1038/nature09941 · Cited by 2,001
Eiraku, M., Watanabe, K., Matsuo-Takasaki, M., Kawada, M., Yonemura, S., Matsumura, M., Wataya, T., Nishiyama, A., Muguruma, K., & Sasai, Y. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.09.002 · Cited by 1,522
Self-formation of optic cups and storable stratified neural retina from human ESCs
Nakano, T., Ando, S., Takata, N., Kawada, M., Muguruma, K., Sekiguchi, K., Saito, K., Yonemura, S., Eiraku, M., & Sasai, Y. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.05.009 · Cited by 1,447
Neurogenic radial glia in the outer subventricular zone of human neocortex
Hansen, D. V., Lui, J. H., Parker, P. R. L., & Kriegstein, A. R. (2010) · Nature · doi:10.1038/nature08845 · Cited by 1,388
Cited by
Sorted by citations
Items 601–700 of 1,035
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
Smart polymers for cell therapy and precision medicine
Huang, H.-J., Tsai, Y., Lin, S., & Hsu, S. (2019) · Journal of Biomedical Science · doi:10.1186/s12929-019-0571-4 · Cited by 102
Therapeutic Plasticity of Neural Stem Cells
Ottoboni, L., von Wunster, B., & Martino, G. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00148 · Cited by 105
Sakalem, M. E., Síbio, M. T. D., da Costa, F. A. D. S., & de Oliveira, M. (2021) · Biotechnology Journal · doi:10.1002/biot.202000463 · Cited by 112
Organoids: a novel modality in disease modeling
Heydari, Z., Moeinvaziri, F., Agarwal, T., Pooyan, P., Shpichka, A. I., Maiti, T. K., Timashev, P. S., Baharvand, H., & Vosough, M. (2021) · Bio-Design and Manufacturing · doi:10.1007/s42242-021-00150-7 · Cited by 106
Neocortical development and epilepsy: insights from focal cortical dysplasia and brain tumours
Blümcke, I., Budday, S., Poduri, A., Lal, D., Kobow, K., & Baulac, S. (2021) · The Lancet Neurology · doi:10.1016/s1474-4422(21)00265-9 · Cited by 100
Duy, P. Q., Weise, S. C., Marini, C., Li, X., Liang, D., Dahl, P. J., Ma, S., Spajic, A., Dong, W., Juusola, J., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01043-3 · Cited by 93
Spatiotemporal, optogenetic control of gene expression in organoids
Legnini, I., Emmenegger, L., Zappulo, A., Rybak‐Wolf, A., Wurmus, R., Oliveras, A., Cerda, C., Boltengagen, A., Hessler, T., Mastrobuoni, G., et al. (2023) · Nature Methods · doi:10.1038/s41592-023-01986-w · Cited by 113
Sun, Z., Chen, Z., Yin, M., Wu, X., Guo, B., Cheng, X., Quan, R., Sun, Y., Zhang, Q., Fan, Y., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.03.007 · Cited by 102
Sustained Pax6 Expression Generates Primate-like Basal Radial Glia in Developing Mouse Neocortex
Wong, F. K., Fei, J., Mora‐Bermúdez, F., Taverna, E., Haffner, C., Fu, J., Anastassiadis, K., Stewart, A. F., & Huttner, W. Β. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002217 · Cited by 101
Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence
Yoon, K., Vissers, C. B., Ming, G., & Song, H. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201802117 · Cited by 96
Airway organoids as models of human disease
van der Vaart, J., & Clevers, H. C. (2020) · Journal of Internal Medicine · doi:10.1111/joim.13075 · Cited by 101
Arzua, 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
The Use of Stem Cell-Derived Organoids in Disease Modeling: An Update
Azar, J. H., Bahmad, H. F., Daher, D., Moubarak, M. M., Hadadeh, O., Monzer, A., Bitar, S. A., Jamal, M., Al‐Sayegh, M., & Abou-Kheir, W. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147667 · Cited by 106
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
Jin-hong, X., Shi, F., Deng, S., Li, H., Lin, X., Huang, Y., Chung, S., Shu, Y., & Shao, Z. (2022) · Nature Biomedical Engineering · doi:10.1038/s41551-022-00963-6 · Cited by 103
In vitro bioengineered model of cortical brain tissue
Chwalek, K., Tang‐Schomer, M. D., Omenetto, F. G., & Kaplan, D. L. (2015) · Nature Protocols · doi:10.1038/nprot.2015.091 · Cited by 97
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
Rai, M., Coleman, Z., Curley, M., Nityanandam, A., Platt, A., Robles‐Murguia, M., Jiao, J., Finkelstein, D., Wang, Y., Xu, B., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.03.005 · Cited by 95
Bioreactor Technologies for Enhanced Organoid Culture
Licata, J. P., Schwab, K. H., Har-el, Y.-E., Gerstenhaber, J. A., & Lelkes, P. I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411427 · Cited by 103
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
Rigamonti, A., Repetti, G. G., Sun, C., Price, F. D., Larrow, D. R., Rapino, F. A., Weisinger, K., Benkler, C., Peterson, Q. P., Davidow, L. S., et al. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.05.010 · Cited by 96
Human organoid cultures: transformative new tools for human virus studies
Ramani, S., Crawford, S. E., Blutt, S. E., & Estes, M. K. (2018) · Current Opinion in Virology · doi:10.1016/j.coviro.2018.04.001 · Cited by 93
Stem cell bioengineering: building from stem cell biology
Tewary, M., Shakiba, N., & Zandstra, P. W. (2018) · Nature Reviews Genetics · doi:10.1038/s41576-018-0040-z · Cited by 97
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
Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform
Sharma, A. D., McCoy, L., Jacobs, E. H., Willey, H., Behn, J. Q., Nguyen, H. T., Bolon, B. N., Curley, J. L., & Moore, M. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-45407-5 · Cited by 97
Microfluidic Organoids-on-a-Chip: Quantum Leap in Cancer Research
Düzağaç, F., Saorin, G., Memeo, L., Canzonieri, V., & Rizzolio, F. (2021) · Cancers · doi:10.3390/cancers13040737 · Cited by 97
Hof, L., Moreth, T., Koch, M., Liebisch, T., Kurtz, M., Tarnick, J., Lissek, S. M., Verstegen, M. M. A., van der Laan, L. J. W., Huch, M., et al. (2021) · BMC Biology · doi:10.1186/s12915-021-00958-w · Cited by 97
Human-specific genomic signatures of neocortical expansion
Florio, M., Borrell, V., & Huttner, W. Β. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.11.004 · Cited by 100
Schwarz, N., Hedrich, U. B. S., Schwarz, H., Ashraf, H. P., Dammeier, N., Auffenberg, E., Bedogni, F., Honegger, J. B., Lerche, H., Wuttke, T. V., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-12527-9 · Cited by 97
Tissue engineering: Still facing a long way ahead
Hassanzadeh, P., Atyabi, F., & Dinarvand, R. (2018) · Journal of Controlled Release · doi:10.1016/j.jconrel.2018.04.024 · Cited by 94
Human cardiomyocytes undergo enhanced maturation in embryonic stem cell-derived organoid transplants
Varzideh, F., Pahlavan, S., Ansari, H., Halvaei, M., Sawa Kostin, D., Feiz, M.-S., Latifi, H., Aghdami, N., Braun, T. W., & Baharvand, H. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.11.033 · Cited by 97
Chadwick, M., Yang, C., Liu, L., Gamboa, C. M., Jara, K., Lee, H., & Sabaawy, H. E. (2020) · iScience · doi:10.1016/j.isci.2020.101365 · Cited by 96
Neural Stem Cells and Methods for Their Generation From Induced Pluripotent Stem Cells in vitro
Galiakberova, A. A., & Dashinimaev, E. B. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00815 · Cited by 100
Organoids of the female reproductive tract
Chumduri, C., & Turco, M. Y. (2021) · Journal of Molecular Medicine · doi:10.1007/s00109-020-02028-0 · Cited by 110
Connecting past and present: single-cell lineage tracing
Chen, C., Liao, Y., & Peng, G. (2022) · Protein & Cell · doi:10.1007/s13238-022-00913-7 · Cited by 99
Modelling metabolic diseases and drug response using stem cells and organoids
Hu, W., & Lazar, M. A. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-022-00733-z · Cited by 99
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
Yao, Q., Cheng, S., Pan, Q., Yu, J., Cao, G., Li, L., & Cao, H. (2024) · MedComm · doi:10.1002/mco2.735 · Cited by 100
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
Vanslambrouck, J. M., Wilson, S. B., Tan, K. S., Groenewegen, E., Rudraraju, R., Neil, J. A., Lawlor, K. T., Mah, S., Scurr, M., Howden, S. E., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33623-z · Cited by 100
Landscape of human organoids: Ideal model in clinics and research
Han, X., Cai, C., Deng, W., Shi, Y., Li, L., Wang, C., Zhang, J., Rong, M., Liu, J., Fang, B., et al. (2024) · The Innovation · doi:10.1016/j.xinn.2024.100620 · Cited by 101
Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward
Nürnberg, E., Vitacolonna, M., Klicks, J., von Molitor, E., Cesetti, T., Keller, F., Bruch, R., Ertongur-Fauth, T., Riedel, K., Scholz, P., et al. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00020 · Cited by 93
Marx, V. (2015) · Nature · doi:10.1038/522373a · Cited by 93
Rapamycin regulates autophagy and cell adhesion in induced pluripotent stem cells
Sotthibundhu, A., McDonagh, K., von Kriegsheim, A., García-Muñoz, A., Klawiter, A., Thompson, K., Chauhan, K. D., Krawczyk, J., McInerney, V., Dockery, P., et al. (2016) · Stem Cell Research & Therapy · doi:10.1186/s13287-016-0425-x · Cited by 93
Cortical progenitor biology: key features mediating proliferation versus differentiation
Uzquiano, A., Gladwyn-Ng, I. E., Nguyen, L., Reiner, O., Götz, M., Matsuzaki, F., & Francis, F. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14338 · Cited by 96
Sánchez‐González, S., Diban, N., & Urtiaga, A. M. (2018) · Membranes · doi:10.3390/membranes8010012 · Cited by 93
Copper Transport and Disease: What Can We Learn from Organoids?
Pierson, H. E., Yang, H., & Lutsenko, S. (2019) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-082018-124242 · Cited by 94
Human cerebral organoids and consciousness: a double-edged sword
Lavazza, A. (2020) · Bioethics News · doi:10.1007/s40592-020-00116-y · Cited by 96
3D cancer models: One step closer to in vitro human studies
Manduca, N., Maccafeo, E., Maria, R. D., Sistigu, A., & Musella, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1175503 · Cited by 103
Qu, S., Xu, R., Yi, G., Li, Z., Zhang, H., Qi, S., & Huang, G. (2024) · Molecular Biomedicine · doi:10.1186/s43556-023-00165-9 · Cited by 106
Edri, R., Yaffe, Y., Ziller, M. J., Mutukula, N., Volkman, R., David, E., Jacob‐Hirsch, J., Malcov, H., Levy, C., Rechavi, G., et al. (2015) · Nature Communications · doi:10.1038/ncomms7500 · Cited by 98
Baillie‐Johnson, P., van den Brink, S., Balayo, T., Turner, D. A., & Arias, A. M. (2015) · Journal of Visualized Experiments · doi:10.3791/53252 · Cited by 97
Synthetic MorphogenesisPreprint
Teague, B. P., Guye, P., & Weiss, R. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a023929 · Cited by 93
Leite, P. E. C., Pereira, M. R., Harris, G., Pamies, D., dos Santos, L. M. G., Granjeiro, J. M., Hogberg, H. T., Hartung, T., & Smirnova, L. (2019) · Particle and Fibre Toxicology · doi:10.1186/s12989-019-0307-3 · Cited by 92
3D culture of murine neural stem cells on decellularized mouse brain sections
Waele, J. D., Reekmans, K., Daans, J., Goossens, H., Berneman, Z. N., & Ponsaerts, P. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.11.025 · Cited by 92
Synthetic scaffolds for 3D cell cultures and organoids: applications in regenerative medicine
Marchini, A., & Gelain, F. (2022) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2021.1932716 · Cited by 91
Three-dimensional cell culture: from evolution to revolution
Alhaque, S., Themis, M., & Rashidi, H. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0216 · Cited by 92
Comprehensive review on the molecular genetics of autosomal recessive primary microcephaly (MCPH)
Naveed, M., Kazmi, S. K., Amin, M., Asif, Z., Islam, U., Shahid, K., & Tehreem, S. (2018) · Genetics Research · doi:10.1017/s0016672318000046 · Cited by 90
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
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
“This organoid recapitulates human cortical development in healthy and disease states (Lancaster et al., 2013).”
BackgroundDerivation of Functional Human Astrocytes from Cerebral Organoids
Dezonne, R. S., Sartore, R., Nascimento, J. M., Saia-Cereda, V. M., Romão, L. F., Alves‐Leon, S. V., de Souza, J. M., Martins‐de‐Souza, D., Rehen, S. K., & Gomes, F. C. A. (2017) · Scientific Reports · doi:10.1038/srep45091 · Cited by 88
Experimental study of tuberculosis: From animal models to complex cell systems and organoids
Fonseca, K. L., Rodrigues, P., Olsson, I. A. S., & Saraiva, M. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006421 · Cited by 90
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
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
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
DNAJB6, a Key Factor in Neuronal Sensitivity to Amyloidogenesis
Thiruvalluvan, A., de Mattos, E. P., Brunsting, J. F., Bakels, R., Serlidaki, D., Barazzuol, L., Conforti, P., Fatima, A., Koyuncu, S., Cattaneo, E. F., et al. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.02.022 · Cited by 89
Allen, M., Huang, B. S., Notaras, M. J., Lodhi, A., Barrio-Alonso, E., Lituma, P. J., Wolujewicz, P., Witztum, J., Longo, F., Chen, M., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01486-x · Cited by 96
FMRP phosphorylation modulates neuronal translation through YTHDF1
Zou, Z., Wei, J., Chen, Y., Kang, Y., Shi, H., Yang, F., Shi, Z., Chen, S., Zhou, Y., Sepich‐Poore, C., et al. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.10.028 · Cited by 90
In vitro Models for Seizure-Liability Testing Using Induced Pluripotent Stem Cells
Grainger, A. I., King, M. C., Nagel, D. A., Parri, H. R., Coleman, M. D., & Hill, E. J. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00590 · Cited by 92
Modeling human development in 3D culture
Ader, M., & Tanaka, E. M. (2014) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2014.06.013 · Cited by 89
RASopathies: unraveling mechanisms with animal models
Jindal, G. A., Goyal, Y., Burdine, R. D., Rauen, K. A., & Shvartsman, S. Y. (2015) · Disease Models & Mechanisms · doi:10.1242/dmm.020339 · Cited by 87
Brennenstuhl, H., Jung‐Klawitter, S., Assmann, B. E., & Opladen, T. (2018) · Neuropediatrics · doi:10.1055/s-0038-1673630 · Cited by 90
Filling the Gap: Neural Stem Cells as A Promising Therapy for Spinal Cord Injury
Pereira, I. M., Marote, A., Salgado, A. J., & Silva, N. A. (2019) · Pharmaceuticals · doi:10.3390/ph12020065 · Cited by 91
Salaris, F., & Rosa, A. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146393 · Cited by 88
Dorsal-ventral patterned neural cyst from human pluripotent stem cells in a neurogenic niche
Zheng, Y., Xue, X., Irizarry, A. M. R., Li, Z., Shao, Y., Zheng, Y., Zhao, G., & Fu, J. (2019) · Science Advances · doi:10.1126/sciadv.aax5933 · Cited by 89
Yavitt, F. M., Brown, T. E., Hushka, E. A., Brown, M. E., Gjorevski, N., Dempsey, P. J., Lütolf, M. P., & Anseth, K. S. (2020) · Advanced Materials · doi:10.1002/adma.201905366 · Cited by 89
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
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
AI‐organoid integrated systems for biomedical studies and applications
Maramraju, S., Kowalczewski, A. C., Kaza, A., Liu, X., Singaraju, J. P., Albert, M. V., Ma, Z., & Yang, H. (2024) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10641 · Cited by 95
Human organoids as 3D in vitro platforms for drug discovery: opportunities and challenges
Wang, D., Villenave, R., Stokar‐Regenscheit, N., & Clevers, H. C. (2025) · Nature Reviews Drug Discovery · doi:10.1038/s41573-025-01317-y · Cited by 111
Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for Neurobiology
McCarroll, S. A., & Hyman, S. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.046 · Cited by 90
Wnt/β‐catenin signaling during early vertebrate neural development
Brafman, D. A., & Willert, K. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22517 · Cited by 95
Controlling Differentiation of Stem Cells for Developing Personalized Organ‐on‐Chip Platforms
Geraili, A., Jafari, P., Hassani, M. S., Araghi, B. H., Mohammadi, M. H., Ghafari, A. M., Tamrin, S. H., Modarres, H. P., Kolahchi, A. R., Ahadian, S., et al. (2017) · Advanced Healthcare Materials · doi:10.1002/adhm.201700426 · Cited by 90
Assessing Toxicity with Human Cell-Based In Vitro Methods
Zink, D., Chuah, J. K. C., & Ying, J. Y. (2020) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2020.01.008 · Cited by 87
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
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
Axial elongation of caudalized human organoids mimics aspects of neural tube development
Libby, A. R. G., Joy, D. A., Elder, N. H., Bulger, E. A., Krakora, M. Z., Gaylord, E. A., Mendoza-Camacho, F. N., Butts, J. C., & McDevitt, T. C. (2021) · Development · doi:10.1242/dev.198275 · Cited by 86
Blood–Brain Barrier Breakdown in Neuroinflammation: Current In Vitro Models
Brandl, S., & Reindl, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612699 · Cited by 97
Concise Review: Induced Pluripotent Stem Cell Research in the Era of Precision Medicine
Hamazaki, T., Rouby, N. M. E., Fredette, N. C., Santostefano, K. E., & Terada, N. (2017) · Stem Cells · doi:10.1002/stem.2570 · Cited by 87
Tubular human brain organoids to model microglia-mediated neuroinflammation
Ao, Z., Cai, H., Wu, Z., Song, S., Karahan, H., Kim, B., Lu, H.-C., Kim, J., Mackie, K., & Guo, F. (2021) · Lab on a Chip · doi:10.1039/d1lc00030f · Cited by 87
Molecular characterization and prospective isolation of human fetal cochlear hair cell progenitors
Roccio, M., Perny, M., Ealy, M., Widmer, H. R., Heller, S., & Senn, P. (2018) · Nature Communications · doi:10.1038/s41467-018-06334-7 · Cited by 88
Innovations 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
JNK Signaling in Stem Cell Self-Renewal and Differentiation
Semba, T., Sammons, R. M., Wang, X., Xie, X., Dalby, K. N., & Ueno, N. T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072613 · Cited by 84
Microphysiological Systems: Design, Fabrication, and Applications
Wang, K., Man, K., Liu, J., Liu, Y., Chen, Q., Zhou, Y., & Yang, Y. S. (2020) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.9b01667 · Cited by 86
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
Iordachescu, A., Hughes, E. A. B., Joseph, S., Hill, E. J., Grover, L. M., & Metcalfe, A. D. (2021) · npj Microgravity · doi:10.1038/s41526-021-00146-8 · Cited by 89
Modafferi, S., Zhong, X., Kleensang, A., Murata, Y., Fagiani, F., Pamies, D., Högberg, H. T., Calabrese, V., Lachman, H. M., Härtung, T., et al. (2021) · Environmental Health Perspectives · doi:10.1289/ehp8580 · Cited by 91
Future regenerative medicine developments and their therapeutic applications
Altyar, A. E., El-Sayed, A., Abdeen, A., Piscopo, M., Mousa, S. A., Najda, A., & Abdel‐Daim, M. M. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.114131 · Cited by 98
Peng, T., Ma, X., Hua, W., Wang, C., Chu, Y., Sun, M., Fermi, V., Hamelmann, S., Lindner, K., Shao, C., et al. (2025) · Cell Stem Cell · doi:10.1016/j.stem.2025.01.002 · Cited by 86
Metadata
- Authors
- 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.
- Affiliations
- Institute of Molecular Biotechnology (AT)
- Institute of Genetics and Cancer (GB)
- Wellcome Sanger Institute (GB)
- St George's, University of London (GB)
- Corresponding author
- Knoblich, Juergen A.
- ORCID
- Venue
- Nature
- Published
- 2013-08-28
- Volume
- 501
- Issue
- 7467
- Pages
- 373-379
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3817409
- OpenAlex
- W2018286352
- Cited by
- 5,372
- References
- 57
- Citations by year
- 2026: 446 · 2025: 575 · 2024: 543 · 2023: 560 · 2022: 544 · 2021: 572 · 2020: 512 · 2019: 383 · 2018: 346 · 2017: 302 · 2016: 239 · 2015: 175 · 2014: 138 · 2013: 31
- FWCI
- 72.04
- 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)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- Funders
- Wellcome Trust (WT 098051)
- Lister Institute of Preventive Medicine
- Österreichischen Akademie der Wissenschaften
- Austrian Science Fund
- Medical Research Council
- 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 › Developmental Biology and Gene Regulation
- Keywords
- brain organoids, human brain development, microcephaly, pluripotent stem cells, induced pluripotent stem cells, three-dimensional organoid culture, cortical development, neuronal differentiation, patient-derived disease model
- MeSH terms
- Animals, Brain, Cerebral Cortex, Humans, Microcephaly, Models, Biological, Neurons, Organoids, Tissue Culture Techniques, Mice, Neurogenesis, Induced Pluripotent Stem Cells, Neural Stem Cells
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