Chromatin accessibility dynamics in a model of human forebrain development

The Sequence Alignment/Map format and SAMtools

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The Human Transcription Factors

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An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues

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Chromatin remodelling complexes in cerebral cortex development and neurodevelopmental disorders

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MYT1L is required for suppressing earlier neuronal development programs in the adult mouse brainPreprint

Chen, J., Fuhler, N. A., Noguchi, K. K., & Dougherty, J. D. (2023) · Genome Research · doi:10.1101/gr.277413.122 · Cited by 19

Gliomas: a reflection of temporal gliogenic principles

Sojka, C., & Sloan, S. A. (2024) · Communications Biology · doi:10.1038/s42003-024-05833-2 · Cited by 18

Epigenetic regulation and factors that influence the effect of iPSCs-derived neural stem/progenitor cells (NS/PCs) in the treatment of spinal cord injury

Yang, Y., Ma, B., Chen, J., Liu, D., Ma, J., Li, B., Hao, J., & Zhou, X. (2024) · Clinical Epigenetics · doi:10.1186/s13148-024-01639-5 · Cited by 18

iPSC toolbox for understanding and repairing disrupted brain circuits in autism

Chiola, S., Edgar, N. U., & Shcheglovitov, A. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01288-7 · Cited by 18

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

Neuronal Differentiation of Induced Pluripotent Stem Cells from Schizophrenia Patients in Two-Dimensional and in Three-Dimensional Cultures Reveals Increased Expression of the Kv4.2 Subunit DPP6 That Contributes to Decreased Neuronal Activity

Naujock, M., Speidel, A., Fischer, S. E., Kizner, V., Dorner‐Ciossek, C., & Gillardon, F. (2020) · Stem Cells and Development · doi:10.1089/scd.2020.0082 · Cited by 18

Epigenetic priming in neurodevelopmental disorders

Ernst, C., & Jefri, M. (2021) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2021.09.005 · Cited by 17

DeepCAGE: Incorporating Transcription Factors in Genome-Wide Prediction of Chromatin Accessibility

Liu, Q., Hua, K., Zhang, X., Wong, W. H., & Jiang, R. (2022) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2021.08.015 · Cited by 18

Probing the molecular and cellular pathological mechanisms of schizophrenia using human induced pluripotent stem cell models

Sebastian, R., Song, Y., & Pak, C. (2022) · Schizophrenia Research · doi:10.1016/j.schres.2022.06.028 · Cited by 16

Present and Future Modeling of Human Psychiatric Connectopathies With Brain Organoids

Urenda, J., Dosso, A. D., Birtele, M., & Quadrato, G. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.12.017 · Cited by 16

Analysis of time-series regulatory networks

Ding, J., & Bar‐Joseph, Z. (2020) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2020.07.005 · Cited by 16

Modeling neurodevelopment in a dish with pluripotent stem cells

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PI3K signaling specifies proximal-distal fate by driving a developmental gene regulatory network in SOX9+ mouse lung progenitors

Khattar, D., Fernandes, S., Snowball, J. M., Guo, M., Gillen, M. C., Jain, S. S., Sinner, D. I., Zacharias, W. J., & Swarr, D. T. (2022) · eLife · doi:10.7554/elife.67954 · Cited by 15

Human PSCs determine the competency of cerebral organoid differentiation via FGF signaling and epigenetic mechanisms

Ideno, H., Imaizumi, K., Shimada, H., Sanosaka, T., Nemoto, A., Kohyama, J., & Okano, H. (2022) · iScience · doi:10.1016/j.isci.2022.105140 · Cited by 15

Navigating Brain Organoid Maturation: From Benchmarking Frameworks to Multimodal Bioengineering Strategies

Huang, J., Zhu, Y., Tang, J., Liu, Y., Lu, M., Zhang, R., & Sun, A. X. (2025) · Biomolecules · doi:10.3390/biom15081118 · Cited by 14

Multiscale Construction, Evaluation, and Application of Organoids

Ma, W., Dong, Z., Zheng, Z., Bai, L., Zhang, X., & Su, J. (2025) · Advanced Science · doi:10.1002/advs.202508534 · Cited by 15

Regulatory landscape in brain development and disease

Spiess, K., & Won, H. (2020) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2020.05.007 · Cited by 14

Impact of schizophrenia GWAS loci converge onto distinct pathways in cortical interneurons vs glutamatergic neurons during development

Liu, D., Zinski, A. L., Mishra, A., Noh, H., Park, G.-H., Qin, Y., Olorife, O., Park, J. M., Abani, C. P., Park, J. S., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01654-z · Cited by 15

A multi-omics approach to visualize early neuronal differentiation from hESCs in 4D

SAMARA, A. A., Spildrejorde, M., Sharma, A., Falck, M., Leithaug, M., Modafferi, S., Bjørnstad, P. M., Acharya, G., Gervin, K., Lyle, R., et al. (2022) · iScience · doi:10.1016/j.isci.2022.105279 · Cited by 14

Global chromatin landscapes identify candidate noncoding modifiers of cardiac rhythm

Bhattacharyya, S., Kollipara, R. K., Orquera-Tornakian, G., Goetsch, S. C., Zhang, M., Perry, C., Li, B., Shelton, J. M., Bhakta, M., Duan, J., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci153635 · Cited by 13

A loss-of-function mutation in human Oxidation Resistance 1 disrupts the spatial–temporal regulation of histone arginine methylation in neurodevelopment

Lin, X., Wang, W., Yang, M., Damseh, N. S., de Sousa, M. M. L., Jacob, F., Lång, A., Kristiansen, E., Pannone, M., Kiššová, M., et al. (2023) · Genome biology · doi:10.1186/s13059-023-03037-1 · Cited by 14

Annotating functional effects of non-coding variants in neuropsychiatric cell types by deep transfer learning

Lai, B., Qian, S., Zhang, H., Zhang, S., Kozlova, A., Duan, J., He, X., & Xu, J. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010011 · Cited by 13

CD4+ T cells from children with active juvenile idiopathic arthritis show altered chromatin features associated with transcriptional abnormalities

Tarbell, E., Jiang, K., Hennon, T., Holmes, L., Williams, S., Fu, Y., Gaffney, P. M., Liu, T., & Jarvis, J. N. (2021) · Scientific Reports · doi:10.1038/s41598-021-82989-5 · Cited by 12

Advances in profiling chromatin architecture shed light on the regulatory dynamics underlying brain disorders

Pratt, B. M., & Won, H. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.08.013 · Cited by 13

Evolutionary divergence in CTCF-mediated chromatin topology drives transcriptional innovation in humans

Wu, X., Xiong, D., Liu, R., Lai, X., Tian, Y., Xie, Z., Chen, L., Hu, L., Duan, J., Gao, X., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58275-7 · Cited by 13

The need for a global effort to attend to human neural organoid and assembloid research

Pașca, S. P., Arlotta, P., Campbell, P., Charo, A., Evans, J. H., III, Farahany, N. A., Gage, F. H., Godfrey‐Smith, P., Hyun, I., Kriegstein, A. R., et al. (2025) · Science · doi:10.1126/science.aeb1510 · Cited by 11

Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications

Schuster, J., Lu, X. H., Dang, Y., Klar, J., Wenz, A. S., Dahl, N., & Chen, X. (2023) · eLife · doi:10.7554/elife.92599 · Cited by 10

DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural NetworkPreprint

Li, Y., Wen, J., Li, G., Chen, J. C., Sun, Q., Liu, W., Guan, W., Lai, B., Szatkiewicz, J., He, X., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2399024/v1 · Cited by 11

Dissecting and improving gene regulatory network inference using single-cell transcriptome dataPreprint

Xue, L., Wu, Y., & Lin, Y. (2023) · Genome Research · doi:10.1101/gr.277488.122 · Cited by 10

Neurodevelopmental disorders: 2021 update

Zamora‐Moratalla, A., de Lagrán, M. M., & Dierssen, M. (2021) · Free Neuropathology · doi:10.17879/freeneuropathology-2021-3268 · Cited by 13

Chromatin accessibility provides a window into the genetic etiology of human brain disease

Bendl, J. M., Fullard, J. F., Girdhar, K., Dong, P., Kosoy, R., Zeng, B., Hoffman, G. E., & Roussos, P. (2025) · Trends in Genetics · doi:10.1016/j.tig.2025.01.001 · Cited by 9

Advancing autism research: Insights from brain organoid modeling

Li, C. V., & Knoblich, J. A. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103030 · Cited by 10

Endocrine-disrupting effects of environmental BPS and PFOS on human brain organoid development

Credico, A. D., Gaggi, G., Bibbò, S., Blenkinsop, T. A., Baldassarre, A. D., & Ghinassi, B. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1692333 · Cited by 9

Migratory cortical interneuron-specific transcriptome abnormalities in schizophrenia

Park, J. M., Liu, D., Park, G.-H., Noh, H., Ni, P., Yin, C., Huang, W., & Chung, S. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.02.054 · Cited by 9

Comparison of chromatin accessibility landscapes during early development of prefrontal cortex between rhesus macaque and human

Yao, X., Lu, Z., Feng, Z., Gao, L., Zhou, X., Li, M., Zhong, S., Wu, Q., Liu, Z., Zhang, H., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31403-3 · Cited by 9

Neural cell isolation from adult macaques for high-throughput analyses and neurosphere cultures

Wei, J.-R., Xiao, D., Tang, L., Xu, N., Liu, R., Shen, Y., Xu, Z., Sang, X., Ge, J., Xiang, M., et al. (2023) · Nature Protocols · doi:10.1038/s41596-023-00820-z · Cited by 9

Rare Does Not Mean Worthless: How Rare Diseases Have Shaped Neurodevelopment Research in the NGS Era

Zaghi, M., Banfi, F., Bellini, E. N., & Sessa, A. (2021) · Biomolecules · doi:10.3390/biom11111713 · Cited by 8

Strategic use of organoids and organs-on-chip as biomimetic tools

Santos, A. K., Scalzo, S., Souza, R. T. V., Santana, P. H. G., Marques, B. L., de Oliveira, L. F., Filho, D. M., Kihara, A. H., Santiago, H. C., Parreira, R. C., et al. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.09.010 · Cited by 9

Mouse brain organoids model in vivo neurodevelopment and function and capture differences to humanPreprint

Sanchez, D. J. L.-D., Lindhout, F. W., Anderson, A. J., Pellegrini, L., & Lancaster, M. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.21.629881 · Cited by 8

Generation and characterization of cortical organoids from iPSC-derived dental pulp stem cells using traditional and innovative approaches

Silva, A. L. T. E., Yokota-Moreno, B. Y., Branquinho, M. S., Salles, G. N., de Souza, T. C., de Carvalho, R. A., Batista, G., Branco, E. V., Griesi‐Oliveira, K., Passos‐Bueno, M. R., et al. (2024) · Neurochemistry International · doi:10.1016/j.neuint.2024.105854 · Cited by 7

Neurobiological Perturbations in Bipolar Disorder Compared With Schizophrenia: Evidence From Cell Cultures and Brain Organoids

Akkouh, I. A., Osete, J. R., Szabó, A., Andreassen, O. A., & Djurovic, S. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.02.012 · Cited by 9

Convergence of the dysregulated regulome in schizophrenia with polygenic risk and evolutionarily constrained enhancers

Dong, P., Voloudakis, G., Fullard, J. F., Hoffman, G. E., & Roussos, P. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02370-y · Cited by 7

CRISPRi screening in cultured human astrocytes uncovers distal enhancers controlling genes dysregulated in Alzheimer’s disease

Green, N. F. O., Sutton, G. J., Pérez‐Burillo, J., Wang, J., Bagot, S., Danon, H. G., Walsh, K., Gokoolparsadh, A., Miles, S. A., Yang, G., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02154-3 · Cited by 6

Organoid analytical toolkits

Jin, Y., Park, S., & Cho, S. (2026) · Nature Reviews Bioengineering · doi:10.1038/s44222-025-00384-5 · Cited by 7

Reconstructing human corticogenesis: Insights from cerebral organoids into neurodevelopment and disease modeling

Tenreiro, M. F., & Muotri, A. R. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.02.018 · Cited by 6

Corticogenesis across species at single‐cell resolution

Park, S. H. E., Ortiz, A. K., & Konopka, G. (2022) · Developmental Neurobiology · doi:10.1002/dneu.22896 · Cited by 6

Profiling Cell Type-Specific Gene Regulatory Regions in Human Cortical Organoids

Schütze, T. M., Bölicke, N., Sameith, K., & Albert, M. (2022) · Neuromethods · doi:10.1007/978-1-0716-2720-4_2 · Cited by 6

Genomic approaches to trace the history of human brain evolution with an emerging opportunity for transposon profiling of ancient humans

Wang, Y., Zhao, B., Choi, J., & Lee, E. A. (2021) · Mobile DNA · doi:10.1186/s13100-021-00250-2 · Cited by 8

APOBEC3C is a novel target for the immune treatment of lower-grade gliomas

Zhao, S., Li, Y., Xu, J., & Shen, L. (2023) · Neurological Research · doi:10.1080/01616412.2023.2287340 · Cited by 5

Recruitment of homodimeric proneural factors by conserved CAT–CAT E-boxes drives major epigenetic reconfiguration in cortical neurogenesis

de Martin, X., Oliva, B., & Santpere, G. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae950 · Cited by 6

Modeling forebrain regional development and connectivity by human brain organoids

Choe, M. S., Lo, C., & Park, I. (2025) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2025.102324 · Cited by 5

A generic reference defined by consensus peaks for single-cell ATAC-seq data analysis

Meng, Q., Wu, X., Chen, W., Zhao, Y., Li, C., Wei, Z., Zeng, X., Li, J., Xi, X., Chen, S., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69461-6 · Cited by 5

Loss of Ezh2 in the medial ganglionic eminence alters interneuron fate, cell morphology and gene expression profiles

Rhodes, C. T., Asokumar, D., Sohn, M., Naskar, S., Elisha, L., Stevenson, P. K., Lee, D. R., Zhang, Y., Rocha, P. P., Dale, R., et al. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1334244 · Cited by 5

Modelling sex differences of neurological disorders in vitro

Castro‐Aldrete, L., Einsiedler, M., Cuní‐López, C., Vanhaelen, Q., Silvestri, A., Ferretti, M. T., de Gennaro, M. E., Putignano, G., Guix, M., Marino, N., et al. (2025) · Nature Reviews Bioengineering · doi:10.1038/s44222-025-00355-w · Cited by 4

Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)

Zhang, K., Zhang, L., Qin, X., Zhang, Y.-W., Xie, W.-J., Wan, R.-D., Fang, Y.-G., & Yang, Q.-E. (2026) · Communications Biology · doi:10.1038/s42003-025-09467-w · Cited by 4

Inter3D: Capture of TAD Reorganization Endows Variant Patterns of Gene Transcription

Ding, T., Fu, S., Zhang, X., Yang, F., Zhang, J., Xu, H., Yang, J., Chen, C., Shi, Y., Bai, Y., et al. (2024) · Genomics Proteomics & Bioinformatics · doi:10.1093/gpbjnl/qzae034 · Cited by 4

Brain regionalization by Polycomb‐group proteins and chromatin accessibility

Eto, H., & Kishi, Y. (2021) · BioEssays · doi:10.1002/bies.202100155 · Cited by 4

Multiplexed analysis of gene expression and chromatin accessibility of human umbilical cord blood using scRNA-Seq and scATAC-Seq

Hou, X., Wang, Y.-L., Shi, W., Hu, W., Zeng, Z., Liu, J., Li, L., Cai, W., Tang, D., & Dai, Y. (2022) · Molecular Immunology · doi:10.1016/j.molimm.2022.10.013 · Cited by 4

A map of enhancer regions in primary human neural progenitor cells using capture STARR-seqPreprint

Gaynor-Gillett, S. C., Cheng, L., Shi, M., Liu, J. J., Wang, G., Spector, M., Guo, Q., Qi, L., Flaherty, M., Wall, M., et al. (2025) · Genome Research · doi:10.1101/gr.279584.124 · Cited by 4

Large-scale discovery of neural enhancers for cis-regulation therapiesPreprint

McDiarmid, T. A., Page, N. F., Chardon, F. M., Daza, R. M., Chen, G. T., Kosicki, M., James, L. M., Nourie, H. C., Cintrón, D. L., Lee, A. S., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.04.686611 · Cited by 4

Pluripotent stem cells-based neural organoids for modelling human brain development and diseases

Tong, L., Tian, P., Wang, R., Niu, S., Wang, R., Ye, Y., Wu, Y., Zhang, W., Wang, Y., Foggetti, A., et al. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01515-6 · Cited by 3

Reciprocal negative feedback between Prrx1 and miR-140-3p regulates rapid chondrogenesis in the regenerating antler

Hu, P., Zhang, G., Ba, H., Ren, J., Li, J., Wang, Z., & Li, C. (2024) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-024-00573-x · Cited by 3

Dynamic Chromatin Accessibility and Gene Expression Regulation During Maize Leaf Development

Wang, Y., Wang, S., Wu, Y., Cheng, J., & Wang, H. (2024) · Genes · doi:10.3390/genes15121630 · Cited by 3

Brain organoids

Glass, M. R., Kyere, F. A., French, D. L., Stein, J. L., & Waxman, E. A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822277-5.00005-5 · Cited by 4

Landscape of human spinal cord cell type diversity at midgestationPreprint

Andersen, J., Thom, N., Shadrach, J. L., Chen, X., Amin, N. D., Yoon, S., Greenleaf, W. J., Müller, F., Pașca, A. M., Kaltschmidt, J. A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.29.473693 · Cited by 3

Human-specific tandem repeat in CACNA1C modulates responses to neuronal stimulationPreprint

Song, J. H. T., Birey, F., Hung, T.-C., Hall, N., Guenther, C. A., Chen, X., Alkuraya, I. F., Tunbridge, E. M., Haerty, W., Pașca, S. P., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.15.676436 · Cited by 3

Modeling amyotrophic lateral sclerosis (ALS) in vitro : from mechanistic studies to translatable drug discovery

Maskell, K. G., Cook, A. L., King, A. E., Dickson, T. C., & Blizzard, C. L. (2026) · Lab on a Chip · doi:10.1039/d5lc00577a · Cited by 2

Reducing methylation of histone 3.3 lysine 4 in the medial ganglionic eminence and hypothalamus recapitulates neurodevelopmental disorder phenotypes

Li, J., Tanzillo, A. F., Pizzirusso, G., Caccavano, A., Chittajallu, R., Sohn, M., Abebe, D. T., Zhang, Y., Pelkey, K. A., Dale, R., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69248-9 · Cited by 2

Methotrexate-induced disruption of the serum-glucocorticoid inducible protein kinase 3 signaling pathway and its effects on brain development

Ham, O., Jung, S., Kim, Y., Woo, D. H., Jeong, J., Kim, W., Kim, S., Quah, Y., Lee, S. J., & Yu, W. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.138438 · Cited by 2

Fundamental signaling pathways for glioblastoma drug resistance and developing robust organoid models for drug discovery

Pratap, A., Lim, E.-J., Kwak, I., & Moon, B.-S. (2022) · Organoid · doi:10.51335/organoid.2022.2.e8 · Cited by 2

Integrating Multimorbidity into a Whole-Body Understanding of Disease Using Spatial Genomics

Gokuladhas, S., Zaied, R. E., Schierding, W. S., Farrow, S. L., Fadason, T., & O'Sullivan, J. M. (2022) · Results and problems in cell differentiation · doi:10.1007/978-3-031-06573-6_5 · Cited by 2

Characterization of Gene Regulatory Elements in Human Fetal Cortical Development: Enhancing Our Understanding of Neurodevelopmental Disorders and Evolution

Guo, Q., Wu, S. J., & Geschwind, D. H. (2023) · Developmental Neuroscience · doi:10.1159/000530929 · Cited by 2

Dual role of ZIC2 during neural induction: from priming transcription factor to enhancer activator

Mariner-Faulí, M., Sánchez-Gaya, V., Robert, S. M., Respuela, P., Cruz-Molina, S., Lobato-Moreno, S., Trovato, M., Prummel, K. D., Noh, K., Zaugg, J. B., et al. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag374 · Cited by 2

Adrenomedullin restores the human cortical interneurons migration defects induced by hypoxia

Puno, A., Michno, W., Li, L., Everitt, A., McCluskey, K., Htun, S., Nagar, D., Choi, J. B., Dai, Y., Park, S., et al. (2026) · eLife · doi:10.1101/2023.05.01.538334 · Cited by 2

DeepCAGE: Incorporating Transcription Factors in Genome-wide Prediction of Chromatin AccessibilityPreprint

Liu, Q., Hua, K., Zhang, X., Wong, W. H., & Jiang, R. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/610642 · Cited by 2

MYT1L is required for suppressing earlier neuronal development programs in the adult mouse brainPreprint

Chen, J., Fuhler, N. A., Noguchi, K., & Dougherty, J. D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.17.512591 · Cited by 2

DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural NetworkPreprint

Wen, J., Li, G., Chen, J. C., Sun, Q., Liu, W., Guan, W., Lai, B., Zhou, H., Szatkiewicz, J., He, X., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.20.521277 · Cited by 2

Single Cell transcriptional analysis of ex vivo models of cortical and hippocampal development identifies unique longitudinal trendsPreprint

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Enhancer-driven gene regulatory network of forebrain human development provides insights into autismPreprint

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