John Hopkings Magazine
26/03/2026
In a bid to better understand, and potentially treat, a host of conditions that affect early cognition, neurodevelopment, and the brain later in life, investigators at Johns Hopkins Medicine and colleagues around (GRIB, Hospital del Mar Research Institute) the world have been mapping the molecular construction of the human brain. These models, which are supported in part by federal and international research grants, are helping researchers study genetic links and pathways involved in a variety of conditions, ranging from autism spectrum disorder to Alzheimer’s disease.
To support this blueprint, Carlo Colantuoni, an adjunct professor of neurology at Johns Hopkins Medicine and the Institute for Genome Sciences at the University of Maryland School of Medicine, and other researchers have, in their most recent study, brought together data from nearly 200 published studies and more than 30 million cells to advance insight about how the neocortex (the outermost layers of the brain) develops and forms over time. This region of the brain is responsible for a variety of functions, including how we think, sense, process and store information, and make decisions.
“Our goal is to understand how the neocortex is built on a cellular level, and identify clues to the earliest stages of developmental delays and brain disorders,” Colantuoni says. “By mapping the cell transitions and genes that give rise to the intricate structure and function of the neocortex, we can better understand, and then attempt to treat, disorders that arise in the womb, during infancy and childhood, and even much later in life.”
This enhanced atlas will help researchers study genetic links for autism spectrum disorder, which affects about 1 in 31, or 3%, of children in the U.S. It can also provide insight into rare conditions like microcephaly, which can begin before birth and drastically affect the growth of the brain. A strength of bringing this information together—it is now available through Nature and Nature Neuroscience—is that researchers can study granular stages of development to identify typical growth patterns and then pinpoint the origins and pathways of neurodevelopmental delays and disease.
In addition to mapping a human model of the neocortex, the authors published a mammal and mouse model. These different atlases show that gene expression programs that began as diffuse networks millions of years ago were more recently focused in human neural stem cells to drive expansion of the human neocortex. This process, the researchers say, helped contribute to and, in part, explains differences in higher human cognitive abilities compared with other animals.
Using the accumulated data, the researchers also charted the maturation of neurons in the human neocortex, a process that has become longer over evolutionary time as the human neocortex and mental capacity have expanded. For example, this type of neural development takes weeks in a mouse but many years in humans. This represents differences in advanced systems that enable the human brain to adapt and learn how to interpret complex social, environmental, and sensory inputs over an extended developmental period.
These resources are now available via an open-access web portal to empower other researchers investigating human brain development and disease. Collectively, says Colantuoni, these and other brain-charting efforts aim to help researchers study mechanisms of brain disease throughout the lifespan and provide a tool to better support and accelerate everyday research.
Researchers without coding expertise can explore the expression patterns of individual genes of interest, chart the coordinated expression of gene modules that work together in specific ways during development, and contribute their own data to expand the resource.
Previous Brain Research Through Advancing Innovative Neurotechnologies (BRAIN) Initiative efforts have generated human and mouse brain cell censuses, which catalog the diversity of cell types in the mammalian brain. Other projects are exploring how opioid use affects the brain of those living with HIV, how hair cells within the inner ear could be regenerated to restore hearing, and how cellular pathways are distributed in dementia, including Alzheimer’s disease, which is estimated to affect more than 7 million U.S. adults, including 1 in 9, or 11%, age 65 and older.
These brain-mapping studies are complemented by broader efforts to chart the entire cellular landscape of the human body, including the Human Cell Atlas, or HCA. The HCA was founded in 2016 with the goal of bringing investigators around the world together to create open-access resources to map every cell in the human body. In 2024, experts published insights from more than 40 papers examining 62 million cells from nearly 10,000 humans.
Research from the HCA and related studies has already led to the discovery of new lung cells, a greater understanding of how the body responds to infections, and identification of networks of cells that work together to help the heart beat, regulate heart rate, and enable communication among organs throughout the body.
“We’re living in an unprecedented time, when advancements in using technology to coordinate and analyze large datasets, work with researchers throughout the world, and leverage insights across disease states is paramount to identifying new treatments that can save and improve lives,” Colantuoni says. “As these initiatives reach major milestones, we’re also seeing that the way investigators can collaborate and use these atlases is just getting started.”
Colantuoni adds that it is critical to recruit more academic and industry partners to invest in these precompetitive data exploration spaces that will greatly expand identification of novel molecular targets for treating brain disorders.
“Combined with AI algorithms to guide large-scale screening in stem cell systems, these resources promise to enable precision tailoring of treatments to help individual patients with neurodevelopmental and neurodegenerative disease,” he says.
To support this vision, Colantuoni and colleagues, including Paul Worley, Jin-Chong Xu, Xiangyu Liao, and Yuelin Lao (all from Johns Hopkins Medicine), Carol A. Barnes (from the University of Arizona), and Matthew Huetelman and Ignazio S. Piras (from TGen, the Translational Genomics Research Institute), have also created an open-data resource focused on Alzheimer’s disease.
Other authors of the neocortical development paper include Shreyash Sonthalia, Ricky S. Adkins, Joshua Orvis, Guangyan Li, Xoel Mato Blanco, Alex Casella, Jinrui Liu, Genevieve Stein-O’Brien, Brian Caffo, Ronna Hertzano, Anup Mahurkar, Jesse Gillis, Jonathan Werner, Shaojie Ma, Nicola Micali, Nenad Sestan, Pasko Rakic, Gabriel Santpere, and Seth A. Ament.
The research described in the new report was supported in part by a PTE federal award, NIH research grants, the NIDCD/NIH Intramural Research Program, international awards, and the Johns Hopkins University Discovery Award. The authors have no disclosures to report.