Development, wiring and function of dopamine neuron subtypes

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

Polymeropoulos, M. H., Lavedan, C., Leroy, E., Ide, S. E., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R., et al. (1997) · Science · doi:10.1126/science.276.5321.2045 · Cited by 8,240

Parkinson's disease

Kalia, L. V., & Lang, A. E. (2015) · The Lancet · doi:10.1016/s0140-6736(14)61393-3 · Cited by 6,184

AGEING AND PARKINSON'S DISEASE: SUBSTANTIA NIGRA REGIONAL SELECTIVITY

FEARNLEY, J. M., & LEES, A. J. (1991) · Brain · doi:10.1093/brain/114.5.2283 · Cited by 3,529

An Essay on the Shaking Palsy

Parkinson, J. (2002) · Journal of Neuropsychiatry · doi:10.1176/jnp.14.2.223 · Cited by 2,856

Slide-seq: A scalable technology for measuring genome-wide expression at high spatial resolution

Rodriques, S. G., Stickels, R. R., Goeva, A., Martin, C. A., Murray, E., Vanderburg, C. R., Welch, J., Chen, L. M., Chen, F., & Macosko, E. Z. (2019) · Science · doi:10.1126/science.aaw1219 · Cited by 2,424

Non-motor features of Parkinson disease

Schapira, A. H. V., Chaudhuri, K. R., & Jenner, P. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.62 · Cited by 2,053

Parkinson's disease

Lees, A. J., Hardy, J., & Revesz, T. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60492-x · Cited by 1,956

Dopamine neurons derived from human ES cells efficiently engraft in animal models of Parkinson’s disease

Kriks, S., Shim, J., Piao, J., Ganat, Y. M., Wakeman, D. R., Xie, Z., Carrillo‐Reid, L., Auyeung, G., Antonacci, C. L., Buch, A., et al. (2011) · Nature · doi:10.1038/nature10648 · Cited by 1,951

The substantia nigra of the human brain

Damier, P., Hirsch, É. C., Agid, Y., & Graybiel, A. M. (1999) · Brain · doi:10.1093/brain/122.8.1437 · Cited by 1,827

Dopamine neuron systems in the brain: An update

Björklund, A., & Dunnett, S. B. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.006 · Cited by 1,777

Striking parallels between the dopaminergic systems of flies and mammals

Jovanoski, K. D., & Waddell, S. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00025-6 · Cited by 1

Molecular heterogeneity of midbrain dopamine neurons

Awatramani, R., & Poulin, J.-F. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00002-5 · Cited by 2

Computational modeling of midbrain dopamine neurons

Canavier, C. C., Knowlton, C., Liss, B., Khaliq, Z., & Roeper, J. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00001-3

Building an action circuit with nigrostriatal dopaminergic neurons and striatonigral neurons

Cai, H., & Gerfen, C. R. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00012-8

Kognitive und neuronale Grundlagen von Motivation, Belohnung und Selbstkontrolle

Goschke, T. (2025) · Springer eBooks · doi:10.1007/978-3-662-69368-1_10

Endocannabinoids regulation of the mesolimbic system

Melis, M., & Brandalise, F. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-13908-6.00011-6

Axon-specific mRNA translation shapes dopaminergic circuit developmentPreprint

Gora, C., Frenette, B., Gelon, P. A., Sephton, C. F., Hussein, S. M. I., Metzakopian, E., & Lévesque, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.25.690389

Merkel cell mechanotransduction facilitates adult neurogenesis and cognition in an enriched environment

Luo, X., Liu, Q., Qin, D., Wang, M., & Guo, W. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2510374122

Rôles de FOXO3 dans la réponse cellulaire au stress et la neurodégénérescence au cours de la maladie Parkinson

Texier, B. (2024) · theses.fr (ABES) · doi:10.70675/44c2147bz67e5z4e37z925az38c78f1151c4

Netrin-1 drives cell-type-specific plasticity of human dopaminergic neurons during circuit integration in a Parkinsonian modelPreprint

Pavan, C., de Lichtenberg, K. H., Gantner, C. W., Frausin, S., Chen, J., Hunt, C. P., Xuereb, B., Hart, E., Chatterton, Z., Halliday, G. M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.01.729439

Neuronal hijacking of cancer niches: integration, remodeling, evolution

Guan, F., Sun, H., Du, Y., Li, D., Huang, M., Li, Y., Li, X., Zhou, X., Cui, S., Long, X., et al. (2026) · Journal of the National Cancer Center · doi:10.1016/j.jncc.2026.05.001

Sensory stimulation triggers different spike responses in serotonin and dopamine neurons in the dorsal midbrain tegmentum

Földi, P., Müller, K., Magyar, D. P., Nagy, G. A., & Hájos, N. (2026) · Scientific Reports · doi:10.1038/s41598-026-66779-5

The role of the subcortical structures in subthreshold depression: evidence from static and dynamic functional connectivity

Zhang, S., Ma, L., Sun, J., Chen, Y., He, Y., Long, Q., Jiao, B., Huang, H., Mo, L., & Lin, J. (2026) · Brain Structure and Function · doi:10.1007/s00429-026-03144-2

Potentiated Maturation of hPSC-Derived Dopaminergic Neurons via Convergent Genetic and Small Molecule Modulation

Park, S., Kim, D., Yoo, S. H., Yeon, G., Lee, J., Cho, M. S., Kim, D., & Kim, D. K. (2026) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-026-00820-6

Mechanisms of Idiopathic Neurodegeneration in Substantia Nigra Neurons: Biochemical, Physiological, and Immuno-Humoral Perspectives

Nikolenko, V. N., Rizaeva, N. A., Oganesyan, M. V., Zubkova, M., Golyshkina, M. S., Orluk, M. A., Pelicer, Y. C., Sabekia, R., Morozow, A., Pires, L. A. S., et al. (2026) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-026-00330-8

Dopamine coated polycaprolactone nanospheres for prochloraz delivery to improve antifungal activity and environmental safety

Yao, J., Wang, Q., Wang, C., Qi, H., Shi, Q., Liu, J., Feng, J., Yang, P., Yu, M., & Xie, X. (2026) · Journal of environmental chemical engineering · doi:10.1016/j.jece.2026.124808

Mapping the Health Burden of Neighbourhood Deprivation: Neurobiological Evidence Across the Life SpanPreprint

Ebneabbasi, A., Warrier, V., Montagnese, M., Romero-García, R., Bethlehem, R. A. I., & Rittman, T. (2026) · medRxiv · doi:10.64898/2026.08.29.26361714

Convergent vulnerability and divergent outcomes of the dopaminergic system in Parkinson’s and Alzheimer’s diseases

Xi, Y.-T., Jia, C.-X., Wang, H. Q., Liu, P., Li, P., Niu, Q., & Yin, Y. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103358

Semiconducting zirconium–cerium oxide nanocomposite derived from Ficus religiosa bark extract for high-performance electrochemical sensing of dopamine

Jarajana, L., Kailasa, S., Kalagadda, V. R., Kalagatur, N. K., Konduri, V. V., Mangamuri, U. K., Arabindi, A., Kiran, G. P. V. S. D. S., & Sudhakar, P. (2026) · Chemical Physics Impact · doi:10.1016/j.chphi.2026.101162

System-level synchronization and subtype-specific modules govern brain-wide serotonin axon innervation

Adams, A. M. J., Wu, K. L., Li, Z., Li, P., Pan, H., 黄祖奇, Migliarini, S., Dear, R., Sun, B., Chan, Z. C.-K., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2611533123

Decoding subtype development and function in human pluripotent stem cell-derived midbrain dopaminergic neuronsPreprint

Yang, D., Choi, S., Piao, J., Evangelisti, A., Yang, Z., Bocchi, V. D., Donohue, S. A., Claros, N., Jungverdorben, J., Sidharta, M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.23.753784

The ontogeny of circadian–social coupling

Confino, S., & Zada, D. (2026) · Trends Open · doi:10.1016/j.treopn.2026.09.004

Dynamic dopamine signaling, prediction error, and microcircuit mechanisms in stress-induced depression-like behaviors

Mahmud, A., & Efremov, L. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1948686

SorCS2 controls Wnt signaling homeostasis during neurodevelopment by regulating Ror2 activity and traffickingPreprint

Salašová, A., Kuncová, L., Yokota, C., Kjær-Sørensen, K., Navis, A. C., Nolte, S., Bernatík, O., Toledo, E. M., Lavický, J., Křivánek, J., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.10.758224

Resilience and vulnerability in the midbrain dopamine system during aging

McMurtrie, G., Mabry, S. J., Glausier, J. R., Rocha, E. M., & Freyberg, Z. (2026) · Trends in Neurosciences · doi:10.1016/j.tins.2026.09.008

Coordinated spatial organization of basal ganglia structures revealed by dopamine subtype projectome mappingPreprint

Moreno-Ramos, O. A., Raj, D. D. A., Vigotsky, A. D., Schonfeld, E., Phelan, E., Singh, A., Jenkins, J. C., Gaertner, Z. A., Gaertner, Z. A., Bolduc, C., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.21.760539

Modeling long-range human nigrostriatal connectivity in vitro reveals striatal target-dependent maturation of dopamine neurons

Corsi, S., Sozzi, E., Bruzelius, A., Scordo, G., Passarello, G. R., Zannino, C., Maraschin, S. T. D. S., Thongkorn, S., Heiskanen, A. R., Kajtez, J., et al. (2026) · The EMBO Journal · doi:10.1038/s44318-026-00942-6

Neuronal Subset-Specific Migration and Axonal Wiring Mechanisms in the Developing Midbrain Dopamine System

Brignani, S., & Pasterkamp, R. J. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00055 · Cited by 47

Wiring up diversity: subset-specific development of midbrain dopaminergic neurons

Brignani, S. (2018) · Utrecht University Repository (Utrecht University)

Single-neuron resolution mapping of dopaminergic connectivity across development, adulthood, and degeneration

Grossouw, L. M., Heijmink, N., Garritsen, O., van de Mheen, T., Naert, W., D’Angelo, R., Rybiczka-Tešulov, M., Adolfs, Y., van Kronenburg, N. C. H., Broekhoven, M. H., et al. (2026) · Neuron · doi:10.1016/j.neuron.2026.07.009 · Cited by 1

Getting connected in the dopamine system

VANDENHEUVEL, D., & Pasterkamp, R. J. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.01.003 · Cited by 187

Subtypes of Midbrain Dopamine Neurons

Subramaniam, M., & Roeper, J. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00016-7 · Cited by 7