<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Johansen NJ</submitter><funding>NIMH NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><pubmed_abstract>The basal ganglia (BG) are conserved brain regions essential for motor control, learning, emotion, and cognition, and are implicated in neurological and psychiatric disease. Yet a unified cross-species taxonomy of BG cell types is lacking, limiting translation of BG circuit mechanisms, interpretation of human genetic risk, and development of cell type-targeted tools. We present a multiomic consensus atlas of 1.8 million nuclei from human, macaque, and marmoset spanning eight BG structures. Integrating cross-species gene expression, open chromatin, and spatial profiling enables definition of conserved and divergent cell types. Alignment to existing mouse and human atlases identifies 61 homologous cell types conserved over 80 million years. We identify a STRd D2 StrioMat Hybrid medium spiny </pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.12.15.694496</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12724601</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cross-species consensus atlas of the primate basal ganglia.</pubmed_title><pmcid>PMC12724601</pmcid><funding_grant_id>UM1 MH130981</funding_grant_id><funding_grant_id>U24 NS133077</funding_grant_id><funding_grant_id>UF1 MH128339</funding_grant_id><funding_grant_id>U24 MH130919</funding_grant_id><funding_grant_id>U24 MH130918</funding_grant_id><funding_grant_id>R01 CA296792</funding_grant_id><funding_grant_id>U24 MH130968</funding_grant_id><pubmed_authors>Sanchez R</pubmed_authors><pubmed_authors>Kalmbach B</pubmed_authors><pubmed_authors>Clark M</pubmed_authors><pubmed_authors>Ding SL</pubmed_authors><pubmed_authors>Huynh G</pubmed_authors><pubmed_authors>Manning A</pubmed_authors><pubmed_authors>Schmitz M</pubmed_authors><pubmed_authors>Liu XP</pubmed_authors><pubmed_authors>DeBerardine M</pubmed_authors><pubmed_authors>James K</pubmed_authors><pubmed_authors>Avola A</pubmed_authors><pubmed_authors>Hodge RD</pubmed_authors><pubmed_authors>Pham T</pubmed_authors><pubmed_authors>Otto S</pubmed_authors><pubmed_authors>Ferrer R</pubmed_authors><pubmed_authors>Rivera AD</pubmed_authors><pubmed_authors>Kapen I</pubmed_authors><pubmed_authors>Bakken TE</pubmed_authors><pubmed_authors>Budzillo A</pubmed_authors><pubmed_authors>Kedzierska KZ</pubmed_authors><pubmed_authors>Fiabane E</pubmed_authors><pubmed_authors>Morrison C</pubmed_authors><pubmed_authors>Schau G</pubmed_authors><pubmed_authors>Yuan D</pubmed_authors><pubmed_authors>Daigle TL</pubmed_authors><pubmed_authors>Turner MA</pubmed_authors><pubmed_authors>Krienen FM</pubmed_authors><pubmed_authors>Dalley R</pubmed_authors><pubmed_authors>Zeng H</pubmed_authors><pubmed_authors>Lein ES</pubmed_authors><pubmed_authors>Gloe J</pubmed_authors><pubmed_authors>Fu Y</pubmed_authors><pubmed_authors>Rocha D</pubmed_authors><pubmed_authors>Guzman J</pubmed_authors><pubmed_authors>Jones DL</pubmed_authors><pubmed_authors>Schembri J</pubmed_authors><pubmed_authors>Sherman J</pubmed_authors><pubmed_authors>Chakka AB</pubmed_authors><pubmed_authors>McMillen D</pubmed_authors><pubmed_authors>Yanny AM</pubmed_authors><pubmed_authors>Freiwald W</pubmed_authors><pubmed_authors>Tran A</pubmed_authors><pubmed_authors>Lee BR</pubmed_authors><pubmed_authors>Ting JT</pubmed_authors><pubmed_authors>Kroes T</pubmed_authors><pubmed_authors>Barlow ST</pubmed_authors><pubmed_authors>Torkelson A</pubmed_authors><pubmed_authors>Keene CD</pubmed_authors><pubmed_authors>Bertagnolli D</pubmed_authors><pubmed_authors>Caceres L</pubmed_authors><pubmed_authors>Levi BP</pubmed_authors><pubmed_authors>Eggermont J</pubmed_authors><pubmed_authors>Goldy J</pubmed_authors><pubmed_authors>Gillis J</pubmed_authors><pubmed_authors>Gouwens N</pubmed_authors><pubmed_authors>Daniel S</pubmed_authors><pubmed_authors>Dan S</pubmed_authors><pubmed_authors>McCue R</pubmed_authors><pubmed_authors>Guilford N</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Mollenkopf T</pubmed_authors><pubmed_authors>Ray PL</pubmed_authors><pubmed_authors>Seeman SC</pubmed_authors><pubmed_authors>Chakrabarty R</pubmed_authors><pubmed_authors>Rajagopal A</pubmed_authors><pubmed_authors>Ho W</pubmed_authors><pubmed_authors>Tieu M</pubmed_authors><pubmed_authors>Long B</pubmed_authors><pubmed_authors>Casper T</pubmed_authors><pubmed_authors>Thijssen J</pubmed_authors><pubmed_authors>Caballero VEN</pubmed_authors><pubmed_authors>French L</pubmed_authors><pubmed_authors>Leytze M</pubmed_authors><pubmed_authors>Sorensen SA</pubmed_authors><pubmed_authors>Vieth A</pubmed_authors><pubmed_authors>Rimorin C</pubmed_authors><pubmed_authors>Sobieski C</pubmed_authors><pubmed_authors>Yao Z</pubmed_authors><pubmed_authors>Lelieveldt B</pubmed_authors><pubmed_authors>Garcia AD</pubmed_authors><pubmed_authors>Jungert M</pubmed_authors><pubmed_authors>Hirschstein D</pubmed_authors><pubmed_authors>Close J</pubmed_authors><pubmed_authors>Kempynck N</pubmed_authors><pubmed_authors>Ng L</pubmed_authors><pubmed_authors>Nguy B</pubmed_authors><pubmed_authors>Hewitt M</pubmed_authors><pubmed_authors>Phillips E</pubmed_authors><pubmed_authors>Shapovalova NV</pubmed_authors><pubmed_authors>Dubuc A</pubmed_authors><pubmed_authors>Smith K</pubmed_authors><pubmed_authors>Miller JA</pubmed_authors><pubmed_authors>Johansen NJ</pubmed_authors><pubmed_authors>Pena N</pubmed_authors><pubmed_authors>Wirthlin M</pubmed_authors><pubmed_authors>Bhandiwad A</pubmed_authors><pubmed_authors>Yazdani F</pubmed_authors><pubmed_authors>Kannan M</pubmed_authors><pubmed_authors>Osumi-Sutherland D</pubmed_authors><pubmed_authors>Dee N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cross-species consensus atlas of the primate basal ganglia.</name><description>The basal ganglia (BG) are conserved brain regions essential for motor control, learning, emotion, and cognition, and are implicated in neurological and psychiatric disease. Yet a unified cross-species taxonomy of BG cell types is lacking, limiting translation of BG circuit mechanisms, interpretation of human genetic risk, and development of cell type-targeted tools. We present a multiomic consensus atlas of 1.8 million nuclei from human, macaque, and marmoset spanning eight BG structures. Integrating cross-species gene expression, open chromatin, and spatial profiling enables definition of conserved and divergent cell types. Alignment to existing mouse and human atlases identifies 61 homologous cell types conserved over 80 million years. We identify a STRd D2 StrioMat Hybrid medium spiny </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-04T03:17:27.809Z</modification><creation>2026-06-04T03:11:37.25Z</creation></dates><accession>S-EPMC12724601</accession><cross_references><pubmed>41446173</pubmed><doi>10.64898/2025.12.15.694496</doi></cross_references></HashMap>