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Search results (374)

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A hippocampal neuroimaging signature of neurovascular insulin signalling links metabolism to mood

Cherix A. et al, (2026)

Regional sex differences in human cortical anatomy vary in their morphometric bases and overlap with sex chromosomal and gonadal influences.

Lee HM. et al, (2026), Nat Commun

Autism-like phenotypes and increased NMDAR2D expression in mice with KDM5B histone lysine demethylase deficiency.

Pérez-Sisqués L. et al, (2026), Sci Adv, 12

Autism subtypes identified using cross-species functional connectivity analyses.

Pagani M. et al, (2026), Nat Neurosci

An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism.

Bradley CA. et al, (2026), Nature

Translating brain anatomy and disease from mouse to human in latent gene expression space

Jaroszynski C. et al, (2026), eBioMedicine, 127, 106259 - 106259

Correction: Using endocrine profiles to explore subgroups among transdiagnostic neurodiverse children and adolescents.

Mo K. et al, (2026), J Neural Transm (Vienna)

Regulation of autism-related self-injurious behavior by electrical stimulation of corticostriatal circuits in mice and humans.

Zhang K. et al, (2026), Sci Adv, 12

The development of dynamic networks supporting attentional flexibility.

Coleman SC. et al, (2026), Dev Cogn Neurosci, 78

Altered Brain Structure in an ATRX-Deficient Mouse Model of Autism Spectrum Disorder.

Quesnel K. et al, (2026), Autism Res, 19

Non-invasive measurement of neurotransmitter-specific glucose metabolism in the human brain using proton-observed proton-edited 13 C-MRS (POPE 13 C-MRS)

Cherix A. et al, (2026)

Macrostructural, microstructural, and cellular effects of neuroinflammation on the mouse brain.

Patel Y. et al, (2026), Brain Behav Immun Health, 52

Enrichment-induced forgetting is associated with white matter microstructure in mice.

Gazdzinski LM. et al, (2026), Behav Brain Res, 497

Probing the Influence of Paternal Diet on Offspring Neuroanatomy With Mouse MRI.

McKnight EGW. et al, (2026), Brain Behav, 16

Enhanced mGluR1 function causes motor deficits and region-specific Purkinje cell dysfunction.

Ibrahim MF. et al, (2026), Brain

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