Sandro Sorbi

UCL Queen Square Institute Of Neurology
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 299 publications

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

Journal: American journal of human genetics

Published: April 20, 2026

Towards the development of a management protocol for subjective cognitive decline: Insights from a cross-sectional and longitudinal analysis of multimodal data from a memory clinic.

Towards the development of a management protocol for subjective cognitive decline: Insights from a cross-sectional and longitudinal analysis of multimodal data from a memory clinic.

Journal: Journal of Alzheimer's disease : JAD

Published: January 28, 2026

Neurodevelopmental effects of genetic frontotemporal dementia mutations revealed by total intracranial volume differences.

Neurodevelopmental effects of genetic frontotemporal dementia mutations revealed by total intracranial volume differences.

Journal: Journal of Alzheimer's disease : JAD

Published: November 19, 2025

Cerebrovascular Reactivity at Rest and Its Association With Cognitive Function in People With Genetic Frontotemporal Dementia.

Cerebrovascular Reactivity at Rest and Its Association With Cognitive Function in People With Genetic Frontotemporal Dementia.

Journal: Neurology

Published: September 04, 2025

Western Hunter-Gatherer genetic ancestry contributes to human longevity in the Italian population.

Western Hunter-Gatherer genetic ancestry contributes to human longevity in the Italian population.

Journal: GeroScience

Published: September 03, 2025

Individualized Atrophy-Based Prediction of Dementia Progression in Familial Frontotemporal Lobar Degeneration With Bayesian Linear Mixed-Effects Modeling.

Individualized Atrophy-Based Prediction of Dementia Progression in Familial Frontotemporal Lobar Degeneration With Bayesian Linear Mixed-Effects Modeling.

Journal: Annals of neurology

Published: July 23, 2025

Composite grey matter fingerprints for genetic frontotemporal dementia.

Composite grey matter fingerprints for genetic frontotemporal dementia.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: July 18, 2025

Italian intersocietal recommendations for restructuring the diagnostic-therapeutic pathway for the implementation and appropriate use of anti-amyloid monoclonal antibodies in Alzheimer's disease.

Italian intersocietal recommendations for restructuring the diagnostic-therapeutic pathway for the implementation and appropriate use of anti-amyloid monoclonal antibodies in Alzheimer's disease.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: July 11, 2025

Accuracy of blood-based neurofilament light to different genetic frontotemporal dementia from primary psychiatric disorders.

Accuracy of blood-based neurofilament light to different genetic frontotemporal dementia from primary psychiatric disorders.

Journal: Journal of Alzheimer's disease : JAD

Published: July 03, 2025

Plasma p-tau181 as a Marker of Conversion to Alzheimer's Disease Dementia and Worsening in Cognitive Functions in Subjective Cognitive Decline and Mild Cognitive Impairment: A Longitudinal Study.

Plasma p-tau181 as a Marker of Conversion to Alzheimer's Disease Dementia and Worsening in Cognitive Functions in Subjective Cognitive Decline and Mild Cognitive Impairment: A Longitudinal Study.

Journal: Annals of clinical and translational neurology

Published: July 01, 2025

The HTT gene influences plasma neurofilament light chain and brain metabolism in prodromal Alzheimer's disease.

The HTT gene influences plasma neurofilament light chain and brain metabolism in prodromal Alzheimer's disease.

Journal: Journal of neurology

Published: June 25, 2025

Genome-wide association studies of binge eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes.

Genome-wide association studies of binge eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes.

Journal: medRxiv : the preprint server for health sciences

Published: May 19, 2025

Showing 1-12 of 299

Last Updated: 09/26/2026