C. Sassi

U. Dirnagl, Marco Foddis, D. Beule, 2019, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

White matter hyperintensities and neurodegenerative dementias

C. Sassi, 2019, Aging.

ABCA7 p.G215S as potential protective factor for Alzheimer's disease

Michelle K. Lupton, W. M. van der Flier, M. Nalls, 2016, Neurobiology of Aging.

Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease

Michelle K. Lupton, A. Singleton, J. Hardy, 2014, Neurobiology of Aging.

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

A. Pavlovic, U. Dirnagl, J. Schleutker, 2021, Scientific Reports.

Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer’s Disease

Michelle K. Lupton, M. Nalls, A. Singleton, 2016, PloS one.

Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3

Michelle K. Lupton, M. Nalls, A. Singleton, 2018, Neurobiology of Aging.

TREM2 Variants in Alz hei mer's Disease

A. Singleton, L. Hazrati, K. Morgan, 2012 .

Shared and oppositely regulated transcriptomic signatures in Huntington's disease and brain ischemia confirm known and unveil novel potential neuroprotective genes

Marco Foddis, M. Holtgrewe, D. Beule, 2021, Neurobiology of Aging.

Individual and temporal variability of the retina after chronic bilateral common carotid artery occlusion (BCCAO)

U. Dirnagl, Marco Foddis, M. Füchtemeier, 2018, PloS one.

A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease

Michelle K. Lupton, D. Hernandez, A. Singleton, 2018, Molecular Psychiatry.

Missense variant in TREML2 protects against Alzheimer's disease

Michelle K. Lupton, A. Singleton, J. Haines, 2014, Neurobiology of Aging.

A comprehensive assessment of benign genetic variability for neurodegenerative disorders

Michelle K. Lupton, D. Hernandez, A. Singleton, 2018, bioRxiv.

TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients

A. Pavlovic, J. Schleutker, R. Guerreiro, 2022, Neurobiology of Aging.

Persistent hiccups as main COVID-19 manifestation with transient cytotoxic lesion of the corpus callosum splenium during the Omicron wave in the post-vaccination era

C. Sassi, S. Habermann, Hans-Michael Schmitt, 2022, Journal of Neurology.

2 Genetics of Parkinson Disease

C. Sassi, 2018 .

Genetics of Parkinson Disease

C. Sassi, 2011 .

Exome sequencing identifies two novel PSEN 1 mutations ( p . L 166 V and p . S 230 R ) in British early onset Alzheimer ’ s

Lupton, Turton, C. Sassi, 2016 .

Investigating APOE, APP-Aβ metabolism genes and Alzheimer’s disease GWAS hits in brain small vessel ischemic disease

U. Dirnagl, Marco Foddis, M. Holtgrewe, 2020, Scientific Reports.

A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy.

A. Singleton, M. Copetti, S. Arcuti, 2016, Journal of Alzheimer's disease : JAD.

Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of Apulia

T. Price, C. Blauwendraat, G. Logroscino, 2021, Scientific Reports.

ABCA7 p.G215S as potential protective factor for Alzheimer's disease

Michelle K. Lupton, W. M. van der Flier, M. Nalls, 2016, Neurobiology of Aging.

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

Erick R. Scott, Michelle K. Lupton, D. Hernandez, 2013, Nature.

Ide copy number variant does not influence lesion size and mortality in two C57BL/6J mouse models of cerebrovascular ischemia nor in human cerebrovascular disease. An exploratory study

A. Pagnamenta, Marco Foddis, D. Beule, 2024, bioRxiv.