I. Leber

发表

Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

Nick C Fox, Alan J. Thomas, D. Hernandez, 2020, Scientific Reports.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

Some effects of carbon dioxide on mortars and concrete

F. A. Blakey, I. Leber, 2017 .

The European Reference Network for Rare Neurological Diseases

E. Bertini, R. Vandenberghe, L. Schöls, 2021, Frontiers in Neurology.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

E. Haan, P. Pietrini, R. Petersen, 2017, Scientific Reports.

Immune-related genetic enrichment in frontotemporal dementia

D. Hernandez, M. Nalls, L. Ferrucci, 2017, bioRxiv.

Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias

A. Dürr, P. Ribai, S. Forlani, 2010, Human mutation.

Association study of the GAB2 gene with the risk of developing Alzheimer's disease

F. Pasquier, J. Lambert, P. Amouyel, 2008, Neurobiology of Disease.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Nature Medicine.

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Brain : a journal of neurology.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Nick C Fox, D. Hernandez, M. Nalls, 2017, Scientific Reports.

Brain dysfunction in gait disorders of Caribbean atypical Parkinsonism and progressive supranuclear palsy patients: A comparative study

S. Lehéricy, M. Welter, S. Rivaud-Pechoux, 2023, NeuroImage: Clinical.

CXCR4 involvement in neurodegenerative diseases

O. Andreassen, G. Schellenberg, A. Dale, 2017, bioRxiv.

Identification of common variants influencing risk of the tauopathy Progressive Supranuclear Palsy

Andrew J. Lees, Allissa Dillman, Li-San Wang, 2011, Nature Genetics.

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

P. Pietrini, R. Desikan, J. Trojanowski, 2019, Scientific Reports.

Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias

A. Dürr, P. Ribai, S. Forlani, 2010, Human mutation.

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

H. Leonard, D. Knopman, C. van Broeckhoven, 2024, American journal of human genetics.