Lena Lilius
Stockholm, AB, Sweden
Last Updated: 09/26/2026
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Found 9 publications
Confirmation of high frequency of C9orf72 mutations in patients with frontotemporal dementia from Sweden.
Journal: Neurobiology of aging
Published: December 11, 2018
Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.
Journal: Acta neuropathologica communications
Published: March 14, 2017
Predicting Cognitive Decline across Four Decades in Mutation Carriers and Non-carriers in Autosomal-Dominant Alzheimer's Disease.
Journal: Journal of the International Neuropsychological Society : JINS
Published: January 13, 2017
Phenotypic variability and neuropsychological findings associated with C9orf72 repeat expansions in a Bulgarian dementia cohort.
Journal: PloS one
Published: October 17, 2016
No common founder for C9orf72 expansion mutation in Sweden.
Journal: Journal of human genetics
Published: April 01, 2016
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.
Journal: The Lancet. Neurology
Published: February 10, 2015
Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
Journal: European journal of human genetics : EJHG
Published: September 03, 2012
Biochemical studies of poly-T variants in the Alzheimer's disease associated TOMM40 gene.
Journal: Journal of Alzheimer's disease : JAD
Published: May 19, 2012
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Last Updated: 09/26/2026