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Lars Lannfelt

Researcher Next ID · RN-021199

Researcher · Medicine

Uppsala University

Uppsala, Sweden

Not currently recruitingFunding unknown
Works count
506
Citation count
40,858
H-index
93
i10-index
283

Research interests

Medicine
Biochemistry, Genetics and Molecular Biology
Alzheimer's disease research and treatments
Dementia and Cognitive Impairment Research
Cholinesterase and Neurodegenerative Diseases
Prion Diseases and Protein Misfolding
Bioinformatics and Genomic Networks

Publications

  • Lecanemab, Aducanumab, and Gantenerumab — Binding Profiles to Different Forms of Amyloid-Beta Might Explain Efficacy and Side Effects in Clinical Trials for Alzheimer's Disease

    Neurotherapeutics · 2022 · 10.1007/s13311-022-01308-6

  • A randomized, double-blind, phase 2b proof-of-concept clinical trial in early Alzheimer’s disease with lecanemab, an anti-Aβ protofibril antibody

    Alzheimer s Research & Therapy · 2021 · https://doi.org/10.1186/s13195-021-00813-8

  • The Amyloid-β Pathway in Alzheimer’s Disease

    Molecular Psychiatry · 2021 · https://doi.org/10.1038/s41380-021-01249-0

  • Alzheimer’s disease pathology propagation by exosomes containing toxic amyloid-beta oligomers

    Acta Neuropathologica · 2018 · 10.1007/s00401-018-1868-1

  • Safety and tolerability of BAN2401 - a clinical study in Alzheimer’s disease with a protofibril selective Aβ antibody

    Alzheimer s Research & Therapy · 2016 · 10.1186/s13195-016-0181-2

  • Accumulation of amyloid-β by astrocytes result in enlarged endosomes and microvesicle-induced apoptosis of neurons

    Molecular Neurodegeneration · 2016 · 10.1186/s13024-016-0098-z

  • η-Secretase processing of APP inhibits neuronal activity in the hippocampus

    Nature · 2015 · 10.1038/nature14864

  • Serial propagation of distinct strains of Aβ prions from Alzheimer’s disease patients

    Proceedings of the National Academy of Sciences · 2014 · 10.1073/pnas.1408900111

  • Cerebrospinal fluid levels of the synaptic protein neurogranin correlates with cognitive decline in prodromal Alzheimer's disease

    Alzheimer s & Dementia · 2014 · 10.1016/j.jalz.2014.10.009

  • Extracellular Alpha-Synuclein Oligomers Modulate Synaptic Transmission and Impair LTP Via NMDA-Receptor Activation

    Journal of Neuroscience · 2012 · 10.1523/jneurosci.0234-12.2012

  • PBT2 Rapidly Improves Cognition in Alzheimer's Disease: Additional Phase II Analyses

    Journal of Alzheimer s Disease · 2010 · 10.3233/jad-2010-1390

  • Stabilization of neurotoxic Alzheimer amyloid-β oligomers by protein engineering

    Proceedings of the National Academy of Sciences · 2010 · 10.1073/pnas.1001740107

  • Safety, efficacy, and biomarker findings of PBT2 in targeting Aβ as a modifying therapy for Alzheimer's disease: a phase IIa, double-blind, randomised, placebo-controlled trial

    The Lancet Neurology · 2008 · https://doi.org/10.1016/s1474-4422(08)70167-4

  • Sensitive ELISA detection of amyloid‐β protofibrils in biological samples

    Journal of Neurochemistry · 2007 · 10.1111/j.1471-4159.2007.04759.x

  • The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation

    Nature Neuroscience · 2001 · 10.1038/nn0901-887

  • Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

    Nature · 1998 · https://doi.org/10.1038/31508

  • Human beta-2 adrenoceptor gene polymorphisms are highly frequent in obesity and associate with altered adipocyte beta-2 adrenoceptor function.

    Journal of Clinical Investigation · 1997 · 10.1172/jci119854

  • Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease

    Nature Medicine · 1996 · https://doi.org/10.1038/nm0896-864

  • The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

    Nature Genetics · 1995 · 10.1038/ng1095-219

  • The Swedish mutation causes early-onset Alzheimer's disease by β-secretase cleavage within the secretory pathway

    Nature Medicine · 1995 · 10.1038/nm1295-1291

  • Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

    Nature · 1995 · https://doi.org/10.1038/376775a0

  • Relative abundance of Alzheimer A beta amyloid peptide variants in Alzheimer disease and normal aging.

    Proceedings of the National Academy of Sciences · 1994 · 10.1073/pnas.91.18.8378

  • Excessive production of amyloid beta-protein by peripheral cells of symptomatic and presymptomatic patients carrying the Swedish familial Alzheimer disease mutation.

    Proceedings of the National Academy of Sciences · 1994 · 10.1073/pnas.91.25.11993

  • APOLIPOPROTEIN-E GENOTYPE AND ALZHEIMERS-DISEASE

    UCL Discovery (University College London) · 1993

  • A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N–terminus of β–amyloid

    Nature Genetics · 1992 · https://doi.org/10.1038/ng0892-345

Current projects

    No projects listed.