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Authors: Marc Cruts
Journal Article
NanoPack: visualizing and processing long-read sequencing data Open Access
Bioinformatics, Volume 34, Issue 15, August 2018, Pages 2666–2669, https://doi.org/10.1093/bioinformatics/bty149
Published: 14 March 2018
Journal Article
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort Open Access
in
Brain
Brain, Volume 139, Issue 2, February 2016, Pages 452–467, https://doi.org/10.1093/brain/awv358
Published: 16 December 2015
Journal Article
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort Open Access
in
Brain
Brain, Volume 134, Issue 3, March 2011, Pages 808–815, https://doi.org/10.1093/brain/awr007
Published: 22 February 2011
Journal Article
Cholesterol and Triglycerides Moderate the Effect of Apolipoprotein E on Memory Functioning in Older Adults Get access
The Journals of Gerontology: Series B, Volume 62, Issue 2, March 2007, Pages P112–P118, https://doi.org/10.1093/geronb/62.2.P112
Published: 01 March 2007
Journal Article
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy Open Access
in
Brain
Brain, Volume 129, Issue 11, November 2006, Pages 2977–2983, https://doi.org/10.1093/brain/awl203
Published: 18 August 2006
Journal Article
Reduced functional brain activity response in cognitively intact apolipoprotein E ε4 carriers Open Access
in
Brain
Brain, Volume 129, Issue 5, May 2006, Pages 1240–1248, https://doi.org/10.1093/brain/awl054
Published: 14 March 2006
Journal Article
Characterization of Ubiquitinated Intraneuronal Inclusions in a Novel Belgian Frontotemporal Lobar Degeneration Family Get access
Journal of Neuropathology & Experimental Neurology, Volume 65, Issue 3, March 2006, Pages 289–301, https://doi.org/10.1097/01.jnen.0000205147.39210.c7
Published: 01 March 2006
Journal Article
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD Open Access
in
Brain
Brain, Volume 129, Issue 4, April 2006, Pages 841–852, https://doi.org/10.1093/brain/awl029
Published: 22 February 2006
Journal Article
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy Get access
Human Molecular Genetics, Volume 14, Issue 21, 1 November 2005, Pages 3281–3292, https://doi.org/10.1093/hmg/ddi361
Published: 29 September 2005
Journal Article
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region Get access
Human Molecular Genetics, Volume 14, Issue 13, 1 July 2005, Pages 1753–1762, https://doi.org/10.1093/hmg/ddi182
Published: 11 May 2005
Journal Article
Alzheimer-associated C allele of the promoter polymorphism −22C>T causes a critical neuron-specific decrease of presenilin 1 expression Get access
Human Molecular Genetics, Volume 12, Issue 8, 15 April 2003, Pages 869–877, https://doi.org/10.1093/hmg/ddg098
Published: 15 April 2003
Journal Article
Pathology of early-onset Alzheimer's disease cases bearing the Thr113–114ins presenilin-1 mutation Get access
in
Brain
Brain, Volume 123, Issue 12, December 2000, Pages 2467–2474, https://doi.org/10.1093/brain/123.12.2467
Published: 01 December 2000
Journal Article
Nonfibrillar diffuse amyloid deposition due to a γ 42‐secretase site mutation points to an essential role for N‐truncated Aβ42 in Alzheimer’s disease Get access
Human Molecular Genetics, Volume 9, Issue 18, 1 November 2000, Pages 2589–2598, https://doi.org/10.1093/hmg/9.18.2589
Published: 01 November 2000
Journal Article
Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692) Get access
in
Brain
Brain, Volume 123, Issue 10, October 2000, Pages 2130–2140, https://doi.org/10.1093/brain/123.10.2130
Published: 01 October 2000
Journal Article
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer’s disease and variable expression Get access
Human Molecular Genetics, Volume 9, Issue 3, 12 February 2000, Pages 325–331, https://doi.org/10.1093/hmg/9.3.325
Published: 12 February 2000
Journal Article
Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease Get access
Human Molecular Genetics, Volume 7, Issue 1, January 1998, Pages 43–51, https://doi.org/10.1093/hmg/7.1.43
Published: 01 January 1998
Journal Article
The presenilin genes: a new gene family involved in Alzheimer disease pathology Get access
Human Molecular Genetics, Volume 5, Issue Supplement_1, September 1996, Pages 1449–1455, https://doi.org/10.1093/hmg/5.Supplement_1.1449
Published: 01 September 1996
Journal Article
Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3 Get access
Human Molecular Genetics, Volume 4, Issue 12, December 1995, Pages 2363–2371, https://doi.org/10.1093/hmg/4.12.2363
Published: 01 December 1995
Journal Article
A yeast artificial chromosome contig from human chromosome 14q24 spanning the Alzheimer's disease locus AD3 Get access
Human Molecular Genetics, Volume 4, Issue 8, August 1995, Pages 1347–1354, https://doi.org/10.1093/hmg/4.8.1347
Published: 01 August 1995
Journal Article
Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3 Get access
Human Molecular Genetics, Volume 4, Issue 8, August 1995, Pages 1355–1364, https://doi.org/10.1093/hmg/4.8.1355
Published: 01 August 1995
