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Marc Cruts

Showing results (71-80 of 85) with videos related to

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JAMA Neurology|February 14, 2017
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat ExpansionSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Human Molecular Genetics|October 1, 2005
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsyRosa Rademakers, Stacey Melquist, Marc Cruts, et al.
Neurogenetics|June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome ProjectAndrea Haworth, Lars Bertram, Paola Carrera, et al.
JAMA Neurology|January 23, 2013
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohortTim Van Langenhove, Julie van der Zee, Ilse Gijselinck, et al.
Nature Communications|September 10, 2014
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European originsShai Carmi, Ken Y Hui, Ethan Kochav, et al.
Neurobiology of Aging|November 18, 2017
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohortJan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
The Lancet. Neurology|December 14, 2011
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification studyIlse Gijselinck, Tim Van Langenhove, Julie van der Zee, et al.
Neurobiology of Aging|March 21, 2018
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementiaStéphanie Philtjens, Sara Van Mossevelde, Julie van der Zee, et al.
Neurology|October 19, 2014
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseJessie Theuns, Aline Verstraeten, Kristel Sleegers, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
JAMA Neurology|February 14, 2017
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat ExpansionSara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, et al.
Human Molecular Genetics|October 1, 2005
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsyRosa Rademakers, Stacey Melquist, Marc Cruts, et al.
Neurogenetics|June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome ProjectAndrea Haworth, Lars Bertram, Paola Carrera, et al.
JAMA Neurology|January 23, 2013
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohortTim Van Langenhove, Julie van der Zee, Ilse Gijselinck, et al.
Nature Communications|September 10, 2014
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European originsShai Carmi, Ken Y Hui, Ethan Kochav, et al.
Neurobiology of Aging|November 18, 2017
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohortJan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
The Lancet. Neurology|December 14, 2011
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification studyIlse Gijselinck, Tim Van Langenhove, Julie van der Zee, et al.
Neurobiology of Aging|March 21, 2018
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementiaStéphanie Philtjens, Sara Van Mossevelde, Julie van der Zee, et al.
Neurology|October 19, 2014
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseJessie Theuns, Aline Verstraeten, Kristel Sleegers, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Pageof 9