Christine Van Broeckhoven

Professor in Moleculaire Biologie en Genetica

Key publications

Dementia in 2013 : frontotemporal lobar degeneration-building on breakthroughs
van der Zee Julie   Van Broeckhoven Christine  
Nature reviews : neurology - ISSN 1759-4758-10:2 (2014) p. 70-72
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The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
Gijselinck Ilse   Van Mossevelde Sara   van der Zee Julie   Sieben Anne   Engelborghs Sebastiaan   De Bleecker J.   Ivanoiu A.   Deryck O.   Edbauer D.   Zhang M.   Heeman Bavo   Bäumer Veerle   Van den Broeck M.   Mattheijssens Maria   Peeters Karin   Rogaeva E.   De Jonghe Peter   Cras Patrick   Martin Jean-Jacques   De Deyn Peter Paul   Cruts Marc   Van Broeckhoven Christine    
Molecular psychiatry - ISSN 1359-4184-21:8 (2016) p. 1112-1124
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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
Gijselinck Ilse   Van Mossevelde Sara   van der Zee Julie   Sieben Anne   Philtjens Stéphanie   Heeman Bavo   Engelborghs Sebastiaan   Vandenbulcke Mathieu   De Baets Greet   Bäumer Veerle   Cuijt Ivy   Van den Broeck Marleen   Peeters Karin   Mattheijssens Maria   Rousseau Frederic   Vandenberghe Rik   De Jonghe Peter   Cras Patrick   De Deyn Peter Paul   Martin Jean-Jacques   Cruts Marc   Van Broeckhoven Christine    
Neurology - ISSN 0028-3878-85:24 (2015) p. 2116-2125
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A family with early-onset Alzheimer's disease and cerebral haemorrhage due to a mutation (codon 692) in the β-amyloid precursor protein gene
van Harskamp Frans   Cras Patrick   Hendriks Lydia   Kros J.M.   Martin Jean-Jacques   Hofman Albert   Van Broeckhoven Christine   van Duijn Cornelia M.  
Alzheimer's disease: biology, diagnosis and therapeutics / Iqbal, K. [edit.]-p. 155-159
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ApoE genotype is a risk factor in nonpresenilin eraly-onset Alzheimer's disease families
Houlden Henry   Crook Richard   Backhovens Hubert   Prihar Guy   Baker Matt   Hutton Mike   Rossor Martin   Martin Jean-Jacques   Van Broeckhoven Christine   Hardy John  
American journal of medical genetics - ISSN 0148-7299-81 (1998) p. 117-121
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Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β-amyloid precursor protein gene
Hendriks Lydia   van Duijn C.M.   Cras Patrick   Cruts Marc   Van Hul Wim   van Harskamp F.   Warren A.   McInnis M.G.   Antonarakis S.E.   Martin Jean-Jacques   Hofman A.   Van Broeckhoven Christine  
Nature genetics - ISSN 1061-4036-1 (1992) p. 218-221
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Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
Van Goethem Gert   Dermaut Bart   Löfgren Ann   Martin Jean-Jacques   Van Broeckhoven Christine  
Nature genetics - ISSN 1061-4036-28 (2001) p. 211-212
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Null mutations in progranulin cause ubiquitine-positive frontotemporal dementia linked to chromosome 17q21
Cruts Marc   Gijselinck Ilse   van der Zee Julie   Engelborghs Sebastiaan   Wils Hans   Pirici Daniel   Rademakers Roos   Vandenberghe R.   Dermaut Bart   Martin Jean-Jacques   van Duijn C.   Peeters Karin   Sciot R.   Santens P.   de Pooter T.   Mattheijssens Maria   Van den Broeck Marleen   Cuijt Ivy   Vennekens K.   De Deyn Peter Paul   Kumar-Singh Samir   Van Broeckhoven Christine  
Nature-442:7105 (2006) p. 920-924
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Genome-wide association study identifies variants at **CLU** and **CR1** associated with Alzheimer's disease
Lambert Jean-Charles   Sleegers Kristel   Bettens Karolien   Engelborghs Sebastiaan   De Deyn Peter Paul   Van Broeckhoven Christine   et al.  
Nature genetics - ISSN 1061-4036-41:10 (2009) p. 1094-1099
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Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites
Brouwers Nathalie   Van Cauwenberghe Caroline   Engelborghs Sebastiaan   Lambert J.-C.   Bettens Karolien   Le Bastard Nathalie   Pasquier F.   Gil Montoya A.   Peeters Karin   Mattheijssens Maria   Vandenberghe R.   De Deyn Peter Paul   Cruts Marc   Amouyel P.   Sleegers Kristel   Van Broeckhoven Christine  
Molecular psychiatry - ISSN 1359-4184-17:2 (2012) p. 223-233
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Both common variations and rare non-synonymous substitutions and small insertion/deletions in **CLU** are associated with increased Alzheimer risk
Bettens Karolien   Brouwers Nathalie   Engelborghs Sebastiaan   Lambert Jean-Charles   Rogeava Ekaterina   Vandenberghe Rik   Le Bastard Nathalie   Pasquier Florence   Vermeulen Steven   Van Dongen Jasper   Mattheijssens Maria   Peeters Karin   Mayeux Richard   St George-Hyslop Peter   Amouyel Philippe   De Deyn Peter Paul   Sleegers Kristel   Van Broeckhoven Christine  
Molecular neurodegeneration - ISSN 1750-1326-7 (2012) p. 1-12
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Full bibliography of this author