Loss of progranulin function in frontotemporal lobar degenerationCRUTS, Marc; VAN BROECKHOVEN, Christine.Trends in genetics (Regular ed.). 2008, Vol 24, Num 4, pp 186-194, issn 0168-9525, 9 p.Article

Pathogenesis of polyglutamine disorders: aggregation revisitedMICHALIK, Andrej; VAN BROECKHOVEN, Christine.Human molecular genetics (Print). 2003, Vol 12, pp R173-R186, issn 0964-6906, NS2Article

Transcriptional regulation of Alzheimer's disease genes : implications for susceptibilityTHEUNS, Jessie; VAN BROECKHOVEN, Christine.Human molecular genetics (Print). 2000, Vol 9, Num 16, pp 2383-2394, issn 0964-6906Article

Molecular genetics of Alzheimer's disease : An updateBROUWERS, Nathalie; SLEEGERS, Kristel; VAN BROECKHOVEN, Christine et al.Annals of medicine (Helsinki). 2008, Vol 40, Num 8, pp 562-583, issn 0785-3890, 22 p.Article

Method to introduce stable, expanded, polyglutamine-encoding CAG/CAA trinucleotide repeats into CAG repeat-containing genesMICHALIK, Andrej; KAZANTSEV, Aleksey; VAN BROECKHOVEN, Christine et al.BioTechniques. 2001, Vol 31, Num 2, pp 250-254, issn 0736-6205, 3 p.Article

Molecular Pathways of Frontotemporal Iobar DegetierationSLEEGERS, Kristel; CRUTS, Marc; VAN BROECKHOVEN, Christine et al.Annual review of neuroscience (Print). 2010, Vol 33, pp 71-88, issn 0147-006X, 18 p.Article

The Genetics of Dementia With Lewy Bodies: What Are We Missing?MEEUS, Bram; THEUNS, Jessie; VAN BROECKHOVEN, Christine et al.Archives of neurology (Chicago). 2012, Vol 69, Num 9, pp 1113-1118, issn 0003-9942, 6 p.Article

Invited Article : The Alzheimer disease-frontotemporal lobar degeneration spectrumVAN DER ZEE, Julie; SLEEGERS, Kristel; VAN BROECKHOVEN, Christine et al.Neurology. 2008, Vol 71, Num 15, pp 1191-1197, issn 0028-3878, 7 p.Article

Hereditary neuralgic amyotrophyMEULEMAN, Jan; TIMMERMAN, Vincent; VAN BROECKHOVEN, Christine et al.Neurogenetics (Oxford. Print). 2001, Vol 3, Num 3, pp 115-118, issn 1364-6745Article

Molecular Pathogenesis of Frontotemporal Lobar Degeneration : Basic Science Seminar in NeurologySLEEGERS, Kristel; KUMAR-SINGH, Samir; CRUTS, Marc et al.Archives of neurology (Chicago). 2008, Vol 65, Num 6, pp 700-704, issn 0003-9942, 5 p.Article

Progressive external ophthalmoplegia and multiple mitochondrial DNA deletionsVAN GOETHEM, Gert; MARTIN, Jean-Jacques; VAN BROECKHOVEN, Christine et al.Acta neurologica belgica. 2002, Vol 102, Num 1, pp 39-42, issn 0300-9009Article

Genetic contributions to individual differences in memory performanceNILSSON, Lars-Göran; VAN BROECKHOVEN, Christine; ADOLFSSON, Rolf et al.European psychologist. 2001, Vol 6, Num 4, pp 264-271, issn 1016-9040Article

SSHSuite: an integrated software package for analysis of large-scale suppression subtractive hybridization dataWECKX, Stefan; DE RIJK, Peter; VAN BROECKHOVEN, Christine et al.BioTechniques. 2004, Vol 36, Num 6, pp 1043-1045, issn 0736-6205, 3 p.Article

SNPbox: a modular software package for large-scale primer designWECKX, Stefan; DE RIJK, Peter; VAN BROECKHOVEN, Christine et al.Bioinformatics (Oxford. Print). 2005, Vol 21, Num 3, pp 385-387, issn 1367-4803, 3 p.Article

The pursuit of susceptibility genes for Alzheimer's disease: progress and prospectsSLEEGERS, Kristel; LAMBERT, Jean-Charles; BERTRAM, Lars et al.Trends in genetics (Regular ed.). 2010, Vol 26, Num 2, pp 84-93, issn 0168-9525, 10 p.Article

Associations between common arginine vasopressin 1b receptor and glucocorticoid receptor gene variants and HPA axis responses to psychosocial stress in a child psychiatric populationVAN WEST, Dirk; DEL-FAVERO, Jurgen; DEBOUTTE, Dirk et al.Psychiatry research (Print). 2010, Vol 179, Num 1, pp 64-68, issn 0165-1781, 5 p.Article

Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathyVAN GOETHEM, Gert; SCHWARTZ, Marianne; LÖFGREN, Ann et al.European journal of human genetics. 2003, Vol 11, Num 7, pp 547-549, issn 1018-4813, 3 p.Article

Parametric and nonparametric genome scan analyses for human handednessVAN AGTMAEL, Tom; FORREST, Susan M; DEL-FAVERO, Jurgen et al.European journal of human genetics. 2003, Vol 11, Num 10, pp 779-783, issn 1018-4813, 5 p.Article

APOE and Lipid Level Synergy Effects on Declarative Memory Functioning in AdulthoodSTERNÄNG, Ola; WAHLIN, Ake; ADOLFSSON, Rolf et al.European psychologist. 2009, Vol 14, Num 4, pp 268-278, issn 1016-9040, 11 p.Article

Trinucleotide repeat expansions: Do they contribute to bipolar disorder?GOOSSENS, Dirk; DEL-FAVERO, Jurgen; VAN BROECKHOVEN, Christine et al.Brain research bulletin. 2001, Vol 56, Num 3-4, pp 243-257, issn 0361-9230Conference Paper

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancyCLAES, Lieve; DEL-FAVERO, Jurgen; CEULEMANS, Berten et al.American journal of human genetics. 2001, Vol 68, Num 6, pp 1327-1332, issn 0002-9297Article

Fractal analysis of amyloid plaques in Alzheimer's disease patients and mouse modelsPIRICI, Daniel; VAN CAUWENBERGHE, Caroline; VAN BROECKHOVEN, Christine et al.Neurobiology of aging. 2011, Vol 32, Num 9, pp 1579-1587, issn 0197-4580, 9 p.Article

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletionsVAN GOETHEM, Gert; DERMAUT, Bart; LÖFGREN, Ann et al.Nature genetics. 2001, Vol 28, Num 3, pp 211-212, issn 1061-4036Article

Current status on Alzheimer disease molecular genetics: from past, to present, to futureBETTENS, Karolien; SLEEGERS, Kristel; VAN BROECKHOVEN, Christine et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R4-R11, NSArticle

Tau is central in the genetic Alzheimer-frontotemporal dementia spectrumDERMAUT, Bart; KUMAR-SINGH, Samir; RADEMAKERS, Rosa et al.Trends in genetics (Regular ed.). 2005, Vol 21, Num 12, pp 664-672, issn 0168-9525, 9 p.Article