L. Sandkuijl

PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36

Cornelia M. van Duijn, Marieke Dekker, Vincenzo Bonifati et al. · The American Journal of Human Genetics · 2001 · 377 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +11

Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling

M.G.E.M. Ausems, J. R. Verbiest, MMP Hermans et al. · European Journal of Human Genetics · 1999 · 302 citations · Full text

Genetic Testing, Mendelian Disorder, Inherited Metabolic Disease +9

Genetic Heterogeneity of Polycystic Kidney Disease in Europe1

Dorien J.M. Peters, L. Sandkuijl · Contributions to nephrology · 2015 · 285 citations

Renal Disease, Medicine, Genetic Epidemiology +6

Involvement of the <i>CACNA1A</i> gene containing region on 19p13 in migraine with and without aura

Gisela M. Terwindt, Roel A. Ophoff, Ronald van Eijk et al. · Neurology · 2001 · 135 citations

Linkage-Disequilibrium Mapping of Disease Genes by Reconstruction of Ancestral Haplotypes in Founder Populations

Susan K. Service, Datian Lang, Nelson B. Freimer et al. · The American Journal of Human Genetics · 1999 · 112 citations · Full text

Haplotype Determination, Linkage Disequilibrium, Genotype-phenotype Association +11