Henneman P, van der Sman-de Beer F, Moghaddam PH, Huijts P, Stalenhoef AF, Kastelein JJ, van Duijn CM, Havekes LM, Frants RR, van Dijk KW, Smelt AH (2009)
The expression of type III hyperlipoproteinemia: involvement of lipolysis genes
Eur J Hum Genet 17: 620

van Himbergen TM, van der Schouw YT, Voorbij HA, van Tits LJ, Stalenhoef AF, Peeters PH, Roest M (2008)
Paraoxonase (PON1) and the risk for coronary heart disease and myocardial infarction in a general population of Dutch women
Atherosclerosis 199: 408

van Himbergen TM, van Tits LJ, Ter Avest E, Roest M, Voorbij HA, de Graaf J, Stalenhoef AF (2008)
Paraoxonase (PON1) is associated with familial combined hyperlipidemia
Atherosclerosis 199: 87

van Himbergen TM, van Tits LJ, Roest M, Stalenhoef AF (2006)
The story of PON1: how an organophosphate-hydrolysing enzyme is becoming a player in cardiovascular medicine
Neth J Med 64: 34

van Tits LJ, van Himbergen TM, Lemmers HL, de Graaf J, Stalenhoef AF (2006)
Proportion of oxidized LDL relative to plasma apolipoprotein B does not change during statin therapy in patients with heterozygous familial hypercholesterolemia
Atherosclerosis 185: 307

van Himbergen TM, Roest M, de Graaf J, Jansen EH, Hattori H, Kastelein JJ, Voorbij HA, Stalenhoef AF, van Tits LJ (2005)
Indications that paraoxonase-1 contributes to plasma high density lipoprotein levels in familial hypercholesterolemia
J Lipid Res 46: 445

van Himbergen TM, van Tits LJ, Hectors MP, de Graaf J, Roest M, Stalenhoef AF (2005)
Paraoxonase-1 and linoleic acid oxidation in familial hypercholesterolemia
Biochemical & Biophysical Research Communications 333: 787

Hoffer MJ, Snieder H, Bredie SJ, Demacker PN, Kastelein JJ, Frants RR, Stalenhoef AF (2000)
The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia
Atherosclerosis 151: 443

Hoffer MJ, Bredie SJ, Snieder H, Reymer PW, Demacker PN, Havekes LM, Boomsma DI, Stalenhoef AF, Frants RR, Kastelein JJ (1998)
Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia
Atherosclerosis 138: 91

Kuivenhoven JA, Stalenhoef AF, Hill JS, Demacker PN, Errami A, Kastelein JJ, Pritchard PH (1996)
Two novel molecular defects in the LCAT gene are associated with fish eye disease
Arterioscler Thromb Vasc Biol 16: 294

Bruin T, Kastelein JJ, Van Diermen DE, Ma Y, Henderson HE, Stuyt PM, Stalenhoef AF, Sturk A, Brunzell JD, Hayden MR (1992)
A missense mutation Pro157 Arg in lipoprotein lipase (LPLNijmegen) resulting in loss of catalytic activity
European Journal of Biochemistry 208: 267