Authors: Clee, SM Zwinderman, AH Engert, JC Zwarts, KY Molhuizen, HOF Roomp, K Jukema, JW van Wijland, M van Dam, M Hudson, TJ Brooks-Wilson, A Genest, J Kastelein, JJ Hayden, MR

Citation: Sm. Clee et al., Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease, CIRCULATION, 103(9), 2001, pp. 1198-1205

Authors: Ayyobi, AF Lacko, AG Murray, K Nair, M Li, M Molhuizen, HOF Pritchard, PH

Citation: Af. Ayyobi et al., Biochemical and compositional analyses of recombinant lecithin : cholesterol acyltransferase (LCAT) obtained from a hepatic source, BBA-MOL C B, 1484(1), 2000, pp. 1-13

Authors: Clee, SM Kastelein, JJP van Dam, M Marcil, M Roomp, K Zwarts, KY Collins, JA Roelants, R Tamasawa, N Stulc, T Suda, T Ceska, R Boucher, B Rondeau, C DeSouich, C Brooks-Wilson, A Molhuizen, HOF Frohlich, J Genest, J Hayden, MR

Citation: Sm. Clee et al., Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes, J CLIN INV, 106(10), 2000, pp. 1263-1270

Authors: Brooks-Wilson, A Marcil, M Clee, SM Zhang, LH Roomp, K van Dam, M Yu, L Brewer, C Collins, JA Molhuizen, HOF Loubser, O Ouelette, BFF Fichter, K Ashbourne-Excoffon, KJD Sensen, CW Scherer, S Mott, S Denis, M Martindale, D Frohlich, J Morgan, K Koop, B Pimstone, S Kastelein, JJP Genest, J Hayden, MR

Citation: A. Brooks-wilson et al., Mutations in ABC1 in Tangier disease and familial high-density lipoproteindeficiency, NAT GENET, 22(4), 1999, pp. 336-345

Authors: Marcil, M Brooks-Wilson, A Clee, SM Roomp, K Zhang, LH Yu, L Collins, JA van Dam, M Molhuizen, HOF Loubster, O Ouellette, BFF Sensen, CW Fichter, K Mott, S Denis, M Boucher, B Pimstone, S Genest, J Kastelein, JJP Hayden, MR

Citation: M. Marcil et al., Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux, LANCET, 354(9187), 1999, pp. 1341-1346