Your search returned the following 7 documents:

7. ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels
   K.Y. Zwarts, Susanne M. Clee, A.H. Zwinderman, J.C. Engert, Roshni Singaraja, O Loubser, E James, Kirsten Roomp, T.J. Hudson, J.W. Jukema, J.J.P. Kastelein, and Michael R. Hayden
   Clinical Genetics 61 (2): 115-125, 2002
   
6. Expression and Functional Analyses of Novel Mutations ot ATP-Binding Cassette Transporter-1 in Japanese Patients with High-Density Lipoprotein Deficiency
   Yoshiharu Nishida, Kenichi Hirano, Kosuke Tsukamoto, Makoto Nagano, Chiaki Ikegami, Kirsten Roomp, Mitsuaki Ishihara, Naoki Sakane, Zhongyan Zhang, Ken-ichi Tsujii, Akifumi Matsuyama, Tohru Ohama, Fumihiko Matsuura, Masato Ishigami, Naohiko Sakai, Hisatoyo Hiraoka, Hiroaki Hattori, Cheryl L. Wellington, Yoshihide Yoshida, Susumu Misugi, Michael R. Hayden, Toru Egashira, Shizuya Yamashita, and Yuji Matsuzawa
   Biochemical and Biophysical Research Communications 290 (2): 713-721, 2002
   
5. Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol
   Cheryl L. Wellington, Yu-Zhou Yang, Stephen Zhou, Susanne M. Clee, Bing Tan, Kenichi Hirano, K.Y. Zwarts, Anita Kwok, Allison Gelfer, Michel Marcil, Scott Newman, Kirsten Roomp, Roshni Singaraja, Jennifer A. Collins, Lin-Hua Zhang, Albert K. Groen, Kees Hovingh, Alison Brownlie, Sherrie Tafuri, Jacques Jr Genest, J.J.P. Kastelein, and Michael R. Hayden
   Journal of Lipid Research 43 (11): 1939-1949, 2002
   
4. Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
   Susanne M. Clee, A.H. Zwinderman, J.C. Engert, K.Y. Zwarts, H.O. Molhuizen, Kirsten Roomp, J.W. Jukema, M van Wijland, M van Dam, T.J. Hudson, A Brooks-Wilson, Jacques Jr Genest, J.J.P. Kastelein, and Michael R. Hayden
   Circulation 103 (9): 1198-205, 2001
   
3. Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
   Susanne M. Clee, J.J.P. Kastelein, M van Dam, Michel Marcil, Kirsten Roomp, K.Y. Zwarts, Jennifer A. Collins, R Roelants, N Tamasawa, T Stulc, T Suda, R Ceska, B Boucher, C Rondeau, C DeSouich, A Brooks-Wilson, H.O. Molhuizen, J Frohlich, Jacques Jr Genest, and Michael R. Hayden
   Journal of Clinical Investigation 106 (10): 1263-70, 2000
   
2. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein
   A Brooks-Wilson, Michel Marcil, Susanne M. Clee, Lin-Hua Zhang, Kirsten Roomp, M van Dam, L Yu, C Brewer, Jennifer A. Collins, H.O. Molhuizen, O Loubser, B.F. Ouelette, K Fichter, K.J. Ashbourne-Excoffon, C.W. Sensen, S Scherer, S Mott, M Denis, D Martindale, J Frohlich, K Morgan, B Koop, S Pimstone, J.J.P. Kastelein, and Michael R. Hayden
   Nature Genetics 22 (4): 336-45, 1999
   
1. Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
   Michel Marcil, A. Brooks-Wilson, Susanne M. Clee, Kirsten Roomp, Lin-Hua Zhang, L. Yu, Jennifer A. Collins, M. van Dam, H. O. Molhuizen, O. Loubser, B. F. Ouelette, C. W. Sensen, K. Fichter, S. Mott, M. Denis, B. Boucher, S. Pimstone, Jacques Genest, J. J. P. Kastelein, and Michael R. Hayden
   The Lancet 354 (9187): 1341-6, 1999