Table of contents

Original articles

• Large scale replication analysis of loci associated with lipid concentrations in a Japanese population (11 March, 2009)

  K Nakayama, T Bayasgalan, K Yamanaka, M Kumada, T Gotoh, N Utsumi, Y Yanagisawa, M Okayama, E Kajii, S Ishibashi, S Iwamoto, The Jichi Community Genetics Team (JCOG)
• Parkin and PINK1 mutations in early-onset Parkinson’s disease: comprehensive screening in publicly available cases and control

  (6 April, 2009)

  J Brooks, J Ding, J Simon-Sanchez, C Paisan-Ruiz, A B Singleton, S W Scholz
• Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders (15 March, 2009)

  S Ben-Shachar, B Lanpher, J R German, M Qasaymeh, L Potocki, S C Sreenath Nagamani, L M Franco, A Malphrus, G W Bottenfield, J E Spence, S Amato, J A Rousseau, B Moghaddam, C Skinner, S A Skinner, S Bernes, N Armstrong, M Shinawi, P Stankiewicz, A Patel, S-W Cheung, J R Lupski, A L Beaudet, T Sahoo
• Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function

  (2 April, 2009) Free

  F Lacbawan, B D Solomon, E Roessler, K El-Jaick, S Domené, J I Vélez, N Zhou, D Hadley, J Z Balog, R Long, A Fryer, W Smith, S Omar, S D McLean, K Clarkson, A Lichty, N J Clegg, M R Delgado, E Levey, E Stashinko, L Potocki, M I VanAllen, J Clayton-Smith, D Donnai, D W Bianchi, P B Juliusson, P R Njølstad, H G Brunner, J C Carey, U Hehr, J Müsebeck, P F Wieacker, A Postra, R C M Hennekam, M-J H van den Boogaard, A van Haeringen, A Paulussen, J Herbergs, C T R M Schrander-Stumpel, A R Janecke, D Chitayat, J Hahn, D M McDonald-McGinn, E H Zackai, W B Dobyns, M Muenke