TABLE OF CONTENTS
Volume 14, Issue 1 (January 2006)
News and Commentaries
Cancer Transcriptomics: Modeling metastasis FREE
Sridhar Ramaswamy
Eur J Hum Genet 14: 1-2; advance online publication, November 16, 2005; doi:10.1038/sj.ejhg.5201525
Mouse models: Psoriasis: an epidermal disease after all? FREE
Johann E Gudjonsson and James T Elder
Eur J Hum Genet 14: 2-4; advance online publication, November 16, 2005; doi:10.1038/sj.ejhg.5201543
Letters
Clock genes as a link between addiction and obesity FREE
Hari Manev and Tolga Uz
Eur J Hum Genet 14: 5; advance online publication, November 16, 2005; doi:10.1038/sj.ejhg.5201524
Comment on 'cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy' FREE
Helen M Bottomley, Louise M Downey, Chris F Inglehearn and Carmel Toomes
Eur J Hum Genet 14: 6-7; advance online publication, November 30, 2005; doi:10.1038/sj.ejhg.5201523
Reply to Bottomley et al FREE
Barkur S Shastry and Michael T Trese
Eur J Hum Genet 14: 7-8; advance online publication, November 16, 2005; doi:10.1038/sj.ejhg.5201518
Reviews
A review of international and UK-based ethical guidelines for researchers conducting nontherapeutic genetic studies in developing countries FREE
Shormila Roy Choudhury and Leslie A Knapp
Eur J Hum Genet 14: 9-16; advance online publication, September 21, 2005; doi:10.1038/sj.ejhg.5201497
Genetics of human heterotaxias FREE
Lirong Zhu, John W Belmont and Stephanie M Ware
Eur J Hum Genet 14: 17-25; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201506
Articles
Analysing DNA patents in relation with diagnostic genetic testing FREE
Birgit Verbeure, Gert Matthijs and Geertrui Van Overwalle
Eur J Hum Genet 14: 26-33; advance online publication, October 12, 2005; doi:10.1038/sj.ejhg.5201503
Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects FREE
Eliana Disabella, Maurizia Grasso, Nicola Marziliano, Silvia Ansaldi, Claudia Lucchelli, Emanuele Porcu, Marilena Tagliani, Andrea Pilotto, Marta Diegoli, Luca Lanzarini, Clara Malattia, Antonio Pelliccia, Anna Ficcadenti, Orazio Gabrielli and Eloisa Arbustini
Eur J Hum Genet 14: 34-38; advance online publication, October 12, 2005; doi:10.1038/sj.ejhg.5201502
Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome FREE
Wolfram Kress, Christian Schropp, Gabriele Lieb, Birgit Petersen, Maria Büsse-Ratzka, Jürgen Kunz, Edeltraut Reinhart, Wolf-Dieter Schäfer, Johanna Sold, Florian Hoppe, Jan Pahnke, Andreas Trusen, Niels Sörensen, Jürgen Krauss and Hartmut Collmann
Eur J Hum Genet 14: 39-48; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201507
Improving the accuracy of BRCA1/2 mutation prediction: validation of the novel country-customized IC software FREE
Carlo Capalbo, Enrico Ricevuto, Annarita Vestri, Tina Sidoni, Amelia Buffone, Enrico Cortesi, Paolo Marchetti, Giovanni Scambia, Silverio Tomao, Christian Rinaldi, Massimo Zani, Sergio Ferraro, Luigi Frati, Isabella Screpanti, Alberto Gulino and Giuseppe Giannini
Eur J Hum Genet 14: 49-54; advance online publication, November 16, 2005; doi:10.1038/sj.ejhg.5201511
Genetic background of HSH in three Polish families and a patient with an X;9 translocation FREE
Reetta Jalkanen, Ewa Pronicka, Henna Tyynismaa, Andre Hanauer, Roxanne Walder and Tiina Alitalo
Eur J Hum Genet 14: 55-62; advance online publication, November 2, 2005; doi:10.1038/sj.ejhg.5201515
Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletion FREE
Chiara Pastrello, Silvana Baglioni, Maria Grazia Tibiletti, Laura Papi, Mara Fornasarig, Alberto Morabito, Marco Agostini, Maurizio Genuardi and Alessandra Viel
Eur J Hum Genet 14: 63-68; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201517
Haplotype analysis of tumour necrosis factor receptor genes in 1p36: no evidence for association with systemic lupus erythematosus FREE
Sapna Chadha, Katie Miller, Lisa Farwell, Steven Sacks, Mark J Daly, John D Rioux and Timothy J Vyse
Eur J Hum Genet 14: 69-78; advance online publication, November 23, 2005; doi:10.1038/sj.ejhg.5201527
Evidence of genetic enrichment for exceptional survival using a family approach: the Leiden Longevity Study FREE
Manja Schoenmaker, Anton J M de Craen, Paul H E M de Meijer, Marian Beekman, Gerard J Blauw, P Eline Slagboom and Rudi G J Westendorp
Eur J Hum Genet 14: 79-84; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201508
Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations FREE
Fiorenza Pompei, Bianca Maria Ciminelli, Cristina Bombieri, Cinzia Ciccacci, Monika Koudova, Silvia Giorgi, Francesca Belpinati, Angela Begnini, Milos Cerny, Marie Des Georges, Mireille Claustres, Claude Ferec, Milan Macek Jr, Guido Modiano and Pier Franco Pignatti
Eur J Hum Genet 14: 85-93; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201498
Association of 
2 adrenergic receptor polymorphisms and related haplotypes with triglyceride and LDL-cholesterol levels FREE
Antonio Petrone, Sara Zavarella, Gianluca Iacobellis, Simona Zampetti, Andrea Vania, Sergio Di Pietro, Andrea Galgani, Frida Leonetti, Umberto Di Mario and Raffaella Buzzetti
Eur J Hum Genet 14: 94-100; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201521
Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin FREE
Chad Garner, Steve Best, Stephan Menzel, Helen Rooks, Tim D Spector and Swee Lay Thein
Eur J Hum Genet 14: 101-108; advance online publication, October 12, 2005; doi:10.1038/sj.ejhg.5201499
Replication of IGF2-INS-TH *5 haplotype effect on obesity in older men and study of related phenotypes FREE
Santiago Rodríguez, Tom R Gaunt, Elaine Dennison, Xiao-he Chen, Holly E Syddall, David I W Phillips, Cyrus Cooper and Ian N M Day
Eur J Hum Genet 14: 109-116; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201505
Genome-wide linkage scan for spontaneous DZ twinning FREE
Catherine Derom, Damini Jawaheer, Wei V Chen, Kim L McBride, Xiangli Xiao, Chris Amos, Peter K Gregersen and Robert Vlietinck
Eur J Hum Genet 14: 117-122; advance online publication, November 16, 2005; doi:10.1038/sj.ejhg.5201522
Short Reports
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample FREE
Francesca Blasi, Elena Bacchelli, Simona Carone, Claudio Toma, Anthony P Monaco, Anthony J Bailey, Elena Maestrini and and the International Molecular Genetic Study of Autism Consortium (IMGSAC)
Eur J Hum Genet 14: 123-126; advance online publication, October 5, 2005; doi:10.1038/sj.ejhg.5201444
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease FREE
Elisabetta Trabetti, Michele Biscuola, Ugo Cavallari, Giovanni Malerba, Domenico Girelli, Oliviero Olivieri, Nicola Martinelli, Roberto Corrocher and Pier Franco Pignatti
Eur J Hum Genet 14: 127-130; advance online publication, October 26, 2005; doi:10.1038/sj.ejhg.5201513
