TABLE OF CONTENTS
Volume 13, Issue 9 (September 2005)
News and Commentaries
Gene Expression: Growing up together may help genes go their separate ways FREE
Vania Parelho and Matthias Merkenschlager
Eur J Hum Genet 13: 993-994; advance online publication, July 6, 2005; doi:10.1038/sj.ejhg.5201464
Research Networks: BioSapiens: a European network for integrated genome annotation FREE
The BioSapiens Network of Excellence
Eur J Hum Genet 13: 994-997; advance online publication, July 13, 2005; doi:10.1038/sj.ejhg.5201470
Letter
Ultraconserved regions in multiple sclerosis FREE
Maria Ban, Mel Maranian, Tai Wai Yeo, Julia Gray, Alastair Compston and Stephen Sawcer
Eur J Hum Genet 13: 998-999; advance online publication, June 29, 2005; doi:10.1038/sj.ejhg.5201457
Articles
Estrogen receptor beta gene variants are associated with increased risk of Alzheimer's disease in women FREE
Mia Pirskanen, Mikko Hiltunen, Arto Mannermaa, Seppo Helisalmi, Maarit Lehtovirta, Tuomo Hänninen and Hilkka Soininen
Eur J Hum Genet 13: 1000-1006; advance online publication, June 8, 2005; doi:10.1038/sj.ejhg.5201447
Combining the case–control methodology with the small size transmission/disequilibrium test for multiallelic markers FREE
Wei Guo and Wing K Fung
Eur J Hum Genet 13: 1007-1012; advance online publication, June 15, 2005; doi:10.1038/sj.ejhg.5201453
Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver–Russell syndrome FREE
Elisabeth Flori, Emmanuelle Girodon, Brigitte Samama, François Becmeur, Brigitte Viville, Françoise Girard-Lemaire, Bérénice Doray, Caroline Schluth, Luc Marcellin, Nelly Boehm, Michel Goossens and Véronique Pingault
Eur J Hum Genet 13: 1013-1018; advance online publication, May 25, 2005; doi:10.1038/sj.ejhg.5201442
Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation FREE
David A Koolen, William Reardon, Elisabeth M Rosser, Didier Lacombe, Jane A Hurst, Caroline J Law, Ernie M H F Bongers, Conny M van Ravenswaaij-Arts, Martijn A R Leisink, Ad Geurts van Kessel, Joris A Veltman and Bert B A de Vries
Eur J Hum Genet 13: 1019-1024; advance online publication, June 29, 2005; doi:10.1038/sj.ejhg.5201456
Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome FREE
Wendy N Cooper, Anita Luharia, Gail A Evans, Hussain Raza, Antonita C Haire, Richard Grundy, Sarah C Bowdin, Andrea Riccio, Gianfranco Sebastio, Jet Bliek, Paul N Schofield, Wolf Reik, Fiona Macdonald and Eamonn R Maher
Eur J Hum Genet 13: 1025-1032; advance online publication, July 6, 2005; doi:10.1038/sj.ejhg.5201463
Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties FREE
David Geneviève, Damien Sanlaville, Laurence Faivre, Marie-Laure Kottler, Marguerite Jambou, Philippe Gosset, Dinane Boustani-Samara, Graziella Pinto, Catherine Ozilou, Geneviève Abeguilé, Arnold Munnich, Serge Romana, Odile Raoul, Valérie Cormier-Daire and Michel Vekemans
Eur J Hum Genet 13: 1033-1039; advance online publication, May 25, 2005; doi:10.1038/sj.ejhg.5201448
Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotype FREE
Elisabet Ars, Bárbara Tazón-Vega, Patricia Ruiz, Carme Nogués, Núria Arnedo, Osvaldo Rajmil and Roser Torra
Eur J Hum Genet 13: 1040-1046; advance online publication, June 15, 2005; doi:10.1038/sj.ejhg.5201452
Nondisease genetic testing: reporting of muscle SNPs shows effects on self-concept and health orientation scales FREE
Erynn S Gordon, Heather A Gordish-Dressman, Joseph Devaney, Priscilla Clarkson, Paul Thompson, Paul Gordon, Linda S Pescatello, Monica J Hubal, Emidio E Pistilli, Gary Gianetti, Bethany Kelsey and Eric P Hoffman
Eur J Hum Genet 13: 1047-1054; advance online publication, June 8, 2005; doi:10.1038/sj.ejhg.5201449
Communication of pharmacogenetic research results to HIV-infected treated patients: standpoints of professionals and patients FREE
Grégoire Moutel, Nathalie Duchange, François Raffi, Lama I Sharara, Ioannis Théodorou, Violaine Noël, Sandrine de Montgolfier, Ingrid Callies, François Bricaire, Christian Hervé, Catherine Leport and the APROCO-COPILOTE Study Group
Eur J Hum Genet 13: 1055-1062; advance online publication, June 15, 2005; doi:10.1038/sj.ejhg.5201450
Pedigree construction and disease confirmation: a pilot study in Wales exploring the role of nonclinical personnel FREE
Vanessa Tempest, Rachel Iredale, Jonathon Gray, Liz France, Sally Anstey and John Steward
Eur J Hum Genet 13: 1063-1070; advance online publication, June 15, 2005; doi:10.1038/sj.ejhg.5201454
Potential harms, anonymization, and the right to withdraw consent to biobank research FREE
Stefan Eriksson and Gert Helgesson
Eur J Hum Genet 13: 1071-1076; advance online publication, June 29, 2005; doi:10.1038/sj.ejhg.5201458
Partners of mutation-carriers for Huntington's disease: forgotten persons? FREE
Marleen Decruyenaere, Gerry Evers-Kiebooms, Andrea Boogaerts, Koen Demyttenaere, René Dom and Jean-Pierre Fryns
Eur J Hum Genet 13: 1077-1085; advance online publication, July 6, 2005; doi:10.1038/sj.ejhg.5201462
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism FREE
Christine Klein, Ana Djarmati, Katja Hedrich, Nora Schäfer, Cesa Scaglione, Roberta Marchese, Norman Kock, Birgitt Schüle, Anja Hiller, Thora Lohnau, Susen Winkler, Karin Wiegers, Robert Hering, Peter Bauer, Olaf Riess, Giovanni Abbruzzese, Paolo Martinelli and Peter P Pramstaller
Eur J Hum Genet 13: 1086-1093; advance online publication, June 22, 2005; doi:10.1038/sj.ejhg.5201455
Short Report
Polymorphism at 3' UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease FREE
Byung-Hoon Jeong, Nam-Ho Kim, Eun-Kyoung Choi, Chaeyoung Lee, Young-Han Song, Jae-Il Kim, Richard I Carp and Yong-Sun Kim
Eur J Hum Genet 13: 1094-1097; advance online publication, June 29, 2005; doi:10.1038/sj.ejhg.5201460
