TABLE OF CONTENTS
Volume 17, Issue 7 (July 2009)
News and Commentary
Breast cancer susceptibility genes analysed into three groups
Genomics and breast cancer: the different levels of inherited susceptibility FREE
Andrew D Beggs and Shirley V Hodgson
Eur J Hum Genet 17: 855-856; advance online publication, December 17, 2008; doi:10.1038/ejhg.2008.235
Viewpoint
Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing
Christine Patch, Jorge Sequeiros and Martina C Cornel
Eur J Hum Genet 17: 857-859; advance online publication, March 4, 2009; doi:10.1038/ejhg.2008.246
Practical Genetics
Hereditary haemorrhagic telangiectasia: a clinical and scientific review FREE
Fatima S Govani and Claire L Shovlin
Eur J Hum Genet 17: 860-871; advance online publication, April 1, 2009; doi:10.1038/ejhg.2009.35
Review
Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information
Gillian Nycum, Denise Avard and Bartha M Knoppers
Eur J Hum Genet 17: 872-880; advance online publication, March 25, 2009; doi:10.1038/ejhg.2009.33
Letters
Angioma serpiginosum is not caused by PORCN mutations
Rudolf Happle
Eur J Hum Genet 17: 881-882; advance online publication, April 1, 2009; doi:10.1038/ejhg.2009.55
Reply to Happle
Gunnar Houge and Raoul C M Hennekam
Eur J Hum Genet 17: 882; advance online publication, April 1, 2009; doi:10.1038/ejhg.2009.49
Articles
Personal genomics services: whose genomes?
David Gurwitz and Yael Bregman-Eschet
Eur J Hum Genet 17: 883-889; advance online publication, March 4, 2009; doi:10.1038/ejhg.2008.254
An international external quality assessment for molecular diagnosis of hereditary recurrent fevers: a 3-year scheme demonstrates the need for improvement
I Touitou, C Rittore, L Philibert, J Yagüe, Y Shinar and I Aksentijevich
Eur J Hum Genet 17: 890-896; advance online publication, January 28, 2009; doi:10.1038/ejhg.2008.253
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses
Antonino Forabosco, Antonio Percesepe and Sandra Santucci
Eur J Hum Genet 17: 897-903; advance online publication, January 21, 2009; doi:10.1038/ejhg.2008.265
An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion
Helle Lybæk, Karen Helene ørstavik, Trine Prescott, Randi Hovland, Harald Breilid, Christine Stansberg, Vidar Martin Steen and Gunnar Houge
Eur J Hum Genet 17: 904-910; advance online publication, January 21, 2009; doi:10.1038/ejhg.2008.261
Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia
Eden V Haverfield, Amanda J Whited, Kristin S Petras, William B Dobyns and Soma Das
Eur J Hum Genet 17: 911-918; advance online publication, December 3, 2008; doi:10.1038/ejhg.2008.213
Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome
Laura Giunti, Valentina Cetica, Ugo Ricci, Sabrina Giglio, Iacopo Sardi, Milena Paglierani, Elena Andreucci, Massimiliano Sanzo, Marco Forni, Anna Maria Buccoliero, Lorenzo Genitori and Maurizio Genuardi
Eur J Hum Genet 17: 919-927; advance online publication, January 21, 2009; doi:10.1038/ejhg.2008.271
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging
Sofia Rodriguez, Fabio Coppedè, Hanna Sagelius and Maria Eriksson
Eur J Hum Genet 17: 928-937; advance online publication, January 28, 2009; doi:10.1038/ejhg.2008.270
The complex interaction between APOE promoter and AD: an Italian case–control study
Alessandra Bizzarro, Davide Seripa, Adele Acciarri, Maria Giovanna Matera, Alberto Pilotto, Francesco Danilo Tiziano, Christina Brahe and Carlo Masullo
Eur J Hum Genet 17: 938-945; advance online publication, January 28, 2009; doi:10.1038/ejhg.2008.263
Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis
Anna C Need, Richard SE Keefe, Dongliang Ge, Iris Grossman, Sam Dickson, Joseph P McEvoy and David B Goldstein
Eur J Hum Genet 17: 946-957; advance online publication, January 21, 2009; doi:10.1038/ejhg.2008.264
Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population
Najaf Amin, Yuri S Aulchenko, Marieke C Dekker, Robert F Ferdinand, Alwin van Spreeken, Alfons H Temmink, Frank C Verhulst, Ben A Oostra and Cornelia M van Duijn
Eur J Hum Genet 17: 958-966; advance online publication, January 21, 2009; doi:10.1038/ejhg.2008.260
An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population
Timothy Tehua Lu, Oscar Lao, Michael Nothnagel, Olaf Junge, Sandra Freitag-Wolf, Amke Caliebe, Miroslava Balascakova, Jaume Bertranpetit, Laurence Albert Bindoff, David Comas, Gunilla Holmlund, Anastasia Kouvatsi, Milan Macek, Isabelle Mollet, Finn Nielsen, Walther Parson, Jukka Palo, Rafal Ploski, Antti Sajantila, Adriano Tagliabracci, Ulrik Gether, Thomas Werge, Fernando Rivadeneira, Albert Hofman, André Gerardus Uitterlinden, Christian Gieger, Heinz-Erich Wichmann, Andreas Ruether, Stefan Schreiber, Christian Becker, Peter Nürnberg, Matthew Roberts Nelson, Manfred Kayser and Michael Krawczak
Eur J Hum Genet 17: 967-975; advance online publication, January 21, 2009; doi:10.1038/ejhg.2008.266
