TABLE OF CONTENTS
Volume 14, Issue 6 (June 2006)
Editorial
Focus on behavioural genetics FREE
Jonathan Flint and Anthony P Monaco
Eur J Hum Genet 14: 647-648; doi:10.1038/sj.ejhg.5201599
News and Commentary
Huntington's Disease: A transcriptional report card from the peripheral blood: Can it measure disease progression in Huntington's disease? FREE
Adel Tabchy and David Housman
Eur J Hum Genet 14: 649-650; advance online publication, March 15, 2006; doi:10.1038/sj.ejhg.5201562
Reviews
The role of mutagenesis in defining genes in behaviour FREE
Sofia I H Godinho and Patrick M Nolan
Eur J Hum Genet 14: 651-659; doi:10.1038/sj.ejhg.5201545
Genetics of affective (mood) disorders FREE
Nick Craddock and Liz Forty
Eur J Hum Genet 14: 660-668; doi:10.1038/sj.ejhg.5201549
Molecular genetic studies of schizophrenia FREE
Brien Riley and Kenneth S Kendler
Eur J Hum Genet 14: 669-680; doi:10.1038/sj.ejhg.5201571
The genetics of developmental dyslexia FREE
Julie Williams and Michael C O'Donovan
Eur J Hum Genet 14: 681-689; doi:10.1038/sj.ejhg.5201575
Genetics of intelligence FREE
Ian J Deary, Frank M Spinath and Timothy C Bates
Eur J Hum Genet 14: 690-700; doi:10.1038/sj.ejhg.5201588
Genetics and pathophysiology of mental retardation FREE
Jamel Chelly, Malik Khelfaoui, Fiona Francis, Beldjord Chérif and Thierry Bienvenu
Eur J Hum Genet 14: 701-713; doi:10.1038/sj.ejhg.5201595
Genetics of autism spectrum disorder FREE
Sabine M Klauck
Eur J Hum Genet 14: 714-720; doi:10.1038/sj.ejhg.5201610
The genetic basis of emotional behaviour in mice FREE
Saffron A G Willis-Owen and Jonathan Flint
Eur J Hum Genet 14: 721-728; doi:10.1038/sj.ejhg.5201569
Molecular genetics of the fruit-fly circadian clock FREE
Ezio Rosato, Eran Tauber and Charalambos P Kyriacou
Eur J Hum Genet 14: 729-738; doi:10.1038/sj.ejhg.5201547
Articles
Deletions of 2q14 that include the homeobox engrailed 1 (EN1) transcription factor are compatible with a normal phenotype FREE
John C K Barber, Viv K Maloney, Beverley Bewes and Emma Wakeling
Eur J Hum Genet 14: 739-743; advance online publication, March 22, 2006; doi:10.1038/sj.ejhg.5201605
Molecular analysis of a human PAX6 homeobox mutant FREE
Angela Valentina D'elia, Cinzia Puppin, Lucia Pellizzari, Annalisa Pianta, Elisa Bregant, Renata Lonigro, Gianluca Tell, Federico Fogolari, Veronica van Heyningen and Giuseppe Damante
Eur J Hum Genet 14: 744-751; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201579
Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15 FREE
Corinna Zogel, Stefan Böhringer, Stephanie Gro
, Raymonda Varon, Karin Buiting and Bernhard Horsthemke
Eur J Hum Genet 14: 752-758; advance online publication, April 5, 2006; doi:10.1038/sj.ejhg.5201602
Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome FREE
Richard Redon, Geneviève Baujat, Damien Sanlaville, Martine Le Merrer, Michel Vekemans, Arnold Munnich, Nigel P Carter, Valérie Cormier-Daire and Laurence Colleaux
Eur J Hum Genet 14: 759-767; advance online publication, March 29, 2006; doi:10.1038/sj.ejhg.5201613
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population FREE
Anne Parle-McDermott, Peadar N Kirke, James L Mills, Anne M Molloy, Christopher Cox, Valerie B O'Leary, Faith Pangilinan, Mary Conley, Laura Cleary, Lawrence C Brody and John M Scott
Eur J Hum Genet 14: 768-772; advance online publication, March 22, 2006; doi:10.1038/sj.ejhg.5201603
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations FREE
Sébastien Albert, Hélène Blons, Laurence Jonard, Delphine Feldmann, Pierre Chauvin, Nathalie Loundon, Annie Sergent-Allaoui, Muriel Houang, Alain Joannard, Sébastien Schmerber, Bruno Delobel, Jacques Leman, Hubert Journel, Hélène Catros, Hélène Dollfus, Marie-Madeleine Eliot, Albert David, Catherine Calais, Valérie Drouin-Garraud, Marie-Françoise Obstoy, Patrice Tran Ba Huy, Didier Lacombe, Françoise Duriez, Christine Francannet, Pierre Bitoun, Christine Petit, Eréa-Noël Garabédian, Rémy Couderc, Sandrine Marlin and Françoise Denoyelle
Eur J Hum Genet 14: 773-779; advance online publication, March 29, 2006; doi:10.1038/sj.ejhg.5201611
Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19 FREE
Marcela Karey Tello-Ruiz, Christine Curley, Terrye DelMonte, Cosmas Giallourakis, Andrew Kirby, Kathryn Miller, Gary Wild, Albert Cohen, Diane Langelier, Anna Latiano, Neils Wedemeyer, Eric Lander, Stefan Schreiber, Vito Annese, Mark J Daly and John D Rioux
Eur J Hum Genet 14: 780-790; advance online publication, March 29, 2006; doi:10.1038/sj.ejhg.5201612
Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity FREE
Tayfun Ozcelik, Elif Uz, Cemaliye B Akyerli, Sevgi Bagislar, Chigdem A Mustafa, Alptekin Gursoy, Nurten Akarsu, Gokce Toruner, Nuri Kamel and Sevim Gullu
Eur J Hum Genet 14: 791-797; advance online publication, April 5, 2006; doi:10.1038/sj.ejhg.5201614
