TABLE OF CONTENTS
Volume 15, Issue 6 (June 2007)
News and Commentary
TNF Polymorphism and Cardiovascular Disease: TNF gene polymorphism and quantitative traits related to cardiovascular disease: getting to the heart of the matter FREE
George D Mellick
Eur J Hum Genet 15: 609-611; advance online publication, March 21, 2007; doi:10.1038/sj.ejhg.5201816
Articles
Communicating genetic information in families – a review of guidelines and position papers FREE
Laura E Forrest, Martin B Delatycki, Loane Skene and MaryAnne Aitken
Eur J Hum Genet 15: 612-618; advance online publication, March 28, 2007; doi:10.1038/sj.ejhg.5201822
Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic review FREE
Ansgar Gerhardus, Henriette Schleberger, Brigitte Schlegelberger and Dorothea Gadzicki
Eur J Hum Genet 15: 619-627; advance online publication, March 7, 2007; doi:10.1038/sj.ejhg.5201806
Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females FREE
Nisa K Renault, Sarah Dyack, Melanie J Dobson, Teresa Costa, Wan L Lam and Wenda L Greer
Eur J Hum Genet 15: 628-637; advance online publication, March 7, 2007; doi:10.1038/sj.ejhg.5201799
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia FREE
Eva Morava, Renate Zeevaert, Eckhard Korsch, Karin Huijben, Suzan Wopereis, Gert Matthijs, Kathelijn Keymolen, Dirk J Lefeber, Linda De Meirleir and Ron A Wevers
Eur J Hum Genet 15: 638-645; advance online publication, March 14, 2007; doi:10.1038/sj.ejhg.5201813
Glycerol kinase deficiency alters expression of genes involved in lipid metabolism, carbohydrate metabolism, and insulin signaling FREE
Lola Rahib, Nicole K MacLennan, Steve Horvath, James C Liao and Katrina M Dipple
Eur J Hum Genet 15: 646-657; advance online publication, April 4, 2007; doi:10.1038/sj.ejhg.5201801
Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation FREE
Laura Torres-Juan, Jordi Rosell, Montse Morla, Catalina Vidal-Pou, Fernando García-Algas, Maria-Angeles de la Fuente, Miguel Juan, Albert Tubau, Daniel Bachiller, Marta Bernues, Angeles Perez-Granero, Nancy Govea, Xavier Busquets and Damian Heine-Suñer
Eur J Hum Genet 15: 658-663; advance online publication, March 21, 2007; doi:10.1038/sj.ejhg.5201819
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families FREE
Linda Köhn, Konstantin Kadzhaev, Marie S I Burstedt, Susann Haraldsson, Bengt Hallberg, Ola Sandgren and Irina Golovleva
Eur J Hum Genet 15: 664-671; advance online publication, March 21, 2007; doi:10.1038/sj.ejhg.5201817
Does apolipoprotein E determine outcome of infection by varicella zoster virus and by Epstein Barr virus? FREE
Matthew A Wozniak, Suzanne J Shipley, Curtis B Dobson, Simon P Parker, Fiona T Scott, Mary Leedham-Green, Judy Breuer and Ruth F Itzhaki
Eur J Hum Genet 15: 672-678; advance online publication, March 14, 2007; doi:10.1038/sj.ejhg.5201812
Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels FREE
Thomas M Barber, Amanda J Bennett, Anna L Gloyn, Christopher J Groves, Ulla Sovio, Aimo Ruokonen, Hannu Martikainen, Anneli Pouta, Saara Taponen, Michael N Weedon, Anna-Liisa Hartikainen, John A H Wass, Marjo-Riitta Järvelin, Eleftheria Zeggini, Stephen Franks and Mark I McCarthy
Eur J Hum Genet 15: 679-684; advance online publication, March 7, 2007; doi:10.1038/sj.ejhg.5201802
Phenotype selection for detecting variable genes: a survey of cardiovascular quantitative traits and TNF locus polymorphism FREE
Mun-Gwan Hong, Anna M Bennet, Ulf de Faire and Jonathan A Prince
Eur J Hum Genet 15: 685-693; advance online publication, March 14, 2007; doi:10.1038/sj.ejhg.5201803
The use of grid computing to drive data-intensive genetic research FREE
Jorge Andrade, Malin Andersen, Anna Sillén, Caroline Graff and Jacob Odeberg
Eur J Hum Genet 15: 694-702; advance online publication, March 21, 2007; doi:10.1038/sj.ejhg.5201815
Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method FREE
Jane Hermanowski, Emmanuelle Bouzigon, Paola Forabosco, Mandy Y Ng, Sheila A Fisher and Cathryn M Lewis
Eur J Hum Genet 15: 703-710; advance online publication, March 21, 2007; doi:10.1038/sj.ejhg.5201818
Short Report
Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome FREE
Jose M Belloso, Iben Bache, Miriam Guitart, Maria Rosa Caballin, Christina Halgren, Maria Kirchhoff, Hans-Hilger Ropers, Niels Tommerup and Zeynep Tümer
Eur J Hum Genet 15: 711-713; advance online publication, March 28, 2007; doi:10.1038/sj.ejhg.5201824
Erratum
A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p FREE
Sreekumar G Pillai, Mathias N Chiano, Nicola J White, Marcy Speer, Kathleen C Barnes, Karin Carlsen, Jorrit Gerritsen, Peter Helms, Warren Lenney, Michael Silverman, Peter Sly, John Sundy, John Tsanakas, Andrea von Berg, Moira Whyte, Shela Varsani, Paul Skelding, Michael Hauser, Jeffery Vance, Margaret Pericak-Vance, Daniel K Burns, Lefkos T Middleton, Shyama R Brewster, Wayne H Anderson and John H Riley
Eur J Hum Genet 15: 714; doi:10.1038/sj.ejhg.5201840
