TABLE OF CONTENTS
Volume 15, Issue 3 (March 2007)
Viewpoint |
Practical Genetics |
Review |
Articles |
Short Reports |
Corrigendum
News and Commentary
Cystic Fibrosis: Cystic fibrosis and lactase persistence: a possible correlation FREE
Guido Modiano, Bianca M Ciminelli and Pier F Pignatti
Eur J Hum Genet 15: 255-259; advance online publication, December 20, 2006; doi:10.1038/sj.ejhg.5201749
Viewpoint
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases? FREE
Catherine Bourgain, Emmanuelle Génin, Nancy Cox and Françoise Clerget-Darpoux
Eur J Hum Genet 15: 260-263; advance online publication, December 13, 2006; doi:10.1038/sj.ejhg.5201753
Practical Genetics
Sotos syndrome FREE
Katrina Tatton-Brown and Nazneen Rahman
Eur J Hum Genet 15: 264-271; advance online publication, September 13, 2006; doi:10.1038/sj.ejhg.5201686
Review
Multiple mutations responsible for frequent genetic diseases in isolated populations FREE
Joël Zlotogora
Eur J Hum Genet 15: 272-278; advance online publication, January 10, 2007; doi:10.1038/sj.ejhg.5201760
Articles
Dopamine transporter, gender, and number of sexual partners among young adults FREE
Guang Guo, Yuying Tong, Cui-Wei Xie and Leslie A Lange
Eur J Hum Genet 15: 279-287; advance online publication, January 24, 2007; doi:10.1038/sj.ejhg.5201763
Africans in Yorkshire? The deepest-rooting clade of the Y phylogeny within an English genealogy FREE
Turi E King, Emma J Parkin, Geoff Swinfield, Fulvio Cruciani, Rosaria Scozzari, Alexandra Rosa, Si-Keun Lim, Yali Xue, Chris Tyler-Smith and Mark A Jobling
Eur J Hum Genet 15: 288-293; advance online publication, January 24, 2007; doi:10.1038/sj.ejhg.5201771
Haplotypes in the human Foxo1a and Foxo3a genes; impact on disease and mortality at old age FREE
Maris Kuningas, Reedik Mägi, Rudi G J Westendorp, P Eline Slagboom, Maido Remm and Diana van Heemst
Eur J Hum Genet 15: 294-301; advance online publication, January 24, 2007; doi:10.1038/sj.ejhg.5201766
Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations FREE
Sheng Gu, Andrew J Pakstis, Hui Li, William C Speed, Judith R Kidd and Kenneth K Kidd
Eur J Hum Genet 15: 302-312; advance online publication, January 3, 2007; doi:10.1038/sj.ejhg.5201751
Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia FREE
Jérémie Nsengimana, Nilesh J Samani, Alistair S Hall, Anthony J Balmforth, Massimo Mangino, Nadira Yuldasheva, Azhar Maqbool, Peter Braund, Paul Burton, D Timothy Bishop, Stephen G Ball and Jennifer H Barrett for the British Heart Foundation Family Heart Study Research Group
Eur J Hum Genet 15: 313-319; advance online publication, December 6, 2006; doi:10.1038/sj.ejhg.5201752
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases FREE
Christopher G Bell, David Meyre, Enrico Petretto, Claire Levy-Marchal, Serge Hercberg, Marie Aline Charles, Cliona Boyle, Jacques Weill, Maïte Tauber, Charles A Mein, Timothy J Aitman, Philippe Froguel and Andrew J Walley
Eur J Hum Genet 15: 320-327; advance online publication, December 13, 2006; doi:10.1038/sj.ejhg.5201754
Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease FREE
Mark S Silverberg, Richard H Duerr, Steven R Brant, Gillian Bromfield, Lisa W Datta, Niraj Jani, Sunanda V Kane, Jerome I Rotter, L Philip Schumm, A Hillary Steinhart, Kent D Taylor, Huiying Yang, Judy H Cho, John D Rioux and Mark J Daly of the NIDDK IBD Genetics Consortium
Eur J Hum Genet 15: 328-335; advance online publication, January 10, 2007; doi:10.1038/sj.ejhg.5201756
Association of PDCD1 polymorphisms with childhood-onset systemic lupus erythematosus FREE
Rafael Velázquez-Cruz, Lorena Orozco, Francisco Espinosa-Rosales, Roberto Carreño-Manjarrez, Eunice Solís-Vallejo, Norma D López-Lara, Ivon K Ruiz-López, Ana L Rodríguez-Lozano, Jesús K Estrada-Gil, Gerardo Jiménez-Sánchez and Vicente Baca
Eur J Hum Genet 15: 336-341; advance online publication, January 17, 2007; doi:10.1038/sj.ejhg.5201767
TCF7L2 polymorphisms are associated with type 2 diabetes in northern Sweden FREE
Sofia Mayans, Kurt Lackovic, Petter Lindgren, Karin Ruikka, Åsa Ågren, Mats Eliasson and Dan Holmberg
Eur J Hum Genet 15: 342-346; advance online publication, January 24, 2007; doi:10.1038/sj.ejhg.5201773
Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3 FREE
Ksenija Fumi
, Robert Belu
i, Mario 
uk, Tea Pavkov, Doris Kloor, Ivo Bari, Ivana Miji and Oliver Vugrek
Eur J Hum Genet 15: 347-351; advance online publication, December 13, 2006; doi:10.1038/sj.ejhg.5201757
Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human FREE
Elke Geuns, Nele De Temmerman, Pierre Hilven, André Van Steirteghem, Inge Liebaers and Martine De Rycke
Eur J Hum Genet 15: 352-361; advance online publication, January 10, 2007; doi:10.1038/sj.ejhg.5201759
A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1 FREE
Melissa Thys, Kris Van Den Bogaert, Vassiliki Iliadou, Kathleen Vanderstraeten, Nele Dieltjens, Isabelle Schrauwen, Wenjie Chen, Nikolaos Eleftheriades, Maria Grigoriadou, Robert Jan Pauw, Cor R W J Cremers, Richard J H Smith, Michael B Petersen and Guy Van Camp
Eur J Hum Genet 15: 362-368; advance online publication, January 10, 2007; doi:10.1038/sj.ejhg.5201761
Progranulin mutations in Dutch familial frontotemporal lobar degeneration FREE
Iraad F Bronner, Patrizia Rizzu, Harro Seelaar, Saskia E van Mil, Burcu Anar, Asma Azmani, Laura Donker Kaat, Sonia Rosso, Peter Heutink and John C van Swieten
Eur J Hum Genet 15: 369-374; advance online publication, January 17, 2007; doi:10.1038/sj.ejhg.5201772
Short Reports
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation FREE
Wei Chen, Lars R Jensen, Jozef Gecz, Jean-Pierre Fryns, Claude Moraine, Arjan de Brouwer, Jamel Chelly, Bettina Moser, H Hilger Ropers and Andreas W Kuss
Eur J Hum Genet 15: 375-378; advance online publication, December 20, 2006; doi:10.1038/sj.ejhg.5201758
FGF10 missense mutations in aplasia of lacrimal and salivary glands (ALSG) FREE
Miriam Entesarian, Johanna Dahlqvist, Vandana Shashi, Christy S Stanley, Babak Falahat, William Reardon and Niklas Dahl
Eur J Hum Genet 15: 379-382; advance online publication, January 10, 2007; doi:10.1038/sj.ejhg.5201762
Partial duplications of the MSH2 and MLH1 genes in hereditary nonpolyposis colorectal cancer FREE
Stephanie Baert-Desurmont, Marie-Pierre Buisine, Emilie Bessenay, Stephanie Frerot, Tonio Lovecchio, Cosette Martin, Sylviane Olschwang, Qing Wang and Thierry Frebourg
Eur J Hum Genet 15: 383-386; advance online publication, January 17, 2007; doi:10.1038/sj.ejhg.5201765
Corrigendum
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia FREE
Daniela Amann-Zalcenstein, Nili Avidan, Kyra Kanyas, Richard P Ebstein, Yoav Kohn, Adnan Hamdan, Edna Ben-Asher, Osnat Karni, Muhammed Mujaheed, Ronnen H Segman, Wolfgang Maier, Fabio Macciardi, Jacques S Beckmann, Doron Lancet and Bernard Lerer
Eur J Hum Genet 15: 387; doi:10.1038/sj.ejhg.5201794
