TABLE OF CONTENTS
Volume 14, Issue 4 (April 2006)
News and Commentary
Ovarian Cancer: Identification of remodeling and spacing factor 1 (rsf-1, HBXAP) at chromosome 11q13 as a putative oncogene in ovarian cancer FREE
Bryan T Hennessy, Meera Nanjundan, Kwai Wa Cheng, Laura Nolden and Gordon B Mills
Eur J Hum Genet 14: 381-383; advance online publication, January 18, 2006; doi:10.1038/sj.ejhg.5201570
Reviews
It's 'back to school' for genetic screening FREE
Alexandra A Gason, Martin B Delatycki, Sylvia A Metcalfe and MaryAnne Aitken
Eur J Hum Genet 14: 384-389; advance online publication, February 15, 2006; doi:10.1038/sj.ejhg.5201581
Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications FREE
Henry T Lynch, C Richard Boland, Gordon Gong, Trudy G Shaw, Patrick M Lynch, Riccardo Fodde, Jane F Lynch and Albert de la Chapelle
Eur J Hum Genet 14: 390-402; advance online publication, February 15, 2006; doi:10.1038/sj.ejhg.5201584
Articles
Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesis FREE
Hitesh Kapadia, Sylvia Frazier-Bowers, Takuya Ogawa and Rena N D'souza
Eur J Hum Genet 14: 403-409; advance online publication, February 15, 2006; doi:10.1038/sj.ejhg.5201574
Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases FREE
Iben Bache, Mads Hjorth, Merete Bugge, Søren Holstebroe, Jørgen Hilden, Lone Schmidt, Karen Brondum-Nielsen, Gert Bruun-Petersen, Peter K A Jensen, Claes Lundsteen, Erik Niebuhr, Kirsten Rasmussen and Niels Tommerup
Eur J Hum Genet 14: 410-417; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201592
Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect FREE
Mireille Cossée, Bénédicte Demeer, Patricia Blanchet, Bernard Echenne, Deepika Singh, Olivier Hagens, Manuela Antin, Sonja Finck, Louis Vallee, Hélène Dollfus, Sridevi Hegde, Kelly Springell, B K Thelma, Geoffrey Woods, Vera Kalscheuer and Jean-Louis Mandel
Eur J Hum Genet 14: 418-425; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201593
An utter refutation of the 'Fundamental Theorem of the HapMap' FREE
Joseph D Terwilliger and Tero Hiekkalinna
Eur J Hum Genet 14: 426-437; advance online publication, February 15, 2006; doi:10.1038/sj.ejhg.5201583
Association study of major risk single nucleotide polymorphisms in the common regulatory region of PARK2 and PACRG genes with leprosy in an Indian population FREE
Dheeraj Malhotra, Katayoon Darvishi, Manmohan Lohra, Himanshu Kumar, Chander Grover, Soni Sood, Belum S N Reddy and Ramesh N K Bamezai
Eur J Hum Genet 14: 438-442; advance online publication, December 14, 2005; doi:10.1038/sj.ejhg.5201563
Influence of serotonin receptor 2A His452Tyr polymorphism on brain temporal structures: a volumetric MR study FREE
Nicola Filippini, Catia Scassellati, Marina Boccardi, Michela Pievani, Cristina Testa, Luisella Bocchio-Chiavetto, Giovanni B Frisoni and Massimo Gennarelli
Eur J Hum Genet 14: 443-449; advance online publication, January 25, 2006; doi:10.1038/sj.ejhg.5201573
Identification of probable genotyping errors by consideration of haplotypes FREE
Tim Becker, Ruta Valentonyte, Peter J P Croucher, Konstantin Strauch, Stefan Schreiber, Jochen Hampe and Michael Knapp
Eur J Hum Genet 14: 450-458; advance online publication, January 25, 2006; doi:10.1038/sj.ejhg.5201565
Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations FREE
Valentina Medici, Silvia Mascheretti, Peter J P Croucher, Monika Stoll, Jochen Hampe, Jochen Grebe, Giacomo C Sturniolo, Camilla Solberg, Jorgen Jahnsen, Bjorn Moum, Stefan Schreiber and Morten H Vatn for the IBSEN group
Eur J Hum Genet 14: 459-468; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201576
The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program FREE
Yen-Pei Christy Chang, James Dae-Ok Kim, Karen Schwander, Dabeeru C Rao, Mike B Miller, Alan B Weder, Richard S Cooper, Nicholas J Schork, Michael A Province, Alanna C Morrison, Sharon L R Kardia, Thomas Quertermous and Aravinda Chakravarti
Eur J Hum Genet 14: 469-477; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201582
3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia FREE
Veronique Vitart, Zrinka Biloglav, Caroline Hayward, Branka Janicijevic, Nina Smolej-Narancic, Lovorka Barac, Marijana Pericic, Irena Martinovic Klaric, Tatjana Skaric-Juric, Maja Barbalic, Ozren Polasek, Ivana Kolcic, Andrew Carothers, Pavao Rudan, Nick Hastie, Alan Wright, Harry Campbell and Igor Rudan
Eur J Hum Genet 14: 478-487; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201589
Role of interferon-
gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study FREE
Francesco Paolo Schena, Giuseppina Cerullo, Diletta Domenica Torres, Francesco Scolari, Marina Foramitti, Antonio Amoroso, Doroti Pirulli, Jürgen Floege, Peter Rene Mertens, Klaus Zerres, Efstathios Alexopoulos, Dimitrios Kirmizis, Leopoldo Zelante and Luigi Bisceglia on behalf of the European IgAN Consortium
Eur J Hum Genet 14: 488-496; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201591
Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands FREE
Thomas D Als, Tove H Jorgensen, Anders D Børglum, Peter A Petersen, Ole Mors and August G Wang
Eur J Hum Genet 14: 497-504; advance online publication, January 25, 2006; doi:10.1038/sj.ejhg.5201578
