TABLE OF CONTENTS
Volume 17, Issue 10 (October 2009)
News and Commentary
Back to the Genome
From genotypes to genometypes: putting the genome back in genome-wide association studies FREE
J H Moore
Eur J Hum Genet 17: 1205-1206; advance online publication, March 11, 2009; doi:10.1038/ejhg.2009.39
Articles
Goltz–Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap
May-Britt Harmsen, Silvia Azzarello-Burri, M Mar García González, Gabriele Gillessen-Kaesbach, Peter Meinecke, Dietmar Müller, Anita Rauch, Eva Rossier, Eva Seemanova, Christiane Spaich, Bernhard Steiner, Dagmar Wieczorek, Martin Zenker and Kerstin Kutsche
Eur J Hum Genet 17: 1207-1215; advance online publication, March 11, 2009; doi:10.1038/ejhg.2009.40
SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions
Claire Beneteau, Hélène Cavé, Anne Moncla, Nathalie Dorison, Arnold Munnich, Alain Verloes and Bruno Leheup
Eur J Hum Genet 17: 1216-1221; advance online publication, April 8, 2009; doi:10.1038/ejhg.2009.44
Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome
Svend Rand-Hendriksen, Rigmor Lundby, Lena Tjeldhorn, Kai Andersen, Jon Offstad, Svein Ove Semb, Hans-Jørgen Smith, Benedicte Paus and Odd Geiran
Eur J Hum Genet 17: 1222-1230; advance online publication, March 18, 2009; doi:10.1038/ejhg.2009.30
Using biological networks to search for interacting loci in genome-wide association studies
Mathieu Emily, Thomas Mailund, Jotun Hein, Leif Schauser and Mikkel Heide Schierup
Eur J Hum Genet 17: 1231-1240; advance online publication, March 11, 2009; doi:10.1038/ejhg.2009.15
The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy
Daniel Vega Møller, Paal Skytt Andersen, Paula Hedley, Mads Kristian Ersbøll, Henning Bundgaard, Johanna Moolman-Smook, Michael Christiansen and Lars Køber
Eur J Hum Genet 17: 1241-1249; advance online publication, March 18, 2009; doi:10.1038/ejhg.2009.34
Evidence for association with hepatocellular carcinoma at the PAPSS1 locus on chromosome 4q25 in a family-based study
Wei-Liang Shih, Ming-Whei Yu, Pei-Jer Chen, Tai-Wei Wu, Chih-Lin Lin, Chun-Jen Liu, Shi-Ming Lin, Dar-In Tai, Shou-Dong Lee and Yun-Fan Liaw
Eur J Hum Genet 17: 1250-1259; advance online publication, April 1, 2009; doi:10.1038/ejhg.2009.48
Y-Chromosome distribution within the geo-linguistic landscape of northwestern Russia
Sheyla Mirabal, Maria Regueiro, Alicia M Cadenas, L Luca Cavalli-Sforza, Peter A Underhill, Dmitry A Verbenko, Svetlana A Limborska and Rene J Herrera
Eur J Hum Genet 17: 1260-1273; advance online publication, March 4, 2009; doi:10.1038/ejhg.2009.6
The interaction index, a novel information-theoretic metric for prioritizing interacting genetic variations and environmental factors
Pritam Chanda, Lara Sucheston, Aidong Zhang and Murali Ramanathan
Eur J Hum Genet 17: 1274-1286; advance online publication, March 18, 2009; doi:10.1038/ejhg.2009.38
Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke
Robin Lemmens, Shérine Abboud, Wim Robberecht, Luc Vanhees, Massimo Pandolfo, Vincent Thijs and An Goris
Eur J Hum Genet 17: 1287-1293; advance online publication, March 25, 2009; doi:10.1038/ejhg.2009.42
The FAS ligand promoter polymorphism, rs763110 (-844C>T), contributes to cancer susceptibility: evidence from 19 case–control studies
Zhizhong Zhang, Lixin Qiu, Meilin Wang, Na Tong, Jin Li and Zhengdong Zhang
Eur J Hum Genet 17: 1294-1303; advance online publication, April 1, 2009; doi:10.1038/ejhg.2009.45
Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15 - Crohn's disease patients
Ana Márquez, Jezabel Varadé, Gema Robledo, Alfonso Martínez, Juan Luis Mendoza, Carlos Taxonera, Miguel Fernández-Arquero, Manuel Díaz-Rubio, María Gómez-García, Miguel Angel López-Nevot, Emilio G de la Concha, Javier Martín and Elena Urcelay
Eur J Hum Genet 17: 1304-1308; advance online publication, April 1, 2009; doi:10.1038/ejhg.2009.50
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
Maria Ban, An Goris, Åslaug R Lorentzen, Amie Baker, Tania Mihalova, Gillian Ingram, David R Booth, Robert N Heard, Graeme J Stewart, Elke Bogaert, Bénédicte Dubois, Hanne F Harbo, Elisabeth G Celius, Anne Spurkland, Richard Strange, Clive Hawkins, Neil P Robertson, Frank Dudbridge, James Wason, Philip L De Jager, David Hafler, John D Rioux, Adrian J Ivinson, Jacob L McCauley, Margaret Pericak-Vance, Jorge R Oksenberg, Stephen L Hauser, David Sexton, Jonathan Haines and Stephen Sawcer , The Wellcome Trust Case–Control Consortium (WTCCC) and Alastair Compston
Eur J Hum Genet 17: 1309-1313; advance online publication, March 18, 2009; doi:10.1038/ejhg.2009.41
The maternal aborigine colonization of La Palma (Canary Islands)
Rosa Fregel, Jose Pestano, Matilde Arnay, Vicente M Cabrera, Jose M Larruga and Ana M González
Eur J Hum Genet 17: 1314-1324; advance online publication, April 1, 2009; doi:10.1038/ejhg.2009.46
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects
Emma Hilton, Jennifer Johnston, Sandra Whalen, Nobuhiko Okamoto, Yoshikazu Hatsukawa, Juntaro Nishio, Hiroshi Kohara, Yoshiko Hirano, Seiji Mizuno, Chiharu Torii, Kenjiro Kosaki, Sylvie Manouvrier, Odile Boute, Rahat Perveen, Caroline Law, Anthony Moore, David Fitzpatrick, Johannes Lemke, Florence Fellmann, François-Guillaume Debray, Florence Dastot-Le-Moal, Marion Gerard, Josiane Martin, Pierre Bitoun, Michel Goossens, Alain Verloes, Albert Schinzel, Deborah Bartholdi, Tanya Bardakjian, Beverly Hay, Kim Jenny, Kathreen Johnston, Michael Lyons, John W Belmont, Leslie G Biesecker, Irina Giurgea and Graeme Black
Eur J Hum Genet 17: 1325-1335; advance online publication, April 15, 2009; doi:10.1038/ejhg.2009.52
Genetic markers and population history: Finland revisited
Jukka U Palo, Ismo Ulmanen, Matti Lukka, Pekka Ellonen and Antti Sajantila
Eur J Hum Genet 17: 1336-1346; advance online publication, April 15, 2009; doi:10.1038/ejhg.2009.53
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection EJHGOpen
Nuala H Sykes, Claudio Toma, Natalie Wilson, Emanuela V Volpi, Inês Sousa, Alistair T Pagnamenta, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini, Anthony J Bailey, Anthony P Monaco and International Molecular Genetic Study of Autism Consortium (IMGSAC)
Eur J Hum Genet 17: 1347-1353; advance online publication, April 22, 2009; doi:10.1038/ejhg.2009.47
Short Reports
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia EJHGOpen
Sonja C Vernes, Kay D MacDermot, Anthony P Monaco and Simon E Fisher
Eur J Hum Genet 17: 1354-1358; advance online publication, April 8, 2009; doi:10.1038/ejhg.2009.43
Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families
Laia Rodriguez-Revenga, Irene Madrigal, Javier Pagonabarraga, Mar Xunclà, Celia Badenas, Jaime Kulisevsky, Beatriz Gomez and Montserrat Milà
Eur J Hum Genet 17: 1359-1362; advance online publication, April 15, 2009; doi:10.1038/ejhg.2009.51
Corrigendum
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 FREE
Lance Doucette, Nancy D Merner, Sandra Cooke, Elizabeth Ives, Dante Galutira, Vanessa Walsh, Tom Walsh, Linda MacLaren, Tracey Cater, Bridget Fernandez, Jane S Green, Edward R Wilcox, Larry Shotland, X C Li, Ming Lee, Mary-Claire King and Terry-Lynn Young
Eur J Hum Genet 17: 1363; doi:10.1038/ejhg.2009.78
