Table of contents


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Editorial

Genomics of common diseases p569

doi:10.1038/ng0507-569


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Correspondence

Reactive oxygen species and the segregation of mtDNA sequence variants pp571 - 572

Brendan J Battersby & Eric A Shoubridge

doi:10.1038/ng0507-571


Reply to "Reactive oxygen species and the segregation of mtDNA sequence variants" p572

José A Enriquez, Raquel Moreno-Loshuertos, Rebeca Acín-Pérez, Nieves Movilla, M Esther Gallardo, Santiago Rodriguez de Córdoba, Acisclo Pérez-Martos & Patricio Fernández-Silva

doi:10.1038/ng0507-572


Inherited epimutation or a haplotypic basis for the propensity to silence? p573

Catherine M Suter & David I K Martin

doi:10.1038/ng0507-573a


Heritable germline epimutations in humans pp573 - 574

Bernhard Horsthemke

doi:10.1038/ng0507-573b


Heritable germline epimutation is not the same as transgenerational epigenetic inheritance pp574 - 575

Suyinn Chong, Neil A Youngson & Emma Whitelaw

doi:10.1038/ng0507-574


Reply to "Heritable germline epimutation is not the same as transgenerational epigenetic inheritance" pp575 - 576

Catherine M Suter & David IK Martin

doi:10.1038/ng0507-575


Reply to "Heritable germline epimutation is not the same as transgenerational epigenetic inheritance" p576

Suet Y Leung, Tsun L Chan & Siu T Yuen

doi:10.1038/ng0507-576


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Book Review

Genes get diabolical p577

doi:10.1038/ng0507-577


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News and Views


Road rage and fruit flies pp581 - 582

Anne F Simon & David E Krantz

doi:10.1038/ng0507-581

See also: Letter by Dierick & Greenspan


MicroRNAs as tumor suppressors pp582 - 583

Scott M Hammond

doi:10.1038/ng0507-582

See also: Letter by Kumar et al.


A quantitative trait locus regulating rice grain width pp583 - 584

Makoto Matsuoka & Motoyuki Ashikari

doi:10.1038/ng0507-583

See also: Article by Song et al.


Touching base p585

doi:10.1038/ng0507-585


Research highlights p587

doi:10.1038/ng0507-587


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Meeting Report

Drosophila researchers focus on human disease p589

Juan Botas

doi:10.1038/ng0507-589


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Brief Communication

Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia pp593 - 595

Idoya Lahortiga, Kim De Keersmaecker, Pieter Van Vlierberghe, Carlos Graux, Barbara Cauwelier, Frederic Lambert, Nicole Mentens, H Berna Beverloo, Rob Pieters, Frank Speleman, Maria D Odero, Marijke Bauters, Guy Froyen, Peter Marynen, Peter Vandenberghe, Iwona Wlodarska, Jules P P Meijerink & Jan Cools

doi:10.1038/ng2025


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Articles

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis pp596 - 604

John D Rioux, Ramnik J Xavier, Kent D Taylor, Mark S Silverberg, Philippe Goyette, Alan Huett, Todd Green, Petric Kuballa, M Michael Barmada, Lisa Wu Datta, Yin Yao Shugart, Anne M Griffiths, Stephan R Targan, Andrew F Ippoliti, Edmond-Jean Bernard, Ling Mei, Dan L Nicolae, Miguel Regueiro, L Philip Schumm, A Hillary Steinhart, Jerome I Rotter, Richard H Duerr, Judy H Cho, Mark J Daly & Steven R Brant

doi:10.1038/ng2032


A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers pp605 - 613

Tong Sun, Yang Gao, Wen Tan, Sufang Ma, Yuankai Shi, Jiarui Yao, Yongli Guo, Ming Yang, Xuemei Zhang, Qingrun Zhang, Changqing Zeng & Dongxin Lin

doi:10.1038/ng2030


Modifiers of epigenetic reprogramming show paternal effects in the mouse pp614 - 622

Suyinn Chong, Nicola Vickaryous, Alyson Ashe, Natasha Zamudio, Neil Youngson, Sarah Hemley, Tomas Stopka, Arthur Skoultchi, Jacqui Matthews, Hamish S Scott, David de Kretser, Moira O'Bryan, Marnie Blewitt & Emma Whitelaw

doi:10.1038/ng2031



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Letters

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 pp631 - 637

Julius Gudmundsson, Patrick Sulem, Andrei Manolescu, Laufey T Amundadottir, Daniel Gudbjartsson, Agnar Helgason, Thorunn Rafnar, Jon T Bergthorsson, Bjarni A Agnarsson, Adam Baker, Asgeir Sigurdsson, Kristrun R Benediktsdottir, Margret Jakobsdottir, Jianfeng Xu, Thorarinn Blondal, Jelena Kostic, Jielin Sun, Shyamali Ghosh, Simon N Stacey, Magali Mouy, Jona Saemundsdottir, Valgerdur M Backman, Kristleifur Kristjansson, Alejandro Tres, Alan W Partin, Marjo T Albers-Akkers, Javier Godino-Ivan Marcos, Patrick C Walsh, Dorine W Swinkels, Sebastian Navarrete, Sarah D Isaacs, Katja K Aben, Theresa Graif, John Cashy, Manuel Ruiz-Echarri, Kathleen E Wiley, Brian K Suarez, J Alfred Witjes, Mike Frigge, Carole Ober, Eirikur Jonsson, Gudmundur V Einarsson, Jose I Mayordomo, Lambertus A Kiemeney, William B Isaacs, William J Catalona, Rosa B Barkardottir, Jeffrey R Gulcher, Unnur Thorsteinsdottir, Augustine Kong & Kari Stefansson

doi:10.1038/ng1999

See also: News and Views by Witte


Multiple regions within 8q24 independently affect risk for prostate cancer pp638 - 644

Christopher A Haiman, Nick Patterson, Matthew L Freedman, Simon R Myers, Malcolm C Pike, Alicja Waliszewska, Julie Neubauer, Arti Tandon, Christine Schirmer, Gavin J McDonald, Steven C Greenway, Daniel O Stram, Loic Le Marchand, Laurence N Kolonel, Melissa Frasco, David Wong, Loreall C Pooler, Kristin Ardlie, Ingrid Oakley-Girvan, Alice S Whittemore, Kathleen A Cooney, Esther M John, Sue A Ingles, David Altshuler, Brian E Henderson & David Reich

doi:10.1038/ng2015

See also: News and Views by Witte


Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 pp645 - 649

Meredith Yeager, Nick Orr, Richard B Hayes, Kevin B Jacobs, Peter Kraft, Sholom Wacholder, Mark J Minichiello, Paul Fearnhead, Kai Yu, Nilanjan Chatterjee, Zhaoming Wang, Robert Welch, Brian J Staats, Eugenia E Calle, Heather Spencer Feigelson, Michael J Thun, Carmen Rodriguez, Demetrius Albanes, Jarmo Virtamo, Stephanie Weinstein, Fredrick R Schumacher, Edward Giovannucci, Walter C Willett, Geraldine Cancel-Tassin, Olivier Cussenot, Antoine Valeri, Gerald L Andriole, Edward P Gelmann, Margaret Tucker, Daniela S Gerhard, Joseph F Fraumeni, Jr, Robert Hoover, David J Hunter, Stephen J Chanock & Gilles Thomas

doi:10.1038/ng2022

See also: News and Views by Witte


Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema pp650 - 654

Aileen Sandilands, Ana Terron-Kwiatkowski, Peter R Hull, Gráinne M O'Regan, Timothy H Clayton, Rosemarie M Watson, Thomas Carrick, Alan T Evans, Haihui Liao, Yiwei Zhao, Linda E Campbell, Matthias Schmuth, Robert Gruber, Andreas R Janecke, Peter M Elias, Maurice A M van Steensel, Ivo Nagtzaam, Michel van Geel, Peter M Steijlen, Colin S Munro, Daniel G Bradley, Colin N A Palmer, Frances J D Smith, W H Irwin McLean & Alan D Irvine

doi:10.1038/ng2020


Estrogen receptor alpha (ESR1) gene amplification is frequent in breast cancer pp655 - 660

Frederik Holst, Phillip R Stahl, Christian Ruiz, Olaf Hellwinkel, Zeenath Jehan, Marc Wendland, Annette Lebeau, Luigi Terracciano, Khawla Al-Kuraya, Fritz Jänicke, Guido Sauter & Ronald Simon

doi:10.1038/ng2006


Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility pp661 - 665

Klaus Dieterich, Ricardo Soto Rifo, Anne Karen Faure, Sylviane Hennebicq, Baha Ben Amar, Mohamed Zahi, Julia Perrin, Delphine Martinez, Bernard Sèle, Pierre-Simon Jouk, Théophile Ohlmann, Sophie Rousseaux, Joel Lunardi & Pierre F Ray

doi:10.1038/ng2027


Direct quantitative trait locus mapping of mammalian metabolic phenotypes in diabetic and normoglycemic rat models pp666 - 672

Marc-Emmanuel Dumas, Steven P Wilder, Marie-Thérèse Bihoreau, Richard H Barton, Jane F Fearnside, Karène Argoud, Lisa D'Amato, Robert H Wallis, Christine Blancher, Hector C Keun, Dorrit Baunsgaard, James Scott, Ulla Grove Sidelmann, Jeremy K Nicholson & Dominique Gauguier

doi:10.1038/ng2026





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Corrigenda

Corrigendum: Differential translation efficiency of orthologous genes is involved in phenotypic divergence of yeast species p688

Orna Man & Yitzhak Pilpel

doi:10.1038/ng0507-688a


Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk p688

Angela Cox, Alison M Dunning, Montserrat Garcia-Closas, Sabapathy Balasubramanian, Malcolm W R Reed, Karen A Pooley, Serena Scollen, Caroline Baynes, Bruce A J Ponder, Stephen Chanock, Jolanta Lissowska, Louise Brinton, Beata Peplonska, Melissa C Southey, John L Hopper, Margaret R E McCredie, Graham G Giles, Olivia Fletcher, Nichola Johnson, Isabel dos Santos Silva, Lorna Gibson, Stig E Bojesen, Børge G Nordestgaard, Christen K Axelsson, Diana Torres, Ute Hamann, Christina Justenhoven, Hiltrud Brauch, Jenny Chang-Claude, Silke Kropp, Angela Risch, Shan Wang-Gohrke, Peter Schürmann, Natalia Bogdanova, Thilo Dörk, Rainer Fagerholm, Kirsimari Aaltonen, Carl Blomqvist, Heli Nevanlinna, Sheila Seal, Anthony Renwick, Michael R Stratton, Nazneen Rahman, Suleeporn Sangrajrang, David Hughes, Fabrice Odefrey, Paul Brennan, Amanda B Spurdle, Georgia Chenevix-Trench, The Kathleen Cunningham Foundation Consortium for Research into Familial Breast Cancer, Jonathan Beesley, Arto Mannermaa, Jaana Hartikainen, Vesa Kataja, Veli-Matti Kosma, Fergus J Couch, Janet E Olson, Ellen L Goode, Annegien Broeks, Marjanka K Schmidt, Frans B L Hogervorst, Laura J Van't Veer, Daehee Kang, Keun-Young Yoo, Dong-Young Noh, Sei-Hyun Ahn, Sara Wedrén, Per Hall, Yen-Ling Low, Jianjun Liu, Roger L Milne, Gloria Ribas, Anna Gonzalez-Neira, Javier Benitez, Alice J Sigurdson, Denise L Stredrick, Bruce H Alexander, Jeffery P Struewing, Paul D P Pharoah & Douglas F Easton, on behalf of the Breast Cancer Association Consortium

doi:10.1038/ng0507-688b


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