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Nature Genetics
ISSUE
January 2006, Volume 38 No 1
Editorial
Commentary
Book Review
News and Views
Research Highlights
Brief Communications
Articles
Letters
About the cover
Editorial Top
Embracing risk p1
doi:10.1038/ng0106-1
Full text | PDF (53K)
Commentary Top
A road map for efficient and reliable human genome epidemiology pp3 - 5
John P A Ioannidis, Marta Gwinn, Julian Little, Julian P T Higgins, Jonine L Bernstein, Paolo Boffetta, Melissa Bondy, Molly S Bray, Paul E Brenchley, Patricia A Buffler, Juan Pablo Casas, Anand Chokkalingam, John Danesh, George Davey Smith, Siobhan Dolan, Ross Duncan, Nelleke A Gruis, Patricia Hartge, Mia Hashibe, David J Hunter, Marjo-Riitta Jarvelin, Beatrice Malmer, Demetrius M Maraganore, Julia A Newton-Bishop, Thomas R O'Brien, Gloria Petersen, Elio Riboli, Georgia Salanti, Daniela Seminara, Liam Smeeth, Emanuela Taioli, Nic Timpson, Andre G Uitterlinden, Paolo Vineis, Nick Wareham, Deborah M Winn, Ron Zimmern, Muin J Khoury & The Human Genome Epidemiology Network and the Network of Investigator Networks
doi:10.1038/ng0106-3
Abstract | Full text | PDF (124K)
Book Review Top
Evolution's secret p7
Reviewed by: Michael A Goldman
doi:10.1038/ng0106-7
Full text | PDF (82K)
News and Views Top
Widening the spectrum of human genetic variation pp9 - 11
Evan E Eichler
doi:10.1038/ng0106-9
Abstract | Full text | PDF (219K)
See also: Letter by Conrad et al.  | Letter by Hinds et al.  | Letter by McCarroll et al.
Amyloid double trouble pp11 - 12
John Hardy
doi:10.1038/ng0106-11
Abstract | Full text | PDF (132K)
See also: Brief Communication by Rovelet-Lecrux et al.
Beyond the beta cell in diabetes pp12 - 13
Andrew T Hattersley
doi:10.1038/ng0106-12
Abstract | Full text | PDF (132K)
See also: Article by Ræder et al.
Confronting ethnicity-specific disease risk pp13 - 15
Hua Tang
doi:10.1038/ng0106-13
Abstract | Full text | PDF (209K)
See also: Letter by Helgadottir et al.
Touching base p17
doi:10.1038/ng0106-17
Full text | PDF (218K)
Research Highlights Top
Research Highlights p19
doi:10.1038/ng0106-19
Full text | PDF (63K)
Brief Communications Top
Defective planar cell polarity in polycystic kidney disease pp21 - 23
Evelyne Fischer, Emilie Legue, Antonia Doyen, Faridabano Nato, Jean-François Nicolas, Vicente Torres, Moshe Yaniv & Marco Pontoglio
Published online: 11 December 2005 | doi:10.1038/ng1701
Abstract | Full text | PDF (293K)  | Supplementary Information
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy pp24 - 26
Anne Rovelet-Lecrux, Didier Hannequin, Gregory Raux, Nathalie Le Meur, Annie Laquerrière, Anne Vital, Cécile Dumanchin, Sébastien Feuillette, Alexis Brice, Martine Vercelletto, Frédéric Dubas, Thierry Frebourg & Dominique Campion
Published online: 20 December 2005 | doi:10.1038/ng1718
Abstract | Full text | PDF (233K)  | Supplementary Information
See also: News and Views by Hardy
Articles Top
Lymphoid cell growth and transformation are suppressed by a key regulatory element of the gene encoding PU.1 pp27 - 37
Frank Rosenbauer, Bronwyn M Owens, Li Yu, Joseph R Tumang, Ulrich Steidl, Jeffery L Kutok, Linda K Clayton, Katharina Wagner, Marina Scheller, Hiromi Iwasaki, Chunhui Liu, Björn Hackanson, Koichi Akashi, Achim Leutz, Thomas L Rothstein, Christoph Plass & Daniel G Tenen
Published online: 27 November 2005 | doi:10.1038/ng1679
Abstract | Full text | PDF (985K)  | Supplementary Information
Homozygous L-SIGN (CLEC4M) plays a protective role in SARS coronavirus infection pp38 - 46
Vera S F Chan, Kelvin Y K Chan, Yongxiong Chen, Leo L M Poon, Annie N Y Cheung, Bojian Zheng, Kwok-Hung Chan, William Mak, Hextan Y S Ngan, Xiaoning Xu, Gavin Screaton, Paul K H Tam, Jonathan M Austyn, Li-Chong Chan, Shea-Ping Yip, Malik Peiris, Ui-Soon Khoo & Chen-Lung S Lin
Published online: 20 December 2005 | doi:10.1038/ng1698
Abstract | Full text | PDF (333K)  | Supplementary Information
Dosage compensation of the active X chromosome in mammals pp47 - 53
Di Kim Nguyen & Christine M Disteche
Published online: 11 December 2005 | doi:10.1038/ng1705
Abstract | Full text | PDF (236K)  | Supplementary Information
Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction pp54 - 62
Helge Ræder, Stefan Johansson, Pål I Holm, Ingfrid S Haldorsen, Eric Mas, Véronique Sbarra, Ingrid Nermoen, Stig Å Eide, Louise Grevle, Lise Bjørkhaug, Jørn V Sagen, Lage Aksnes, Oddmund Søvik, Dominique Lombardo, Anders Molven & Pål Rasmus Njølstad
Published online: 20 December 2005 | doi:10.1038/ng1708
Abstract | Full text | PDF (492K)  | Supplementary Information
See also: News and Views by Hattersley
A positive signal from the fertilization of the egg cell sets off endosperm proliferation in angiosperm embryogenesis pp63 - 67
Moritz K Nowack, Paul E Grini, Marc J Jakoby, Marcel Lafos, Csaba Koncz & Arp Schnittger
Published online: 27 November 2005 | doi:10.1038/ng1694
Abstract | Full text | PDF (367K)  | Supplementary Information
Letters Top
A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction pp68 - 74
Anna Helgadottir, Andrei Manolescu, Agnar Helgason, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Daniel F Gudbjartsson, Solveig Gretarsdottir, Kristinn P Magnusson, Gudmundur Gudmundsson, Andrew Hicks, Thorlakur Jonsson, Struan F A Grant, Jesus Sainz, Stephen J O'Brien, Sigurlaug Sveinbjornsdottir, Einar M Valdimarsson, Stefan E Matthiasson, Allan I Levey, Jerome L Abramson, Murdach P Reilly, Viola Vaccarino, Megan L Wolfe, Vilmundur Gudnason, Arshed A Quyyumi, Eric J Topol, Daniel J Rader, Gudmundur Thorgeirsson, Jeffrey R Gulcher, Hakon Hakonarson, Augustine Kong & Kari Stefansson
Published online: 10 November 2005 | doi:10.1038/ng1692
Abstract | Full text | PDF (155K)  | Supplementary Information
See also: News and Views by Tang
A high-resolution survey of deletion polymorphism in the human genome pp75 - 81
Donald F Conrad, T Daniel Andrews, Nigel P Carter, Matthew E Hurles & Jonathan K Pritchard
Published online: 04 December 2005 | doi:10.1038/ng1697
Abstract | Full text | PDF (286K)  | Supplementary Information
See also: News and Views by Eichler | Letter by Hinds et al.  | Letter by McCarroll et al.
Common deletions and SNPs are in linkage disequilibrium in the human genome pp82 - 85
David A Hinds, Andrew P Kloek, Michael Jen, Xiyin Chen & Kelly A Frazer
Published online: 04 December 2005 | doi:10.1038/ng1695
Abstract | Full text | PDF (197K)  | Supplementary Information
See also: News and Views by Eichler | Letter by Conrad et al.  | Letter by McCarroll et al.
Common deletion polymorphisms in the human genome pp86 - 92
Steven A McCarroll, Tracy N Hadnott, George H Perry, Pardis C Sabeti, Michael C Zody, Jeffrey C Barrett, Stephanie Dallaire, Stacey B Gabriel, Charles Lee, Mark J Daly, David M Altshuler & The International HapMap Consortium
Published online: 04 December 2005 | doi:10.1038/ng1696
Abstract | Full text | PDF (342K)  | Supplementary Information
See also: News and Views by Eichler | Letter by Conrad et al.  | Letter by Hinds et al.
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type pp93 - 100
Jordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, Carole Doré, Janet L Atkinson, David Watkins, Chantal F Morel, T Mary Fujiwara, Emily Moras, Angela R Hosack, Gail V Dunbar, Hana Antonicka, Vince Forgetta, C Melissa Dobson, Daniel Leclerc, Roy A Gravel, Eric A Shoubridge, James W Coulton, Pierre Lepage, Johanna M Rommens, Kenneth Morgan & David S Rosenblatt
Published online: 27 November 2005 | doi:10.1038/ng1683
Abstract | Full text | PDF (632K)  | Supplementary Information
Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality pp101 - 106
Ryuichi Ono, Kenji Nakamura, Kimiko Inoue, Mie Naruse, Takako Usami, Noriko Wakisaka-Saito, Toshiaki Hino, Rika Suzuki-Migishima, Narumi Ogonuki, Hiromi Miki, Takashi Kohda, Atsuo Ogura, Minesuke Yokoyama, Tomoko Kaneko-Ishino & Fumitoshi Ishino
Published online: 11 December 2005 | doi:10.1038/ng1699
Abstract | Full text | PDF (452K)  | Supplementary Information
Genetic analysis of cavefish reveals molecular convergence in the evolution of albinism pp107 - 111
Meredith E Protas, Candace Hersey, Dawn Kochanek, Yi Zhou, Horst Wilkens, William R Jeffery, Leonard I Zon, Richard Borowsky & Clifford J Tabin
Published online: 11 December 2005 | doi:10.1038/ng1700
Abstract | Full text | PDF (401K)  | Supplementary Information
Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification pp112 - 117
Maria Immacolata Ferrante, Alessandro Zullo, Adriano Barra, Sabrina Bimonte, Nadia Messaddeq, Michèle Studer, Pascal Dollé & Brunella Franco
Published online: 27 November 2005 | doi:10.1038/ng1684
Abstract | Full text | PDF (614K)  | Supplementary Information
Nras loss induces metastatic conversion of Rb1-deficient neuroendocrine thyroid tumor pp118 - 123
Chiaki Takahashi, Bernardo Contreras, Tsuyoshi Iwanaga, Yujiro Takegami, Anke Bakker, Roderick T Bronson, Makoto Noda, Massimo Loda, Jennifer L Hunt & Mark E Ewen
Published online: 20 December 2005 | doi:10.1038/ng1703
Abstract | Full text | PDF (560K)  | Supplementary Information
Genome-wide transcription analyses in rice using tiling microarrays pp124 - 129
Lei Li, Xiangfeng Wang, Viktor Stolc, Xueyong Li, Dongfen Zhang, Ning Su, Waraporn Tongprasit, Songgang Li, Zhukuan Cheng, Jun Wang & Xing Wang Deng
Published online: 20 December 2005 | doi:10.1038/ng1704
Abstract | Full text | PDF (623K)  | Supplementary Information
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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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