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Nature Genetics

Articles from the last few issues of Nature Genetics © Nature Publishing Group
  • Variation in KLK genes, prostate-specific antigen and risk of prostate cancer
    Nature Genetics, Vol. 40, No. 9., pp. 1032-1034.
    by Jiyoung Ahn, Sonja I Berndt, Sholom Wacholder, Peter Kraft, Adam S Kibel, Meredith Yeager, Demetrius Albanes, Edward Giovannucci, Meir J Stampfer, Jarmo Virtamo, Michael J Thun, Heather S Feigelson, Geraldine Cancel-Tassin, Olivier Cussenot, Gilles Thomas, David J Hunter, Joseph F Fraumeni, Robert N Hoover, Stephen J Chanock, Richard B Hayes
  • Reply to “Variation in KLK genes, prostate-specific antigen and risk of prostate cancer”
    Nature Genetics, Vol. 40, No. 9., pp. 1035-1036.
    by Rosalind Eeles, Graham Giles, David Neal, Kenneth Muir, Douglas F Easton
  • High anxiety
    Nature Genetics, Vol. 40, No. 9., pp. 1038-1038.
    by Misha Angrist
  • Psychiatric genetics gets a boost
    Nature Genetics, Vol. 40, No. 9., pp. 1042-1044.
    by Brion S Maher, Brien P Riley, Kenneth S Kendler
  • Casting a wider net for diabetes susceptibility genes
    Nature Genetics, Vol. 40, No. 9., pp. 1039-1040.
    by Mark I Mccarthy
  • Hedgehog in Wnterland
    Nature Genetics, Vol. 40, No. 9., pp. 1040-1041.
    by Dennis Roop, Rune Toftgård
  • A wiki for the life sciences where authorship matters
    Nat Genet, Vol. 40, No. 9. (2008), pp. 1047-1051.
    by Robert Hoffmann
  • Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
    Nature Genetics, Vol. 40, No. 9. (17 August 2008), pp. 1056-1058.
    by Manuel AR Ferreira, Michael C O'Donovan, Yan A Meng, Ian R Jones, Douglas M Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H Perlis, Elaine K Green, Jordan W Smoller, Detelina Grozeva, Jennifer Stone, Ivan Nikolov, Kimberly Chambert, Marian L Hamshere, Vishwajit L Nimgaonkar, Valentina Moskvina, Michael E Thase, Sian Caesar, Gary S Sachs, Jennifer Franklin, Katherine Gordon-Smith, Kristin G Ardlie, Stacey B Gabriel, Christine Fraser, Brendan Blumenstiel, Matthew Defelice, Gerome Breen, Michael Gill, Derek W Morris, Amanda Elkin, Walter J Muir, Kevin A Mcghee, Richard Williamson, Donald J Macintyre, Alan W Maclean, David St Clair, Michelle Robinson, Margaret Van Beck, Ana CP Pereira, Radhika Kandaswamy, Andrew Mcquillin, David A Collier, Nicholas J Bass, Allan H Young, Jacob Lawrence, Nicol I Ferrier, Adebayo Anjorin, Anne Farmer, David Curtis, Edward M Scolnick, Peter Mcguffin, Mark J Daly, Aiden P Corvin, Peter A Holmans, Douglas H Blackwood, Hugh M Gurling, Michael J Owen, Shaun M Purcell, Pamela Sklar, Nick Craddock
  • Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus
    Nature Genetics, Vol. 40, No. 9. (01 August 2008), pp. 1059-1061.
    by Robert R Graham, Chris Cotsapas, Leela Davies, Rachel Hackett, Christopher J Lessard, Joanlise M Leon, Noel P Burtt, Candace Guiducci, Melissa Parkin, Casey Gates, Robert M Plenge, Timothy W Behrens, Joan E Wither, John D Rioux, Paul R Fortin, Deborah C Graham, Andrew K Wong, Timothy J Vyse, Mark J Daly, David Altshuler, Kathy L Moser, Patrick M Gaffney
  • Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus
    Nature Genetics, Vol. 40, No. 9. (01 August 2008), pp. 1062-1064.
    by Stacy L Musone, Kimberly E Taylor, Timothy T Lu, Joanne Nititham, Ricardo C Ferreira, Ward Ortmann, Nataliya Shifrin, Michelle A Petri, Ilyas M Kamboh, Susan Manzi, Michael F Seldin, Peter K Gregersen, Timothy W Behrens, Averil Ma, Pui-Yan Kwok, Lindsey A Criswell
  • Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum
    Nature Genetics, Vol. 40, No. 9. (10 August 2008), pp. 1065-1067.
    by Juliane Najm, Denise Horn, Isabella Wimplinger, Jeffrey A Golden, Victor V Chizhikov, Jyotsna Sudi, Susan L Christian, Reinhard Ullmann, Alma Kuechler, Carola A Haas, Armin Flubacher, Lawrence R Charnas, Gökhan Uyanik, Ulrich Frank, Eva Klopocki, William B Dobyns, Kerstin Kutsche
  • Identification of loci associated with schizophrenia by genome-wide association and follow-up
    Nature Genetics, Vol. 40, No. 9. (30 July 2008), pp. 1053-1055.
    by Michael C O'Donovan, Nicholas Craddock, Nadine Norton, Hywel Williams, Timothy Peirce, Valentina Moskvina, Ivan Nikolov, Marian Hamshere, Liam Carroll, Lyudmila Georgieva, Sarah Dwyer, Peter Holmans, Jonathan L Marchini, Chris CA Spencer, Bryan Howie, Hin-Tak Leung, Annette M Hartmann, Hans-Jürgen Möller, Derek W Morris, Yongyong Shi, Guoyin Feng, Per Hoffmann, Peter Propping, Catalina Vasilescu, Wolfgang Maier, Marcella Rietschel, Stanley Zammit, Johannes Schumacher, Emma M Quinn, Thomas G Schulze, Nigel M Williams, Ina Giegling, Nakao Iwata, Masashi Ikeda, Ariel Darvasi, Sagiv Shifman, Lin He, Jubao Duan, Alan R Sanders, Douglas F Levinson, Pablo V Gejman, Sven Cichon, Markus M Nöthen, Michael Gill, Aiden Corvin, Dan Rujescu, George Kirov, Michael J Owen
  • Detection of sharing by descent, long-range phasing and haplotype imputation
    Nature Genetics, Vol. 40, No. 9. (17 August 2008), pp. 1068-1075.
    by Augustine Kong, Gisli Masson, Michael L Frigge, Arnaldur Gylfason, Pasha Zusmanovich, Gudmar Thorleifsson, Pall I Olason, Andres Ingason, Stacy Steinberg, Thorunn Rafnar, Patrick Sulem, Magali Mouy, Frosti Jonsson, Unnur Thorsteinsdottir, Daniel F Gudbjartsson, Hreinn Stefansson, Kari Stefansson
    posted by 1 person caseybrown
  • Max-independent functions of Myc in Drosophila melanogaster
    Nature Genetics, Vol. 40, No. 9. (01 August 2008), pp. 1084-1091.
    by Dominik Steiger, Michael Furrer, Daniela Schwinkendorf, Peter Gallant
  • Evolutionary toggling of the MAPT 17q21.31 inversion region
    Nature Genetics, Vol. 40, No. 9. (10 August 2008), pp. 1076-1083.
    by Michael C Zody, Zhaoshi Jiang, Hon-Chung Fung, Francesca Antonacci, Ladeana W Hillier, Maria F Cardone, Tina A Graves, Jeffrey M Kidd, Ze Cheng, Amr Abouelleil, Lin Chen, John Wallis, Jarret Glasscock, Richard K Wilson, Amy D Reily, Jaime Duckworth, Mario Ventura, John Hardy, Wesley C Warren, Evan E Eichler
  • A developmental framework for dissected leaf formation in the Arabidopsis relative Cardamine hirsuta
    Nature Genetics, Vol. 40, No. 9. (10 August 2008), pp. 1136-1141.
    by Michalis Barkoulas, Angela Hay, Evagelia Kougioumoutzi, Miltos Tsiantis
  • tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia
    Nature Genetics, Vol. 40, No. 9. (17 August 2008), pp. 1113-1118.
    by Birgit S Budde, Yasmin Namavar, Peter G Barth, Bwee T Poll-The, Gudrun Nürnberg, Christian Becker, Fred van Ruissen, Marian AJ Weterman, Kees Fluiter, Erik, Eleonora Aronica, Marjo S van der Knaap, Wolfgang Höhne, Mohammad R Toliat, Yanick J Crow, Maja Steinlin, Thomas Voit, Filip Roelens, Wim Brussel, Knut Brockmann, Marten Kyllerman, Eugen Boltshauser, Gerhard Hammersen, Michèl Willemsen, Lina Basel-Vanagaite, Ingeborg Krägeloh-Mann, Linda S de Vries, Laszlo Sztriha, Francesco Muntoni, Colin D Ferrie, Roberta Battini, Raoul CM Hennekam, Eugenio Grillo, Frits A Beemer, Loes ME Stoets, Bernd Wollnik, Peter Nürnberg, Frank Baas
  • Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis
    Nature Genetics, Vol. 40, No. 9. (10 August 2008), pp. 1103-1106.
    by Sylvia Hofmann, Andre Franke, Annegret Fischer, Gunnar Jacobs, Michael Nothnagel, Karoline I Gaede, Manfred Schürmann, Joachim Müller-Quernheim, Michael Krawczak, Philip Rosenstiel, Stefan Schreiber
  • Pathological responses to oncogenic Hedgehog signaling in skin are dependent on canonical Wnt/β-catenin signaling
    Nature Genetics, Vol. 40, No. 9. (01 August 2008), pp. 1130-1135.
    by Steven H Yang, Thomas Andl, Vladimir Grachtchouk, Aiqin Wang, Jianhong Liu, Li-Jyun Syu, Jenny Ferris, Timothy S Wang, Adam B Glick, Sarah E Millar, Andrzej A Dlugosz
  • ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation
    Nature Genetics, Vol. 40, No. 9. (01 August 2008), pp. 1119-1123.
    by Carine Le Goff, Fanny Morice-Picard, Nathalie Dagoneau, Lauren W Wang, Claire Perrot, Yanick J Crow, Florence Bauer, Elisabeth Flori, Catherine Prost-Squarcioni, Deborah Krakow, Gaoxiang Ge, Daniel S Greenspan, Damien Bonnet, Martine Le Merrer, Arnold Munnich, Suneel S Apte, Valérie Cormier-Daire
  • Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
    Nat Genet, Vol. 40, No. 9. (2008), pp. 1107-1112.
    by Steven A Mccarroll, Alan Huett, Petric Kuballa, Shannon D Chilewski, Aimee Landry, Philippe Goyette, Michael C Zody, Jennifer L Hall, Steven R Brant, Judy H Cho, Richard H Duerr, Mark S Silverberg, Kent D Taylor, John D Rioux, David Altshuler, Mark J Daly, Ramnik J Xavier
  • A common sequence motif associated with recombination hot spots and genome instability in humans
    Nature Genetics, Vol. 40, No. 9. (24 August 2008), pp. 1124-1129.
    by Simon Myers, Colin Freeman, Adam Auton, Peter Donnelly, Gil Mcvean
  • SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
    Nature Genetics, Vol. 40, No. 9. (17 August 2008), pp. 1098-1102.
    by Hiroyuki Unoki, Atsushi Takahashi, Takahisa Kawaguchi, Kazuo Hara, Momoko Horikoshi, Gitte Andersen, Daniel PK Ng, Johan Holmkvist, Knut Borch-Johnsen, Torben Jørgensen, Annelli Sandbæk, Torsten Lauritzen, Torben Hansen, Siti Nurbaya, Tatsuhiko Tsunoda, Michiaki Kubo, Tetsuya Babazono, Hiroshi Hirose, Matsuhiko Hayashi, Yasuhiko Iwamoto, Atsunori Kashiwagi, Kohei Kaku, Ryuzo Kawamori, Shyong E Tai, Oluf Pedersen, Naoyuki Kamatani, Takashi Kadowaki, Ryuichi Kikkawa, Yusuke Nakamura, Shiro Maeda
  • Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus
    Nature Genetics, Vol. 40, No. 9. (17 August 2008), pp. 1092-1097.
    by Kazuki Yasuda, Kazuaki Miyake, Yukio Horikawa, Kazuo Hara, Haruhiko Osawa, Hiroto Furuta, Yushi Hirota, Hiroyuki Mori, Anna Jonsson, Yoshifumi Sato, Kazuya Yamagata, Yoshinori Hinokio, He-Yao Wang, Toshihito Tanahashi, Naoto Nakamura, Yoshitomo Oka, Naoko Iwasaki, Yasuhiko Iwamoto, Yuichiro Yamada, Yutaka Seino, Hiroshi Maegawa, Atsunori Kashiwagi, Jun Takeda, Eiichi Maeda, Hyoung D Shin, Young M Cho, Kyong S Park, Hong K Lee, Maggie CY Ng, Ronald CW Ma, Wing-Yee So, Juliana CN Chan, Valeriya Lyssenko, Tiinamaija Tuomi, Peter Nilsson, Leif Groop, Naoyuki Kamatani, Akihiro Sekine, Yusuke Nakamura, Ken Yamamoto, Teruhiko Yoshida, Katsushi Tokunaga, Mitsuo Itakura, Hideichi Makino, Kishio Nanjo, Takashi Kadowaki, Masato Kasuga
  • Victor A. McKusick 1921–2008
    Nature Genetics, Vol. 40, No. 9., pp. 1037-1037.
    by David L Rimoin
  • Putting science over supposition in the arena of personalized genomics
    Nature Genetics, Vol. 40, No. 8., pp. 939-942.
    by Colleen M Mcbride, Sharon H Alford, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody
    posted by 1 person reyez
  • Famed biologist lost to Stalin's terror
    Nature Genetics, Vol. 40, No. 8., pp. 930-930.
    by Vadim Birstein
  • H19 in the pouch
    Nature Genetics, Vol. 40, No. 8., pp. 932-933.
    by Marisa S Bartolomei, Sebastien Vigneau, Michael J O'Neill
  • One PRDM is not enough for germ cell development
    Nature Genetics, Vol. 40, No. 8., pp. 934-935.
    by Elizabeth K Bikoff, Elizabeth J Robertson
  • Mapping the strand-specific transcriptome of fission yeast
    Nature Genetics, Vol. 40, No. 8., pp. 935-936.
    by Thomas R Gingeras
  • Dark skin mutations shed light on inherited anemia
    Nature Genetics, Vol. 40, No. 8., pp. 931-932.
    by Philip J Mason, Monica Bessler
  • Common nonsynonymous variants in PCSK1 confer risk of obesity
    Nature Genetics, Vol. 40, No. 8. (06 July 2008), pp. 943-945.
    by Michael Benzinou, John WM Creemers, Helene Choquet, Stephane Lobbens, Christian Dina, Emmanuelle Durand, Audrey Guerardel, Philippe Boutin, Beatrice Jouret, Barbara Heude, Beverley Balkau, Jean Tichet, Michel Marre, Natascha Potoczna, Fritz Horber, Catherine Le Stunff, Sebastien Czernichow, Annelli Sandbaek, Torsten Lauritzen, Knut Borch-Johnsen, Gitte Andersen, Wieland Kiess, Antje Körner, Peter Kovacs, Peter Jacobson, Lena MS Carlsson, Andrew J Walley, Torben Jørgensen, Torben Hansen, Oluf Pedersen, David Meyre, Philippe Froguel
  • Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
    Nature Genetics, Vol. 40, No. 8. (11 July 2008), pp. 949-951.
    by Deborah JG Mackay, Jonathan LA Callaway, Sophie M Marks, Helen E White, Carlo L Acerini, Susanne E Boonen, Pinar Dayanikli, Helen V Firth, Judith A Goodship, Andreas P Haemers, Johanne MD Hahnemann, Olga Kordonouri, Ahmed F Masoud, Elsebet Oestergaard, John Storr, Sian Ellard, Andrew T Hattersley, David O Robinson, Karen I Temple
  • Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension
    Nature Genetics, Vol. 40, No. 8. (29 June 2008), pp. 952-954.
    by Michal Pravenec, Paul C Churchill, Monique C Churchill, Ondrej Viklicky, Ludmila Kazdova, Timothy J Aitman, Enrico Petretto, Norbert Hubner, Caroline A Wallace, Heike Zimdahl, Vaclav Zidek, Vladimir Landa, Joseph Dunbar, Anil Bidani, Karen Griffin, Nathan Qi, Martina Maxova, Vladimir Kren, Petr Mlejnek, Jiaming Wang, Theodore W Kurtz
  • PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
    Nat Genet, Vol. 40, No. 8. (2008), pp. 946-948.
    by Barbara Schormair, David Kemlink, Darina Roeske, Gertrud Eckstein, Lan Xiong, Peter Lichtner, Stephan Ripke, Claudia Trenkwalder, Alexander Zimprich, Karin Stiasny-Kolster, Wolfgang Oertel, Cornelius G Bachmann, Walter Paulus, Birgit Hogl, Birgit Frauscher, Viola Gschliesser, Werner Poewe, Ines Peglau, Pavel Vodicka, Jana Vavrova, Karel Sonka, Sona Nevsimalova, Jacques Montplaisir, Gustavo Turecki, Guy Rouleau, Christian Gieger, Thomas Illig, H-Erich Wichmann, Florian Holsboer, Bertram Muller-Myhsok, Thomas Meitinger, Juliane Winkelmann
  • Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
    Nature Genetics, Vol. 40, No. 8. (29 June 2008), pp. 955-962.
    by Jeffrey C Barrett, Sarah Hansoul, Dan L Nicolae, Judy H Cho, Richard H Duerr, John D Rioux, Steven R Brant, Mark S Silverberg, Kent D Taylor, Michael M Barmada, Alain Bitton, Themistocles Dassopoulos, Lisa W Datta, Todd Green, Anne M Griffiths, Emily O Kistner, Michael T Murtha, Miguel D Regueiro, Jerome I Rotter, Philip L Schumm, Hillary A Steinhart, Stephan R Targan, Ramnik J Xavier, Cécile Libioulle, Cynthia Sandor, Mark Lathrop, Jacques Belaiche, Olivier Dewit, Ivo Gut, Simon Heath, Debby Laukens, Myriam Mni, Paul Rutgeerts, André Van Gossum, Diana Zelenika, Denis Franchimont, Jean-Pierre Hugot, Martine de Vos, Severine Vermeire, Edouard Louis, Lon R Cardon, Carl A Anderson, Hazel Drummond, Elaine Nimmo, Tariq Ahmad, Natalie J Prescott, Clive M Onnie, Sheila A Fisher, Jonathan Marchini, Jilur Ghori, Suzannah Bumpstead, Rhian Gwilliam, Mark Tremelling, Panos Deloukas, John Mansfield, Derek Jewell, Jack Satsangi, Christopher G Mathew, Miles Parkes, Michel Georges, Mark J Daly
  • Dynamic transcriptome of Schizosaccharomyces pombe shown by RNA-DNA hybrid mapping
    Nat Genet, Vol. 40, No. 8. (2008), pp. 977-986.
    by Natalie Dutrow, David A Nix, Derick Holt, Brett Milash, Brian Dalley, Erick Westbroek, Timothy J Parnell, Bradley R Cairns
  • High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi
    Nature Genetics, Vol. 40, No. 8. (27 July 2008), pp. 987-993.
    by Kathryn E Holt, Julian Parkhill, Camila J Mazzoni, Philippe Roumagnac, François-Xavier Weill, Ian Goodhead, Richard Rance, Stephen Baker, Duncan J Maskell, John Wain, Christiane Dolecek, Mark Achtman, Gordon Dougan
    posted by 2 people Stew aconesa
  • Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects
    Nature Genetics, Vol. 40, No. 8. (20 July 2008), pp. 963-970.
    by Kelly A Mcgowan, Jun Z Li, Christopher Y Park, Veronica Beaudry, Holly K Tabor, Amit J Sabnis, Weibin Zhang, Helmut Fuchs, Martin H de Angelis, Richard M Myers, Laura D Attardi, Gregory S Barsh
  • Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians
    Nature Genetics, Vol. 40, No. 8. (29 June 2008), pp. 971-976.
    by Guillaume Smits, Andrew J Mungall, Sam Griffiths-Jones, Paul Smith, Delphine Beury, Lucy Matthews, Jane Rogers, Andrew J Pask, Geoff Shaw, John L Vandeberg, John R Mccarrey, Marilyn B Renfree, Wolf Reik, Ian Dunham
  • Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis
    Nature Genetics, Vol. 40, No. 8. (11 July 2008), pp. 994-998.
    by Yoshinari Miyamoto, Dongquan Shi, Masahiro Nakajima, Kouichi Ozaki, Akihiro Sudo, Akihiro Kotani, Atsumasa Uchida, Toshihiro Tanaka, Naoshi Fukui, Tatsuhiko Tsunoda, Atsushi Takahashi, Yusuke Nakamura, Qing Jiang, Shiro Ikegawa
  • Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia
    Nature Genetics, Vol. 40, No. 8. (29 June 2008), pp. 999-1003.
    by Matthew J Rock, Jean Prenen, Vincent A Funari, Tara L Funari, Barry Merriman, Stanley F Nelson, Ralph S Lachman, William R Wilcox, Soraya Reyno, Roberto Quadrelli, Alicia Vaglio, Grzegorz Owsianik, Annelies Janssens, Thomas Voets, Shiro Ikegawa, Toshiro Nagai, David L Rimoin, Bernd Nilius, Daniel H Cohn
  • A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse
    Nat Genet, Vol. 40, No. 8. (2008), pp. 1004-1009.
    by Rosengren, Anna Golovko, Elisabeth Sundstrom, Ino Curik, Johan Lennartsson, Monika H Seltenhammer, Thomas Druml, Matthew Binns, Carolyn Fitzsimmons, Gabriella Lindgren, Kaj Sandberg, Roswitha Baumung, Monika Vetterlein, Sara Stromberg, Manfred Grabherr, Claire Wade, Kerstin Lindblad-Toh, Fredrik Ponten, Carl-Henrik Heldin, Johann Solkner, Leif Andersson
    posted by 1 person oelemento
  • Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease
    Nature Genetics, Vol. 40, No. 8. (06 July 2008), pp. 1010-1015.
    by Sakura Saburi, Ian Hester, Evelyne Fischer, Marco Pontoglio, Vera Eremina, Manfred Gessler, Sue E Quaggin, Robert Harrison, Richard Mount, Helen Mcneill
  • Deletion in a gene associated with grain size increased yields during rice domestication
    Nat Genet, Vol. 40, No. 8. (2008), pp. 1023-1028.
    by Ayahiko Shomura, Takeshi Izawa, Kaworu Ebana, Takeshi Ebitani, Hiromi Kanegae, Saeko Konishi, Masahiro Yano
    posted by 1 person jmjimenez
  • Critical function of Prdm14 for the establishment of the germ cell lineage in mice
    Nature Genetics, Vol. 40, No. 8. (11 July 2008), pp. 1016-1022.
    by Masashi Yamaji, Yoshiyuki Seki, Kazuki Kurimoto, Yukihiro Yabuta, Mihoko Yuasa, Mayo Shigeta, Kaori Yamanaka, Yasuhide Ohinata, Mitinori Saitou
  • Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
    Nature Genetics, Vol. 40, No. 8., pp. 1029-1029.
    by Daniel F Gudbjartsson, Patrick Sulem, Simon N Stacey, Alisa M Goldstein, Thorunn Rafnar, Bardur Sigurgeirsson, Kristrun R Benediktsdottir, Kristin Thorisdottir, Rafn Ragnarsson, Steinunn G Sveinsdottir, Veronica Magnusson, Annika Lindblom, Konstantinos Kostulas, Rafael Botella-Estrada, Virtudes Soriano, Pablo Juberías, Matilde Grasa, Berta Saez, Raquel Andres, Dominique Scherer, Peter Rudnai, Eugene Gurzau, Kvetoslava Koppova, Lambertus A Kiemeney, Margret Jakobsdottir, Stacy Steinberg, Agnar Helgason, Solveig Gretarsdottir, Margaret A Tucker, José I Mayordomo, Eduardo Nagore, Rajiv Kumar, Johan Hansson, Jon H Olafsson, Jeffrey Gulcher, Augustine Kong, Unnur Thorsteinsdottir, Kari Stefansson
  • ESR1 gene amplification in breast cancer: a common phenomenon?
    Nature Genetics, Vol. 40, No. 7., pp. 806-807.
    by Lindsay A Brown, Jeremy Hoog, Suet-Feung Chin, Yu Tao, Abd A Zayed, Koei Chin, Andrew E Teschendorff, John F Quackenbush, John C Marioni, Samuel Leung, Charles M Perou, Torsten O Neilsen, Matthew Ellis, Joe W Gray, Philip S Bernard, David G Huntsman, Carlos Caldas
    posted by 1 person caseybrown
  • Reply to “ESR1 gene amplification in breast cancer: a common phenomenon?”
    Nature Genetics, Vol. 40, No. 7., pp. 810-812.
    by Frederik Holst, Phillip Stahl, Olaf Hellwinkel, Ana-Maria Dancau, Antje Krohn, Laura Wuth, Christian Heupel, Annette Lebeau, Luigi Terracciano, Khawla Al-Kuraya, Fritz Jänicke, Guido Sauter, Ronald Simon
    posted by 1 person caseybrown
  • ESR1 gene amplification in breast cancer: a common phenomenon?
    Nature Genetics, Vol. 40, No. 7., pp. 807-808.
    by Hugo M Horlings, Anna Bergamaschi, Silje H Nordgard, Young H Kim, Wonshik Han, Dong-Young Noh, Keyan Salari, Simon A Joosse, Fabien Reyal, Ole C Lingjaerde, Vessela N Kristensen, Anne-Lise Børresen-Dale, Jonathan Pollack, Marc J van de Vijver
    posted by 1 person caseybrown
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