Works matching IS 10614036 AND DT 2010 AND VI 42 AND IP 8

Results: 22

Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 655, doi. 10.1038/ng.631
By:
- Hirschfield, Gideon M.;
- Xiangdong Liu;
- Younghun Han;
- Gorlov, Ivan P.;
- Yan Lu;
- Chun Xu;
- Yue Lu;
- Wei Chen;
- Juran, Brian D.;
- Coltescu, Catalina;
- Mason, Andrew L.;
- Milkiewicz, Piotr;
- Myers, Robert P.;
- Odin, Joseph A.;
- Luketic, Velimir A.;
- Speiciene, Danute;
- Vincent, Catherine;
- Levy, Cynthia;
- Gregersen, Peter K.;
- Jinyi Zhang
Publication type:
Article
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 658, doi. 10.1038/ng.627
By:
- Xiangdong Liu;
- Invernizzi, Pietro;
- Yue Lu;
- Kosoy, Roman;
- Yan Lu;
- Bianchi, Ilaria;
- Podda, Mauro;
- Chun Xu;
- Gang Xie;
- Macciardi, Fabio;
- Selmi, Carlo;
- Lupoli, Sara;
- Shigeta, Russell;
- Ransom, Michael;
- Lleo, Ana;
- Lee, Annette T.;
- Mason, Andrew L.;
- Myers, Robert P.;
- Peltekian, Kevork M.;
- Ghent, Cameron N.
Publication type:
Article
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 661, doi. 10.1038/ng.626
By:
- Conde, Lucia;
- Halperin, Eran;
- Akers, Nicholas K.;
- Brown, Kevin M.;
- Smedby, Karin E.;
- Rothman, Nathaniel;
- Nieters, Alexandra;
- Slager, Susan L.;
- Brooks-Wilson, Angela;
- Agana, Luz;
- Riby, Jacques;
- Jianjun Liu;
- Adami, Hans-Olov;
- Darabi, Hatef;
- Hjalgrim, Henrik;
- Hui-Qi Low;
- Humphreys, Keith;
- Melbye, Mads;
- Chang, Ellen T.;
- Glimelius, Bengt
Publication type:
Article
Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 665, doi. 10.1038/ng.620
By:
- Nikoloski, Gorica;
- Langemeijer, Saskia M. C.;
- Kuiper, Roland P.;
- Knops, Ruth;
- Massop, Marion;
- Tönnissen, Evelyn R. L. T. M.;
- Van der Heijden, Adrian;
- Scheele, Theresia N.;
- Vandenberghe, Peter;
- de Witte, Theo;
- van der Reijden, Bert A.;
- Jansen, Joop H.
Publication type:
Article
Preempting and preventing drug-induced liver injury.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 650, doi. 10.1038/ng0810-650
By:
- Aithal, Guruprasad P.;
- Daly, Ann K.
Publication type:
Article
Research highlights.
Published in:
2010
Publication type:
Abstract
Androgen-induced TOP2B-mediated double-strand breaks and prostate cancer gene rearrangements.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 668, doi. 10.1038/ng.613
By:
- Haffner, Michael C.;
- Aryee, Martin J.;
- Toubaji, Antoun;
- Esopi, David M.;
- Albadine, Roula;
- Gurel, Bora;
- Isaacs, William B.;
- Bova, G. Steven;
- Wennuan Liu;
- Jianfeng Xu;
- Meeker, Alan K.;
- Netto, George;
- De Marzo, Angelo M.;
- Nelson, William G.;
- Yegnasubramanian, Srinivasan
Publication type:
Article
Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 688, doi. 10.1038/ng.623
By:
- Bezzina, Connie R.;
- Pazoki, Raha;
- Bardai, Abdennasser;
- Marsman, Roos F.;
- de Jong, Jonas S. S. G.;
- Blom, Marieke T.;
- Scicluna, Brendon P.;
- Jukema, J. Wouter;
- Bindraban, Navin R.;
- Lichtner, Peter;
- Pfeufer, Arne;
- Bishopric, Nanette H.;
- Roden, Dan M.;
- Meitinger, Thomas;
- Chugh, Sumeet S.;
- Myerburg, Robert J.;
- Jouven, Xavier;
- Kääb, Stefan;
- Dekker, Lukas R. C.;
- Tan, Hanno L.
Publication type:
Article
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 692, doi. 10.1038/ng.622
By:
- Gretarsdottir, Solveig;
- Baas, Annette F.;
- Thorleifsson, Gudmar;
- Holm, Hilma;
- den Heijer, Martin;
- de Vries, Jean-Paul P. M.;
- Kranendonk, Steef E.;
- Zeebregts, Clark J. A. M.;
- van Sterkenburg, Steven M.;
- Geelkerken, Robert H.;
- van Rij, Andre M.;
- Williams, Michael J. A.;
- Boll, Albert P. M.;
- Kostic, Jelena P.;
- Jonasdottir, Adalbjorg;
- Jonasdottir, Aslaug;
- Walters, G. Bragi;
- Masson, Gisli;
- Sulem, Patrick;
- Saemundsdottir, Jona
Publication type:
Article
Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 698, doi. 10.1038/ng.625
By:
- Remmers, Elaine F.;
- Cosan, Fulya;
- Kirino, Yohei;
- Ombrello, Michael J.;
- Abaci, Neslihan;
- Satorius, Colleen;
- Le, Julie M.;
- Yang, Barbara;
- Korman, Benjamin D.;
- Cakiris, Aris;
- Aglar, Oznur;
- Emrence, Zeliha;
- Azakli, Hulya;
- Ustek, Duran;
- Tugal-Tutkun, Ilknur;
- Akman-Demir, Gulsen;
- Wei Chen;
- Amos, Christopher I.;
- Dizon, Michael B.;
- Kose, Afet Akdag
Publication type:
Article
Matriptase initiates activation of epidermal pro-kallikrein and disease onset in a mouse model of Netherton syndrome.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 676, doi. 10.1038/ng.629
By:
- Sales, Katiuchia Uzzun;
- Masedunskas, Andrius;
- Bey, Alexandra L.;
- Rasmussen, Amber L.;
- Weigert, Roberto;
- List, Karin;
- Szabo, Roman;
- Overbeek, Paul A.;
- Bugge, Thomas H.
Publication type:
Article
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 684, doi. 10.1038/ng.628
By:
- Johansen, Christopher T.;
- Jian Wang;
- Lanktree, Matthew B.;
- Henian Cao;
- McIntyre, Adam D.;
- Ban, Matthew R.;
- Martins, Rebecca A.;
- Kennedy, Brooke A.;
- Hassell, Reina G.;
- Visser, Maartje E.;
- Schwartz, Stephen M.;
- Voight, Benjamin F.;
- Elosua, Roberto;
- Salomaa, Veikko;
- O'Donnell, Christopher J.;
- Dallinga-Thie, Geesje M.;
- Anand, Sonia S.;
- Yusuf, Salim;
- Huff, Murray W.;
- Kathiresan, Sekar
Publication type:
Article
Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.
Published in:
2010
By:
- Beaty, Terri H;
- Murray, Jeffrey C;
- Marazita, Mary L;
- Munger, Ronald G;
- Hetmanski, Ingo Ruczinski Jacqueline B;
- Liang, Kung Yee;
- Wu, Tao;
- Murray, Tanda;
- Fallin, M Daniele;
- Redett, Richard A;
- Raymond, Gerald;
- Schwender, Holger;
- Jin, Shin C;
- Cooper, Margaret E;
- Dunnwald, Martine;
- Mansilla, Maria A;
- Leslie, Elizabeth;
- Bullard, Stephen;
- Lidral, Andrew C;
- Moreno, Lina M
Publication type:
Correction Notice
A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 707, doi. 10.1038/ng.612
By:
- Uno, Satoko;
- Zembutsu, Hitoshi;
- Hirasawa, Akira;
- Takahashi, Atsushi;
- Kubo, Michiaki;
- Akahane, Tomoko;
- Aoki, Daisuke;
- Kamatani, Naoyuki;
- Hirata, Koichi;
- Nakamura, Yusuke
Publication type:
Article
Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 703, doi. 10.1038/ng.624
By:
- Mizuki, Nobuhisa;
- Meguro, Akira;
- Ota, Masao;
- Ohno, Shigeaki;
- Shiota, Tomoko;
- Kawagoe, Tatsukata;
- Ito, Norihiko;
- Kera, Jiro;
- Okada, Eiichi;
- Yatsu, Keisuke;
- Yeong-Wook Song;
- Eun-Bong Lee;
- Kitaichi, Nobuyoshi;
- Namba, Kenichi;
- Horie, Yukihiro;
- Takeno, Mitsuhiro;
- Sugita, Sunao;
- Mochizuki, Manabu;
- Bahram, Seiamak;
- Ishigatsubo, Yoshiaki
Publication type:
Article
A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 711, doi. 10.1038/ng.632
By:
- Singer, Jonathan B.;
- Lewitzky, Steve;
- Leroy, Elisabeth;
- Fan Yang;
- Xiaojun Zhao;
- Klickstein, Lloyd;
- Wright, Timothy M.;
- Meyer, Joanne;
- Paulding, Charles A.
Publication type:
Article
Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 715, doi. 10.1038/ng.619
By:
- Barretina, Jordi;
- Taylor, Barry S.;
- Banerji, Shantanu;
- Ramos, Alexis H.;
- Lagos-Quintana, Mariana;
- DeCarolis, Penelope L.;
- Shah, Kinjal;
- Socci, Nicholas D.;
- Weir, Barbara A.;
- Ho, Alan;
- Chiang, Derek Y.;
- Reva, Boris;
- Mermel, Craig H.;
- Getz, Gad;
- Antipin, Yevgenyi;
- Beroukhim, Rameen;
- Major, John E.;
- Hatton, Charles;
- Nicoletti, Richard;
- Hanna, Megan
Publication type:
Article
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 722, doi. 10.1038/ng.621
By:
- Ernst, Thomas;
- Chase, Andrew J.;
- Score, Joannah;
- Hidalgo-Curtis, Claire E.;
- Bryant, Catherine;
- Jones, Amy V.;
- Waghorn, Katherine;
- Zoi, Katerina;
- Ross, Fiona M;
- Reiter, Andreas;
- Hochhaus, Andreas;
- Drexler, Hans G.;
- Duncombe, Andrew;
- Cervantes, Francisco;
- Oscier, David;
- Boultwood, Jacqueline;
- Grand, Francis H.;
- Cross, Nicholas C. P.
Publication type:
Article
Collaborative genomics for human health and cooperation in the Mediterranean region.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 641, doi. 10.1038/ng0810-641
By:
- Özçelik, Tayfun;
- Kanaan, Moien;
- Avraham, Karen B.;
- Yannoukakos, Drakoulis;
- Mégarbané, André;
- Tadmouri, Ghazi O.;
- Middleton, Lefkos;
- Romeo, Giovanni;
- King, Mary-Claire;
- Levy-Lahad, Ephrat
Publication type:
Article
Basin of attraction.
Published in:
2010
Publication type:
Editorial
On the origin of prostate fusion oncogenes.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 647, doi. 10.1038/ng0810-647
By:
- Bartek, Jiri;
- Hamerlik, Petra;
- Lukas, Jiri
Publication type:
Article
Variation across the allele frequency spectrum.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 648, doi. 10.1038/ng0810-648
By:
- Gloyn, Anna L.;
- McCarthy, Mark I.
Publication type:
Article