Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 14

Results: 20
    1
    2

    Fine mapping of the association with obesity at the FTO locus in African-derived populations.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. 2907, doi. 10.1093/hmg/ddq178
    By:
    • Hassanein, Mohamed T.;
    • Lyon, Helen N.;
    • Nguyen, Thutrang T.;
    • Akylbekova, Ermeg L.;
    • Waters, Kevin;
    • Lettre, Guillaume;
    • Tayo, Bamidele;
    • Forrester, Terrence;
    • Sarpong, Daniel F.;
    • Stram, Dan O.;
    • Butler, Johannah L.;
    • Wilks, Rainford;
    • Liu, Jiankang;
    • Le Marchand, Loic;
    • Kolonel, Laurence N.;
    • Zhu, Xiaofeng;
    • Henderson, Brian;
    • Cooper, Richard;
    • McKenzie, Colin;
    • Taylor, Herman A.
    Publication type:
    Article
    3

    A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. 2780, doi. 10.1093/hmg/ddq179
    By:
    • Yu, Tao;
    • Li, Zhongyou;
    • Jia, Zhengping;
    • Clapcote, Steven J.;
    • Liu, Chunhong;
    • Li, Shaomin;
    • Asrar, Suhail;
    • Pao, Annie;
    • Chen, Rongqing;
    • Fan, Ni;
    • Carattini-Rivera, Sandra;
    • Bechard, Allison R.;
    • Spring, Shoshana;
    • Henkelman, R. Mark;
    • Stoica, George;
    • Matsui, Sei-Ichi;
    • Nowak, Norma J.;
    • Roder, John C.;
    • Chen, Chu;
    • Bradley, Allan
    Publication type:
    Article
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    6

    Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. 2917, doi. 10.1093/hmg/ddq196
    By:
    • Garcia-Barceló, Maria-Mercè;
    • Yeung, Ming-Yiu;
    • Miao, Xiao-Ping;
    • Tang, Clara Sze-Man;
    • Chen, Guo;
    • So, Man-Ting;
    • Ngan, Elly Sau-Wai;
    • Lui, Vincent Chi-Hang;
    • Chen, Yan;
    • Liu, Xue-Lai;
    • Hui, Kenneth-Jeremy W.S.;
    • Li, Long;
    • Guo, Wei-Hong;
    • Sun, Xiao-Bin;
    • Tou, Jin-Fa;
    • Chan, Kin-Wai;
    • Wu, Xuan-Zhao;
    • Song, You-Qiang;
    • Chan, Danny;
    • Cheung, Kenneth
    Publication type:
    Article
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    10
    11

    Subscription Page.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. NP, doi. 10.1093/hmg/ddq244
    Publication type:
    Article
    12
    13

    The RET51/FKBP52 complex and its involvement in Parkinson disease.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. 2804, doi. 10.1093/hmg/ddq181
    By:
    • Fusco, Daniela;
    • Vargiolu, Manuela;
    • Vidone, Michele;
    • Mariani, Elisa;
    • Pennisi, Lucia Fiammetta;
    • Bonora, Elena;
    • Capellari, Sabina;
    • Dirnberger, Dietmar;
    • Baumeister, Ralf;
    • Martinelli, Paolo;
    • Romeo, Giovanni
    Publication type:
    Article
    14

    A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. 2877, doi. 10.1093/hmg/ddq173
    By:
    • Acuña-Alonzo, Víctor;
    • Flores-Dorantes, Teresa;
    • Kruit, Janine K.;
    • Villarreal-Molina, Teresa;
    • Arellano-Campos, Olimpia;
    • Hünemeier, Tábita;
    • Moreno-Estrada, Andrés;
    • Ortiz-López, Ma Guadalupe;
    • Villamil-Ramírez, Hugo;
    • León-Mimila, Paola;
    • Villalobos-Comparan, Marisela;
    • Jacobo-Albavera, Leonor;
    • Ramírez-Jiménez, Salvador;
    • Sikora, Martin;
    • Zhang, Lin-Hua;
    • Pape, Terry D.;
    • Granados-Silvestre, Ma de Ángeles;
    • Montufar-Robles, Isela;
    • Tito-Alvarez, Ana M.;
    • Zurita-Salinas, Camilo
    Publication type:
    Article
    15

    Common variants in CASP3 confer susceptibility to Kawasaki disease.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. 2898, doi. 10.1093/hmg/ddq176
    By:
    • Onouchi, Yoshihiro;
    • Ozaki, Kouichi;
    • Buns, Jane C.;
    • Shimizu, Chisato;
    • Hamada, Hiromichi;
    • Honda, Takafumi;
    • Terai, Masaru;
    • Honda, Akihito;
    • Takeuchi, Takashi;
    • Shibuta, Shoichi;
    • Suenaga, Tomohiro;
    • Suzuki, Hiroyuki;
    • Higashi, Kouji;
    • Yasukawa, Kumi;
    • Suzuki, Yoichi;
    • Sasago, Kumiko;
    • Kemmotsu, Yasushi;
    • Takatsuki, Shinichi;
    • Saji, Tsutomu;
    • Yoshikawa, Tetsushi
    Publication type:
    Article
    16

    Contents Page.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. NP, doi. 10.1093/hmg/ddq240
    Publication type:
    Article
    17
    18

    Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. 2886, doi. 10.1093/hmg/ddq174
    By:
    • Wang, Xianshu;
    • Pankratz, V. Shane;
    • Fredericksen, Zachary;
    • Tarrell, Robert;
    • Karaus, Mary;
    • McGuffog, Lesley;
    • Pharaoh, Paul D.P.;
    • Ponder, Bruce A.J.;
    • Dunning, Alison M.;
    • Peock, Susan;
    • Cook, Margaret;
    • Oliver, Clare;
    • Frost, Debra;
    • Sinilnikova, Olga M.;
    • Stoppa-Lyonnet, Dominique;
    • Mazoyer, Sylvie;
    • Houdayer, Claude;
    • Hogervorst, Frans B.L.;
    • Hooning, Maartje J.;
    • Ligtenberg, Marjolijn J.
    Publication type:
    Article
    19

    Cover Page.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. NP, doi. 10.1093/hmg/ddq238
    Publication type:
    Article
    20

    Editorial Board.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 14, p. NP, doi. 10.1093/hmg/ddq242
    Publication type:
    Article