Works matching IS 09646906 AND DT 2016 AND VI 25 AND IP 23


Results: 20
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    CORRIGENDUM.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 23, p. 5286, doi. 10.1093/hmg/ddw390
    Publication type:
    Article
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    PNPLA3 overexpression results in reduction of proteins predisposing to fibrosis.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 23, p. 5212, doi. 10.1093/hmg/ddw341
    By:
    • Pingitore, Piero;
    • Dongiovanni, Paola;
    • Motta, Benedetta Maria;
    • Meroni, Marica;
    • Massimo Lepore, Saverio;
    • Mancina, Rosellina Margherita;
    • Pelusi, Serena;
    • Russo, Cristina;
    • Caddeo, Andrea;
    • Rossi, Giorgio;
    • Montalcini, Tiziana;
    • Pujia, Arturo;
    • Wiklund, Olov;
    • Valenti, Luca;
    • Romeo, Stefano
    Publication type:
    Article
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    Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 23, p. 5083, doi. 10.1093/hmg/ddw337
    By:
    • Qiumin Tan;
    • Yalamanchili, Hari Krishna;
    • Jeehye Park;
    • De Maio, Antonia;
    • Hsiang-Chih Lu;
    • Ying-Wooi Wan;
    • White, Joshua J.;
    • Bondar, Vitaliy V.;
    • Sayegh, Layal S.;
    • Xiuyun Liu;
    • Yan Gao;
    • Sillitoe, Roy V.;
    • Orr, Harry T.;
    • Zhandong Liu;
    • Huda Y. Zoghbi
    Publication type:
    Article
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    Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 23, p. 5265, doi. 10.1093/hmg/ddw333
    By:
    • Sze-man Tang, Clara;
    • Hongsheng Gui;
    • Kapoor, Ashish;
    • Jeong-Hyun Kim;
    • Luzón-Toro, Berta;
    • Pelet, Anna;
    • Burzynski, Grzegorz;
    • Lantieri, Francesca;
    • Man-ting So;
    • Berrios, Courtney;
    • Hyoung Doo Shin;
    • Fernandez, Raquel M.;
    • Thuy-Linh Le;
    • Verheij, Joke B. G. M.;
    • Matera, Ivana;
    • Cherny, Stacey S.;
    • Nandakumar, Priyanka;
    • Hyun Sub Cheong;
    • Antiñolo, Guillermo;
    • Amiel, Jeanne
    Publication type:
    Article
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    Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 23, p. 5244, doi. 10.1093/hmg/ddw324
    By:
    • Heming Wang;
    • Cade, Brian E.;
    • Chen, Han;
    • Gleason, Kevin J.;
    • Saxena, Richa;
    • Tao Feng;
    • Larkin, Emma K.;
    • Vasan, Ramachandran S.;
    • Honghuang Lin;
    • Patel, Sanjay R.;
    • Tracy, Russell P.;
    • Yongmei Liu;
    • Gottlieb, Daniel J.;
    • Below, Jennifer E.;
    • Hanis, Craig L.;
    • Petty, Lauren E.;
    • Sunyaev, Shamil R.;
    • Frazier-Wood, Alexis C.;
    • Rotter, Jerome I.;
    • Post, Wendy
    Publication type:
    Article
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    Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 23, p. 5234, doi. 10.1093/hmg/ddw289
    By:
    • Yi-Hsiang Hsu;
    • Guo Li;
    • Ching-Ti Liu;
    • Brody, Jennifer A.;
    • Karasik, David;
    • Wen-Chi Chou;
    • Demissie, Serkalem;
    • Nandakumar, Kannabiran;
    • Yanhua Zhou;
    • Chia-Ho Cheng;
    • Gill, Richard;
    • Gibbs, Richard A.;
    • Muzny, Donna;
    • Santibanez, Jireh;
    • Estrada, Karol;
    • Rivadeneira, Fernando;
    • Harris, Tamara;
    • Gudnason, Vilmundur;
    • Uitterlinden, Andre;
    • Psaty, Bruce M.
    Publication type:
    Article
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