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  • Corrigendum: TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.

    Published in:
    2011
    By:
    • Davis, Erica E;
    • Zhang, Qi;
    • Liu, Qin;
    • Diplas, Bill H;
    • Davey, Lisa M;
    • Hartley, Jane;
    • Stoetzel, Corinne;
    • Szymanska, Katarzyna;
    • Ramaswami, Gokul;
    • Logan, Clare V;
    • Muzny, Donna M;
    • Young, Alice C;
    • Wheeler, David A;
    • Cruz, Pedro;
    • Morgan, Margaret;
    • Lewis, Lora R;
    • Cherukuri, Praveen;
    • Maskeri, Baishali;
    • Hansen, Nancy F;
    • Mullikin, James C
    Publication type:
    Correction Notice

  • TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.

    Published in:
    Nature Genetics, 2011, v. 43, n. 3, p. 189, doi. 10.1038/ng.756
    By:
    • Davis, Erica E.;
    • Qi Zhang;
    • Qin Liu;
    • Diplas, Bill H.;
    • Davey, Lisa M.;
    • Hartley, Jane;
    • Stoetzel, Corinne;
    • Szymanska, Katarzyna;
    • Ramaswami, Gokul;
    • Logan, Clare V.;
    • Muzny, Donna M.;
    • Young, Alice C.;
    • Wheeler, David A.;
    • Cruz, Pedro;
    • Morgan, Margaret;
    • Lewis, Lora R.;
    • Cherukuri, Praveen;
    • Maskeri, Baishali;
    • Hansen, Nancy F.;
    • Mullikin, James C.
    Publication type:
    Article

  • A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.

    Published in:
    Nature Genetics, 2009, v. 41, n. 6, p. 739, doi. 10.1038/ng.366
    By:
    • Khanna, Hemant;
    • Davis, Erica E.;
    • Murga-Zamalloa, Carlos A.;
    • Estrada-Cuzcano, Alejandro;
    • Lopez, Irma;
    • den Hollander, Anneke I.;
    • Zonneveld, Marijke N.;
    • Othman, Mohammad I.;
    • Waseem, Naushin;
    • Chakarova, Christina F.;
    • Maubaret, Cecilia;
    • Diaz-Font, Anna;
    • MacDonald, Ian;
    • Muzny, Donna M;
    • Wheeler, David A.;
    • Morgan, Margaret;
    • Lewis, Lora R.;
    • Logan, Clare V.;
    • Tan, Perciliz L.;
    • Beer, Michael A.
    Publication type:
    Article

  • Integrating common and rare genetic variation in diverse human populations.

    Published in:
    Nature, 2010, v. 467, n. 7311, p. 52, doi. 10.1038/nature09298
    By:
    • Altshuler, David M.;
    • Gibbs, Richard A.;
    • Peltonen, Leena;
    • Dermitzakis, Emmanouil;
    • Schaffner, Stephen F.;
    • Yu, Fuli;
    • Bonnen, Penelope E.;
    • de Bakker, Paul I. W.;
    • Deloukas, Panos;
    • Gabriel, Stacey B.;
    • Gwilliam, Rhian;
    • Hunt, Sarah;
    • Inouye, Michael;
    • Jia, Xiaoming;
    • Palotie, Aarno;
    • Parkin, Melissa;
    • Whittaker, Pamela;
    • Chang, Kyle;
    • Hawes, Alicia;
    • Lewis, Lora R.
    Publication type:
    Article

  • The finished DNA sequence of human chromosome 12.

    Published in:
    Nature, 2006, v. 440, n. 7082, p. 346, doi. 10.1038/nature04569
    By:
    • Scherer, Steven E.;
    • Muzny, Donna M.;
    • Buhay, Christian J.;
    • Chen, Rui;
    • Cree, Andrew;
    • Yan Ding;
    • Dugan-Rocha, Shannon;
    • Gill, Rachel;
    • Gunaratne, Preethi;
    • Harris, R. Alan;
    • Hawes, Alicia C.;
    • Hernandez, Judith;
    • Hodgson, Anne V.;
    • Hume, Jennifer;
    • Jackson, Andrew;
    • Khan, Ziad Mohid;
    • Kovar-Smith, Christie;
    • Lewis, Lora R.;
    • Lozado, Ryan J.;
    • Metzker, Michael L.
    Publication type:
    Article

  • Comprehensive molecular characterization of human colon and rectal cancer.

    Published in:
    Nature, 2012, v. 487, n. 7407, p. 330, doi. 10.1038/nature11252
    By:
    • Muzny, Donna M.;
    • Bainbridge, Matthew N.;
    • Chang, Kyle;
    • Dinh, Huyen H.;
    • Drummond, Jennifer A.;
    • Fowler, Gerald;
    • Kovar, Christie L.;
    • Lewis, Lora R.;
    • Morgan, Margaret B.;
    • Newsham, Irene F.;
    • Reid, Jeffrey G.;
    • Santibanez, Jireh;
    • Shinbrot, Eve;
    • Trevino, Lisa R.;
    • Wu, Yuan-Qing;
    • Wang, Min;
    • Gunaratne, Preethi;
    • Donehower, Lawrence A.;
    • Creighton, Chad J.;
    • Wheeler, David A.
    Publication type:
    Article