Found: 14

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  • Rates of contributory de novo mutation in high and low-risk autism families.

    Published in:
    Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02533-z
    By:
    • Yoon, Seungtai;
    • Munoz, Adriana;
    • Yamrom, Boris;
    • Lee, Yoon-ha;
    • Andrews, Peter;
    • Marks, Steven;
    • Wang, Zihua;
    • Reeves, Catherine;
    • Winterkorn, Lara;
    • Krieger, Abba M.;
    • Buja, Andreas;
    • Pradhan, Kith;
    • Ronemus, Michael;
    • Baldwin, Kristin K.;
    • Levy, Dan;
    • Wigler, Michael;
    • Iossifov, Ivan
    Publication type:
    Article

  • Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm.

    Published in:
    Nucleic Acids Research, 2011, v. 39, n. 10, p. e65, doi. 10.1093/nar/gkr068
    By:
    • Magi, Alberto;
    • Benelli, Matteo;
    • Yoon, Seungtai;
    • Roviello, Franco;
    • Torricelli, Francesca
    Publication type:
    Article

  • Microduplications of 16p11.2 are associated with schizophrenia.

    Published in:
    Nature Genetics, 2009, v. 41, n. 11, p. 1223, doi. 10.1038/ng.474
    By:
    • McCarthy, Shane E.;
    • Makarov, Vladimir;
    • Kirov, George;
    • Addington, Anjene M.;
    • McClellan, Jon;
    • Seungtai Yoon;
    • Perkins, Diana O.;
    • Dickel, Diane E.;
    • Kusenda, Mary;
    • Krastoshevsky, Olga;
    • Krause, Verena;
    • Kumar, Ravinesh A.;
    • Grozeva, Detelina;
    • Malhotra, Dheeraj;
    • Walsh, Tom;
    • Zackai, Elaine H.;
    • Kaplan, Paige;
    • Ganesh, Jaya;
    • Krantz, Ian D.;
    • Spinner, Nancy B.
    Publication type:
    Article

  • Characterization of <i>SLITRK1</i> Variation in Obsessive-Compulsive Disorder.

    Published in:
    PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070376
    By:
    • Ozomaro, Uzoezi;
    • Cai, Guiqing;
    • Kajiwara, Yuji;
    • Yoon, Seungtai;
    • Makarov, Vladimir;
    • Delorme, Richard;
    • Betancur, Catalina;
    • Ruhrmann, Stephan;
    • Falkai, Peter;
    • Grabe, Hans Jörgen;
    • Maier, Wolfgang;
    • Wagner, Michael;
    • Lennertz, Leonhard;
    • Moessner, Rainald;
    • Murphy, Dennis L.;
    • Buxbaum, Joseph D.;
    • Züchner, Stephan;
    • Grice, Dorothy E.
    Publication type:
    Article

  • Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia.

    Published in:
    Human Genetics, 2012, v. 131, n. 3, p. 435, doi. 10.1007/s00439-011-1086-6
    By:
    • Marti-Masso, Jose;
    • Ruiz-Martínez, Javier;
    • Makarov, Vladimir;
    • Munain, Adolfo;
    • Gorostidi, Ana;
    • Bergareche, Alberto;
    • Yoon, Seungtai;
    • Buxbaum, Joseph;
    • Paisán-Ruiz, Coro
    Publication type:
    Article

  • Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.

    Published in:
    2011
    By:
    • Vacic, Vladimir;
    • McCarthy, Shane;
    • Malhotra, Dheeraj;
    • Murray, Fiona;
    • Chou, Hsun-Hua;
    • Peoples, Aine;
    • Makarov, Vladimir;
    • Yoon, Seungtai;
    • Bhandari, Abhishek;
    • Corominas, Roser;
    • Iakoucheva, Lilia M.;
    • Krastoshevsky, Olga;
    • Krause, Verena;
    • Larach-Walters, Verónica;
    • Welsh, David K.;
    • Craig, David;
    • Kelsoe, John R.;
    • Gershon, Elliot S.;
    • Leal, Suzanne M.;
    • Aquila, Marie Dell
    Publication type:
    Correction Notice

  • Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.

    Published in:
    Nature, 2011, v. 471, n. 7339, p. 499, doi. 10.1038/nature09884
    By:
    • Vacic, Vladimir;
    • McCarthy, Shane;
    • Malhotra, Dheeraj;
    • Murray, Fiona;
    • Chou, Hsun-Hua;
    • Peoples, Aine;
    • Makarov, Vladimir;
    • Yoon, Seungtai;
    • Bhandari, Abhishek;
    • Corominas, Roser;
    • Iakoucheva, Lilia M.;
    • Krastoshevsky, Olga;
    • Krause, Verena;
    • Larach-Walters, Verónica;
    • Welsh, David K.;
    • Craig, David;
    • Kelsoe, John R.;
    • Gershon, Elliot S.;
    • Leal, Suzanne M.;
    • Aquila, Marie Dell
    Publication type:
    Article

  • Mapping copy number variation by population-scale genome sequencing.

    Published in:
    Nature, 2011, v. 470, n. 7332, p. 59, doi. 10.1038/nature09708
    By:
    • Mills, Ryan E.;
    • Walter, Klaudia;
    • Stewart, Chip;
    • Handsaker, Robert E.;
    • Chen, Ken;
    • Alkan, Can;
    • Abyzov, Alexej;
    • Yoon, Seungtai Chris;
    • Kai Ye;
    • Cheetham, R. Keira;
    • Chinwalla, Asif;
    • Conrad, Donald F.;
    • Yutao Fu;
    • Grubert, Fabian;
    • Hajirasouliha, Iman;
    • Hormozdiari, Fereydoun;
    • Iakoucheva, Lilia M.;
    • Iqbal, Zamin;
    • Shuli Kang;
    • Kidd, Jeffrey M.
    Publication type:
    Article

  • The contribution of de novo coding mutations to autism spectrum disorder.

    Published in:
    Nature, 2014, v. 515, n. 7526, p. 216, doi. 10.1038/nature13908
    By:
    • Iossifov, Ivan;
    • Ronemus, Michael;
    • Levy, Dan;
    • Yamrom, Boris;
    • Lee, Yoon-ha;
    • Wang, Zihua;
    • Marks, Steven;
    • Andrews, Peter;
    • Leotta, Anthony;
    • Kendall, Jude;
    • Hakker, Inessa;
    • Rosenbaum, Julie;
    • Ma, Beicong;
    • Rodgers, Linda;
    • Troge, Jennifer;
    • Yoon, Seungtai;
    • Schatz, Michael C.;
    • McCombie, W. Richard;
    • Wigler, Michael;
    • Grabowska, Ewa
    Publication type:
    Article

  • A tumour suppressor network relying on the polyamine-hypusine axis.

    Published in:
    Nature, 2012, v. 487, n. 7406, p. 244, doi. 10.1038/nature11126
    By:
    • Scuoppo, Claudio;
    • Miething, Cornelius;
    • Lindqvist, Lisa;
    • Reyes, José;
    • Ruse, Cristian;
    • Appelmann, Iris;
    • Yoon, Seungtai;
    • Krasnitz, Alexander;
    • Teruya-Feldstein, Julie;
    • Pappin, Darryl;
    • Pelletier, Jerry;
    • Lowe, Scott W.
    Publication type:
    Article

  • Patterns and rates of exonic de novo mutations in autism spectrum disorders.

    Published in:
    Nature, 2012, v. 485, n. 7397, p. 242, doi. 10.1038/nature11011
    By:
    • Neale, Benjamin M.;
    • Kou, Yan;
    • Liu, Li;
    • Ma'ayan, Avi;
    • Samocha, Kaitlin E.;
    • Sabo, Aniko;
    • Lin, Chiao-Feng;
    • Stevens, Christine;
    • Wang, Li-San;
    • Makarov, Vladimir;
    • Polak, Paz;
    • Yoon, Seungtai;
    • Maguire, Jared;
    • Crawford, Emily L.;
    • Campbell, Nicholas G.;
    • Geller, Evan T.;
    • Valladares, Otto;
    • Schafer, Chad;
    • Liu, Han;
    • Zhao, Tuo
    Publication type:
    Article

  • Principal components ancestry adjustment for Genetic Analysis Workshop 17 data.

    Published in:
    BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S66
    By:
    • Jing Jin;
    • Cerise, Jane E.;
    • Sun Jung Kang;
    • Eun Jung Yoon;
    • Seungtai Yoon;
    • Mendell, Nancy R.;
    • Finch, Stephen J.
    Publication type:
    Article

  • Identification of genes and variants associated with quantitative traits using Bayesian factor screening.

    Published in:
    BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S4
    By:
    • Pradhan, Kith;
    • Yoon, Seungtai Chris;
    • Tao Wang;
    • Kenny Ye
    Publication type:
    Article

  • AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.

    Published in:
    Bioinformatics, 2012, v. 28, n. 5, p. 724, doi. 10.1093/bioinformatics/bts032
    By:
    • Makarov, Vladimir;
    • O'Grady, Tina;
    • Cai, Guiqing;
    • Lihm, Jayon;
    • Buxbaum, Joseph D.;
    • Yoon, Seungtai
    Publication type:
    Article