Search Results - Cheryl Roe

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  1. 1
    Genetic studies of stuttering in a founder population

    Genetic studies of stuttering in a founder population by Jacqueline K. Wittke‐Thompson, Nicoline Ambrose, Ehud Yairi, Cheryl Roe, Edwin H. Cook, Carole Ober, Nancy J. Cox

    Published 2006
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  2. 2
    Genetic Architecture of Transcript-Level Variation in Humans

    Genetic Architecture of Transcript-Level Variation in Humans by Shiwei Duan, R. Stephanie Huang, Wei Zhang, Wasim K. Bleibel, Cheryl Roe, Tyson A. Clark, Tina X. Chen, Anthony Schweitzer, John E. Blume, Nancy J. Cox, M. Eileen Dolan

    Published 2008
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  3. 3
    Identification of Type 2 Diabetes Genes in Mexican Americans Through Genome-Wide Association Studies

    Identification of Type 2 Diabetes Genes in Mexican Americans Through Genome-Wide Association Studies by M. Geoffrey Hayes, Anna Pluzhnikov, Kazuaki Miyake, Ying Sun, Maggie Ng, Cheryl Roe, Jennifer E. Below, Raluca Nicolae, Anuar Konkashbaev, Graeme I. Bell, Nancy J. Cox, Craig L. Hanis

    Published 2007
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  4. 4
    New Complexities in the Genetics of Stuttering: Significant Sex-Specific Linkage Signals

    New Complexities in the Genetics of Stuttering: Significant Sex-Specific Linkage Signals by Rathi Suresh, Nicoline Ambrose, Cheryl Roe, Anna Pluzhnikov, Jacqueline K. Wittke‐Thompson, Maggie C. Y. Ng, Xiaolin Wu, Edwin H. Cook, Cecilia Lundström, Marie Garsten, Ruth Ezrati, Ehud Yairi, Nancy J. Cox

    Published 2006
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  5. 5
    Evidence for a Susceptibility Locus on Chromosome 10p15 in Early-Onset Obsessive-Compulsive Disorder

    Evidence for a Susceptibility Locus on Chromosome 10p15 in Early-Onset Obsessive-Compulsive Disorder by Gregory L. Hanna, Jeremy Veenstra‐VanderWeele, Nancy J. Cox, Michelle Van Etten, Daniel Fischer, Joseph A. Himle, Nancy Chiu Bivens, Xiaolin Wu, Cheryl Roe, Kathleen Hennessy, Diane E. Dickel, Bennett Leventhal, Edwin H. Cook

    Published 2007
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  6. 6
    Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations

    Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations by Daniel P. Howrigan, Samuel A. Rose, Kaitlin E. Samocha, Menachem Fromer, Felecia Cerrato, Wei J. Chen, Claire Churchhouse, Kimberly Chambert, Sharon D. Chandler, Mark J. Daly, Ashley Dumont, Giulio Genovese, Hai‐Gwo Hwu, Nan M. Laird, Jack A. Kosmicki, Jennifer L. Moran, Cheryl Roe, Tarjinder Singh, Shi‐Heng Wang, Stephen V. Faraone, Stephen J. Glatt, Steven A. McCarroll, Ming T. Tsuang, Benjamin M. Neale

    Published 2020
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