Hasil Pencarian - Bernie Devlin

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  1. 1
    De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

    De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types oleh Siwei Chen, Jiebiao Wang, Ercument Cicek, Kathryn Roeder, Haiyuan Yu, Bernie Devlin

    Diterbitkan 2020-10-01
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  2. 2
    Evaluating and improving health equity and fairness of polygenic scores

    Evaluating and improving health equity and fairness of polygenic scores oleh Tianyu Zhang, Geyu Zhou, Lambertus Klei, Peng Liu, Alexandra Chouldechova, Hongyu Zhao, Kathryn Roeder, Max G’Sell, Bernie Devlin

    Diterbitkan 2024-04-01
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  3. 3
    Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

    Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder oleh Sean C. Piantadosi, Lora L. McClain, Lambertus Klei, Jiebiao Wang, Brittany L. Chamberlain, Sara A. Springer, David A. Lewis, Bernie Devlin, Susanne E. Ahmari

    Diterbitkan 2021-03-01
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  4. 4
    Testing for an unusual distribution of rare variants.

    Testing for an unusual distribution of rare variants. oleh Benjamin M Neale, Manuel A Rivas, Benjamin F Voight, David Altshuler, Bernie Devlin, Marju Orho-Melander, Sekar Kathiresan, Shaun M Purcell, Kathryn Roeder, Mark J Daly

    Diterbitkan 2011-03-01
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  5. 5
    Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk

    Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotyp... oleh Brandon C. McKinney, Lora L. McClain, Christopher M. Hensler, Yue Wei, Lambertus Klei, David A. Lewis, Bernie Devlin, Jiebiao Wang, Ying Ding, Robert A. Sweet

    Diterbitkan 2022-08-01
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  6. 6
    Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.

    Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. oleh Xin He, Stephan J Sanders, Li Liu, Silvia De Rubeis, Elaine T Lim, James S Sutcliffe, Gerard D Schellenberg, Richard A Gibbs, Mark J Daly, Joseph D Buxbaum, Matthew W State, Bernie Devlin, Kathryn Roeder

    Diterbitkan 2013-01-01
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  7. 7
    How rare and common risk variation jointly affect liability for autism spectrum disorder

    How rare and common risk variation jointly affect liability for autism spectrum disorder oleh Lambertus Klei, Lora Lee McClain, Behrang Mahjani, Klea Panayidou, Silvia De Rubeis, Anna-Carin Säll Grahnat, Gun Karlsson, Yangyi Lu, Nadine Melhem, Xinyi Xu, Abraham Reichenberg, Sven Sandin, Christina M. Hultman, Joseph D. Buxbaum, Kathryn Roeder, Bernie Devlin

    Diterbitkan 2021-10-01
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  8. 8
    Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder

    Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder oleh Behrang Mahjani, Silvia De Rubeis, Christina Gustavsson Mahjani, Maureen Mulhern, Xinyi Xu, Lambertus Klei, F. Kyle Satterstrom, Jack Fu, Michael E. Talkowski, Abraham Reichenberg, Sven Sandin, Christina M. Hultman, Dorothy E. Grice, Kathryn Roeder, Bernie Devlin, Joseph D. Buxbaum

    Diterbitkan 2021-10-01
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  9. 9
    Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.

    Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. oleh Li Liu, Aniko Sabo, Benjamin M Neale, Uma Nagaswamy, Christine Stevens, Elaine Lim, Corneliu A Bodea, Donna Muzny, Jeffrey G Reid, Eric Banks, Hillary Coon, Mark Depristo, Huyen Dinh, Tim Fennel, Jason Flannick, Stacey Gabriel, Kiran Garimella, Shannon Gross, Alicia Hawes, Lora Lewis, Vladimir Makarov, Jared Maguire, Irene Newsham, Ryan Poplin, Stephan Ripke, Khalid Shakir, Kaitlin E Samocha, Yuanqing Wu, Eric Boerwinkle, Joseph D Buxbaum, Edwin H Cook, Bernie Devlin, Gerard D Schellenberg, James S Sutcliffe, Mark J Daly, Richard A Gibbs, Kathryn Roeder

    Diterbitkan 2013-04-01
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  10. 10
    Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

    Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex oleh Donna M. Werling, Sirisha Pochareddy, Jinmyung Choi, Joon-Yong An, Brooke Sheppard, Minshi Peng, Zhen Li, Claudia Dastmalchi, Gabriel Santpere, André M.M. Sousa, Andrew T.N. Tebbenkamp, Navjot Kaur, Forrest O. Gulden, Michael S. Breen, Lindsay Liang, Michael C. Gilson, Xuefang Zhao, Shan Dong, Lambertus Klei, A. Ercument Cicek, Joseph D. Buxbaum, Homa Adle-Biassette, Jean-Leon Thomas, Kimberly A. Aldinger, Diana R. O’Day, Ian A. Glass, Noah A. Zaitlen, Michael E. Talkowski, Kathryn Roeder, Matthew W. State, Bernie Devlin, Stephan J. Sanders, Nenad Sestan

    Diterbitkan 2020-04-01
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  11. 11
    De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder

    De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder oleh Shan Dong, Michael F. Walker, Nicholas J. Carriero, Michael DiCola, A. Jeremy Willsey, Adam Y. Ye, Zainulabedin Waqar, Luis E. Gonzalez, John D. Overton, Stephanie Frahm, John F. Keaney, III, Nicole A. Teran, Jeanselle Dea, Jeffrey D. Mandell, Vanessa Hus Bal, Catherine A. Sullivan, Nicholas M. DiLullo, Rehab O. Khalil, Jake Gockley, Zafer Yuksel, Sinem M. Sertel, A. Gulhan Ercan-Sencicek, Abha R. Gupta, Shrikant M. Mane, Michael Sheldon, Andrew I. Brooks, Kathryn Roeder, Bernie Devlin, Matthew W. State, Liping Wei, Stephan J. Sanders

    Diterbitkan 2014-10-01
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  12. 12
    Genetic associations with psychosis and affective disturbance in Alzheimer's disease

    Genetic associations with psychosis and affective disturbance in Alzheimer's disease oleh Inga Margret Antonsdottir, Byron Creese, Lambertus Klei, Mary Ann A. DeMichele‐Sweet, Elise A. Weamer, Pablo Garcia‐Gonzalez, Marta Marquie, Mercè Boada, Emilio Alarcón‐Martín, Sergi Valero, NIA‐LOAD Family Based Study Consortium, Alzheimer's Disease Genetics Consortium (ADGC), AddNeuroMed Consortium, Yushi Liu, Basavaraj Hooli, Dag Aarsland, Geir Selbaek, Sverre Bergh, Arvid Rongve, Ingvild Saltvedt, Håvard K. Skjellegrind, Bo Engdahl, Ole A. Andreassen, Barbara Borroni, Patrizia Mecocci, Yehani Wedatilake, Richard Mayeux, Tatiana Foroud, Agustín Ruiz, Oscar L. Lopez, M. Ilyas Kamboh, Clive Ballard, Bernie Devlin, Constantine Lyketsos, Robert A. Sweet

    Diterbitkan 2024-04-01
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