Rezultaty - James S. Sutcliffe

Redukuj rezultaty
  1. 1
    Enhanced activity of human serotonin transporter variants associated with autism

    Enhanced activity of human serotonin transporter variants associated with autism od Harish C. Prasad, Jennifer A. Steiner, James S. Sutcliffe, Randy Blakely

    Wydane 2008
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  2. 2
    Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

    Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder od Jerry L. Campbell, Chun Li, James S. Sutcliffe, Antonio M. Persico, Pat Levitt

    Wydane 2008
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  3. 3
    Shorter sleep duration is associated with social impairment and comorbidities in ASD

    Shorter sleep duration is associated with social impairment and comorbidities in ASD od Olivia J. Veatch, James S. Sutcliffe, Zachary Warren, Brendan T Keenan, Melissa H. Potter, Beth A. Malow

    Wydane 2017
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  4. 4
    Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility

    Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility od Lauren A. Weiss, Gülüm Kosova, Ryan Delahanty, Lan Jiang, Edwin H. Cook, Carole Ober, James S. Sutcliffe

    Wydane 2006
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  5. 5
    Appetitive behavior, compulsivity, and neurochemistry in Prader-Willi syndrome

    Appetitive behavior, compulsivity, and neurochemistry in Prader-Willi syndrome od Anastasia Dimitropoulos, Irene D. Feurer, Elizabeth Roof, Wendy L. Stone, Merlin G. Butler, James S. Sutcliffe, Travis Thompson

    Wydane 2000
    Dokumenty pełnotekstowe
    Revisão
    Dodaj do listy ulubionych książek
    Zapisane w:
  6. 6
    Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder

    Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder od Jerry L. Campbell, Dibyadeep Datta, Shaine T. Jones, Evon Batey Lee, James S. Sutcliffe, Elizabeth A. D. Hammock, Pat Levitt

    Wydane 2011
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  7. 7
    Genetic analysis of biological pathway data through genomic randomization

    Genetic analysis of biological pathway data through genomic randomization od Brian L. Yaspan, William S. Bush, Eric S. Torstenson, Deqiong Ma, Margaret A. Pericak‐Vance, Marylyn D. Ritchie, James S. Sutcliffe, Jonathan L. Haines

    Wydane 2011
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  8. 8
    Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors

    Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors od James S. Sutcliffe, Ryan Delahanty, Harish C. Prasad, Jacob L. McCauley, Qiao Han, Lan Jiang, Chun Li, Susan E. Folstein, Randy Blakely

    Wydane 2005
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  9. 9
    Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

    Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates od Jacob L. McCauley, Chun Li, Lan Jiang, Lana M. Olson, Genea Crockett, Kimberly Gainer, Susan E. Folstein, Jonathan L. Haines, James S. Sutcliffe

    Wydane 2005
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  10. 10
    Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

    Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism od Ryan Delahanty, Jing‐Qiong Kang, Camille W. Brune, Emily O. Kistner, Eric Courchesne, Nancy J. Cox, Edwin H. Cook, Robert L. Macdonald, James S. Sutcliffe

    Wydane 2009
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  11. 11
    Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase

    Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase od Harish C. Prasad, Chong-Bin Zhu, Jacob L. McCauley, Devadoss J. Samuvel, Sammanda Ramamoorthy, Richard C. Shelton, William A. Hewlett, James S. Sutcliffe, Randy Blakely

    Wydane 2005
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  12. 12
    Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism

    Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism od Rui Chen, Lea K. Davis, Stephen J. Guter, Qiang Wei, Suma Jacob, Melissa H. Potter, Nancy J. Cox, Edwin H. Cook, James S. Sutcliffe, Bingshan Li

    Wydane 2017
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  13. 13
    Contribution of SHANK3 Mutations to Autism Spectrum Disorder

    Contribution of SHANK3 Mutations to Autism Spectrum Disorder od Rainald Moessner, Christian R. Marshall, James S. Sutcliffe, Jennifer Skaug, Dalila Pinto, John B. Vincent, Lonnie Zwaigenbaum, Bridget A. Fernandez, Wendy Roberts, Peter Szatmari, Stephen W. Scherer

    Wydane 2007
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  14. 14
    A Novel Human<i>CAMK2A</i>Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors

    A Novel Human<i>CAMK2A</i>Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors od Jason R. Stephenson, Xiaohan Wang, Tyler L. Perfitt, Walker P. Parrish, Brian C. Shonesy, Christian R. Marks, Douglas P. Mortlock, Terunaga Nakagawa, James S. Sutcliffe, Roger Colbran

    Wydane 2017
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  15. 15
    A genetic variant that disrupts <i>MET</i> transcription is associated with autism

    A genetic variant that disrupts <i>MET</i> transcription is associated with autism od Jerry L. Campbell, James S. Sutcliffe, Philip J. Ebert, Roberto Militerni, Carmela Bravaccio, Simona Trillo, Maurizio Elia, Cindy Schneider, Raun D. Melmed, Roberto Sacco, Antonio M. Persico, Pat Levitt

    Wydane 2006
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  16. 16
    The E6–AP Ubiquitin–Protein Ligase (<i>UBE3A</i>) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region

    The E6–AP Ubiquitin–Protein Ligase (<i>UBE3A</i>) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region od James S. Sutcliffe, Yong‐hui Jiang, Robert‐Jan H. Galjaard, Toshinobu Matsuura, Ping Fang, Takeo Kubota, Susan L. Christian, Jan Bressler, B.M. Cattanach, David H. Ledbetter, Arthur L. Beaudet

    Wydane 1997
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Carta
    Dodaj do listy ulubionych książek
    Zapisane w:
  17. 17
    De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder

    De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder od Peter J. Hamilton, Nicholas G. Campbell, Shruti Sharma, Kevin Erreger, Freja Herborg, Christine Saunders, Andrea N. Belovich, Mark J. Daly, Richard A. Gibbs, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Elaine T. Lim, Benjamin M. Neale, Kathryn Roeder, A Sabó, Gerard D. Schellenberg, Christine Stevens, James S. Sutcliffe, Michelle A. Sahai, Edwin H. Cook, Ulrik Gether, Hassane S. Mchaourab, H Matthies, James S. Sutcliffe, Aurelio Galli

    Wydane 2013
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  18. 18
    A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data

    A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data od Quan Wang, Rui Chen, Feixiong Cheng, Qiang Wei, Ying Ji, Yang Hai, Xue Zhong, Ran Tao, Zhexing Wen, James S. Sutcliffe, Chunyu Liu, Edwin H. Cook, Nancy J. Cox, Bingshan Li

    Wydane 2019
    Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  19. 19
    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 od Xin He, Stephan 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

    Wydane 2013
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:
  20. 20
    SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking

    SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking od Erica Bowton, Christine Saunders, India A. Reddy, Nicholas G. Campbell, Peter J. Hamilton, L. Keith Henry, Hilary Coon, Dhananjay Sakrikar, Jeremy Veenstra‐VanderWeele, Randy Blakely, James S. Sutcliffe, H Matthies, Kevin Erreger, Aurelio Galli

    Wydane 2014
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
    Dodaj do listy ulubionych książek
    Zapisane w:

Narzędzie wyszukiwania: