Ngā hua rapu - James S. Sutcliffe
- E whakaatu ana i te 1 - 20 hua o te 51
- Haere ki te Whārangi Whai Ake
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Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder mā Jerry L. Campbell, Dibyadeep Datta, Shaine T. Jones, Evon Batey Lee, James S. Sutcliffe, Elizabeth A. D. Hammock, Pat Levitt
I whakaputaina 2011Artigo -
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Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors mā James S. Sutcliffe, Ryan Delahanty, Harish C. Prasad, Jacob L. McCauley, Qiao Han, Lan Jiang, Chun Li, Susan E. Folstein, Randy Blakely
I whakaputaina 2005Artigo -
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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates mā Jacob L. McCauley, Chun Li, Lan Jiang, Lana M. Olson, Genea Crockett, Kimberly Gainer, Susan E. Folstein, Jonathan L. Haines, James S. Sutcliffe
I whakaputaina 2005Artigo -
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Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase mā 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
I whakaputaina 2005Artigo -
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Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism mā 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
I whakaputaina 2017Artigo -
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Contribution of SHANK3 Mutations to Autism Spectrum Disorder mā 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
I whakaputaina 2007Artigo -
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A Novel Human<i>CAMK2A</i>Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors mā 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
I whakaputaina 2017Artigo -
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A genetic variant that disrupts <i>MET</i> transcription is associated with autism mā 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
I whakaputaina 2006Artigo -
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The E6–AP Ubiquitin–Protein Ligase (<i>UBE3A</i>) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region mā 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
I whakaputaina 1997Carta -
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De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder mā 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
I whakaputaina 2013Artigo -
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A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data mā 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
I whakaputaina 2019Artigo -
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Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes mā 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
I whakaputaina 2013Artigo -
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SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking mā 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
I whakaputaina 2014Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Genetics
Gene
Autism
Psychiatry
Psychology
Medicine
Genotype
Genome
Mutation
Single-nucleotide polymorphism
Neuroscience
Autism spectrum disorder
Copy-number variation
Developmental psychology
Phenotype
Receptor
Computational biology
Allele
Exome sequencing
Genetic association
Proband
Serotonin
Computer science
Exome
Gene duplication
Candidate gene
Chromosome
Clinical psychology
Genome-wide association study