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K Lowe

Showing results (251-260 of 267) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|May 7, 2019
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsyZhongbo Chen, Jason A Chen, Aleksey Shatunov, et al.
Brain : a Journal of Neurology|May 29, 2021
Impact of autism genetic risk on brain connectivity: a mechanism for the female protective effectKatherine E Lawrence, Leanna M Hernandez, Emily Fuster, et al.
Molecular Neurodegeneration|August 10, 2018
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseasesJason A Chen, Zhongbo Chen, Hyejung Won, et al.
Nucleic Acids Research|October 1, 2015
ANISEED 2015: a digital framework for the comparative developmental biology of ascidiansMatija Brozovic, Cyril Martin, Christelle Dantec, et al.
Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Plos Genetics|February 7, 2009
Genome-wide association studies in an isolated founder population from the Pacific Island of KosraeJennifer K Lowe, Julian B Maller, Itsik Pe'er, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Nucleic Acids Research|November 18, 2017
ANISEED 2017: extending the integrated ascidian database to the exploration and evolutionary comparison of genome-scale datasetsMatija Brozovic, Christelle Dantec, Justine Dardaillon, et al.
Pageof 27

Showing results (251-260 of 267) with videos related to

Sort By:
Pageof 27
Movement Disorders : Official Journal of the Movement Disorder Society|May 7, 2019
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsyZhongbo Chen, Jason A Chen, Aleksey Shatunov, et al.
Brain : a Journal of Neurology|May 29, 2021
Impact of autism genetic risk on brain connectivity: a mechanism for the female protective effectKatherine E Lawrence, Leanna M Hernandez, Emily Fuster, et al.
Molecular Neurodegeneration|August 10, 2018
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseasesJason A Chen, Zhongbo Chen, Hyejung Won, et al.
Nucleic Acids Research|October 1, 2015
ANISEED 2015: a digital framework for the comparative developmental biology of ascidiansMatija Brozovic, Cyril Martin, Christelle Dantec, et al.
Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Plos Genetics|February 7, 2009
Genome-wide association studies in an isolated founder population from the Pacific Island of KosraeJennifer K Lowe, Julian B Maller, Itsik Pe'er, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Nucleic Acids Research|November 18, 2017
ANISEED 2017: extending the integrated ascidian database to the exploration and evolutionary comparison of genome-scale datasetsMatija Brozovic, Christelle Dantec, Justine Dardaillon, et al.
Pageof 27