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Holly A Stessman

Showing results (1-10 of 7) with videos related to

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Cell|March 4, 2014
A genotype-first approach to defining the subtypes of a complex diseaseHolly A Stessman, Raphael Bernier, Evan E Eichler
Methods in Molecular Biology (Clifton, N.J.)|November 9, 2016
Targeted Capture and High-Throughput Sequencing Using Molecular Inversion Probes (MIPs)Stuart Cantsilieris, Holly A Stessman, Jay Shendure, et al.
Nature Genetics|May 12, 2015
Excess of rare, inherited truncating mutations in autismNiklas Krumm, Tychele N Turner, Carl Baker, et al.
American Journal of Human Genetics|January 11, 2016
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNATychele N Turner, Fereydoun Hormozdiari, Michael H Duyzend, et al.
Neurology|November 6, 2015
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlationsDong-Hui Chen, Aurélie Méneret, Jennifer R Friedman, et al.
Cell|July 8, 2014
Disruptive CHD8 mutations define a subtype of autism early in developmentRaphael Bernier, Christelle Golzio, Bo Xiong, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Cell|March 4, 2014
A genotype-first approach to defining the subtypes of a complex diseaseHolly A Stessman, Raphael Bernier, Evan E Eichler
Methods in Molecular Biology (Clifton, N.J.)|November 9, 2016
Targeted Capture and High-Throughput Sequencing Using Molecular Inversion Probes (MIPs)Stuart Cantsilieris, Holly A Stessman, Jay Shendure, et al.
Nature Genetics|May 12, 2015
Excess of rare, inherited truncating mutations in autismNiklas Krumm, Tychele N Turner, Carl Baker, et al.
American Journal of Human Genetics|January 11, 2016
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNATychele N Turner, Fereydoun Hormozdiari, Michael H Duyzend, et al.
Neurology|November 6, 2015
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlationsDong-Hui Chen, Aurélie Méneret, Jennifer R Friedman, et al.
Cell|July 8, 2014
Disruptive CHD8 mutations define a subtype of autism early in developmentRaphael Bernier, Christelle Golzio, Bo Xiong, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Pageof 1