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Charlotte N Henrichsen

Showing results (1-10 of 11) with videos related to

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Human Molecular Genetics|March 20, 2009
Copy number variants, diseases and gene expressionCharlotte N Henrichsen, Evelyne Chaignat, Alexandre Reymond
Current Opinion in Genetics & Development|October 5, 2007
Side effects of genome structural changesAlexandre Reymond, Charlotte N Henrichsen, Louise Harewood, et al.
Plos Computational Biology|February 10, 2011
Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndromeCharlotte N Henrichsen, Gábor Csárdi, Marie-Thérèse Zabot, et al.
Genome Research|November 19, 2010
Copy number variation modifies expression time coursesEvelyne Chaignat, Emilie Aït Yahya-Graison, Charlotte N Henrichsen, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromesStefania Gimelli, Jacqueline Chrast, Anwar Baban, et al.
American Journal of Human Genetics|July 11, 2006
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genesGiuseppe Merla, Cédric Howald, Charlotte N Henrichsen, et al.
Nature Genetics|March 10, 2009
Segmental copy number variation shapes tissue transcriptomesCharlotte N Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, et al.
Genome Research|June 15, 2007
Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regionsFrance Denoeud, Philipp Kapranov, Catherine Ucla, et al.
Plos Biology|January 27, 2011
A high-resolution anatomical atlas of the transcriptome in the mouse embryoGraciana Diez-Roux, Sandro Banfi, Marc Sultan, et al.
Nature|June 16, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project, Ewan Birney, John A Stamatoyannopoulos, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|March 20, 2009
Copy number variants, diseases and gene expressionCharlotte N Henrichsen, Evelyne Chaignat, Alexandre Reymond
Current Opinion in Genetics & Development|October 5, 2007
Side effects of genome structural changesAlexandre Reymond, Charlotte N Henrichsen, Louise Harewood, et al.
Plos Computational Biology|February 10, 2011
Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndromeCharlotte N Henrichsen, Gábor Csárdi, Marie-Thérèse Zabot, et al.
Genome Research|November 19, 2010
Copy number variation modifies expression time coursesEvelyne Chaignat, Emilie Aït Yahya-Graison, Charlotte N Henrichsen, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromesStefania Gimelli, Jacqueline Chrast, Anwar Baban, et al.
American Journal of Human Genetics|July 11, 2006
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genesGiuseppe Merla, Cédric Howald, Charlotte N Henrichsen, et al.
Nature Genetics|March 10, 2009
Segmental copy number variation shapes tissue transcriptomesCharlotte N Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, et al.
Genome Research|June 15, 2007
Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regionsFrance Denoeud, Philipp Kapranov, Catherine Ucla, et al.
Plos Biology|January 27, 2011
A high-resolution anatomical atlas of the transcriptome in the mouse embryoGraciana Diez-Roux, Sandro Banfi, Marc Sultan, et al.
Nature|June 16, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project, Ewan Birney, John A Stamatoyannopoulos, et al.
Pageof 2