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Elizabeth K Ruzzo

Showing results (1-10 of 17) with videos related to

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Nature Neuroscience|March 22, 2016
Schizophrenia genetics complements its mechanistic understandingElizabeth K Ruzzo, Daniel H Geschwind
Genome Biology|March 31, 2012
Modifier genetics in neuropsychiatric disease: challenges and opportunitiesElizabeth K Ruzzo, Andrea L Pappas, David B Goldstein
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.
Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.
American Journal of Human Genetics|September 4, 2012
Using ERDS to infer copy-number variants in high-coverage genomesMingfu Zhu, Anna C Need, Yujun Han, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 7, 2015
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disabilityGali Heimer, Danit Oz-Levi, Eran Eyal, et al.
American Journal of Human Genetics|November 27, 2012
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.
Cell|August 10, 2019
Inherited and De Novo Genetic Risk for Autism Impacts Shared NetworksElizabeth K Ruzzo, Laura Pérez-Cano, Jae-Yoon Jung, et al.
Human Molecular Genetics|January 14, 2009
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophyMegan L Landsverk, Elizabeth K Ruzzo, Heather C Mefford, et al.
Neuron|July 16, 2019
A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestationDamon Polioudakis, Luis de la Torre-Ubieta, Justin Langerman, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Nature Neuroscience|March 22, 2016
Schizophrenia genetics complements its mechanistic understandingElizabeth K Ruzzo, Daniel H Geschwind
Genome Biology|March 31, 2012
Modifier genetics in neuropsychiatric disease: challenges and opportunitiesElizabeth K Ruzzo, Andrea L Pappas, David B Goldstein
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.
Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.
American Journal of Human Genetics|September 4, 2012
Using ERDS to infer copy-number variants in high-coverage genomesMingfu Zhu, Anna C Need, Yujun Han, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 7, 2015
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disabilityGali Heimer, Danit Oz-Levi, Eran Eyal, et al.
American Journal of Human Genetics|November 27, 2012
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.
Cell|August 10, 2019
Inherited and De Novo Genetic Risk for Autism Impacts Shared NetworksElizabeth K Ruzzo, Laura Pérez-Cano, Jae-Yoon Jung, et al.
Human Molecular Genetics|January 14, 2009
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophyMegan L Landsverk, Elizabeth K Ruzzo, Heather C Mefford, et al.
Neuron|July 16, 2019
A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestationDamon Polioudakis, Luis de la Torre-Ubieta, Justin Langerman, et al.
Pageof 2