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Sahar Esmaeeli-Nieh

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

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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 1, 2014
Epileptic encephalopathies: new genes and new pathwaysSahar Esmaeeli Nieh, Elliott H Sherr
European Journal of Medical Genetics|April 14, 2009
Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian populationAli Reza Pouya, Seyedeh Sedigheh Abedini, Neda Mansoorian, et al.
American Journal of Human Genetics|September 12, 2007
A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardationMohammad Mahdi Motazacker, Benjamin Rainer Rost, Tim Hucho, et al.
Human Genetics|November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephalyMasoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
American Journal of Human Genetics|May 1, 2012
Mutations in NSUN2 cause autosomal-recessive intellectual disabilityLia Abbasi-Moheb, Sara Mertel, Melanie Gonsior, et al.
Plos Genetics|May 12, 2016
BOD1 Is Required for Cognitive Function in Humans and DrosophilaSahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, et al.
Plos Genetics|October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaSamin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Nature|September 23, 2011
Deep sequencing reveals 50 novel genes for recessive cognitive disordersHossein Najmabadi, Hao Hu, Masoud Garshasbi, et al.
Pageof 2

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

Sort By:
Pageof 2
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 1, 2014
Epileptic encephalopathies: new genes and new pathwaysSahar Esmaeeli Nieh, Elliott H Sherr
European Journal of Medical Genetics|April 14, 2009
Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian populationAli Reza Pouya, Seyedeh Sedigheh Abedini, Neda Mansoorian, et al.
American Journal of Human Genetics|September 12, 2007
A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardationMohammad Mahdi Motazacker, Benjamin Rainer Rost, Tim Hucho, et al.
Human Genetics|November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephalyMasoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
American Journal of Human Genetics|May 1, 2012
Mutations in NSUN2 cause autosomal-recessive intellectual disabilityLia Abbasi-Moheb, Sara Mertel, Melanie Gonsior, et al.
Plos Genetics|May 12, 2016
BOD1 Is Required for Cognitive Function in Humans and DrosophilaSahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, et al.
Plos Genetics|October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaSamin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Nature|September 23, 2011
Deep sequencing reveals 50 novel genes for recessive cognitive disordersHossein Najmabadi, Hao Hu, Masoud Garshasbi, et al.
Pageof 2