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A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

Journal of medical genetics, 2010-12, Vol.47 (12), p.823-828

2010

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Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy

Annals of neurology, 2015-08, Vol.78 (2), p.323-328

2015

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Mental Retardation/Intellectual Disability

Encyclopedia of the Neurological Sciences, 2014, p.1090-1094

Second Edition, 2014

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Epileptic Encephalopathies: New Genes and New Pathways

Neurotherapeutics, 2014-10, Vol.11 (4), p.796-806

2014

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BOD1 Is Required for Cognitive Function in Humans and Drosophila

PLoS genetics, 2016-05, Vol.12 (5), p.e1006022-e1006022

2016

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Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria

PLoS genetics, 2013-10, Vol.9 (10), p.e1003823-e1003823

2013

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De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy

Annals of clinical and translational neurology, 2015-06, Vol.2 (6), p.623-635

2015

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A Defect in the Ionotropic Glutamate Receptor 6 Gene ( GRIK2) Is Associated with Autosomal Recessive Mental Retardation

American journal of human genetics, 2007-10, Vol.81 (4), p.792-798

2007

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De novo mutations in epileptic encephalopathies

Nature (London), 2013-09, Vol.501 (7466), p.217-221

2013

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Nature (London), 2011-10, Vol.478 (7367), p.57-63

2011

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Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American journal of human genetics, 2012-05, Vol.90 (5), p.847-855

2012

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Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population

European journal of medical genetics, 2009-07, Vol.52 (4), p.170-173

2009

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A defect in the lonotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

American journal of human genetics, 2007-10, Vol.81 (4), p.792-798

2007

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SNP array-based homozygosity mapping reveals MCPH71 deletion in family with autosomal recessive mental retardation and mild microcephaly

Human genetics, 2006, Vol.118 (6), p.708-715

2006

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SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

Human genetics, 2006-02, Vol.118 (6), p.708-715

2006

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A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy

Mental Retardation/Intellectual Disability

Epileptic Encephalopathies: New Genes and New Pathways

BOD1 Is Required for Cognitive Function in Humans and Drosophila

Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria

De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

A Defect in the Ionotropic Glutamate Receptor 6 Gene ( GRIK2) Is Associated with Autosomal Recessive Mental Retardation

De novo mutations in epileptic encephalopathies

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population

A defect in the lonotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

SNP array-based homozygosity mapping reveals MCPH71 deletion in family with autosomal recessive mental retardation and mild microcephaly

Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria: e1003823

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

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