Gene networks associated with non-syndromic intellectual disability
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Title
Gene networks associated with non-syndromic intellectual disability
Authors
Keywords
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Journal
JOURNAL OF NEUROGENETICS
Volume 32, Issue 1, Pages 6-14
Publisher
Informa UK Limited
Online
2017-12-04
DOI
10.1080/01677063.2017.1404058
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- (2016) Jans S. van Ool et al. EPILEPSY & BEHAVIOR
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- (2014) Toshiyuki Yamamoto et al. JOURNAL OF HUMAN GENETICS
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- (2014) M Sokolowski et al. MOLECULAR PSYCHIATRY
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- (2014) Kaitlin E Samocha et al. NATURE GENETICS
- XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing
- (2013) Amélie Piton et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2013) Sirisha Peddibhotla et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genetics and the investigation of developmental delay/intellectual disability
- (2013) M. Srour et al. ARCHIVES OF DISEASE IN CHILDHOOD
- X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome
- (2013) R. S. Møller et al. HUMAN GENETICS
- Loss of Predominant Shank3 Isoforms Results in Hippocampus-Dependent Impairments in Behavior and Synaptic Transmission
- (2013) M. Kouser et al. JOURNAL OF NEUROSCIENCE
- Quantitative analysis of locomotor defects in neonatal mice lacking proprioceptive feedback
- (2013) Marisela A. Dallman et al. PHYSIOLOGY & BEHAVIOR
- Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophy
- (2012) Fadi F Hamdan et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Reduced Excitatory Neurotransmission and Mild Autism-Relevant Phenotypes in Adolescent Shank3 Null Mutant Mice
- (2012) M. Yang et al. JOURNAL OF NEUROSCIENCE
- New mutations and sporadic intellectual disability
- (2012) Jozef Gecz et al. LANCET
- Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
- (2012) Anita Rauch et al. LANCET
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- (2012) Andrea de Bartolomeis et al. MOLECULAR NEUROBIOLOGY
- RIM genes differentially contribute to organizing presynaptic release sites
- (2012) P. S. Kaeser et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability
- (2011) Fadi F. Hamdan et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2011) M. Mondin et al. JOURNAL OF NEUROSCIENCE
- Mutationsde novodeSYNGAP1associées à la déficience intellectuelle non syndromique
- (2011) Fadi F. Hamdan et al. M S-MEDECINE SCIENCES
- Spatio-temporal transcriptome of the human brain
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- (2011) Hossein Najmabadi et al. NATURE
- Proteins Encoded in Genomic Regions Associated with Immune-Mediated Disease Physically Interact and Suggest Underlying Biology
- (2011) Elizabeth J. Rossin et al. PLoS Genetics
- Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
- (2010) Feng Li et al. European Journal of Medical Genetics
- The genetic basis of non-syndromic intellectual disability: a review
- (2010) Liana Kaufman et al. Journal of Neurodevelopmental Disorders
- Ephrin-A5 and EphA5 Interaction Induces Synaptogenesis during Early Hippocampal Development
- (2010) Yukio Akaneya et al. PLoS One
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- (2009) Fadi F. Hamdan et al. ANNALS OF NEUROLOGY
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- (2009) Roger E. Stevenson et al. Developmental Disabilities Research Reviews
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- (2009) Da-Ting Lin et al. NATURE NEUROSCIENCE
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- (2009) A. LaMora et al. NEUROSCIENCE
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- Genetic polymorphisms in the dopamine-2 receptor (DRD2), dopamine-3 receptor (DRD3), and dopamine transporter (SLC6A3) genes in schizophrenia: Data from an association study
- (2009) Pilar A. Sáiz et al. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
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- (2008) F. Anne Stephenson et al. MOLECULAR MEMBRANE BIOLOGY
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