Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment
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Title
Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment
Authors
Keywords
Language, Alleles, Sequence motif analysis, Variant genotypes, Europe, Children, Islands, Chile (country)
Journal
PLoS Genetics
Volume 11, Issue 3, Pages e1004925
Publisher
Public Library of Science (PLoS)
Online
2015-03-18
DOI
10.1371/journal.pgen.1004925
References
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- (2014) Fabiola Ceroni et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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- (2014) R. Nudel et al. GENES BRAIN AND BEHAVIOR
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- (2013) Nuala H Simpson et al. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
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- Genome-wide association study of shared components of reading disability and language impairment
- (2013) J. D. Eicher et al. GENES BRAIN AND BEHAVIOR
- A genome-wide association study for reading and language abilities in two population cohorts
- (2013) M. Luciano et al. GENES BRAIN AND BEHAVIOR
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- A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
- (2012) Pablo Cingolani et al. FLY
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- Differential confounding of rare and common variants in spatially structured populations
- (2012) Iain Mathieson et al. NATURE GENETICS
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- (2012) Miriam Kos et al. PLoS One
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- (2011) Heather C. Whalley et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
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- (2011) Anna C. Cummings et al. ANNALS OF HUMAN GENETICS
- DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits
- (2011) Tom S. Scerri et al. BIOLOGICAL PSYCHIATRY
- Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population
- (2011) Pia Villanueva et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- CNTNAP2variants affect early language development in the general population
- (2011) A. J. O. Whitehouse et al. GENES BRAIN AND BEHAVIOR
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- (2011) Brian J O'Roak et al. NATURE GENETICS
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- (2011) Raghothama Chaerkady et al. PROTEOMICS
- Taxometric Analyses of Specific Language Impairment in 6-Year-Old Children
- (2011) Christine A. Dollaghan JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
- Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes
- (2011) Santhosh Girirajan et al. PLoS Genetics
- Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects
- (2010) D. F. Newbury et al. BEHAVIOR GENETICS
- A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Is Associated with Increased Risk for Selective Mutism and Social Anxiety-Related Traits
- (2010) Murray B. Stein et al. BIOLOGICAL PSYCHIATRY
- THE CAMBRIDGE LANGUAGE AND SPEECH PROJECT (CLASP). L DETECTION OF LANGUAGE DIFFICULTIES AT 36 TO 39 MONTHS
- (2010) V. Burden et al. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads
- (2010) G. Lunter et al. GENOME RESEARCH
- Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
- (2010) Denise Horn et al. HUMAN MUTATION
- Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
- (2010) Beate Peter et al. Journal of Neurodevelopmental Disorders
- NFX1 Plays a Role in Human Papillomavirus Type 16 E6 Activation of NF B Activity
- (2010) M. Xu et al. JOURNAL OF VIROLOGY
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
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- (2008) Sonja C. Vernes et al. NEW ENGLAND JOURNAL OF MEDICINE
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- (2007) M. Falcaro et al. GENES BRAIN AND BEHAVIOR
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