Published in Epigenetics on January 16, 2014
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders. Mol Syndromol (2015) 1.00
The interplay between DNA methylation and sequence divergence in recent human evolution. Nucleic Acids Res (2015) 0.81
Epigenetics and nutritional environmental signals. Integr Comp Biol (2014) 0.80
The Age of the Father. Mol Syndromol (2017) 0.75
Evolution of the Human Nervous System Function, Structure, and Development. Cell (2017) 0.75
The placental gateway of maternal transgenerational epigenetic inheritance. J Genet (2017) 0.75
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods (2001) 414.27
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol (2002) 82.19
Mauve: multiple alignment of conserved genomic sequence with rearrangements. Genome Res (2004) 28.63
Initial sequence of the chimpanzee genome and comparison with the human genome. Nature (2005) 25.67
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Nat Genet (2003) 25.57
progressiveMauve: multiple genome alignment with gene gain, loss and rearrangement. PLoS One (2010) 24.31
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nat Genet (2007) 20.22
The faculty of language: what is it, who has it, and how did it evolve? Science (2002) 13.18
Conserved role of intragenic DNA methylation in regulating alternative promoters. Nature (2010) 9.81
A forkhead-domain gene is mutated in a severe speech and language disorder. Nature (2001) 9.25
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet (2008) 7.13
Paleontological evidence to date the tree of life. Mol Biol Evol (2006) 6.46
Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet (1991) 5.95
High-resolution analysis of parent-of-origin allelic expression in the mouse brain. Science (2010) 5.91
Molecular evolution of FOXP2, a gene involved in speech and language. Nature (2002) 5.89
CTCF-promoted RNA polymerase II pausing links DNA methylation to splicing. Nature (2011) 5.50
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am J Hum Genet (2008) 5.44
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. N Engl J Med (2006) 5.28
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet (2008) 5.28
A functional genetic link between distinct developmental language disorders. N Engl J Med (2008) 4.99
Elevated gene expression levels distinguish human from non-human primate brains. Proc Natl Acad Sci U S A (2003) 4.69
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. Mol Psychiatry (2007) 3.44
Sperm methylation profiles reveal features of epigenetic inheritance and evolution in primates. Cell (2011) 3.39
Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood. Genome Biol (2012) 3.31
Body mass and encephalization in Pleistocene Homo. Nature (1997) 3.25
DNA methylation and mutation. Mutat Res (1993) 3.23
Evolution of primate gene expression. Nat Rev Genet (2006) 3.04
Human-specific transcriptional networks in the brain. Neuron (2012) 2.80
Prefrontal cortex in humans and apes: a comparative study of area 10. Am J Phys Anthropol (2001) 2.71
Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage. Genome Res (2010) 2.61
FOXP2 as a molecular window into speech and language. Trends Genet (2009) 2.59
Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Mol Psychiatry (2010) 2.59
Sequencing the chimpanzee genome: insights into human evolution and disease. Nat Rev Genet (2003) 2.41
Genomic imprinting mechanisms in mammals. Mutat Res (2008) 2.28
Induced gene expression in human brain after the split from chimpanzee. Trends Genet (2003) 2.19
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet (2006) 2.14
A comparison of RNA-Seq and high-density exon array for detecting differential gene expression between closely related species. Nucleic Acids Res (2010) 2.07
Lymphocytes as a neural probe: potential for studying psychiatric disorders. Prog Neuropsychopharmacol Biol Psychiatry (2004) 2.03
Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. J Physiol (2003) 2.01
Comparing the human and chimpanzee genomes: searching for needles in a haystack. Genome Res (2005) 1.95
A genome-wide study of DNA methylation patterns and gene expression levels in multiple human and chimpanzee tissues. PLoS Genet (2011) 1.92
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. Neurogenetics (2009) 1.58
CNTNAP2 variants affect early language development in the general population. Genes Brain Behav (2011) 1.41
Differential GC content between exons and introns establishes distinct strategies of splice-site recognition. Cell Rep (2012) 1.41
The 'big bang' theory of the origin of psychosis and the faculty of language. Schizophr Res (2008) 1.36
Decoding the genetics of speech and language. Curr Opin Neurobiol (2012) 1.35
Shining a light on CNTNAP2: complex functions to complex disorders. Eur J Hum Genet (2013) 1.34
Intergenic and repeat transcription in human, chimpanzee and macaque brains measured by RNA-Seq. PLoS Comput Biol (2010) 1.33
Comparative primate genomics. Annu Rev Genomics Hum Genet (2004) 1.33
Divergent whole-genome methylation maps of human and chimpanzee brains reveal epigenetic basis of human regulatory evolution. Am J Hum Genet (2012) 1.31
Differences in human and chimpanzee gene expression patterns define an evolving network of transcription factors in brain. Proc Natl Acad Sci U S A (2009) 1.31
A model for genomic imprinting in the social brain: juveniles. Evolution (2010) 1.20
Human epigenome data reveal increased CpG methylation in alternatively spliced sites and putative exonic splicing enhancers. DNA Cell Biol (2011) 1.18
A model for genomic imprinting in the social brain: adults. Evolution (2010) 1.13
What does CNTNAP2 reveal about autism spectrum disorder? Trends Mol Med (2012) 1.12
Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human. Hum Mol Genet (2007) 1.10
Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate cortices. Mol Biol Evol (2009) 1.07
Recent advances in the genetics of language impairment. Genome Med (2010) 1.06
Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals. Am J Med Genet B Neuropsychiatr Genet (2011) 1.01
Internodal specializations of myelinated axons in the central nervous system. Cell Tissue Res (2001) 0.99
FOXP2 targets show evidence of positive selection in European populations. Am J Hum Genet (2013) 0.94
Genomic imprinting--roles and regulation in development. Endocr Dev (2007) 0.92
A pipeline to determine RT-QPCR control genes for evolutionary studies: application to primate gene expression across multiple tissues. PLoS One (2010) 0.92
Unity and diversity in human language. Philos Trans R Soc Lond B Biol Sci (2011) 0.91
Response execution in lexical decision tasks obscures sex-specific lateralization effects in language processing: evidence from event-related potential measures during word reading. Cereb Cortex (2005) 0.87
The ontogenesis of language impairment in autism: a neuropsychological perspective. Neuropsychol Rev (2011) 0.84
Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices. Cytogenet Genome Res (2012) 0.82
Severe Intellectual Disability Associated with Recessive Defects in CNTNAP2 and NRXN1. Mol Syndromol (2011) 0.81
When epigenetics meets alternative splicing: the roles of DNA methylation and GC architecture. Epigenomics (2013) 0.81
A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices. Cytogenet Genome Res (2012) 0.80
Genome-wide DNA methylation analyses in the brain reveal four differentially methylated regions between humans and non-human primates. BMC Evol Biol (2012) 0.79
The speech gene FOXP2 is not imprinted. J Med Genet (2012) 0.77
The paleoneurology of language. Ann N Y Acad Sci (1976) 0.76
The parental antagonism theory of language evolution: preliminary evidence for the proposal. Hum Biol (2011) 0.76