| case report | Q2782326 |
| scholarly article | Q13442814 |
| P50 | author | Raul Torres-Ruiz | Q47252193 |
| P2093 | author name string | Antonio Benítez-Burraco | |
| Ma Salud Jiménez-Romero | |||
| Sandra Rodríguez-Perales | |||
| Isabel Espejo-Portero | |||
| Raúl Torres-Ruiz | |||
| Maite Fernández-Urquiza | |||
| Montserrat Barcos-Martínez | |||
| P2860 | cites work | The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia | Q21092504 |
| Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain | Q21144946 | ||
| Wnt/wingless signaling requires BCL9/legless-mediated recruitment of pygopus to the nuclear beta-catenin-TCF complex | Q24294443 | ||
| Mean length of utterance levels in 6-month intervals for children 3 to 9 years with and without language impairments | Q24605578 | ||
| Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder | Q24624740 | ||
| Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities | Q24647145 | ||
| Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain | Q24648621 | ||
| Poly(ADP-ribosyl)ation directs recruitment and activation of an ATP-dependent chromatin remodeler | Q24655668 | ||
| Prenatal diazepam exposure: effects on auditory temporal resolution in rats. | Q50594571 | ||
| KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. | Q50695616 | ||
| Prenatal exposure to anxiolytics and hypnotics and language competence at 3 years of age | Q86423685 | ||
| Human-specific transcriptional regulation of CNS development genes by FOXP2 | Q24655742 | ||
| Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes | Q24655755 | ||
| Autism spectrum disorders and neuropathology of the cerebellum | Q26853603 | ||
| High-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathies | Q28506691 | ||
| The lhx2 transcription factor controls thalamocortical axonal guidance by specific regulation of robo1 and robo2 receptors | Q28591967 | ||
| Possible functional links among brain- and skull-related genes selected in modern humans | Q28648399 | ||
| Convergent differential regulation of SLIT-ROBO axon guidance genes in the brains of vocal learners | Q28649912 | ||
| Globularity and language-readiness: generating new predictions by expanding the set of genes of interest | Q28651479 | ||
| The Genotype-Tissue Expression (GTEx) project | Q28657968 | ||
| BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies | Q28943394 | ||
| STRING v10: protein-protein interaction networks, integrated over the tree of life | Q29615545 | ||
| Consensus paper: Language and the cerebellum: an ongoing enigma | Q30410137 | ||
| The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia | Q30482949 | ||
| Understanding violations of Gricean maxims in preschoolers and adults | Q30656284 | ||
| Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment | Q33601252 | ||
| Efficient Recreation of t(11;22) EWSR1-FLI1+ in Human Stem Cells Using CRISPR/Cas9. | Q33659569 | ||
| Evolution of genetic and genomic features unique to the human lineage | Q33900428 | ||
| Epigenome-wide DNA methylation in hearing ability: new mechanisms for an old problem | Q34128248 | ||
| Common variants in the BCL9 gene conferring risk of schizophrenia | Q34169123 | ||
| CHD1L Regulated PARP1-Driven Pluripotency and Chromatin Remodeling During the Early-Stage Cell Reprogramming | Q34486397 | ||
| Novel genetic causes for cerebral visual impairment | Q34493173 | ||
| Analysis of whole genome biomarker expression in blood and brain | Q34994239 | ||
| Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population | Q36192989 | ||
| Aristaless Related Homeobox (ARX) Interacts with β-Catenin, BCL9, and P300 to Regulate Canonical Wnt Signaling | Q36253912 | ||
| Autism traits in individuals with agenesis of the corpus callosum | Q36763173 | ||
| Bridging the Gap between Genes and Language Deficits in Schizophrenia: An Oscillopathic Approach. | Q37194932 | ||
| 1q21.1 Microduplication expression in adults | Q37278755 | ||
| New findings in the genetics of schizophrenia | Q37321993 | ||
| Arx is a direct target of Dlx2 and thereby contributes to the tangential migration of GABAergic interneurons | Q37352456 | ||
| CHD1L: a novel oncogene | Q37597560 | ||
| Neuropsychological profile of agenesis of the corpus callosum: a systematic review | Q38073289 | ||
| Gestational Diabetes: Long-Term Central Nervous System Developmental and Cognitive Sequelae | Q38255225 | ||
| The homeobox protein Six3 interacts with the Groucho corepressor and acts as a transcriptional repressor in eye and forebrain formation | Q38300039 | ||
| Analysis of transcriptional codes for zebrafish dopaminergic neurons reveals essential functions of Arx and Isl1 in prethalamic dopaminergic neuron development. | Q38324172 | ||
| Preschoolers can recognize violations of the Gricean maxims | Q38387574 | ||
| Diabetes in Pregnancy and Childhood Cognitive Development: A Systematic Review | Q38849105 | ||
| Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder | Q38884466 | ||
| Language deficits in schizophrenia and autism as related oscillatory connectomopathies: An evolutionary account | Q38913624 | ||
| Advances in Dyslexia Genetics-New Insights Into the Role of Brain Asymmetries. | Q39101919 | ||
| The Oscillopathic Nature of Language Deficits in Autism: From Genes to Language Evolution. | Q39104650 | ||
| Clinical phenotype of the recurrent 1q21.1 copy-number variant | Q39132862 | ||
| Comparison of gene expression profiles in the blood, hippocampus and prefrontal cortex of rats | Q39495606 | ||
| FoxG1 and TLE2 act cooperatively to regulate ventral telencephalon formation | Q39720362 | ||
| Increased expression of Slit2 and its receptors Robo1 and Robo4 in reactive astrocytes of the rat hippocampus after transient forebrain ischemia. | Q40110332 | ||
| New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum | Q41930382 | ||
| Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes. | Q42063621 | ||
| Constitutive scaffolding of multiple Wnt enhanceosome components by Legless/BCL9. | Q42316186 | ||
| A co-dependent requirement of xBcl9 and Pygopus for embryonic body axis development in Xenopus | Q42462232 | ||
| β-catenin promoter ChIP-chip reveals potential schizophrenia and bipolar disorder gene network | Q42976183 | ||
| Explicit Oral Narrative Intervention for Students with Williams Syndrome | Q47552074 | ||
| Beta-catenin in schizophrenia: Possibly deleterious novel mutation. | Q48152731 | ||
| Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain | Q48225682 | ||
| Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain. | Q48544028 | ||
| Evaluating the comparability of gene expression in blood and brain | Q48623627 | ||
| Human ROBO1 regulates interaural interaction in auditory pathways. | Q48701284 | ||
| Prenatal and perinatal risks for late language emergence in a population-level sample of twins at age 2. | Q49355108 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P304 | page(s) | 163 | |
| P577 | publication date | 2018-06-05 | |
| P1433 | published in | Frontiers in pediatrics | Q27725038 |
| P1476 | title | Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome. | |
| P478 | volume | 6 |
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