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The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers.
- Published in:
- Scientific Reports, 2016, p. 20911, doi. 10.1038/srep20911
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- Article
Neurogenomics of speech and language disorders: the road ahead.
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- Genome Biology, 2013, v. 14, n. 4, p. 204, doi. 10.1186/gb-2013-14-4-204
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- Article
Molecular evolution of FOXP2, a gene involved in speech and language.
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- Nature, 2002, v. 418, n. 6900, p. 869, doi. 10.1038/nature01025
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- Article
The eloquent ape: genes, brains and the evolution of language.
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- Nature Reviews Genetics, 2006, v. 7, n. 1, p. 9, doi. 10.1038/nrg1747
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- Article
Functional characterization of TBR1 variants in neurodevelopmental disorder.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-32053-6
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- Article
Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29496-2
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- Article
Absolute pitch exhibits phenotypic and genetic overlap with synesthesia.
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- Human Molecular Genetics, 2013, v. 22, n. 10, p. 2097, doi. 10.1093/hmg/ddt059
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- Article
The DISC1 promoter: characterization and regulation by FOXP2.
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- Human Molecular Genetics, 2012, v. 21, n. 13, p. 2862, doi. 10.1093/hmg/dds111
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- Article
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.
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- Human Molecular Genetics, 2010, v. 19, n. 24, p. 4848, doi. 10.1093/hmg/ddq415
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- Article
Functional genetic analysis of mutations implicated in a human speech and language disorder.
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- Human Molecular Genetics, 2006, v. 15, n. 21, p. 3154, doi. 10.1093/hmg/ddl392
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- Article
Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12–q11.
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- Human Molecular Genetics, 2003, v. 12, n. 24, p. 3225, doi. 10.1093/hmg/ddg362
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- Article
De novo TBR1 mutations in sporadic autism disrupt protein functions.
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- Nature Communications, 2014, v. 5, n. 9, p. 4954, doi. 10.1038/ncomms5954
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- Article
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.
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- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1702, doi. 10.1038/ejhg.2015.66
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- Article
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
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- European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1370, doi. 10.1038/ejhg.2014.296
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- Article
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.
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- European Journal of Human Genetics, 2015, v. 23, n. 9, p. 1113, doi. 10.1038/ejhg.2014.275
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- Article
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
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- European Journal of Human Genetics, 2014, v. 22, n. 10, p. 1165, doi. 10.1038/ejhg.2014.4
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- Article
Persistence and transmission of recessive deafness and sign language: new insights from village sign languages.
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- European Journal of Human Genetics, 2013, v. 21, n. 9, p. 894, doi. 10.1038/ejhg.2012.292
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- Article
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
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- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 361, doi. 10.1038/ejhg.2012.166
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- Article
The Association Between Stuttering Burden and Psychosocial Aspects of Life in Adults.
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- Journal of Speech, Language & Hearing Research, 2024, v. 67, n. 5, p. 1385, doi. 10.1044/2024_JSLHR-23-00562
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- Article
On the other hand: including left-handers in cognitive neuroscience and neurogenetics.
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- Nature Reviews Neuroscience, 2014, v. 15, n. 3, p. 193, doi. 10.1038/nrn3679
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- Article
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
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- European Journal of Human Genetics, 2009, v. 17, n. 10, p. 1354, doi. 10.1038/ejhg.2009.43
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- Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
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- 2012
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- Correction notice
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
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- Nature Genetics, 2011, v. 43, n. 6, p. 585, doi. 10.1038/ng.835
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- Article
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill.
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- PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003751
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- Article
Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain.
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- PLoS Genetics, 2011, v. 7, n. 7, p. 1, doi. 10.1371/journal.pgen.1002145
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- Article
Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 7, p. 555, doi. 10.1002/ajmg.b.32258
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- Article
Loss of Intercalated Cells (ITCs) in the Mouse Amygdala of Tshz1 Mutants Correlates with Fear, Depression, and Social Interaction Phenotypes.
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- Journal of Neuroscience, 2018, v. 38, n. 5, p. 1160, doi. 10.1523/JNEUROSCI.1412-17.2017
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- Article
The genetics of situs inversus without primary ciliary dyskinesia.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-60589-z
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- Article
Neuroimaging genomics as a window into the evolution of human sulcal organization.
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- Cerebral Cortex, 2024, v. 34, n. 3, p. 1, doi. 10.1093/cercor/bhae078
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- Article
Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew.
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- Cerebral Cortex, 2021, v. 31, n. 9, p. 4151, doi. 10.1093/cercor/bhab075
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- Article
The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area.
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- Cerebral Cortex, 2021, v. 31, n. 4, p. 1873, doi. 10.1093/cercor/bhaa327
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- Article
Associations of HLA alleles with specific language impairment.
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- Journal of Neurodevelopmental Disorders, 2014, v. 6, n. 1, p. 1
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- Article
A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: A Preliminary Study.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0096374
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- Article
Foxp2 Mutations Impair Auditory-Motor Association Learning.
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- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033130
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- Article
Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults.
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- Brain Structure & Function, 2022, v. 227, n. 2, p. 561, doi. 10.1007/s00429-021-02220-z
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- Article
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release.
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- Brain Structure & Function, 2018, v. 223, n. 9, p. 4211, doi. 10.1007/s00429-018-1746-6
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- Article
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
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- Nature Genetics, 2002, v. 30, n. 1, p. 86, doi. 10.1038/ng792
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- Article
A major susceptibility locus for leprosy in India maps to chromosome 10p13.
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- Nature Genetics, 2001, v. 27, n. 4, p. 439, doi. 10.1038/86958
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- Article
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family.
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- Human Genetics, 2021, v. 140, n. 8, p. 1183, doi. 10.1007/s00439-021-02289-w
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- Article
The developmental origins of genetic factors influencing language and literacy: Associations with early‐childhood vocabulary.
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- Journal of Child Psychology, 2021, v. 62, n. 6, p. 728, doi. 10.1111/jcpp.13327
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- Article
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
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- Scientific Reports, 2017, p. 46105, doi. 10.1038/srep46105
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- Article
A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.
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- Frontiers in Behavioral Neuroscience, 2016, v. 10, p. 1, doi. 10.3389/fnbeh.2016.00197
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- Article
Toward Robust Functional Neuroimaging Genetics of Cognition.
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- Journal of Neuroscience, 2019, v. 39, n. 44, p. 8778, doi. 10.1523/JNEUROSCI.0888-19.2019
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- Article
A forkhead-domain gene is mutated in a severe speech and language disorder.
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- Nature, 2001, v. 413, n. 6855, p. 519, doi. 10.1038/35097076
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- Article
Molecular networks of the FOXP2 transcription factor in the brain.
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- EMBO Reports, 2021, v. 22, n. 8, p. 1, doi. 10.15252/embr.202152803
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- Article
Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies.
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- NPJ Science of Learning, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41539-021-00101-y
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- Article
Region-specific Foxp2 deletions in cortex, striatum or cerebellum cannot explain vocalization deficits observed in spontaneous global knockouts.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-78531-8
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- Article
Exome-wide analysis implicates rare protein-altering variants in human handedness.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46277-w
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- Article
Structural models of genome-wide covariance identify multiple common dimensions in autism.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46128-8
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- Article
Patterns of Gray Matter Abnormalities in Schizophrenia Based on an International Mega-analysis.
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- Schizophrenia Bulletin, 2015, v. 41, n. 5, p. 1133, doi. 10.1093/schbul/sbu177
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- Article