| P50 | author | Sara Mascheretti | Q50631458 |
| | Manuela Sironi | Q56460432 |
| | Alessandra Mozzi | Q57656900 |
| | Rachele Cagliani | Q81579912 |
| | Franca Rosa Guerini | Q89825958 |
| | Mario Clerici | Q37839199 |
| | Diego Forni | Q42256688 |
| P2093 | author name string | Cecilia Marino | |
| | Massimo Molteni | |
| | Stefania Riva | |
| | Valentina Riva | |
| P2860 | cites work | No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes | Q43864082 |
| | Heterozygote advantage of the MTHFR C677T polymorphism on specific cognitive performance in elderly Chinese males without dementia | Q44201962 |
| | FOXP2 variation modulates functional hemispheric asymmetries for speech perception | Q45389379 |
| | FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder | Q47742684 |
| | An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia. | Q50589590 |
| | The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration. | Q52297325 |
| | Variants in SNAP25 are targets of natural selection and influence verbal performances in women. | Q53093415 |
| | Human-specific transcriptional regulation of CNS development genes by FOXP2 | Q24655742 |
| | Neurobiological Basis of Language Learning Difficulties. | Q26740046 |
| | The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles. | Q27317078 |
| | A forkhead-domain gene is mutated in a severe speech and language disorder | Q28190379 |
| | Convergent transcriptional specializations in the brains of humans and song-learning birds | Q28650360 |
| | A new multipoint method for genome-wide association studies by imputation of genotypes | Q29547209 |
| | Functional and evolutionary insights into human brain development through global transcriptome analysis | Q29617082 |
| | Prevalence of specific language impairment in kindergarten children. | Q30371988 |
| | Enhanced procedural learning of speech sound categories in a genetic variant of FOXP2. | Q30398496 |
| | Transcriptional landscape of the prenatal human brain | Q33926910 |
| | Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. | Q33957708 |
| | Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations. | Q33994158 |
| | Deciphering the genetic basis of speech and language disorders | Q34170013 |
| | Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. | Q34248551 |
| | Language fMRI abnormalities associated with FOXP2 gene mutation | Q34269471 |
| | Improving language and literacy is a matter of time | Q34342502 |
| | Qualitative analysis of verbal fluency output: review and comparison of several scoring methods | Q34383592 |
| | Molecular genetics of speech and language disorders | Q35000031 |
| | A dual-route approach to orthographic processing | Q35033369 |
| | Imaging genetics of FOXP2 in dyslexia | Q35679721 |
| | Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development | Q35985503 |
| | Age-Related Differences and Heritability of the Perisylvian Language Networks | Q36064385 |
| | Toward epigenetic and gene regulation models of specific language impairment: looking for links among growth, genes, and impairments | Q36499887 |
| | Decoding the genetics of speech and language | Q38066309 |
| | Molecular genetics of dyslexia: an overview | Q38153350 |
| | Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample | Q38271952 |
| | Dough, tough, cough, rough: A "fast" fMRI localizer of component processes in reading | Q38386117 |
| | The role of speed of processing, rapid naming, and phonological awareness in reading achievement | Q38419414 |
| | Assessing the effects of common variation in the FOXP2 gene on human brain structure | Q41561119 |
| P433 | issue | 5 | |
| P304 | page(s) | 578-586 | |
| P577 | publication date | 2017-04-24 | |
| P1433 | published in | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | Q15762380 |
| P1476 | title | A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples | |
| P478 | volume | 174 | |