| 36823321 | Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. | Nat Genet | 2023 |
| 37761888 | The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait. | Genes (Basel) | 2023 |
| 37214935 | Phonological Awareness Mediates the Relationship between DCDC2 and Reading Performance with the Influence of Home Environment. | Res Sq | 2023 |
| 34623748 | D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. | Am J Med Genet A | 2022 |
| 35998220 | Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. | Proc Natl Acad Sci U S A | 2022 |
| 36266505 | Discovery of 42 genome-wide significant loci associated with dyslexia. | Nat Genet | 2022 |
| 36223729 | Orthographic Depth May Influence the Degree of Severity of Maze Learning Performance in Children at Risk for Reading Disorder. | Dev Neurosci | 2022 |
| 36016658 | Dyslexia associated gene <i>KIAA0319</i> regulates cell cycle during human neuroepithelial cell development. | Front Cell Dev Biol | 2022 |
| 34186533 | Identifying Dyslexia: Link between Maze Learning and Dyslexia Susceptibility Gene, DCDC2, in Young Children. | Dev Neurosci | 2021 |
| 34970657 | Sex-specific associations between traumatic experiences and resting-state functional connectivity in the Philadelphia Neurodevelopmental Cohort. | JCPP Adv | 2021 |
| 31411106 | Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes. | Child Neuropsychol | 2020 |
| 32682798 | The temporal dynamics of first and second language processing: ERPs to spoken words in Mandarin-English bilinguals. | Neuropsychologia | 2020 |
| 32486976 | <i>DCDC2</i> READ1 regulatory element: how temporal processing differences may shape language. | Proc Biol Sci | 2020 |
| 30737034 | Genetics of bronchopulmonary dysplasia: When things do not match up, it is only the beginning. | J Pediatr | 2019 |
| 32523329 | Causal Attribution Profiles as a Function of Reading Skills, Hyperactivity, and Inattention. | Sci Stud Read | 2019 |
| 29666269 | Worldwide distribution of the <i>DCDC2</i> READ1 regulatory element and its relationship with phoneme variation across languages. | Proc Natl Acad Sci U S A | 2018 |
| 32523322 | Achievement attributions are associated with specific rather than general learning delays. | Learn Individ Differ | 2018 |
| 29894888 | Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexia. | Dev Cogn Neurosci | 2018 |
| 30631481 | A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children. | NPJ Sci Learn | 2018 |
| 29391653 | Reading-Related Causal Attributions for Success and Failure: Dynamic Links With Reading Skill. | Read Res Q | 2018 |
| 26755569 | Executive Functions Contribute Uniquely to Reading Competence in Minority Youth. | J Learn Disabil | 2017 |
| 28866788 | Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. | Hum Genet | 2017 |
| 27859682 | A method for integrating neuroimaging into genetic models of learning performance. | Genet Epidemiol | 2017 |
| 25953057 | Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. | Brain Imaging Behav | 2016 |
| 26660103 | The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles. | J Med Genet | 2016 |
| 27535846 | Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders. | Hum Genet | 2016 |
| 26183468 | Anxiety is related to indices of cortical maturation in typically developing children and adolescents. | Brain Struct Funct | 2016 |
| 25937488 | The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. | Neuroimage | 2016 |
| 25448322 | Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders. | Autism Res | 2015 |
| 26471062 | What is the basis for a genetic approach in neonatal disorders? | Semin Perinatol | 2015 |
| 25778907 | The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. | Genes Brain Behav | 2015 |
| 25821911 | Family income, parental education and brain structure in children and adolescents. | Nat Neurosci | 2015 |
| 24219608 | The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING). | Neuropsychology | 2014 |
| 24926531 | The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia. | Cortex | 2014 |
| 24509779 | Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. | Hum Genet | 2014 |
| 22669497 | Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study. | Brain Imaging Behav | 2013 |
| 23916419 | Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments. | Mol Genet Metab | 2013 |
| 24024963 | Genome-wide association study of shared components of reading disability and language impairment. | Genes Brain Behav | 2013 |
| 23691092 | Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. | PLoS One | 2013 |
| 23746548 | Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. | Am J Hum Genet | 2013 |
| 23122624 | Prenatal exposure to nicotine and impaired reading performance. | J Pediatr | 2013 |
| 21881542 | DCDC2 genetic variants and susceptibility to developmental dyslexia. | Psychiatr Genet | 2012 |
| 23169628 | Long-term influence of normal variation in neonatal characteristics on human brain development. | Proc Natl Acad Sci U S A | 2012 |
| 23150548 | Multimodal imaging of the self-regulating developing brain. | Proc Natl Acad Sci U S A | 2012 |
| 22750057 | Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability. | Neuroimage | 2012 |
| 22902750 | Neuroanatomical assessment of biological maturity. | Curr Biol | 2012 |
| 22524164 | Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies. | Int J Pediatr Endocrinol | 2012 |
| 22343285 | Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. | Proc Natl Acad Sci U S A | 2012 |
| 20850766 | The impact of environmental and genetic factors on neonatal late-onset sepsis. | J Pediatr | 2011 |
| 21507613 | Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia. | Schizophr Res | 2011 |