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Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.
Human Molecular Genetics|April 17, 2021
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measuresAngela Martinelli, Mabel L Rice, Joel B Talcott, et al.
Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.
Genes, Brain, and Behavior|March 18, 2015
Lack of replication for the myosin-18B association with mathematical ability in independent cohortsK A Pettigrew, S F Fajutrao Valles, K Moll, et al.
Child Development|August 2, 2025
Learning Variability Network Exchange (LEVANTE): A Global Framework for Measuring Children's Learning Variability Through Collaborative Data SharingMichael C Frank, Heidi A Baumgartner, Mika Braginsky, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research|March 1, 2019
The future of WRRF modelling - outlook and challengesPusker Regmi, Heather Stewart, Youri Amerlinck, et al.
Child Development|February 13, 2023
Language and reading impairments are associated with increased prevalence of non-right-handednessFilippo Abbondanza, Philip S Dale, Carol A Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2022
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 peopleElse Eising, Nazanin Mirza-Schreiber, Eveline L de Zeeuw, et al.
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