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Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation.
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In: Journal of neurodevelopmental disorders, vol 14, iss 1 (2022)
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| 2 |
Development of thalamus mediates paternal age effect on offspring reading: A preliminary investigation.
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In: Human brain mapping, vol 42, iss 14 (2021)
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| 3 |
Pre-treatment clinical and gene expression patterns predict developmental change in early intervention in autism.
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In: Molecular psychiatry, vol 26, iss 12 (2021)
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| 4 |
Translating genomic education materials into languages other than English: A scoping review protocol ...
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| 5 |
Genetic testing and eHealth usage among Deaf women.
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In: Journal of genetic counseling, vol 28, iss 5 (2019)
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| 6 |
Metformin treatment in young children with fragile X syndrome.
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In: Molecular genetics & genomic medicine, vol 7, iss 11 (2019)
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| 7 |
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
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In: Genetics in medicine : official journal of the American College of Medical Genetics, vol 21, iss 8 (2019)
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| 8 |
Dumb or smart asses? Donkey's (Equus asinus) cognitive capabilities share the heritability and variation patterns of human's (Homo sapiens) cognitive capabilities
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| 10 |
Curvilinear Association Between Language Disfluency and FMR1 CGG Repeat Size Across the Normal, Intermediate, and Premutation Range.
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In: Frontiers in genetics, vol 9, iss AUG (2018)
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| 11 |
Assessing the accuracy of perceptions of intelligence based on heritable facial features
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| 12 |
Assessing the accuracy of perceptions of intelligence based on heritable facial features
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| 13 |
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.
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In: Brain imaging and behavior, vol 10, iss 1 (2016)
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| 14 |
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.
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In: Brain imaging and behavior, vol 10, iss 1 (2016)
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| 15 |
Healing Our Race-Linked Wounds
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In: Carroy U "Cuf" Ferguson, Ph.D. (2015)
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| 16 |
Examining the Genetic Underpinnings of Commonly Comorbid Language Disorders
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| 17 |
List of sequences used for the phylogenetic analysis of FoxP subfamily members ...
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| 18 |
Insertion mutants of the Drosophila FoxP gene affect isoform expression and flight performance ...
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| 19 |
Deficiency ED5438 uncovers the FoxP³⁹⁵⁵ self-learning phenotype ...
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| 20 |
The mutant line FoxP³⁹⁵⁵ was impaired in operant self- but not world-learning ...
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