Publications:

Neuroimaging genetics studies of specific reading disability and developmental language disorder: A review.

Language And Linguistics Compass

Landi, Nicole N; Perdue, Meaghan M

Publication Date: 2019-09

Variant appearance in text: rs9295626

PubMed Link: 31844423

Variant Present in the following documents:

• Main text

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Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.

Brain Imaging And Behavior

Eicher, John D JD; Montgomery, Angela M AM; Akshoomoff, Natacha N; Amaral, David G DG; Bloss, Cinnamon S CS; Libiger, Ondrej O; Schork, Nicholas J NJ; Darst, Burcu F BF; Casey, B J BJ; Chang, Linda L; Ernst, Thomas T; Frazier, Jean J; Kaufmann, Walter E WE; Keating, Brian B; Kenet, Tal T; Kennedy, David D; Mostofsky, Stewart S; Murray, Sarah S SS; Sowell, Elizabeth R ER; Bartsch, Hauke H; Kuperman, Joshua M JM; Brown, Timothy T TT; Hagler, Donald J DJ; Dale, Anders M AM; Jernigan, Terry L TL; Gruen, Jeffrey R JR; ,

Publication Date: 2016-03

Variant appearance in text: rs9295626

PubMed Link: 25953057

Variant Present in the following documents:

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The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains.

Genes, Brain, And Behavior

Eicher, J D JD; Stein, C M CM; Deng, F F; Ciesla, A A AA; Powers, N R NR; Boada, R R; Smith, S D SD; Pennington, B F BF; Iyengar, S K SK; Lewis, B A BA; Gruen, J R JR

Publication Date: 2015-04

Variant appearance in text: rs9295626

PubMed Link: 25778907

Variant Present in the following documents:

• Main text
• GBB-14-377.pdf

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A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children.

Behavioral And Brain Functions : Bbf

Lim, Cadmon King-Poo CK; Wong, Amabel May-Bo AM; Ho, Connie Suk-Han CS; Waye, Mary Mui-Yee MM

Publication Date: 2014-07-11

Variant appearance in text: rs9295626

PubMed Link: 25015435

Variant Present in the following documents:

• Main text
• 1744-9081-10-23.pdf

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Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ.

Human Genetics

Eicher, John D JD; Powers, Natalie R NR; Miller, Laura L LL; Mueller, Kathryn L KL; Mascheretti, Sara S; Marino, Cecilia C; Willcutt, Erik G EG; DeFries, John C JC; Olson, Richard K RK; Smith, Shelley D SD; Pennington, Bruce F BF; Tomblin, J Bruce JB; Ring, Susan M SM; Gruen, Jeffrey R JR

Publication Date: 2014-07

Variant appearance in text: rs9295626

PubMed Link: 24509779

Variant Present in the following documents:

• Main text
• 439_2014_Article_1427.pdf

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