ORA - Oxford University Research Archive

1 - 10 of 10

1

Journal article

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.

Vernes, SC, Spiteri, E, Nicod, J, et al.
2007-12-05

2

Journal article

A functional genetic link between distinct developmental language disorders.

Vernes, SC, Newbury, DF, Abrahams, BS, et al.
2008-11-05

3

Journal article

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.

Vernes, SC, Oliver, PL, Spiteri, E, et al.
2011-07-05

4

Journal article

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.

Scerri, TS, Fisher, SE, Francks, C, et al.
2004-11-05

5

Journal article

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.

Francks, C, Maegawa, S, Laurén, J, et al.
2007-12-05

6

Journal article

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Simpson, NH, Addis, L, Brandler, WM, et al.
2014-04-05

7

Journal article

Functional genetic analysis of mutations implicated in a human speech and language disorder.

Vernes, SC, Nicod, J, Elahi, FM, et al.
2006-11-05

8

Journal article

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

Francks, C, Paracchini, S, Smith, SD, et al.
2004-12-05

9

Journal article

LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells

Francks, C, Maegawa, S, Laurén, J, et al.
2007-12-05

10

Journal article

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill

Brandler, WM, Morris, AP, Evans, DM, et al.
2013-09-12

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