Imaging genetics of FOXP2 in dyslexia (Q35679721)

9 August 2017

Imaging genetics of FOXP2 in dyslexia (English)

1 reference

9 August 2017

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11

Sven Cichon

0 references

Bertram Müller-Myhsok

10

Bertram Müller-Myhsok

0 references

Per Hoffmann

Per Hoffmann

8

0 references

Peter Ahnert

Peter Ahnert

7

0 references

Christiane Wolf

5

Christiane Wolf

1 reference

9 August 2017

Arndt Wilcke

1

1 reference

9 August 2017

Carolin Ligges

2

1 reference

9 August 2017

Jana Burkhardt

3

1 reference

9 August 2017

Michael Alexander

4

1 reference

9 August 2017

Elfi Quente

6

1 reference

9 August 2017

Albert Becker

9

1 reference

9 August 2017

Johannes Boltze

12

1 reference

9 August 2017

Holger Kirsten

13

1 reference

9 August 2017

7 September 2011

1 reference

European Journal of Human Genetics

9 August 2017

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9 August 2017

20

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9 August 2017

2

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9 August 2017

224-229

1 reference

https://scigraph.springernature.com/pub.10.1038/ejhg.2011.160

9 August 2017

0 references

cites work

The songbird as a model for the generation and learning of complex sequential behaviors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

FOXP2 as a molecular window into speech and language

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

A functional genetic link between distinct developmental language disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

The multiple roles of CUX1: insights from mouse models and cell-based assays

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Survey of fMRI results regarding a phonological deficit in children and adults with dyslexia: fundamental deficit or indication of compensation?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

CalcDalton: a tool for multiplex genotyping primer design for single-base extension reactions using cleavable primers

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Analysis of transcriptional regulation of the small leucine rich proteoglycans.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Imaging genetic influences in human brain function

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Genosnip: SNP genotyping by MALDI-TOF MS using photocleavable oligonucleotides

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Language fMRI abnormalities associated with FOXP2 gene mutation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Mapping the genetic variation of executive attention onto brain activity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Links between signal transduction, transcription and adhesion in epithelial bud development

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Serotonin transporter genetic variation and the response of the human amygdala

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

A forkhead-domain gene is mutated in a severe speech and language disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Dyslexia: cultural diversity and biological unity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Hes1 and Hes5 as notch effectors in mammalian neuronal differentiation.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Neural basis of an inherited speech and language disorder.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Functional disruption in the organization of the brain for reading in dyslexia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Cloning and characterization of an ATBF1 isoform that expresses in a neuronal differentiation-dependent manner

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

ATBF1, a multiple-homeodomain zinc finger protein, selectively down-regulates AT-rich elements of the human alpha-fetoprotein gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Local and transient expression of E-cadherin involved in mouse embryonic brain morphogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Right handed Neandertals: Vindija and beyond

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

The role of gene DCDC2 in German dyslexics.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

A meta-analysis of functional neuroimaging studies of dyslexia.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Robustness of single-base extension against mismatches at the site of primer attachment in a clinical assay.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

PAWE-3D: visualizing power for association with error in case-control genetic studies of complex traits.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

FOXP2 polymorphisms in patients with schizophrenia.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3260915

Dopamine-dependent facilitation of LTP induction in hippocampal CA1 by exposure to spatial novelty

25 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2011.160

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/EJHG.2011.160

1 reference

9 August 2017

1 reference

9 August 2017

1 reference