(Q39828938)

15 September 2017

title

A null mutation in TNIK defines a novel locus for intellectual disability (English)

1 reference

15 September 2017

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8

Fowzan S Alkuraya

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15 September 2017

5

Dorota Monies

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15 September 2017

Shams Anazi

1

1 reference

15 September 2017

Hanan E Shamseldin

2

1 reference

15 September 2017

Dhekra AlNaqeb

3

1 reference

15 September 2017

Mohamed Abouelhoda

4

1 reference

15 September 2017

Mustafa A Salih

6

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15 September 2017

Khalid Al-Rubeaan

7

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15 September 2017

publication date

22 April 2016

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15 September 2017

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15 September 2017

volume

135

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15 September 2017

issue

7

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15 September 2017

page(s)

773-778

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https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

15 September 2017

1 reference

Discovery of rare homozygous mutations from studies of consanguineous pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

The application of next-generation sequencing in the autozygosity mapping of human recessive diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Human knockout research: new horizons and opportunities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Organization of TNIK in dendritic spines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

TNiK is required for postsynaptic and nuclear signaling pathways and cognitive function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

TNIK, a novel member of the germinal center kinase family that activates the c-Jun N-terminal kinase pathway and regulates the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Genome sequencing identifies major causes of severe intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

MINK and TNIK differentially act on Rap2-mediated signal transduction to regulate neuronal structure and AMPA receptor function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Signaling by the germinal center kinase family of protein kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

The kinase TNIK is an essential activator of Wnt target genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Agonistic and antagonistic roles for TNIK and MINK in non-canonical and canonical Wnt signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

DISC1: a key lead in studying cortical development and associated brain disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Semiquantitative proteomic analysis of rat forebrain postsynaptic density fractions by mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

The Traf2- and Nck-interacting kinase as a putative effector of Rap2 to regulate actin cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

The psychiatric disease risk factors DISC1 and TNIK interact to regulate synapse composition and function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1671-9

10.1007/S00439-016-1671-9

21 January 2018

Identifiers

DOI

1 reference

15 September 2017

1 reference