Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism (Q39980288)

16 September 2017

title

Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism (English)

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MAP/microtubule affinity regulating kinase 1

16 September 2017

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GOA release 2020-03-11

4

Frédéric Tores

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Anne Philippi

Anne Philippi

Aude-Marie Lepagnol-Bestel

11

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Aude-Marie Lepagnol-Bestel

3

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Alain Chédotal

Alain Chedotal

12

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Nicolas Ramoz

Nicolas Ramoz

14

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Philip Gorwood

Philip Gorwood

13

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Gilles Maussion

Gilles Maussion

1

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author name string

Jérôme Carayol

2

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16 September 2017

Frédéric Tores

4

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16 September 2017

Yann Loe-Mie

5

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16 September 2017

Ulla Milbreta

6

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16 September 2017

Francis Rousseau

7

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16 September 2017

Karine Fontaine

8

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16 September 2017

Julie Renaud

9

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16 September 2017

Jean-Marie Moalic

10

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16 September 2017

Jörg Hager

15

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16 September 2017

Michel Simonneau

16

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16 September 2017

publication date

20 May 2008

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16 September 2017

published in

Human Molecular Genetics

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16 September 2017

volume

17

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16 September 2017

issue

16

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16 September 2017

page(s)

2541-2551

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Genetics of austim: complex aetiology for a heterogeneous disorder

16 September 2017

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Autism as a paradigmatic complex genetic disorder

21 January 2018

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

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Major changes in our DNA lead to major changes in our thinking

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Symptom domains in autism and related conditions: evidence for familiality

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Genetic links between brain development and brain evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

MARK/PAR1 kinase is a regulator of microtubule-dependent transport in axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Protein kinase MARK/PAR-1 is required for neurite outgrowth and establishment of neuronal polarity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

mRNA transport in dendrites: RNA granules, motors, and tracks.

21 January 2018

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Neuronal polarity: from extracellular signals to intracellular mechanisms

21 January 2018

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Microtubule affinity-regulating kinase 2 functions downstream of the PAR-3/PAR-6/atypical PKC complex in regulating hippocampal neuronal polarity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Neuropathological findings in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Altered neuregulin 1-erbB4 signaling contributes to NMDA receptor hypofunction in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Reconstructing the evolutionary history of microcephalin, a gene controlling human brain size

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Adaptive evolution of ASPM, a major determinant of cerebral cortical size in humans

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Familial factors influence level of functioning in pervasive developmental disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

An overview of the KIN1/PAR-1/MARK kinase family

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Polarity-regulating kinase partitioning-defective 1/microtubule affinity-regulating kinase 2 negatively regulates development of dendrites on hippocampal neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Crucial importance of PKC-beta(I) in LFA-1-mediated locomotion of activated T cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Increased expression of protein kinase C beta activates ERK3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Phospholipase Cbeta4 and protein kinase Calpha and/or protein kinase CbetaI are involved in the induction of long term depression in cerebellar Purkinje cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

A clustered plasticity model of long-term memory engrams

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Pervasive Developmental Disorders in Preschool Children

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Efficiency and power in genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Granule cell behavior on laminin in cerebellar microexplant cultures

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

Cdh1-APC controls axonal growth and patterning in the mammalian brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN154

21 January 2018

Identifiers

DOI

10.1093/HMG/DDN154

1 reference

16 September 2017

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