(Q28511185)

26 June 2017

title

TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons (English)

1 reference

Teashirt zinc finger family member 3

26 June 2017

0 references

1 reference

GOA release 2020-03-11

author

Nenad Sestan

26

0 references

Mehdi Metwaly

Mehdi Metwaly

5

0 references

Emeric Dubois

Emeric Dubois

24

0 references

Kenneth Y. Kwan

Kenneth Y Kwan

9

0 references

Lydia Kerkerian-Le Goff

Lydia Kerkerian-Le Goff

28

0 references

Marwan Shinawi

Marwan Shinawi

14

0 references

Adrian S. Woolf

Adrian S Woolf

21

0 references

Nenad Sestan

26

Nenad Sestan

1 reference

26 June 2017

3

Joris Andrieux

1 reference

26 June 2017

Xavier Caubit

1

1 reference

26 June 2017

Paolo Gubellini

2

1 reference

26 June 2017

Bernard Jacq

6

1 reference

26 June 2017

Ahmed Fatmi

7

1 reference

26 June 2017

Laurence Had-Aissouni

8

1 reference

26 June 2017

Pascal Salin

10

1 reference

26 June 2017

Michèle Carlier

11

1 reference

26 June 2017

Agne Liedén

12

1 reference

26 June 2017

Eva Rudd

13

1 reference

26 June 2017

Catherine Vincent-Delorme

15

1 reference

26 June 2017

Jean-Marie Cuisset

16

1 reference

26 June 2017

Marie-Pierre Lemaitre

17

1 reference

26 June 2017

Fatimetou Abderrehamane

18

1 reference

26 June 2017

Bénédicte Duban

19

1 reference

26 June 2017

Jean-François Lemaitre

20

1 reference

26 June 2017

Detlef Bockenhauer

22

1 reference

26 June 2017

Dany Severac

23

1 reference

26 June 2017

Ying Zhu

25

1 reference

26 June 2017

Laurent Fasano

29

1 reference

26 June 2017

Pierre L Roubertoux

4

1 reference

26 June 2017

Alistair N Garratt

27

1 reference

26 June 2017

language of work or name

English

0 references

publication date

26 September 2016

1 reference

26 June 2017

1 reference

26 June 2017

volume

48

1 reference

26 June 2017

issue

11

1 reference

26 June 2017

page(s)

1359-1369

1 reference

TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions

26 June 2017

cites work

1 reference

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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

19 March 2017

1 reference

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Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfate

19 March 2017

1 reference

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Fast gapped-read alignment with Bowtie 2

19 March 2017

1 reference

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Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Teashirt 3 regulates development of neurons involved in both respiratory rhythm and airflow control

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Common genetic variants on 5p14.1 associate with autism spectrum disorders

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

FOXG1 is responsible for the congenital variant of Rett syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

SOX5 controls the sequential generation of distinct corticofugal neuron subtypes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Ctip2 controls the differentiation of medium spiny neurons and the establishment of the cellular architecture of the striatum

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Fezl regulates the differentiation and axon targeting of layer 5 subcortical projection neurons in cerebral cortex

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Fezl is required for the birth and specification of corticospinal motor neurons

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Neuronal subtype-specific genes that control corticospinal motor neuron development in vivo

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Emx1 and Emx2 cooperate to regulate cortical size, lamination, neuronal differentiation, development of cortical efferents, and thalamocortical pathfinding

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Spatio-temporal transcriptome of the human brain

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

PANTHER version 10: expanded protein families and functions, and analysis tools.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Metabolic, synaptic and behavioral impact of 5-week chronic deep brain stimulation in hemiparkinsonian rats.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Satb2 Regulates the Differentiation of Both Callosal and Subcerebral Projection Neurons in the Developing Cerebral Cortex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Modeling transformations of neurodevelopmental sequences across mammalian species

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Corticostriatal connectivity and its role in disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Anatomic and molecular development of corticostriatal projection neurons in mice

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Neuroscience. The emerging biology of autism spectrum disorders

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Renal malformations associated with mutations of developmental genes: messages from the clinic

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Ciliary neurotrophic factor protects striatal neurons against excitotoxicity by enhancing glial glutamate uptake

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Simple behavioral assessment of mouse olfaction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Expression patterns of the three Teashirt-related genes define specific boundaries in the developing and postnatal mouse forebrain.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Autism and abnormal development of brain connectivity.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Automated apparatus for quantitation of social approach behaviors in mice.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

A genomewide screen for autism susceptibility loci

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Development of projection neuron types, axon pathways, and patterned connections of the mammalian cortex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

An automated method for studying exploratory and stereotyped behaviour in rats

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Functional and structural connectivity of frontostriatal circuitry in Autism Spectrum Disorder

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Membrane properties and synaptic responses of rat striatal neurones in vitro

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Development of tone response thresholds, latencies and tuning in the mouse inferior colliculus

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

[Genetic Basis of Congenital Anomalies of the Kidney and Urinary Tract].

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Complex autism spectrum disorder in a patient with a 17q12 microduplication

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Refining the phenotype associated with MEF2C haploinsufficiency.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

SFARI Gene: an evolving database for the autism research community.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Acute effects of ethanol on social behavior of adolescent and adult rats: role of familiarity of the test situation

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5083212

Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patients

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27668656

12 December 2020

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/27668656

12 December 2020

inferred from PubMed ID database lookup

Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systems

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27668656

12 December 2020

inferred from PubMed ID database lookup

1 reference

7 January 2021

Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb

1 reference

7 January 2021

19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias

1 reference

7 January 2021

19q13 microdeletion syndrome: Further refining the critical region.

1 reference

7 January 2021

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG.3681

1 reference

Dimensions Publication ID

26 June 2017

1047364476

0 references

PMC publication ID

5083212

0 references

1 reference