(Q36589721)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference

10 November 2020

Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

0 references

0 references

9 references

13 March 2019

22 April 2019

25 April 2019

28 September 2019

28 November 2019

11 December 2019

15 December 2019

19 December 2019

10 November 2020

1 reference

28 September 2019

1 reference

28 November 2019

cytoskeletal proteins

1 reference

11 December 2019

1 reference

15 December 2019

1 reference

19 December 2019

neurodevelopmental disorder

1 reference

neuronal cell adhesion molecules

inferred from title

1 reference

Erratum: Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism

10 November 2020

corrigendum / erratum

0 references

author

Raymond A. Clarke

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Valsamma Eapen

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

author name string

S Lee

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

language of work or name

1 reference

4 September 2012

10 references

13 March 2019

22 April 2019

25 April 2019

28 September 2019

28 November 2019

11 December 2019

15 December 2019

19 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

10 November 2020

Translational Psychiatry

10 references

13 March 2019

22 April 2019

25 April 2019

28 September 2019

28 November 2019

11 December 2019

15 December 2019

19 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

10 November 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

page(s)

e158

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

12 February 2020

copyright license

9 references

13 March 2019

22 April 2019

25 April 2019

28 September 2019

28 November 2019

11 December 2019

15 December 2019

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on focus list of Wikimedia project

10 November 2020

ScienceSource

0 references

cites work

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9 September 2017

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9 September 2017

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9 September 2017

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Mitochondrial peptidase IMMP2L mutation causes early onset of age-associated disorders and impairs adult stem cell self-renewal

9 September 2017

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Slitrks as emerging candidate genes involved in neuropsychiatric disorders

9 September 2017

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The genetics of Tourette disorder

9 September 2017

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Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation

9 September 2017

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Neurexins, neuroligins and LRRTMs: synaptic adhesion getting fishy

9 September 2017

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The Genetics of Child Psychiatric Disorders: Focus on Autism and Tourette Syndrome

9 September 2017

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9 September 2017

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Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry

9 September 2017

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Trans-synaptic interaction of GluRdelta2 and Neurexin through Cbln1 mediates synapse formation in the cerebellum

9 September 2017

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Neurexins physically and functionally interact with GABA(A) receptors

9 September 2017

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L-histidine decarboxylase and Tourette's syndrome

9 September 2017

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Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred

9 September 2017

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Tourette syndrome is associated with recurrent exonic copy number variants

9 September 2017

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Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

9 September 2017

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The role of SAP97 in synaptic glutamate receptor dynamics

9 September 2017

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Contributions of the environment and environmentally vulnerable physiology to autism spectrum disorders

9 September 2017

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Three hypotheses for developmental defects that may underlie some forms of autism spectrum disorder

9 September 2017

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Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication

9 September 2017

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LRRTM2 functions as a neurexin ligand in promoting excitatory synapse formation

9 September 2017

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Epigenetics and the environmental regulation of the genome and its function

9 September 2017

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Decreased number of parvalbumin and cholinergic interneurons in the striatum of individuals with Tourette syndrome

9 September 2017

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The genetics of Tourette syndrome: a review.

9 September 2017

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Tourette syndrome in children and adolescents: special considerations

9 September 2017

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The international prevalence, epidemiology, and clinical phenomenology of Tourette syndrome: a cross-cultural perspective

9 September 2017

1 reference

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Linkage analysis of Tourette syndrome in a large Utah pedigree

9 September 2017

1 reference

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Instantaneous modulation of gamma oscillation frequency by balancing excitation with inhibition

9 September 2017

1 reference

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

9 September 2017

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High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

9 September 2017

1 reference

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New genomic structure for prostate cancer specific gene PCA3 within BMCC1: implications for prostate cancer detection and progression

9 September 2017

1 reference

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An unbiased expression screen for synaptogenic proteins identifies the LRRTM protein family as synaptic organizers

9 September 2017

1 reference

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Nested genes and increasing organizational complexity of metazoan genomes

9 September 2017

1 reference

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Histamine in the nervous system

9 September 2017

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Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome

9 September 2017

1 reference

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Non-random retention of protein-coding overlapping genes in Metazoa

9 September 2017

1 reference

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Familial deletion within NLGN4 associated with autism and Tourette syndrome

9 September 2017

1 reference

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A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice

9 September 2017

1 reference

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

9 September 2017

1 reference

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Development of cortical GABAergic circuits and its implications for neurodevelopmental disorders

9 September 2017

1 reference

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Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.

9 September 2017

1 reference

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Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families

9 September 2017

1 reference

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Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses

9 September 2017

1 reference

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Collision events between RNA polymerases in convergent transcription studied by atomic force microscopy

9 September 2017

1 reference

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Neuroligins determine synapse maturation and function

9 September 2017

1 reference

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AMIGO and friends: an emerging family of brain-enriched, neuronal growth modulating, type I transmembrane proteins with leucine-rich repeats (LRR) and cell adhesion molecule motifs

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Caudate volumes in childhood predict symptom severity in adults with Tourette syndrome

9 September 2017

1 reference

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Sequence variants in SLITRK1 are associated with Tourette's syndrome

9 September 2017

1 reference

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Altered parvalbumin-positive neuron distribution in basal ganglia of individuals with Tourette syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Nested genes in the human genome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

The delta2 glutamate receptor: a key molecule controlling synaptic plasticity and structure in Purkinje cells.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Synapse-associated protein-97 isoform-specific regulation of surface AMPA receptors and synaptic function in cultured neurons

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

A novel gene family encoding leucine-rich repeat transmembrane proteins differentially expressed in the nervous system

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

A stoichiometric complex of neurexins and dystroglycan in brain

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Significant linkage for Tourette syndrome in a large French Canadian family

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Tourette's disorder: epidemiology and comorbidity in primary school children

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Neurexophilin binding to alpha-neurexins. A single LNS domain functions as an independently folding ligand-binding unit

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Distinct expression of Cbln family mRNAs in developing and adult mouse brains.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Tourette's syndrome in a black woman with associated triple X and 9p mosaicism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Tourette syndrome and autistic disorder: a significant relationship

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

The inheritance of Gilles de la Tourette's syndrome and associated behaviors. Evidence for autosomal dominant transmission

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Lrrn1 is required for formation of the midbrain-hindbrain boundary and organiser through regulation of affinity differences between midbrain and hindbrain cells in chick.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Input normalization by global feedforward inhibition expands cortical dynamic range

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

The OMgp gene, a second growth suppressor within the NF1 gene

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Persistent multiple climbing fiber innervation of cerebellar Purkinje cells in mice lacking mGluR1.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

GluRδ2 assembles four neurexins into trans-synaptic triad to trigger synapse formation.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Glutamate receptor δ1 induces preferentially inhibitory presynaptic differentiation of cortical neurons by interacting with neurexins through cerebellin precursor protein subtypes

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Bidirectional transcription from human LRRTM2/CTNNA1 and LRRTM1/CTNNA2 gene loci leads to expression of N-terminally truncated CTNNA1 and CTNNA2 isoforms

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Autism, genetics and synaptic function alterations

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Tourette syndrome and comorbid pervasive developmental disorders.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

An individual with Gilles de la Tourette syndrome and Smith-Magenis microdeletion syndrome: is chromosome 17p11.2 a candidate region for Tourette syndrome putative susceptibility genes?

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

A patient with both Gilles de la Tourette's syndrome and chromosome 22q11 deletion syndrome: clue to the genetics of Gilles de la Tourette's syndrome?

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Cbln1 is essential for synaptic integrity and plasticity in the cerebellum

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Sexual dimorphism and developmental regulation of substantia nigra function

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Bilineal transmission in Tourette syndrome.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

Obsessive compulsive symptoms in Gilles de la Tourette syndrome and obsessive compulsive disorder: differences by diagnosis and family history

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3565204

An investigation of candidate regions for association with bipolar disorder

20 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FTP.2012.75

Genetic and clinical analysis of a large Dutch Gilles de la Tourette family

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FTP.2012.75

Cbln family proteins promote synapse formation by regulating distinct neurexin signaling pathways in various brain regions

21 January 2018

1 reference

12 December 2020

Gene location in Tourette syndrome

1 reference

12 December 2020

Father-to-son transmission of 6;17 translocation in Tourette's syndrome

1 reference

12 December 2020

9p monosomy in a patient with Gilles de la Tourette's syndrome

1 reference

12 December 2020

Multiple childhood behavioral disorders (Tourette syndrome, multiple tics, ADD and OCD) presenting in a family with a balanced chromosome translocation (t1;8)(q21.1;q22.1)

1 reference

12 December 2020

Linkage analysis and exclusion of regions of chromosomes 3 and 8 in Gilles de la Tourette syndrome following the identification of a balanced reciprocal translocation 46 XY, t(3:8)(p21.3 q24.1) in a case of Tourette syndrome

1 reference

12 December 2020

A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. The Tourette Syndrome Association International Consortium for Genetics

1 reference

12 December 2020

Association ofSLITRK1to Gilles de la Tourette Syndrome

1 reference

12 December 2020

Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region

1 reference

12 December 2020

Candidate region for Gilles de la Tourette syndrome at 7q31

1 reference

12 December 2020

Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22

1 reference

12 December 2020

Evidence for autosomal dominant transmission in Tourette's syndrome. United Kingdom cohort study

1 reference

12 December 2020

Identifiers

DOI

10.1038/TP.2012.75

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

PubMed publication ID

22948383

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22948383%20AND%20SRC:MED&resulttype=core&format=json