(Q24306625)

G protein-coupled receptor 155

1 reference

Janus kinase and microtubule interacting protein 1

1 reference

cognition

1 reference

author

Daniel Geschwind

11

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Christa Lese Martin

2

Christa L Martin

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Yuhei Nishimura

Yuhei Nishimura

1

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Sandra Pellegrini

Sandra Pellegrini

8

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Marian Sigman

6

Marian Sigman

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author name string

Araceli Vazquez-Lopez

3

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Sarah J Spence

4

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Ana Isabel Alvarez-Retuerto

5

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Corinna Steindler

7

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N Carolyn Schanen

9

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Stephen T Warren

Fragile X and autism: a multicenter survey.

10

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language of work or name

English

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publication date

15 July 2007

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published in

Human Molecular Genetics

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volume

16

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page(s)

1682-98

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issue

14

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cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Estimate of the prevalence of chromosome 15q11-q13 duplications

1 reference

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7 January 2021

Gene expression analysis of peripheral blood leukocytes from discordant sib-pairs with schizophrenia and bipolar disorder reveals points of convergence between genetic and functional genomic approaches

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families

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https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Toward a developmental neurobiology of autism.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Rank products: a simple, yet powerful, new method to detect differentially regulated genes in replicated microarray experiments

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

The mGluR theory of fragile X mental retardation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Global up-regulation of chromosome 21 gene expression in the developing down syndrome brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Matching strategies in cognitive research with individuals with high-functioning autism: current practices, instrument biases, and recommendations.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Genetics of austim: complex aetiology for a heterogeneous disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

RNA and microRNAs in fragile X mental retardation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Altered IMPA2 gene expression and calcium homeostasis in bipolar disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Molecular characterization of bipolar disorder by comparing gene expression profiles of postmortem brains of major mental disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Autism as a disorder of neural information processing: directions for research and targets for therapy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Ca2+ activity at GABAB receptors constitutively promotes metabotropic glutamate signaling in the absence of GABA.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Significance analysis of microarrays applied to the ionizing radiation response

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Marlin-1, a novel RNA-binding protein associates with GABA receptors

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Jamip1 (marlin-1) defines a family of proteins interacting with janus kinases and microtubules.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

A genomewide screen for autism susceptibility loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

A genomewide screen of 345 families for autism-susceptibility loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Evidence for sex-specific risk alleles in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Replication of autism linkage: fine-mapping peak at 17q21.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21q

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

miRBase: microRNA sequences, targets and gene nomenclature

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

QGRS Mapper: a web-based server for predicting G-quadruplexes in nucleotide sequences

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Autistic spectrum disorder and the fragile X premutation.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Lessons from fragile X regarding neurobiology, autism, and neurodegeneration

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Autism as a paradigmatic complex genetic disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Comparison and evaluation of methods for generating differentially expressed gene lists from microarray data.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Statistical tests for differential expression in cDNA microarray experiments

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

DAVID: Database for Annotation, Visualization, and Integrated Discovery

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

Bioconductor: open software development for computational biology and bioinformatics

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

The genetics of autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021

TM4: a free, open-source system for microarray data management and analysis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM116

7 January 2021