| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1038061275 |
| P356 | DOI | 10.1007/S00439-006-0284-0 |
| P698 | PubMed publication ID | 17211639 |
| P50 | author | Hans-Hilger Ropers | Q20607814 |
| Vera M. Kalscheuer | Q28468812 | ||
| Niels Tommerup | Q30004359 | ||
| David FitzPatrick | Q41066804 | ||
| P2093 | author name string | Erik Niebuhr | |
| Fikret Erdogan | |||
| Luitgard M Neumann | |||
| Corinna Menzel | |||
| Andreas Tzschach | |||
| Sarah A Shoichet | |||
| Ger Arkesteijn | |||
| Reinhard Ullmann | |||
| Merete Bugge | |||
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| P433 | issue | 3-4 | |
| P921 | main subject | autism | Q38404 |
| P304 | page(s) | 501-509 | |
| P577 | publication date | 2007-01-09 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation | |
| P478 | volume | 121 |
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| Q36950691 | An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk |
| Q24629598 | Autism genome-wide copy number variation reveals ubiquitin and neuronal genes |
| Q33638384 | Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology |
| Q37166261 | Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder. |
| Q37433978 | Balanced translocations in mental retardation |
| Q34697737 | Chapter 15: disease gene prioritization |
| Q45331171 | Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients. |
| Q48095556 | Characterization of human cortical gene expression in relation to glucose utilization |
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| Q33906205 | Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1;q21.3) in a family co-segregating with mental retardation, language delay, and microcephaly |
| Q37235652 | Copy-number variations associated with autism spectrum disorder |
| Q33802577 | DIA1R is an X-linked gene related to Deleted In Autism-1. |
| Q53554100 | De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review. |
| Q52647146 | De novo single exon deletion of AUTS2 in a patient with speech and language disorder: a review of disrupted AUTS2 and further evidence for its role in neurodevelopmental disorders. |
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| Q50307316 | Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder |
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| Q24655403 | Epigenomic profiling reveals DNA-methylation changes associated with major psychosis |
| Q36595094 | Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus |
| Q27325418 | Function and regulation of AUTS2, a gene implicated in autism and human evolution |
| Q34539953 | Genetic copy number variation and general cognitive ability |
| Q55089250 | Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line. |
| Q28943526 | Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption |
| Q33587483 | Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies |
| Q34350428 | Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes. |
| Q28732207 | Genomic analysis of wig-1 pathways |
| Q35960747 | Genomic sister-disorders of neurodevelopment: an evolutionary approach |
| Q47251188 | Glycosphingolipid metabolic reprogramming drives neural differentiation |
| Q30393988 | Heterozygous Disruption of Autism susceptibility candidate 2 Causes Impaired Emotional Control and Cognitive Memory |
| Q46259543 | Human accelerated regions and other human-specific sequence variations in the context of evolution and their relevance for brain development |
| Q52663263 | Identification of disrupted AUTS2 and EPHA6 genes by array painting in a patient carrying a de novo balanced translocation t(3;7) with intellectual disability and neurodevelopment disorder. |
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| Q58612599 | Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24 |
| Q24305646 | Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders |
| Q37223275 | Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus |
| Q38067378 | Neocortical arealization: evolution, mechanisms, and open questions |
| Q33737231 | Neuronal Migration and AUTS2 Syndrome |
| Q33601252 | Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment |
| Q43900215 | Parental origin of de novo cytogenetically balanced reciprocal non-Robertsonian translocations |
| Q34600208 | Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene |
| Q34872499 | Rare SERINC2 variants are specific for alcohol dependence in individuals of European descent |
| Q34247422 | Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis |
| Q41768169 | Rare de novo germline copy-number variation in testicular cancer |
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| Q41380903 | Transcriptional Complexity and Distinct Expression Patterns of auts2 Paralogs in Danio rerio. |
| Q33931065 | Transcriptional dysregulation of neocortical circuit assembly in ASD |
| Q36096140 | Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies |
| Q39074170 | Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. |
| Q24301463 | WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome |
| Q38346550 | Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly |
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