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Times Cited: 14
Times Cited: 14
Times Cited
Times Co-cited
Similarity
Subcategories of restricted and repetitive behaviors in children with autism spectrum disorders.
Somer L Bishop, Vanessa Hus, Amie Duncan, Marisela Huerta, Katherine Gotham, Andrew Pickles, Abba Kreiger, Andreas Buja, Sabata Lund, Catherine Lord. J Autism Dev Disord 2013
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Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders.
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Most genetic risk for autism resides with common variation.
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Restricted and repetitive behaviors in autism spectrum disorders: a review of research in the last decade.
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Evidence for three subtypes of repetitive behavior in autism that differ in familiality and association with other symptoms.
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Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
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Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8.
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders.
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Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R.
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Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions.
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Development of restricted and repetitive behaviors from 15 to 77 months: Stability of two distinct subtypes?
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Development of Two Dimensional Measures of Restricted and Repetitive Behavior in Parents and Children.
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Age-related differences in restricted repetitive behaviors in autism spectrum disorders.
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Repetitive behavior profiles in Asperger syndrome and high-functioning autism.
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Short report: relationship between restricted and repetitive behaviours in children with autism spectrum disorder and their parents.
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Autism spectrum disorders and autistic traits: a decade of new twin studies.
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Autism spectrum disorders and autistic traits share genetics and biology.
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Identification of common genetic risk variants for autism spectrum disorder.
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Autism as a strongly genetic disorder: evidence from a British twin study.
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Finding the missing heritability of complex diseases.
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
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14
Synaptic, transcriptional and chromatin genes disrupted in autism.
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Chromosome conformation elucidates regulatory relationships in developing human brain.
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The Adult Repetitive Behaviours Questionnaire-2 (RBQ-2A): A Self-Report Measure of Restricted and Repetitive Behaviours.
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The autism-spectrum quotient (AQ): evidence from Asperger syndrome/high-functioning autism, males and females, scientists and mathematicians.
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The Simons Simplex Collection: a resource for identification of autism genetic risk factors.
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ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains.
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Genetic heterogeneity between the three components of the autism spectrum: a twin study.
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An atlas of genetic correlations across human diseases and traits.
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14
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.