ROBIN KOCHEL to DNA Copy Number Variations
This is a "connection" page, showing publications ROBIN KOCHEL has written about DNA Copy Number Variations.
Connection Strength
0.839
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The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. J Autism Dev Disord. 2017 Mar; 47(3):549-562.
Score: 0.182
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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants. Am J Psychiatry. 2021 01 01; 178(1):77-86.
Score: 0.118
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Language characterization in 16p11.2 deletion and duplication syndromes. Am J Med Genet B Neuropsychiatr Genet. 2020 09; 183(6):380-391.
Score: 0.115
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Developmental trajectories for young children with 16p11.2 copy number variation. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun; 174(4):367-380.
Score: 0.091
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The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition. Biol Psychiatry. 2016 07 15; 80(2):129-139.
Score: 0.083
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Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med. 2016 Apr; 18(4):341-9.
Score: 0.081
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Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers. Autism Res. 2020 08; 13(8):1300-1310.
Score: 0.057
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Psychiatric disorders in children with 16p11.2 deletion and duplication. Transl Psychiatry. 2019 01 16; 9(1):8.
Score: 0.052
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The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions. JAMA Psychiatry. 2015 Feb; 72(2):119-26.
Score: 0.039
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Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. JAMA Psychiatry. 2016 Jan; 73(1):20-30.
Score: 0.021