ROBIN KOCHEL to Adult
This is a "connection" page, showing publications ROBIN KOCHEL has written about Adult.
Connection Strength
0.221
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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: 0.043
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Understanding Vaccine Hesitancy Among Parents of Children With Autism Spectrum Disorder and Parents of Children With Non-Autism Developmental Delays. J Child Neurol. 2021 09; 36(10):911-918.
Score: 0.023
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Parent-led, stepped-care cognitive-behavioral therapy for youth with autism and co-occurring anxiety: study rationale and method. Braz J Psychiatry. 2020 Nov-Dec; 42(6):638-645.
Score: 0.022
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Evaluating Two Common Strategies for Research Participant Recruitment Into Autism Studies: Observational Study. J Med Internet Res. 2020 09 24; 22(9):e16752.
Score: 0.022
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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: 0.021
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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: 0.015
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Expression of the broad autism phenotype in simplex autism families from the Simons Simplex Collection. J Autism Dev Disord. 2014 Oct; 44(10):2392-9.
Score: 0.014
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Lack of evidence for increased genetic loading for autism among families of affected females: a replication from family history data in two large samples. Autism. 2007 May; 11(3):279-86.
Score: 0.009
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How many doctors does it take to make an autism spectrum diagnosis? Autism. 2006 Sep; 10(5):439-51.
Score: 0.008
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Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication. J Autism Dev Disord. 2016 Aug; 46(8):2734-2748.
Score: 0.008
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The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med. 2016 11; 18(11):1111-1118.
Score: 0.008
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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: 0.008
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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: 0.008
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Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med. 2016 Apr; 18(4):341-9.
Score: 0.007
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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. J Med Genet. 2012 Oct; 49(10):660-8.
Score: 0.006