ROBIN KOCHEL to Female
This is a "connection" page, showing publications ROBIN KOCHEL has written about Female.
Connection Strength
0.345
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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: 0.028
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It takes two! Exploring sex differences in parenting neurobiology and behaviour. J Neuroendocrinol. 2019 09; 31(9):e12721.
Score: 0.026
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Simons Variation in Individuals Project (Simons VIP): a genetics-first approach to studying autism spectrum and related neurodevelopmental disorders. Neuron. 2012 Mar 22; 73(6):1063-7.
Score: 0.016
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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: 0.015
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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: 0.014
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Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome. J Autism Dev Disord. 2020 Jul; 50(7):2491-2500.
Score: 0.014
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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: 0.014
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Beliefs in vaccine as causes of autism among SPARK cohort caregivers. Vaccine. 2020 02 11; 38(7):1794-1803.
Score: 0.014
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Using latent class analysis to identify treatment-use subgroups among parents of children with autism spectrum disorder. Autism Res. 2019 05; 12(5):843-854.
Score: 0.013
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Psychiatric disorders in children with 16p11.2 deletion and duplication. Transl Psychiatry. 2019 01 16; 9(1):8.
Score: 0.013
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Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder. J Autism Dev Disord. 2017 Nov; 47(11):3600-3607.
Score: 0.012
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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: 0.011
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Brief Report: Further Examination of Self-Injurious Behaviors in Children and Adolescents with Autism Spectrum Disorders. J Autism Dev Disord. 2016 May; 46(5):1872-9.
Score: 0.011
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Parental report of vaccine receipt in children with autism spectrum disorder: Do rates differ by pattern of ASD onset? Vaccine. 2016 Mar 08; 34(11):1335-42.
Score: 0.010
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Early Intervention Before Autism Diagnosis in Children Referred to a Regional Autism Clinic. J Dev Behav Pediatr. 2016 Jan; 37(1):15-9.
Score: 0.010
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Emergence of autism spectrum disorder in children from simplex families: relations to parental perceptions of etiology. J Autism Dev Disord. 2015 May; 45(5):1451-63.
Score: 0.010
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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: 0.010
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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: 0.009
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Parent-Led Cognitive Behavioral Teletherapy for Anxiety in Autistic Youth: A Randomized Trial Comparing Two Levels of Therapist Support. Behav Ther. 2024 May; 55(3):499-512.
Score: 0.009
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Utility of the social communication questionnaire-current and social responsiveness scale as teacher-report screening tools for autism spectrum disorders. J Autism Dev Disord. 2012 Aug; 42(8):1705-16.
Score: 0.008
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Emotional and behavioral adjustment in typically developing siblings of children with autism spectrum disorders. J Autism Dev Disord. 2012 Jul; 42(7):1393-402.
Score: 0.008
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Level of functioning in autism spectrum disorders: phenotypic congruence among affected siblings. J Autism Dev Disord. 2008 Jul; 38(6):1019-27.
Score: 0.006
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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: 0.006
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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: 0.006
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How many doctors does it take to make an autism spectrum diagnosis? Autism. 2006 Sep; 10(5):439-51.
Score: 0.005
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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: 0.005
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The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med. 2016 11; 18(11):1111-1118.
Score: 0.005
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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: 0.005
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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: 0.005
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Cognitive Profiles in Youth with Autism Spectrum Disorder: An Investigation of Base Rate Discrepancies using the Differential Ability Scales--Second Edition. J Autism Dev Disord. 2015 Jul; 45(7):1978-88.
Score: 0.005
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Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med. 2016 Apr; 18(4):341-9.
Score: 0.005
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Psychotropic medication use among children with autism spectrum disorders within the Simons Simplex Collection: are core features of autism spectrum disorder related? Autism. 2014 Nov; 18(8):933-42.
Score: 0.004
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TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Am J Hum Genet. 2013 Aug 08; 93(2):197-210.
Score: 0.004
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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: 0.004
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A multisite study of the clinical diagnosis of different autism spectrum disorders. Arch Gen Psychiatry. 2012 Mar; 69(3):306-13.
Score: 0.004
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Kawasaki syndrome: a controlled study of an outbreak in Wisconsin. Am J Epidemiol. 1986 Aug; 124(2):306-16.
Score: 0.001