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ROBIN KOCHEL to Humans

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This is a "connection" page, showing publications ROBIN KOCHEL has written about Humans.
ROBIN KOCHEL
Connection Strength
0.430
Humans
  1. Vaccine Hesitancy and Attributions for Autism among Racially and Ethnically Diverse Groups of Parents of Children with Autism Spectrum Disorder: A Pilot Study. Autism Res. 2020 10; 13(10):1790-1796.
    View in: PubMed
    Score: 0.020
  2. Language characterization in 16p11.2 deletion and duplication syndromes. Am J Med Genet B Neuropsychiatr Genet. 2020 09; 183(6):380-391.
    View in: PubMed
    Score: 0.020
  3. On measuring regression in autism spectrum disorder: A commentary. Neurosci Biobehav Rev. 2019 09; 104:116-117.
    View in: PubMed
    Score: 0.018
  4. It takes two! Exploring sex differences in parenting neurobiology and behaviour. J Neuroendocrinol. 2019 09; 31(9):e12721.
    View in: PubMed
    Score: 0.018
  5. Musings on the puzzle piece. Autism. 2016 Feb; 20(2):250.
    View in: PubMed
    Score: 0.014
  6. Developmental regression in children: Current and future directions. Cortex. 2023 12; 169:5-17.
    View in: PubMed
    Score: 0.012
  7. An initial trial of OPT-In-Early: An online training program for caregivers of autistic children. Autism. 2023 08; 27(6):1601-1615.
    View in: PubMed
    Score: 0.012
  8. Stepped-Care Cognitive Behavioral Therapy in Children on the Autism Spectrum with Co-occurring Anxiety. J Autism Dev Disord. 2024 Jan; 54(1):93-108.
    View in: PubMed
    Score: 0.011
  9. 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.
    View in: PubMed
    Score: 0.011
  10. Utilization of a Best Practice Alert (BPA) at Point-of-Care for Recruitment into a US-Based Autism Research Study. J Autism Dev Disord. 2023 Jan; 53(1):359-369.
    View in: PubMed
    Score: 0.011
  11. Use of a Best Practice Alert (BPA) to Increase Diversity Within a US-Based Autism Research Cohort. J Autism Dev Disord. 2023 Jan; 53(1):370-377.
    View in: PubMed
    Score: 0.011
  12. 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.
    View in: PubMed
    Score: 0.010
  13. 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.
    View in: PubMed
    Score: 0.010
  14. Evaluating Two Common Strategies for Research Participant Recruitment Into Autism Studies: Observational Study. J Med Internet Res. 2020 09 24; 22(9):e16752.
    View in: PubMed
    Score: 0.010
  15. Beliefs about causes of autism and vaccine hesitancy among parents of children with autism spectrum disorder. Vaccine. 2020 09 11; 38(40):6327-6333.
    View in: PubMed
    Score: 0.010
  16. Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome. J Autism Dev Disord. 2020 Jul; 50(7):2491-2500.
    View in: PubMed
    Score: 0.010
  17. Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers. Autism Res. 2020 08; 13(8):1300-1310.
    View in: PubMed
    Score: 0.010
  18. Beliefs in vaccine as causes of autism among SPARK cohort caregivers. Vaccine. 2020 02 11; 38(7):1794-1803.
    View in: PubMed
    Score: 0.009
  19. Screening and Referral Practices for Autism Spectrum Disorder in Primary Pediatric Care. Pediatrics. 2019 10; 144(4).
    View in: PubMed
    Score: 0.009
  20. Towards a consensus on developmental regression. Neurosci Biobehav Rev. 2019 12; 107:3-5.
    View in: PubMed
    Score: 0.009
  21. 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.
    View in: PubMed
    Score: 0.009
  22. Psychiatric disorders in children with 16p11.2 deletion and duplication. Transl Psychiatry. 2019 01 16; 9(1):8.
    View in: PubMed
    Score: 0.009
  23. Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder. J Autism Dev Disord. 2017 Nov; 47(11):3600-3607.
    View in: PubMed
    Score: 0.008
  24. The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. J Autism Dev Disord. 2017 Mar; 47(3):549-562.
    View in: PubMed
    Score: 0.008
  25. 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.
    View in: PubMed
    Score: 0.007
  26. 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.
    View in: PubMed
    Score: 0.007
  27. Early Intervention Before Autism Diagnosis in Children Referred to a Regional Autism Clinic. J Dev Behav Pediatr. 2016 Jan; 37(1):15-9.
    View in: PubMed
    Score: 0.007
  28. Self-motion perception in autism is compromised by visual noise but integrated optimally across multiple senses. Proc Natl Acad Sci U S A. 2015 May 19; 112(20):6461-6.
    View in: PubMed
    Score: 0.007
  29. 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.
    View in: PubMed
    Score: 0.007
  30. 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.
    View in: PubMed
    Score: 0.007
  31. 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.
    View in: PubMed
    Score: 0.007
  32. 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.
    View in: PubMed
    Score: 0.006
  33. 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.
    View in: PubMed
    Score: 0.006
  34. Emotional and behavioral adjustment in typically developing siblings of children with autism spectrum disorders. J Autism Dev Disord. 2012 Jul; 42(7):1393-402.
    View in: PubMed
    Score: 0.006
  35. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. Proc Natl Acad Sci U S A. 2012 May 22; 109(21):7974-81.
    View in: PubMed
    Score: 0.006
  36. 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.
    View in: PubMed
    Score: 0.005
  37. Some, but not complete, reassurance on the safety of folic acid fortification. Am J Clin Nutr. 2010 Dec; 92(6):1287-8.
    View in: PubMed
    Score: 0.005
  38. Person Ability Scores as an Alternative to Norm-Referenced Scores as Outcome Measures in Studies of Neurodevelopmental Disorders. Am J Intellect Dev Disabil. 2020 11 01; 125(6):475-480.
    View in: PubMed
    Score: 0.005
  39. Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia. Eur J Hum Genet. 2011 Feb; 19(2):152-6.
    View in: PubMed
    Score: 0.005
  40. The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations. Autism Res. 2009 Apr; 2(2):98-108.
    View in: PubMed
    Score: 0.004
  41. Level of functioning in autism spectrum disorders: phenotypic congruence among affected siblings. J Autism Dev Disord. 2008 Jul; 38(6):1019-27.
    View in: PubMed
    Score: 0.004
  42. Visual systemizing preference in children with autism: A randomized controlled trial of intranasal oxytocin. Dev Psychopathol. 2018 05; 30(2):511-521.
    View in: PubMed
    Score: 0.004
  43. 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.
    View in: PubMed
    Score: 0.004
  44. Developmental trajectories for young children with 16p11.2 copy number variation. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun; 174(4):367-380.
    View in: PubMed
    Score: 0.004
  45. How many doctors does it take to make an autism spectrum diagnosis? Autism. 2006 Sep; 10(5):439-51.
    View in: PubMed
    Score: 0.004
  46. Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication. J Autism Dev Disord. 2016 Aug; 46(8):2734-2748.
    View in: PubMed
    Score: 0.004
  47. The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med. 2016 11; 18(11):1111-1118.
    View in: PubMed
    Score: 0.004
  48. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. JAMA Psychiatry. 2016 Jan; 73(1):20-30.
    View in: PubMed
    Score: 0.004
  49. 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.
    View in: PubMed
    Score: 0.004
  50. 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.
    View in: PubMed
    Score: 0.003
  51. Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med. 2016 Apr; 18(4):341-9.
    View in: PubMed
    Score: 0.003
  52. The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population. Biol Psychiatry. 2015 May 01; 77(9):785-93.
    View in: PubMed
    Score: 0.003
  53. 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.
    View in: PubMed
    Score: 0.003
  54. 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.
    View in: PubMed
    Score: 0.003
  55. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. J Med Genet. 2012 Oct; 49(10):660-8.
    View in: PubMed
    Score: 0.003
  56. A multisite study of the clinical diagnosis of different autism spectrum disorders. Arch Gen Psychiatry. 2012 Mar; 69(3):306-13.
    View in: PubMed
    Score: 0.003
  57. Kawasaki syndrome: a controlled study of an outbreak in Wisconsin. Am J Epidemiol. 1986 Aug; 124(2):306-16.
    View in: PubMed
    Score: 0.000
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.