Connection

ROBIN KOCHEL to Female

This is a "connection" page, showing publications ROBIN KOCHEL has written about Female.
Connection Strength

0.345
  1. 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: 0.028
  2. It takes two! Exploring sex differences in parenting neurobiology and behaviour. J Neuroendocrinol. 2019 09; 31(9):e12721.
    View in: PubMed
    Score: 0.026
  3. 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: 0.016
  4. 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: 0.015
  5. 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: 0.014
  6. Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome. J Autism Dev Disord. 2020 Jul; 50(7):2491-2500.
    View in: PubMed
    Score: 0.014
  7. 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: 0.014
  8. Beliefs in vaccine as causes of autism among SPARK cohort caregivers. Vaccine. 2020 02 11; 38(7):1794-1803.
    View in: PubMed
    Score: 0.014
  9. 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: 0.013
  10. Psychiatric disorders in children with 16p11.2 deletion and duplication. Transl Psychiatry. 2019 01 16; 9(1):8.
    View in: PubMed
    Score: 0.013
  11. Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder. J Autism Dev Disord. 2017 Nov; 47(11):3600-3607.
    View in: PubMed
    Score: 0.012
  12. The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. J Autism Dev Disord. 2017 Mar; 47(3):549-562.
    View in: PubMed
    Score: 0.011
  13. 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: 0.011
  14. 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: 0.010
  15. 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: 0.010
  16. 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: 0.010
  17. 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: 0.010
  18. 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: 0.009
  19. 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: 0.009
  20. 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: 0.008
  21. 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: 0.008
  22. 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: 0.006
  23. 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: 0.006
  24. 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: 0.006
  25. How many doctors does it take to make an autism spectrum diagnosis? Autism. 2006 Sep; 10(5):439-51.
    View in: PubMed
    Score: 0.005
  26. 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: 0.005
  27. The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med. 2016 11; 18(11):1111-1118.
    View in: PubMed
    Score: 0.005
  28. 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: 0.005
  29. 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: 0.005
  30. 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: 0.005
  31. Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med. 2016 Apr; 18(4):341-9.
    View in: PubMed
    Score: 0.005
  32. 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: 0.004
  33. 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: 0.004
  34. 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: 0.004
  35. 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: 0.004
  36. Kawasaki syndrome: a controlled study of an outbreak in Wisconsin. Am J Epidemiol. 1986 Aug; 124(2):306-16.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.