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Journal of Autism and Developmental Disorders|September 1, 2017
Gene Disrupting Mutations Associated with Regression in Autism Spectrum DisorderRobin P Goin-Kochel, Sandy Trinh, Shelley Barber, et al.Autism : the International Journal of Research and Practice|September 24, 2015
Musings on the puzzle pieceRobin P Goin-KochelVaccine|January 12, 2020
Beliefs in vaccine as causes of autism among SPARK cohort caregiversEric Fombonne, Robin P Goin-Kochel, Brian J O'Roak, et al.Autism : the International Journal of Research and Practice|May 5, 2007
Lack of evidence for increased genetic loading for autism among families of affected females: a replication from family history data in two large samplesRobin P Goin-Kochel, Anna Abbacchi, John N Constantino, et al.Proceedings of the National Academy of Sciences of the United States of America|May 6, 2015
Self-motion perception in autism is compromised by visual noise but integrated optimally across multiple sensesAdam Zaidel, Robin P Goin-Kochel, Dora E AngelakiJournal of Autism and Developmental Disorders|October 31, 2007
Level of functioning in autism spectrum disorders: phenotypic congruence among affected siblingsRobin P Goin-Kochel, Carla A Mazefsky, Brien P RileyJournal of Autism and Developmental Disorders|December 7, 2011
Utility of the social communication questionnaire-current and social responsiveness scale as teacher-report screening tools for autism spectrum disordersG Thomas Schanding, Kerri P Nowell, Robin P Goin-KochelAutism : the International Journal of Research and Practice|August 31, 2006
How many doctors does it take to make an autism spectrum diagnosis?Robin P Goin-Kochel, Virginia H Mackintosh, Barbara J MyersJournal of Neuroendocrinology|April 30, 2019
It takes two! Exploring sex differences in parenting neurobiology and behaviourPurva Rajhans, Robin P Goin-Kochel, Lane Strathearn, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 12, 2020
Language characterization in 16p11.2 deletion and duplication syndromesSo Hyun Kim, LeeAnne Green-Snyder, Catherine Lord, et al.Pageof 15