World's Best Scientists 2026 revealed!

D-Index & Metrics

Psychology

D-Index
35
Citations
6702
World Ranking
9760
National Ranking
5158

Overview

Robin P. Goin-Kochel is affiliated with Baylor College of Medicine in the United States. Their research primarily focuses on neurodevelopmental disorders, with a special emphasis on autism spectrum disorder and associated genetic and environmental factors.

Their work covers several main fields of study, including:

  • Neuroscience
  • Psychology
  • Medicine

Subfields of particular interest in their research include:

  • Cognitive Neuroscience
  • Clinical Psychology
  • Genetics
  • Psychiatry and Mental Health
  • Health

The scientist's main topics of investigation are:

  • Autism Spectrum Disorder Research
  • Family and Disability Support Research
  • Genetics and Neurodevelopmental Disorders
  • Child Nutrition and Feeding Issues
  • Child and Adolescent Psychosocial and Emotional Development
  • Vaccine Coverage and Hesitancy
  • Genomic variations and chromosomal abnormalities

Among their recent papers are:

  • "A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants," 2021, American Journal of Psychiatry
  • "Person Ability Scores as an Alternative to Norm-Referenced Scores as Outcome Measures in Studies of Neurodevelopmental Disorders," 2020, American Journal on Intellectual and Developmental Disabilities
  • "Beliefs in vaccine as causes of autism among SPARK cohort caregivers," 2020, Vaccine
  • "Beliefs about causes of autism and vaccine hesitancy among parents of children with autism spectrum disorder," 2020, Vaccine
  • "Language characterization in 16p11.2 deletion and duplication syndromes," 2020, American Journal of Medical Genetics Part B Neuropsychiatric Genetics

The scientist frequently publishes in these venues:

  • Journal of Autism and Developmental Disorders
  • American Journal on Intellectual and Developmental Disabilities
  • Vaccine
  • Autism Research
  • Journal of Clinical and Translational Science

Collaborations have been a key aspect of their work, with frequent co-authors including:

  • Leandra N. Berry
  • Sarah S. Mire
  • Eric A. Storch
  • Wendy K. Chung
  • Sophie C. Schneider

Best Publications

  • A multisite study of the clinical diagnosis of different autism spectrum disorders

    Catherine Lord;Eva Petkova;Eva Petkova;Vanessa Hus;Weijin Gan

  • “My greatest joy and my greatest heart ache:” Parents’ own words on how having a child in the autism spectrum has affected their lives and their families’ lives

    Barbara J. Myers;Virginia H. Mackintosh;Robin P. Goin-Kochel

  • SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research

    Pamela Feliciano;Amy M. Daniels;LeeAnne Green Snyder;Amy Beaumont

  • How many doctors does it take to make an autism spectrum diagnosis

    Robin P Goin-Kochel;Virginia H Mackintosh;Barbara J Myers

  • A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

    Flore Zufferey;Elliott H. Sherr;Noam D. Beckmann;Ellen Hanson

  • Parental reports on the use of treatments and therapies for children with autism spectrum disorders

    Robin P. Goin-Kochel;Barbara J. Myers;Virginia H. Mackintosh

  • Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.

    Debra D'Angelo;Sébastien Lebon;Qixuan Chen;Sandra Martin-Brevet

  • The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population

    Ellen Hanson;Raphael Bernier;Ken Porche;Frank I. Jackson

  • Parental reports on the efficacy of treatments and therapies for their children with autism spectrum disorders

    Robin P. Goin-Kochel;Virginia H. Mackintosh;Barbara J. Myers

  • Clinical phenotype of the recurrent 1q21.1 copy-number variant.

    Raphael Bernier;Kyle J. Steinman;Beau Reilly;Arianne Stevens Wallace

  • “What Do You Like/Dislike About the Treatments You’re Currently Using?”: A Qualitative Study of Parents of Children With Autism Spectrum Disorders

    Virginia H. Mackintosh;Robin P. Goin-Kochel;Barbara J. Myers

  • Psychiatric disorders in children with 16p11.2 deletion and duplication.

    Maria Niarchou;Maria Niarchou;Samuel J. R. A. Chawner;Joanne L. Doherty;Anne M. Maillard

  • A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

    Patrícia B. S. Celestino-Soper;Sara Violante;Sara Violante;Emily L. Crawford;Rui Luo

  • The Role of Parental Cognitive, Behavioral, and Motor Profiles in Clinical Variability in Individuals With Chromosome 16p11.2 Deletions

    Andres Moreno-De-Luca;David W. Evans;David W. Evans;K. B. Boomer;Ellen Hanson;Ellen Hanson

  • Utility of the Social Communication Questionnaire-Current and Social Responsiveness Scale as Teacher-Report Screening Tools for Autism Spectrum Disorders

    G. Thomas Schanding;Kerri P. Nowell;Robin P. Goin-Kochel

  • Self-motion perception in autism is compromised by visual noise but integrated optimally across multiple senses.

    Adam Zaidel;Robin P. Goin-Kochel;Dora E. Angelaki

  • The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.

    Loyse Hippolyte;Anne M. Maillard;Borja Rodriguez-Herreros;Aurélie Pain

  • Emotional and Behavioral Adjustment in Typically Developing Siblings of Children with Autism Spectrum Disorders

    Allison G. Dempsey;Ashlie Llorens;Christie Brewton;Simmi Mulchandani

  • A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.

    Samuel J R A Chawner;Joanne L Doherty;Richard J L Anney;Kevin M Antshel

  • The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations.

    Robin P. Goin-Kochel;Anne E. Porter;Sarika U. Peters;Marwan Shinawi

  • Congenital Versus Regressive Onset of Autism Spectrum Disorders Parents' Beliefs About Causes

    Robin P. Goin-Kochel;Barbara J. Myers

  • The complex behavioral phenotype of 15q13.3 microdeletion syndrome.

    Mark N. Ziats;Robin P. Goin-Kochel;Robin P. Goin-Kochel;Leandra N. Berry;Leandra N. Berry;May Ali;May Ali

Frequent Co-Authors

Raphael Bernier
Raphael Bernier University of Washington
Wendy K. Chung
Wendy K. Chung Columbia University
Stephen M. Kanne
Stephen M. Kanne Weill Cornell Medicine
David H. Ledbetter
David H. Ledbetter University of Florida
Christa Lese Martin
Christa Lese Martin Geisinger Health System
Arthur L. Beaudet
Arthur L. Beaudet Baylor College of Medicine
Jacques S. Beckmann
Jacques S. Beckmann University of Lausanne
Jill A. Rosenfeld
Jill A. Rosenfeld Baylor College of Medicine
James S. Sutcliffe
James S. Sutcliffe Vanderbilt University
Michael John Owen
Michael John Owen Cardiff University

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