Reid Robison
American data scientist and physician
Reid Robison's AcademicInfluence.com Rankings


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Computer Science Philosophy
Reid Robison's Degrees
- Doctorate Medicine University of Utah
- PhD Data Science Stanford University
Why Is Reid Robison Influential?
(Suggest an Edit or Addition)According to Wikipedia, Reid Robison is an American board-certified psychiatrist known primarily for his work with psychedelic medicines. As an early adopter and researcher of the use of ketamine in psychiatry, Robison has made significant contributions to ketamine-assisted psychotherapy and other treatment modalities using ketamine for mental health conditions. He previously served as coordinating investigator for a study on MDMA-assisted psychotherapy for eating disorders, sponsored by the Multidisciplinary Association for Psychedelic Studies , and he continues to lead research and psychiatric clinical trials involving psychedelics. To date, Robison has guided thousands of ketamine-assisted therapy sessions and Spravato dosing sessions. He currently serves as Medical Director of Center for Change, an eating disorder treatment center in Utah, and Chief Clinical Officer of Numinus, a Vancouver-based mental health company focused on psychedelic research and treatments. Robison is an adjunct professor at both the University of Utah and Brigham Young University.
Reid Robison's Published Works
Published Works
- Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder (2011) (337)
- Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency. (2011) (233)
- Methamphetamine/amphetamine abuse and risk of Parkinson's disease in Utah: a population-based assessment. (2015) (136)
- Gender differences in 2 clinical trials of adults with attention-deficit/hyperactivity disorder: a retrospective data analysis. (2008) (94)
- TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations (2015) (87)
- Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications. (2011) (61)
- Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees (2010) (58)
- Psychometric properties of the Wender-Reimherr Adult Attention Deficit Disorder Scale. (2013) (50)
- Long-term open-label response to atomoxetine in adult ADHD: influence of sex, emotional dysregulation, and double-blind response to atomoxetine (2011) (44)
- Methylphenidate Transdermal System in Adult ADHD and Impact on Emotional and Oppositional Symptoms (2011) (44)
- Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders (2010) (43)
- Emotional Self-Regulation in Adults With Attention-Deficit / Hyperactivity Disorder ( ADHD ) : The Relative Contributions of Emotional Impulsiveness and ADHD Symptoms to Adaptive Impairments in Major Life Activities (2010) (42)
- Genome-wide linkage in Utah autism pedigrees (2009) (40)
- Personality disorder in ADHD Part 1: Assessment of personality disorder in adult ADHD using data from a clinical trial of OROS methylphenidate. (2010) (22)
- SeqHBase: a big data toolset for family based sequencing data analysis (2015) (21)
- Oppositional Defiant Disorder in Adults With ADHD (2013) (19)
- Integrating precision medicine in the study and clinical treatment of a severely mentally ill person (2013) (18)
- Personality disorders in ADHD Part 2: The effect of symptoms of personality disorder on response to treatment with OROS methylphenidate in adults with ADHD. (2010) (15)
- KBG syndrome involving a single-nucleotide duplication in ANKRD11 (2016) (13)
- Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine (2017) (12)
- SCN8A mutation in a child presenting with seizures and developmental delays (2016) (12)
- The Use of Emotional Dysregulation as an Endophenotype for Genetic studies in Adults with Attention-Deficit Hyperactivity Disorder (2010) (11)
- A unified theory of autism revisited: linkage evidence points to chromosome X using a high‐risk subset of AGRE families (2010) (10)
- The effect of personality disorder symptoms on response to treatment with methylphenidate transdermal system in adults with attention-deficit/hyperactivity disorder. (2012) (9)
- Massively parallel sequencing identifies a previously unrecognized X-linked disorder resulting in lethality in male infants owing to amino-terminal acetyltransferase deficiency (2011) (8)
- A variant in TAF1 is associated with a new syndrome with severe intellectual disability and characteristic dysmorphic features (2015) (6)
- Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43)) (2011) (5)
- A case series of group-based ketamine-assisted psychotherapy for patients in residential treatment for eating disorders with comorbid depression and anxiety disorders (2022) (4)
- Ketamine as a Novel Psychopharmacotherapy for Eating Disorders: Evidence and Future Directions (2022) (4)
- No evidence for IL1RAPL1 involvement in selected high‐risk autism pedigrees from the AGRE data set (2011) (2)
- Supplementary video of subject M.A for Integrating precision medicine in the study and clinical treatment of a severely mentally ill person. PeerJ 1:e177 (2013) (2)
- Whole exome sequencing reveals the genetic basis of a case of idiopathic hemolytic anemia and suggests candidate rare variants for ADHD in a Utah pedigree (2012) (1)
- Title : KBG syndrome involving a single base insertion in ANKRD 11 (2016) (0)
- Toward a methodology for evaluating DNA variants in nuclear families (2021) (0)
- Using VAAST and massively parallel sequencing to characterize a novel disorder caused by protein N-terminal acetyltransferase deficiency (2012) (0)
- Whole Genome Sequencing Analysis of an Idiopathic Intellectual Disability Syndrome (2013) (0)
- Massively parallel sequencing identifies a previously unrecognized X-linked disorder resulting in lethality in male infants owing to amino-terminal acetyltransferase deficiency (2011) (0)
- Toward more accurate variant calling for “personal genomes” (2013) (0)
- Comprehensive whole genome sequencing of a three generation pedigree : genetic components of a new syndrome with Severe Developmental Delay and Dysmorphic Features (2014) (0)
- ResearchGenome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders (2015) (0)
- Researchlinkage using the Social Responsiveness Scale in Utah autism pedigrees (2010) (0)
- Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine (2017) (0)
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What Schools Are Affiliated With Reid Robison?
Reid Robison is affiliated with the following schools: