Bryan H. King

ORCID: 0000-0003-1203-784X
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About
Contact & Profiles
Research Areas
  • Autism Spectrum Disorder Research
  • Attention Deficit Hyperactivity Disorder
  • Genetics and Neurodevelopmental Disorders
  • Family and Disability Support Research
  • Child Nutrition and Feeding Issues
  • Child and Adolescent Psychosocial and Emotional Development
  • Obsessive-Compulsive Spectrum Disorders
  • Child Development and Digital Technology
  • Behavioral and Psychological Studies
  • Suicide and Self-Harm Studies
  • Epigenetics and DNA Methylation
  • Adolescent and Pediatric Healthcare
  • Schizophrenia research and treatment
  • RNA modifications and cancer
  • Neurotransmitter Receptor Influence on Behavior
  • Immunotherapy and Immune Responses
  • Immune Cell Function and Interaction
  • HIV Research and Treatment
  • Acute Lymphoblastic Leukemia research
  • Ion channel regulation and function
  • Biochemical and Molecular Research
  • Neuroendocrine regulation and behavior
  • Infant Health and Development
  • RNA and protein synthesis mechanisms
  • Electroconvulsive Therapy Studies

New York University
2010-2025

University of California, San Francisco
2016-2025

Seattle Children's Hospital
2010-2023

University of Washington
2010-2023

Bunnell (United States)
2023

Seattle University
2009-2021

Memorial Sloan Kettering Cancer Center
2015-2021

St George's, University of London
2021

UCSF Benioff Children's Hospital
2017-2021

Polatis (United Kingdom)
2017

BackgroundTuberous sclerosis complex is highly variable in clinical presentation and findings. Disease manifestations continue to develop over the lifetime of an affected individual. Accurate diagnosis fundamental implementation appropriate medical surveillance treatment. Although significant advances have been made past 15 years understanding treatment tuberous complex, current diagnostic criteria not critically evaluated or updated since last consensus conference 1998.MethodsThe 2012...

10.1016/j.pediatrneurol.2013.08.001 article EN cc-by-nc-nd Pediatric Neurology 2013-09-20

Tuberous sclerosis complex is a genetic disorder affecting every organ system, but disease manifestations vary significantly among affected individuals. The diverse and varied presentations progression can be life-threatening with significant impact on cost quality of life. Current surveillance management practices are highly variable region country, reflective the fact that last consensus recommendations occurred in 1998 an updated, comprehensive standard lacking incorporates latest...

10.1016/j.pediatrneurol.2013.08.002 article EN cc-by-nc-nd Pediatric Neurology 2013-09-19

Comparative genomics allow us to search the human genome for segments that were extensively changed in last approximately 5 million years since divergence from our common ancestor with chimpanzee, but are highly conserved other species and thus likely be functional. We found 202 genomic elements vertebrates show evidence of significantly accelerated substitution rates human. These mostly non-coding DNA, often near genes associated transcription DNA binding. Resequencing confirmed five most...

10.1371/journal.pgen.0020168 article EN cc-by PLoS Genetics 2006-10-10

<h3>Context</h3> Selective serotonin reuptake inhibitors are widely prescribed for children with autism spectrum disorders. <h3>Objectives</h3> To determine the efficacy and safety of citalopram hydrobromide therapy repetitive behavior in <h3>Design</h3> National Institutes Health–sponsored randomized controlled trial. <h3>Setting</h3> Six academic centers, including Mount Sinai School Medicine, North Shore–Long Island Jewish Health System, University Carolina at Chapel Hill, California Los...

10.1001/archgenpsychiatry.2009.30 article EN Archives of General Psychiatry 2009-06-01
Hope Northrup Mary E. Aronow E. Martina Bebin John J. Bissler Thomas N. Darling and 95 more Petrus J. de Vries Michael Frost Zoë Fuchs Elizabeth S. Gosnell Nishant Gupta Anna Jansen Sergiusz Jóźwiak J.C. Kingswood Timothy K. Knilans Francis X. McCormack Ashley J. Pounders Steven L. Roberds David Rodriguez‐Buritica Jonathan Roth Julian R. Sampson Steven Sparagana Elizabeth A. Thiele Howard L. Weiner James W. Wheless Alexander J. Towbin Darcy A. Krueger Nicholas M. P. Annear Mary E. Aronow Ute Bartels E. Martina Bebin Moncef Berhouma John J. Bissler Klemens Budde Anna W. Byars Harry T. Chugani Edward W. Cowen Peter B. Crino Paolo Curatolo Thomas N. Darling Petrus de Vries Daniel F. Dilling David W. Dunn Rosemary Ekong Kevin C. Ess David Neal Franz Michael Frost Zoë Fuchs Elizabeth S. Gosnell Lisa M. Guay‐Woodford Nishant Gupta Luciana A. Haddad Anne Halbert Adelaide A. Hebert Elizabeth P. Henske Gregory L. Holmes Dena Hook John C. Hulbert Anna Jansen Simon R. Johnson Sergiusz Jóźwiak Bryan H. King J.C. Kingswood Timothy K. Knilans Mary Kay Koenig Bruce R. Korf Darcy A. Krueger David J. Kwiatkowski Francis X. McCormack Joel Moss David Mowat Kate Mowrey Rima Nabbout Mark Nellist Hope Northrup Finbar O’Callaghan Uday Patel Ashley J. Pounders E. Steve Roach Steven L. Roberds David Rodriguez‐Buritica Robb L. Romp Jonathan Roth Micaela Rozenberg Stephen J. Ruoss Mustafa Şahin Julian R. Sampson Joshua Samuels Matthias Sauter Catherine Smith Keyomaurs Soltani Steven Sparagana Shoba Srivastava Clare Stuart Joyce Teng Elizabeth A. Thiele Alexander J. Towbin Andrew T. Trout Agnies M. van Eeghen Stephanie Vanclooster Henry Z. Wang

Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disease affecting multiple body systems with wide variability in presentation. In 2013, Pediatric Neurology published articles outlining updated diagnostic criteria and recommendations for surveillance management of manifestations. Advances knowledge approvals new therapies necessitated a revision those recommendations.Chairs working group cochairs from the 2012 International TSC Consensus Group were invited to meet...

10.1016/j.pediatrneurol.2021.07.011 article EN cc-by-nc-nd Pediatric Neurology 2021-07-24

Mammalian cells possess two amino acid-sensing kinases: general control nonderepressible 2 (GCN2) and mechanistic target of rapamycin complex 1 (mTORC1). Their combined effects orchestrate cellular adaptation to acid levels, but how their activities are coordinated remains poorly understood. Here, we demonstrate an important link between GCN2 mTORC1 signaling. Upon deprivation various acids, activated up-regulates ATF4 induce expression the stress response protein Sestrin2, which is required...

10.1101/gad.269324.115 article EN Genes & Development 2015-11-05

OBJECTIVES: To compare 2 short-term, community caregiver training interventions for preschool-aged children with Autism Spectrum Disorder who had low resources. Low resource was defined by the US Department of Housing and Urban Development low-income index or 1 “indicator,” (eg, Medicaid eligibility). Child outcomes focused on joint engagement, attention, play. METHODS: Participants included 112 families a child met criteria being low-resourced were randomly assigned to 3-month...

10.1542/peds.2013-3229 article EN PEDIATRICS 2014-06-24

Background: Although randomized clinical trials (RCTs) have investigated several treatments for social communication difficulties and repetitive behavior in autism, none has yet shown consistent superiority over placebo. Placebo response autism RCTs may impede the ability to detect meaningful treatment effects. Objective: We sought identify individual-level predictors of placebo Study Oxytocin Autism improve Reciprocal Social Behaviors (SOARS-B), a 24-week RCT intranasal oxytocin impairment...

10.1089/cap.2024.0131 article EN Journal of Child and Adolescent Psychopharmacology 2025-02-19

This paper summarizes a conference held at the National Institute of Child Health and Human Development on December 6-7, 1999, self-injurious behavior [SIB] in developmental disabilities. Twenty-six top researchers U.S. from this field representing 13 different disciplines discussed environmental mechanisms, epidemiology, behavioral pharmacological intervention strategies, neurochemical substrates, genetic syndromes which SIB is prominent phenotype, neurobiological neurodevelopmental factors...

10.1002/1098-2779(200102)7:1<3::aid-mrdd1002>3.0.co;2-# article EN Mental Retardation and Developmental Disabilities Research Reviews 2001-02-01

Hyperactivity, impulsiveness, and distractibility are common problems in children with autism spectrum disorder (ASD). Extended-release guanfacine is approved for attention deficit hyperactivity but not well studied ASD.In a multisite, randomized clinical trial, extended-release was compared placebo ASD accompanied by hyperactivity, distractibility.Sixty-two subjects (boys, N=53; girls, N=9; mean age=8.5 years [SD=2.25]) were randomly assigned to (N=30) or (N=32) 8 weeks. The group showed...

10.1176/appi.ajp.2015.15010055 article EN American Journal of Psychiatry 2015-08-28
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