Donald B Bailey


Ontology type: schema:Person     


Person Info

NAME

Donald B

SURNAME

Bailey

Publications in SciGraph latest 50 shown

  • 2018-12 Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol in TRIALS
  • 2018-02 Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment in GENETICS IN MEDICINE
  • 2017-09-29 Fragile X syndrome in NATURE REVIEWS DISEASE PRIMERS
  • 2016-12 Mavoglurant in adolescents with fragile X syndrome: analysis of Clinical Global Impression-Improvement source data from a double-blind therapeutic study followed by an open-label, long-term extension study in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2016-12 Developmental profiles of infants with an FMR1 premutation in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2016-10 Family Communication and Cascade Testing for Fragile X Syndrome in JOURNAL OF GENETIC COUNSELING
  • 2016-06 Infant Development in Fragile X Syndrome: Cross-Syndrome Comparisons in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2015-11 Autism Symptoms Across Adulthood in Men with Fragile X Syndrome: A Cross-Sectional Analysis in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2015-06 Reading and Phonological Skills in Boys with Fragile X Syndrome in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2015-03 DSM-5 Changes and the Prevalence of Parent-Reported Autism Spectrum Symptoms in Fragile X Syndrome in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2015-02 Developing a utility index for the Aberrant Behavior Checklist (ABC-C) for fragile X syndrome in QUALITY OF LIFE RESEARCH
  • 2014-12 Associated features in females with an FMR1 premutation in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2013-04 Can a decision aid enable informed decisions in neonatal nursery recruitment for a fragile X newborn screening study? in GENETICS IN MEDICINE
  • 2013-02 Design and Evaluation of a Decision Aid for Inviting Parents to Participate in a Fragile X Newborn Screening Pilot Study in JOURNAL OF GENETIC COUNSELING
  • 2012-01 Video Analysis of Sensory-Motor Features in Infants with Fragile X Syndrome at 9–12 Months of Age in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2012-01 Caregiver opinions about fragile X population screening in GENETICS IN MEDICINE
  • 2011-09 Caregiver opinions about fragile X population screening in GENETICS IN MEDICINE
  • 2011-07 Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening in GENETICS IN MEDICINE
  • 2003-09 Screening for Fragile X Syndrome: Parent attitudes and perspectives in GENETICS IN MEDICINE
  • 2002 Fragile X Syndrome and Autism in THE RESEARCH BASIS FOR AUTISM INTERVENTION
  • 2001-04 Autistic Behavior, FMR1 Protein, and Developmental Trajectories in Young Males with Fragile X Syndrome in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2000-02 Early Development, Temperament, and Functional Impairment in Autism and Fragile X Syndrome in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 1998-12 Autistic Behavior in Young Boys with Fragile X Syndrome in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 1991-02 Scaling and attainment of goals in family-focused early intervention in COMMUNITY MENTAL HEALTH JOURNAL
  • 1991 Evaluating Programme Impact: Levels of Certainty in EARLY INTERVENTION STUDIES FOR YOUNG CHILDREN WITH SPECIAL NEEDS
  • 1988 Essential Elements of the Assessment Process in ASSESSMENT OF YOUNG DEVELOPMENTALLY DISABLED CHILDREN
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