Rebecca Wilson

发表

The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy

J. Frazier, R. Boada, P. Zeitler, 2015, Journal of multidisciplinary healthcare.

Neurodevelopmental delay: Case definition & guidelines for data collection, analysis, and presentation of immunization safety data

S. Kochhar, N. Boghossian, V. Burton, 2019, Vaccine.

Early symptoms of autism spectrum disorder (ASD) in 1–8 year old children with sex chromosome trisomies (XXX, XXY, XYY), and the predictive value of joint attention

S. van Rijn, H. Swaab, N. Tartaglia, 2022, European Child & Adolescent Psychiatry.

Supporting students with sex chromosome aneuploidies in educational settings: Results of a nationwide survey.

L. Pyle, R. Boada, S. Davis, 2021, Journal of school psychology.

Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome.

S. Davis, P. Zeitler, N. Tartaglia, 2016, Advances in pediatrics.

Revisiting recombinant 8 syndrome

Laura Pickler, A. Tsai, Rebecca Wilson, 2011, American journal of medical genetics. Part A.

Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY

Judith S Miller, D. Hessl, J. Ross, 2017, Journal of developmental and behavioral pediatrics : JDBP.

Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS)

D. Loesch, P. Hagerman, S. Jacquemont, 2006, Journal of the Neurological Sciences.

Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis

Kristen Wigby, N. Tartaglia, S. Howell, 2016, American journal of medical genetics. Part A.

Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention

S. van Rijn, S. Davis, N. Tartaglia, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

ReviewA review of trisomy X ( 47 , XXX )

N. Tartaglia, S. Howell, Rebecca Wilson, 2015 .

A review of trisomy X (47,XXX)

N. Tartaglia, S. Howell, Rebecca Wilson, 2010, Orphanet journal of rare diseases.

Reviewof trisomy X (47,XXX)

N. Tartaglia, S. Howell, Rebecca Wilson, 2010 .

An Investigation of the Relationship Between Cortical Connectivity and Schizotypy in the General Population

C. Pantelis, L. Phillips, M. Seal, 2011, The Journal of nervous and mental disease.

Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies

L. Pyle, R. Boada, S. Davis, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Cognitive impairment in a 65-year-old male with the fragile X-associated tremor-ataxia syndrome (FXTAS).

J. Brunberg, P. Hagerman, S. Jacquemont, 2006, Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology.

Improving Access to Diagnostic Evaluations for Developmental Disabilities Through an Initial Assessment Model.

J. Dempsey, Rebecca Wilson, Lindsey DeVries, 2023, Journal of Developmental and Behavioral Pediatrics.

Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis

T. Simon, N. Tartaglia, K. Angkustsiri, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome).

N. Tartaglia, S. Howell, J. Janusz, 2010, Pediatric endocrinology reviews : PER.

Impairment of executive cognitive functioning in males with fragile X‐associated tremor/ataxia syndrome

D. Loesch, P. Hagerman, D. Hessl, 2007, Movement disorders : official journal of the Movement Disorder Society.

Cognitive Impairment in a 65-year-old Male With the Fragile X-associated Tremor-Ataxia Syndrome (FXTAS)

J. Brunberg, P. Hagerman, S. Jacquemont, 2006 .