Angela Morgan

Severe speech impairment is a distinguishing feature of FOXP1-related disorder

Ruth O Braden, David J Amor, Simon E Fisher, Cristina Mei, Candace T Myers, Heather Mefford, Deepak Gill, Siddharth Srivastava, Lindsay C Swanson, Himanshu Goel, Ingrid E Scheffer, Angela T Morgan

Journal article  |  2021  |  DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

AIM: To delineate the speech and language phenotype of a cohort of individuals with FOXP1-related disorder. METHOD: We administere..

A Modeling-Guided Case Study of Disordered Speech in Minimally Verbal Children With Autism Spectrum Disorder

Karen Chenausky, Amanda Brignell, Angela T Morgan, Andrea C Norton, Helen B Tager-Flusberg, Gottfried Schlaug, Frank H Guenther

Journal article  |  2021  |  AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY

Purpose Understanding what limits speech development in minimally verbal (MV) children with autism spectrum disorder (ASD) is impo..

Early Intervention for Children Aged 0 to 2 Years With or at High Risk of Cerebral Palsy International Clinical Practice Guideline Based on Systematic Reviews

Catherine Morgan, Linda Fetters, Lars Adde, Nadia Badawi, Ada Bancale, Roslyn N Boyd, Olena Chorna, Giovanni Cioni, Diane L Damiano, Johanna Darrah, Linda S de Vries, Stacey Dusing, Christa Einspieler, Ann-Christin Eliasson, Donna Ferriero, Darcy Fehlings, Hans Forssberg, Andrew M Gordon, Susan Greaves, Andrea Guzzetta, et al.

Journal article  |  2021  |  JAMA PEDIATRICS

Importance: Cerebral palsy (CP) is the most common childhood physical disability. Early intervention for children younger than 2 y..

Speech and language deficits are central to SETBP1 haploinsufficiency disorder

Angela Morgan, Ruth Braden, Maggie MK Wong, Estelle Colin, David Amor, Frederique Liegeois, Siddharth Srivastava, Adam Vogel, Varoona Bizaoui, Kara Ranguin, Simon E Fisher, Bregje W van Bon

Journal article  |  2021  |  EUROPEAN JOURNAL OF HUMAN GENETICS

Expressive communication impairment is associated with haploinsufficiency of SETBP1, as reported in small case series. Heterozygou..

Clinical delineation of SETBP1 haploinsufficiency disorder

Nadieh A Jansen, Ruth O Braden, Siddharth Srivastava, Erin F Otness, Gaetan Lesca, Massimiliano Rossi, Mathilde Nizon, Raphael A Bernier, Chloe Quelin, Arie van Haeringen, Tjitske Kleefstra, Maggie MK Wong, Sandra Whalen, Simon E Fisher, Angela T Morgan, Bregje W van Bon

Journal article  |  2021  |  EUROPEAN JOURNAL OF HUMAN GENETICS

SETBP1 haploinsufficiency disorder (MIM#616078) is caused by haploinsufficiency of SETBP1 on chromosome 18q12.3, but there has not..

Speech, Language, and Oromotor Skills in Patients With Polymicrogyria

Ruth O Braden, Jessica O Boyce, Chloe A Stutterd, Kate Pope, Himanshu Goel, Richard J Leventer, Ingrid E Scheffer, Angela T Morgan

Journal article  |  2021  |  NEUROLOGY

OBJECTIVE: To determine whether specific speech, language, and oromotor profiles are associated with different patterns of polymic..

Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome (Mar, 10.1038/s41431-020-00761-1, 2021)

Amanda Brignell, Conway Gu, Alison Holm, Bronwyn Carrigg, Daisy A Sheppard, David J Amor, Angela T Morgan

Journal article  |  2021  |  EUROPEAN JOURNAL OF HUMAN GENETICS

In the text of the original article linked to this correction article, we the authors incorrectly wrote “receptive” which has been..

Interventions for children and adolescents who stutter: A systematic review, meta-analysis, and evidence map.

Amanda Brignell, Michelle Krahe, Martin Downes, Elaina Kefalianos, Sheena Reilly, Angela Morgan

Journal article  |  2021  |  J Fluency Disord

PURPOSE: This systematic review critically appraises and maps the evidence for stuttering interventions in childhood and adolescen..

Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variants

Abdulla Alawadhi, Angela T Morgan, Bettina E Mucha, Ingrid E Scheffer, Kenneth A Myers

Journal article  |  2021  |  EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Heterozygous pathogenic WAC variants cause Desanto-Shinawi syndrome; affected patients have dysmorphic features, developmental imp..

Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome

Amanda Brignell, Conway Gu, Alison Holm, Bronwyn Carrigg, Daisy A Sheppard, David J Amor, Angela T Morgan

Journal article  |  2020  |  EUROPEAN JOURNAL OF HUMAN GENETICS

Communication difficulties are a core feature of Phelan-McDermid syndrome (PMS). However, a specific speech and language phenotype..