Publications by authors named "Lottie D Morison"

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Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2.
Lottie D Morison, Ruth Braden, David J Amor, Angela T Morgan

Am J Med Genet A· December 2025

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Schinzel-Giedion syndrome: communication, feeding and motor skills in 16 individuals.
Lottie D Morison, Nuala Summerfield, Dana Bradley, Bregje W van Bon, Angela T Morgan

Neurogenetics· August 2025

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Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders.
Emma K Baker, Miya St John, Ruth Braden, Lottie D Morison, Elana J Forbes

Dev Med Child Neurol· July 2025

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Understanding speech and language in KIF1A-associated neurological disorder.
Lottie D Morison, Adam P Vogel, John Christodoulou, Wendy A Gold, Dylan Verden

Eur J Hum Genet· May 2025

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Speech, Language and Non-verbal Communication in CLN2 and CLN3 Batten Disease.
Lottie D Morison, Ineka T Whiteman, Adam P Vogel, Lisa Tilbrook, Michael C Fahey

J Inherit Metab Dis· January 2025

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Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention.
Elana J Forbes, Lottie D Morison, Fatma Lelik, Tegan Howell, Simone Debono

Am J Med Genet B Neuropsychiatr Genet· September 2024

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Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling

J Med Genet· May 2024

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Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorder.
Lottie D Morison, Olivia Van Reyk, Emma Baker, Lyse Ruaud, Nathalie Couque

Eur J Med Genet· April 2024

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Correction: CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases.
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre

Eur J Hum Genet· December 2023

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CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases.
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre

Eur J Hum Genet· July 2023

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In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting .
Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, Irene Steiner-Wilke, Brigitte Vollmer

J Med Genet· June 2023

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Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments.
Lottie D Morison, Ruth O Braden, David J Amor, Amanda Brignell, Bregje W M van Bon

Eur J Hum Genet· July 2022

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