Lottie D Morison

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 11

Top Topics

Left Ventricular

Intellectual Disability

Top Venues

Journal of medical genetics

European journal of human genetics : EJHG

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics (2024)
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics 61 (6) (2024)
Elana J Forbes, Lottie D Morison, Fatma Lelik, Tegan Howell, Simone Debono, Himanshu Goel, Pauline Burger, Jean-Louis Mandel, David Geneviève, David J Amor, Angela T Morgan
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2024)
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics 61 (6) (2024)
Elana J Forbes, Lottie D Morison, Fatma Lelik, Tegan Howell, Simone Debono, Himanshu Goel, Pauline Burger, Jean-Louis Mandel, David Geneviève, David J Amor, Angela T Morgan
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 195 (6) (2024)
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics 61 (6) (2024)
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre, Fiona Bruinsma, Marie Vincent, Marie-Line Jacquemont, Natalie L Dykzeul, David Genevieve, David J Amor, Angela T Morgan
Correction: CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European journal of human genetics : EJHG (2023)
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre, Fiona Bruinsma, Marie Vincent, Marie-Line Jacquemont, Natalie L Dykzeul, David Genevieve, David J Amor, Angela T Morgan
CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European journal of human genetics : EJHG (2023)
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre, Fiona Bruinsma, Marie Vincent, Marie-Line Jacquemont, Natalie L Dykzeul, David Genevieve, David J Amor, Angela T Morgan
CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European journal of human genetics : EJHG (2023)
Lottie D Morison, Ruth O Braden, David J Amor, Amanda Brignell, Bregje W M van Bon, Angela T Morgan
Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments. European journal of human genetics : EJHG 30 (7) (2022)
Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, Irene Steiner-Wilke, Brigitte Vollmer, Katrin Schulze, Tracy Briggs, Ruth Braden, Adam P Vogel, Daisy Thompson-Lake, Chirag Patel, Edward Blair, Himanshu Goel, Samantha Turner, Ute Moog, Angelika Riess, Frederique Liegeois, David A Koolen, David J Amor, Tjitske Kleefstra, Simon E Fisher, Christiane Zweier, Angela T Morgan
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 . Journal of medical genetics (2022)