Amelle Shillington

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 11

Top Topics

Respiratory Failure

Duchenne Muscular Dystrophy

Pseudomonas Aeruginosa

Top Venues

Journal of developmental and behavioral pediatrics : JDBP

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

Journal of autism and developmental disorders

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

Publications

Katherine J Zappia, Amelle Shillington, Cara Fosdick, Craig A Erickson, Martine A Lamy, Kelli C Dominick
Neurodevelopmental Disorders Including Autism Spectrum Disorder and Intellectual Disability as a Risk Factor for Delayed Diagnosis of Catatonia. Journal of developmental and behavioral pediatrics : JDBP 45 (2) (2024)
Katherine J Zappia, Amelle Shillington, Cara Fosdick, Craig A Erickson, Martine A Lamy, Kelli C Dominick
Neurodevelopmental Disorders Including Autism Spectrum Disorder and Intellectual Disability as a Risk Factor for Delayed Diagnosis of Catatonia. Journal of developmental and behavioral pediatrics : JDBP 45 (2) (2024)
Katherine J Zappia, Amelle Shillington, Cara Fosdick, Craig A Erickson, Martine A Lamy, Kelli C Dominick
Neurodevelopmental Disorders Including Autism Spectrum Disorder and Intellectual Disability as a Risk Factor for Delayed Diagnosis of Catatonia. Journal of developmental and behavioral pediatrics : JDBP 45 (2) (2024)
Katherine J Zappia, Amelle Shillington, Cara Fosdick, Craig A Erickson, Martine A Lamy, Kelli C Dominick
Neurodevelopmental Disorders Including Autism Spectrum Disorder and Intellectual Disability as a Risk Factor for Delayed Diagnosis of Catatonia. Journal of developmental and behavioral pediatrics : JDBP 45 (2) (2024)
Katherine J Zappia, Amelle Shillington, Cara Fosdick, Craig A Erickson, Martine A Lamy, Kelli C Dominick
Neurodevelopmental Disorders Including Autism Spectrum Disorder and Intellectual Disability as a Risk Factor for Delayed Diagnosis of Catatonia. Journal of developmental and behavioral pediatrics : JDBP (2024)
Amelle Shillington, Katherine J Zappia, Lori White, Cara Fosdick, Craig A Erickson, Martine Lamy, Kelli C Dominick
Genetic syndromes are prevalent in patients with comorbid neurodevelopmental disorders and catatonia. American journal of medical genetics. Part A (2023)
Soha Sewani, Mahshid S Azamian, Bryce A Mendelsohn, Frederic Tran Mau-Them, Manon Réda, Sophie Nambot, Bertrand Isidor, Jasper J van der Smagt, Joseph J Shen, Amelle Shillington, Lori White, Houda Zghal Elloumi, Peter R Baker, Shayna Svihovec, Kathleen Brown, Yvonne Koopman-Keemink, Mariette J V Hoffer, Inge M M Lakeman, Elise Brischoux-Boucher, Maria Kinali, Xiaonan Zhao, Seema R Lalani, Daryl A Scott
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variants. American journal of medical genetics. Part A (2023)
Stephanie Oates, Michael Absoud, Sushma Goyal, Sophie Bayley, Jennifer Baulcomb, Annemarie Sims, Amy Riddett, Katrina Allis, Charlotte Brasch-Andersen, Meena Balasubramanian, Renkui Bai, Bert Callewaert, Ulrike Hüffmeier, Diana Le Duc, Maximilian Radtke, Christian M Korff, Joanna Kennedy, Karen Jaqueline Low, Rikke Steensjerre Moller, Jens Erik Klint Nielsen, Bernt Popp, Lina Quteineh, Gitte Rønde, Bitten Schönewolf-Greulich, Amelle Shillington, Matthew R G Taylor, Emily Todd, Pernille Mathiesen Torring, Zeynep Tümer, Georgia Vasileiou, T Michael Yates, Christiane Zweier, Richard E Rosch, M Albert Basson, Deb K Pal
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. Clinical genetics 100 (4) (2021)
Amelle Shillington, Alonso Zea Vera, Tanya Perry, Robert Hopkin, Cameron Thomas, David Cooper, Kristen Suhrie
Clinical RNA sequencing confirms compound heterozygous intronic variants in RYR1 in a patient with congenital myopathy, respiratory failure, neonatal brain hemorrhage, and d-transposition of the great arteries. Molecular genetics & genomic medicine 9 (10) (2021)
Amelle Shillington, Martine Lamy, Marissa Vawter-Lee, Craig Erickson, Howard Saal, Davide Comoletti, Katherine Abell
Case Report: Is Catatonia a Clinical Feature of the Natural Progression of NLGN2-Related Neurodevelopmental Disorder? Journal of autism and developmental disorders (2020)
Amelle Shillington, Ernest V Pedapati, Robert J Hopkin, Kristen Suhrie
Early behavioral and developmental interventions in ADNP-syndrome: A case report of SWI/SNF-related neurodevelopmental syndrome. Molecular genetics & genomic medicine 8 (6) (2020)