All Stories

  1. How genetic findings in cerebral palsy can impact treatment

    Article • EBioMedicine, August 2024, Elsevier

    Sara Lewis

  2. eIF2α phosphorylation evokes dystonia-like movements with D2-receptor and cholinergic origin and abnormal neuronal connectivity

    Article • May 2024, Cold Spring Harbor Laboratory Press

    Sara Lewis

  3. Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders

    Article • Annals of Clinical and Translational Neurology, January 2024, Wiley

    Sara Lewis

  4. TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions

    Article • Brain, September 2023, Oxford University Press (OUP)

    Sara Lewis

  5. Clinical actionability of genetic findings in cerebral palsy

    Article • September 2023, Cold Spring Harbor Laboratory Press

    Sara Lewis

  6. AGAP1-associated endolysosomal trafficking abnormalities link gene–environment interactions in neurodevelopmental disorders

    Article • Disease Models & Mechanisms, September 2023, The Company of Biologists

    Sara Lewis

  7. Intrathecal magnesium delivery for Mg++-insensitive NMDA receptor activity due to GRIN1 mutation

    Article • Orphanet Journal of Rare Diseases, August 2023, Springer Science + Business Media

    Sara Lewis

  8. A transposase-derived gene required for human brain development

    Article • April 2023, Cold Spring Harbor Laboratory Press

    Sara Lewis

  9. Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy

    Article • JAMA Neurology, December 2022, American Medical Association (AMA)

    Sara Lewis

  10. Underrepresentation of the term cerebral palsy in clinical genetics databases

    Article • American Journal of Medical Genetics Part A, August 2022, Wiley

    Sara Lewis

  11. Mutation in ZDHHC15 Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual Disability

    Article • Neurology Genetics, August 2021, Wolters Kluwer Health

    Sara Lewis

  12. Insights From Genetic Studies of Cerebral Palsy

    Article • Frontiers in Neurology, January 2021, Frontiers

    Sara Lewis

  13. Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

    Article • Nature Genetics, January 2021, Springer Science + Business Media

    Sara Lewis

  14. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

    Article • Nature Genetics, September 2020, Springer Science + Business Media

    Sara Lewis

  15. Cataplexy in Patients Harboring the KCNMA1 p.N999S Mutation

    Article • Movement Disorders Clinical Practice, August 2020, Wiley

    Sara Lewis

  16. Damaging de novo missense variants inEEF1A2lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy

    Article • Human Mutation, April 2020, Hindawi Publishing Corporation

    Sara Lewis

  17. Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy

    Article • Journal of Child Neurology, April 2019, SAGE Publications

    Alastair MacLennan, Sara Lewis, Dr Carlos Santos Ocaña

  18. Spontaneous alternation: A potential gateway to spatial working memory in Drosophila

    Article • Neurobiology of Learning and Memory, July 2017, Elsevier

    Sara Lewis