Alastair H. Maclennan
72 King William Road
North Adelaide, SA 5006, Australia
North Adelaide, SA 5006, Australia
Last Updated: 09/26/2026
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Found 50 publications
Genetic diagnostic yield by MRI pattern in children with cerebral palsy: a population-based study.
Journal: EBioMedicine
Published: June 17, 2025
Application of multiple mosaic callers improves post-zygotic mutation detection from exome sequencing data.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 21, 2023
All Patients With a Cerebral Palsy Diagnosis Merit Genomic Sequencing.
Journal: JAMA pediatrics
Published: March 06, 2023
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 23, 2022
Transgenerational adverse effects of valproate? A patient report from 90 affected families.
Journal: Birth defects research
Published: September 23, 2021
All cases of cerebral palsy warrant genomic screening.
Journal: Developmental medicine and child neurology
Published: June 11, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss.
Journal: American journal of human genetics
Published: May 28, 2021
Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing.
Journal: NPJ genomic medicine
Published: April 27, 2021
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Journal: Nature genetics
Published: January 12, 2021
Definition and diagnosis of cerebral palsy in genetic studies: a systematic review.
Journal: Developmental medicine and child neurology
Published: April 23, 2020
Last Updated: 09/26/2026