Christopher J. Lelliott
Cambridge, ENG CB101SA, United Kingdom
Last Updated: 09/26/2026
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Found 42 publications
Knockout or inhibition of USP30 protects dopaminergic neurons in a Parkinson's disease mouse model.
Journal: Nature communications
Published: December 16, 2022
Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes.
Journal: Brain : a journal of neurology
Published: November 02, 2022
YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 10, 2022
Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.
Journal: International journal of molecular sciences
Published: July 27, 2022
What is the most appropriate covariate in ANCOVA when analysing metabolic rate?
Journal: Nature metabolism
Published: December 14, 2021
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice.
Journal: PLoS genetics
Published: September 26, 2021
A Positively Selected MAGEE2 LoF Allele Is Associated with Sexual Dimorphism in Human Brain Size and Shows Similar Phenotypes in Magee2 Null Mice.
Journal: Molecular biology and evolution
Published: August 31, 2021
PDZD8 Disruption Causes Cognitive Impairment in Humans, Mice, and Fruit Flies.
Journal: Biological psychiatry
Published: August 05, 2021
Publisher Correction: Accelerating functional gene discovery in osteoarthritis.
Journal: Nature communications
Published: May 29, 2021
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects.
Journal: American journal of human genetics
Published: April 24, 2020
Last Updated: 09/26/2026