Hood Mugalaasi
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
The SINEs were there: identification of a pathogenic Alu insertion in a patient with DICER1-related tumour predisposition.
Journal: Journal of medical genetics
Published: November 13, 2025
Correction to: The Cancer Research UK Stratified Medicine Programme as a model for delivering personalised cancer care.
Journal: British journal of cancer
Published: January 25, 2023
The Cancer Research UK Stratified Medicine Programme as a model for delivering personalised cancer care.
Journal: British journal of cancer
Published: November 16, 2022
A pilot of Blood-First diagnostic cell free DNA (cfDNA) next generation sequencing (NGS) in patients with suspected advanced lung cancer.
Journal: Lung cancer (Amsterdam, Netherlands)
Published: December 13, 2021
Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis.
Journal: Histopathology
Published: September 10, 2021
Syringomatous tumour of the nipple: histological, immunophenotypical and genomic characteristics.
Journal: Pathology
Published: September 08, 2021
Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation.
Journal: Brain sciences
Published: May 30, 2018
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.
Journal: Brain : a journal of neurology
Published: July 16, 2017
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.
Journal: BMC medical genetics
Published: October 20, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026