Glen Brice

St George's University Of London
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage.

A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage.

Journal: Nature cancer

Published: June 24, 2021

Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort.

Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort.

Journal: PloS one

Published: June 10, 2021

Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Journal: Nature communications

Published: April 28, 2019

Human venous valve disease caused by mutations in FOXC2 and GJC2.

Human venous valve disease caused by mutations in FOXC2 and GJC2.

Journal: The Journal of experimental medicine

Published: June 08, 2016

EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.

EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.

Journal: The Journal of clinical investigation

Published: December 14, 2015

The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome.

The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome.

Journal: European journal of human genetics : EJHG

Published: March 24, 2015

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Journal: Nature communications

Published: March 04, 2015

The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.

The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.

Journal: European journal of human genetics : EJHG

Published: September 21, 2014

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

Journal: European journal of human genetics : EJHG

Published: May 25, 2013

Genital lymphoedema due to ano-genital granulomatosis.

Genital lymphoedema due to ano-genital granulomatosis.

Journal: International journal of STD & AIDS

Published: March 22, 2013

A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.

A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.

Journal: Clinical genetics

Published: February 20, 2013

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.

Journal: Clinical genetics

Published: February 17, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026