Lara Olabi-Al

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 11 publications

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype.

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 13, 2020

GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of Gα/11 Mosaicism and the Associated Clinical Diagnoses.

GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of Gα/11 Mosaicism and the Associated Clinical Diagnoses.

Journal: The Journal of investigative dermatology

Published: June 29, 2019

Does the gene matter? Genotype-phenotype and genotype-outcome associations in congenital melanocytic naevi.

Does the gene matter? Genotype-phenotype and genotype-outcome associations in congenital melanocytic naevi.

Journal: The British journal of dermatology

Published: May 02, 2019

Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy.

Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy.

Journal: The Journal of clinical investigation

Published: November 15, 2017

Extending the spectrum of AKT1 mosaicism: not just the Proteus syndrome.

Extending the spectrum of AKT1 mosaicism: not just the Proteus syndrome.

Journal: The British journal of dermatology

Published: February 02, 2016

Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt Signaling.

Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt Signaling.

Journal: The Journal of investigative dermatology

Published: July 17, 2015

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis.

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis.

Journal: The Journal of investigative dermatology

Published: June 29, 2015

The role and interaction of imprinted genes in human fetal growth.

The role and interaction of imprinted genes in human fetal growth.

Journal: Philosophical transactions of the Royal Society of London. Series B, Biological sciences

Published: January 21, 2015

Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt Signaling.

Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt Signaling.

Journal: The Journal of investigative dermatology

Published: January 12, 2015

Next-generation sequencing of nevus spilus-type congenital melanocytic nevus: exquisite genotype-phenotype correlation in mosaic RASopathies.

Next-generation sequencing of nevus spilus-type congenital melanocytic nevus: exquisite genotype-phenotype correlation in mosaic RASopathies.

Journal: The Journal of investigative dermatology

Published: April 23, 2014

Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight.

Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight.

Journal: PloS one

Published: November 01, 2013

Showing 1-11 of 11

Last Updated: 09/26/2026