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List of works by Neil Rajan

A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds.

scientific article published in November 2013

A novel link between keratoderma and cardiomyopathy: contiguous gene deletion involving the desmoglein gene cluster

scientific article published on 13 April 2017

A tale of two sisters: identical IL36RN mutations and discordant phenotypes.

scientific article published on 4 July 2015

Basal cell carcinoma arising in association with trichoepithelioma in a case of Brooke‐Spiegler syndrome with a novel genetic mutation in CYLD

scientific article published on August 9, 2012

Basaloid follicular proliferations, brain tumours and SUFU

scientific article published on 25 June 2020

CYLD GeneticTesting for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas

scientific article published on 19 February 2015

CYLD in health and disease

scientific article published in June 2023

Clinical outcomes and response of patients applying topical therapy for pyoderma gangrenosum: A prospective cohort study

scientific article

Cutaneous immune-related adverse events in patients with melanoma treated with checkpoint inhibitors

scientific article published on 04 January 2021

Cutaneous xanthomatosis: a novel presentation of hypercholesterolaemia in primary sclerosing cholangitis

scientific article published on 01 July 2006

Demonstration of gastrointestinal venous malformations in blue rubber bleb naevus syndrome using capsule endoscopy.

scientific article published on 26 June 2008

Development and validation of LC-MS/MS with in-source collision-induced dissociation for the quantification of pegcantratinib in human skin tumors

scientific article published on 23 January 2017

Diverse assays from a single skin punch biopsy to assess topical drug intervention

scientific article published on 20 January 2019

Dry skin and blistering in childhood.

scientific article published on October 2016

Dysregulated TRK signalling is a therapeutic target in CYLD defective tumours

scientific article published on 09 May 2011

Enucleation of cylindromas in Brooke-Spiegler syndrome: a novel surgical technique

scientific article published in December 2014

Familial cylindromatosis and brooke-spiegler syndrome: a review of current therapeutic approaches and the surgical challenges posed by two affected families

scientific article published on 06 April 2009

Human cowpox: presentation and investigation in an era of bioterrorism

scientific article published on 01 October 2005

Huriez syndrome caused by a large deletion that abrogates the skin-specific isoform of SMARCAD1

scientific article published on 05 January 2021

Idiopathic infantile pyoderma gangrenosum with stridor responsive to infliximab

scientific article published on January 2009

Impetiginized eczema arising within a port-wine stain of the arm

scientific article published on 01 September 2006

Infiltrative recurrent eccrine spiradenoma of the anterior neck treated using Mohs micrographic surgery.

scientific article

Inherited pulmonary cylindromas: extending the phenotype of CYLD mutation carriers

scientific article published on 29 May 2018

Inherited skin tumour syndromes

scientific article published in December 2017

Mesenteric cysts in naevoid basal cell carcinoma syndrome: a mimic of metastatic disease.

scientific article published on 16 October 2015

Milia: a useful clinical marker of CYLD mutation carrier status

scientific article published on 12 October 2017

Multifocal capillary malformations in an older, asymptomatic child with a novel RASA1 mutation

scientific article published on 30 June 2015

Multiple Facial Trichoepitheliomas and Vulval Cysts: Extending the Phenotypic Spectrum in CYLD Cutaneous Syndrome.

scientific article published in August 2017

Overexpression of MYB drives proliferation of CYLD-defective cylindroma cells

scientific article published on 11 March 2016

Phacomatosis pigmentokeratotica and precocious puberty associated with HRAS mutation

scientific article

Pre-emptive intra-auricular electrosurgical resurfacing of cylindromas to prevent conductive deafness in CYLD cutaneous syndrome

scientific article published on 27 July 2020

Public engagement lectures targeting prospective medical students: an opportunity for dermatology

scientific article published on 02 October 2018

Reading through genetic 'stop signs': a therapeutic strategy in genetic skin disease

scientific article published on 09 February 2020

Squamous cell carcinoma arising within a facial port-wine stain treated by mohs micrographic surgical excision

scientific article published on 01 June 2006

Squamous cell carcinomas in linear epidermal naevi

scientific article published on 28 June 2018

The cylindromatosis gene product, CYLD, interacts with MIB2 to regulate notch signalling

scientific article published on December 2014

The punch and graft technique: a novel method of surgical treatment for chondrodermatitis nodularis helicis.

scientific article published on 2 August 2007

Transcriptomic profiling of human skin biopsies in the clinical trial setting: A protocol for high quality RNA extraction from skin tumours.

scientific article published on 23 April 2018

Transition from cylindroma to spiradenoma in CYLD-defective tumours is associated with reduced DKK2 expression

scientific article published on 19 May 2011

Tropomyosin Receptor Antagonism in Cylindromatosis (TRAC), an early phase trial of a topical tropomyosin kinase inhibitor as a treatment for inherited CYLD defective skin tumours: study protocol for a randomised controlled trial

scientific article published on 07 March 2017

Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction

scientific article

Understanding Inherited Cylindromas: Clinical Implications of Gene Discovery

scientific article published on January 2017

p63 and smooth muscle actin expression in low-grade spiradenocarcinomas in a case of CYLD cutaneous syndrome

scientific article published on 19 July 2018