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A Surveillance Model for Skin Cancer in Organ Transplant Recipients: A 22‐Year Prospective Study in an Ethnically Diverse Population

American journal of transplantation, 2013-01, Vol.13 (1), p.119-129

2013

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Keratinocyte skin cancers in the spotlight

British journal of dermatology (1951), 2017-08, Vol.177 (2), p.334-335

2017

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Treatment of post-transplant premalignant skin disease: a randomized intrapatient comparative study of 5-fluorouracil cream and topical photodynamic therapy

British journal of dermatology (1951), 2007-02, Vol.156 (2), p.320-328

2007

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Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer

British journal of dermatology (1951), 2005-07, Vol.153 (1), p.11-17

2005

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Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

Nature (London), 1997-05, Vol.387 (6628), p.80-83

1997

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Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma

Oncogene, 2011-11, Vol.30 (46), p.4666-4677

2011

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High levels of type VII collagen expression in recessive dystrophic epidermolysis bullosa cutaneous squamous cell carcinoma keratinocytes increases PI3K and MAPK signalling, cell migration and invasion

British journal of dermatology (1951), 2014-06, Vol.170 (6), p.1256-1265

2014

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Increased risk of skin cancer associated with the presence of epidermodysplasia verruciformis human papillomavirus types in normal skin

British journal of dermatology (1951), 2004-05, Vol.150 (5), p.949-957

2004

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Role of a p53 polymorphism in the development of human papillomavirus-associated cancer

Nature (London), 1998-05, Vol.393 (6682), p.229-234

1998

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Epidemiology of basal and cutaneous squamous cell carcinoma in the U.K. 2013–15: a cohort study

British journal of dermatology (1951), 2019-09, Vol.181 (3), p.474-482

2019

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Advanced cutaneous squamous cell carcinoma – a pressing case for treatment

Journal of the European Academy of Dermatology and Venereology, 2019-12, Vol.33 (S8), p.3-5

Leigh, I.M.

2019

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Progress in skin cancer: the U.K. experience

British journal of dermatology (1951), 2014-09, Vol.171 (3), p.443-445

Leigh, I. M.

2014

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Pioneers in Dermatology and Venereology: an interview with Prof. Irene M. Leigh

Journal of the European Academy of Dermatology and Venereology, 2020-01, Vol.34 (1), p.14-16

Leigh, I.M.

2020

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Human papillomavirus infection and non-melanoma skin cancer in immunosuppressed and immunocompetent individuals

Journal of medical virology, 2000-07, Vol.61 (3), p.289-297

2000

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Imiquimod cream 5% for recalcitrant cutaneous warts in immunosuppressed individuals

British journal of dermatology (1951), 2005-01, Vol.152 (1), p.122-129

2005

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Human Papillomavirus Infections in Nonmelanoma Skin Cancers From Renal Transplant Recipients and Nonimmunosuppressed Patients

JNCI : Journal of the National Cancer Institute, 1996-06, Vol.88 (12), p.802-811

1996

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Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndrome

Journal of medical genetics, 2006-02, Vol.43 (2), p.e05-e05

2006

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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Nature genetics, 1996-08, Vol.13 (4), p.450-457

1996

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Multiple Epidermal Connexins are Expressed in Different Keratinocyte Subpopulations Including Connexin 31

Journal of investigative dermatology, 2001-10, Vol.117 (4), p.958-964

2001

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Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations

British journal of dermatology (1951), 2003-07, Vol.149 (1), p.46-58

2003

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Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

Nature genetics, 1997-10, Vol.17 (2), p.240-244

1997

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Overexpression of the Axl tyrosine kinase receptor in cutaneous SCC-derived cell lines and tumours

British journal of cancer, 2006-05, Vol.94 (10), p.1446-1451

2006

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Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Muscle & nerve, 2007-01, Vol.35 (1), p.24-35

2007

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Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

Nature genetics, 1997-08, Vol.16 (4), p.372-374

1997

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Azathioprine: friend or foe?

British journal of dermatology (1951), 2019-05, Vol.180 (5), p.961-963

2019

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A Surveillance Model for Skin Cancer in Organ Transplant Recipients: A 22‐Year Prospective Study in an Ethnically Diverse Population

Keratinocyte skin cancers in the spotlight

Treatment of post-transplant premalignant skin disease: a randomized intrapatient comparative study of 5-fluorouracil cream and topical photodynamic therapy

Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma

High levels of type VII collagen expression in recessive dystrophic epidermolysis bullosa cutaneous squamous cell carcinoma keratinocytes increases PI3K and MAPK signalling, cell migration and invasion

Increased risk of skin cancer associated with the presence of epidermodysplasia verruciformis human papillomavirus types in normal skin

Role of a p53 polymorphism in the development of human papillomavirus-associated cancer

Epidemiology of basal and cutaneous squamous cell carcinoma in the U.K. 2013–15: a cohort study

Advanced cutaneous squamous cell carcinoma – a pressing case for treatment

Progress in skin cancer: the U.K. experience

Pioneers in Dermatology and Venereology: an interview with Prof. Irene M. Leigh

Human papillomavirus infection and non-melanoma skin cancer in immunosuppressed and immunocompetent individuals

Imiquimod cream 5% for recalcitrant cutaneous warts in immunosuppressed individuals

Human Papillomavirus Infections in Nonmelanoma Skin Cancers From Renal Transplant Recipients and Nonimmunosuppressed Patients

Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndrome

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Multiple Epidermal Connexins are Expressed in Different Keratinocyte Subpopulations Including Connexin 31

Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

Overexpression of the Axl tyrosine kinase receptor in cutaneous SCC-derived cell lines and tumours

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

Azathioprine: friend or foe?

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