PubRank

Andrew P South

Author PubWeight™ 40.89‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma. Proc Natl Acad Sci U S A 2011 3.10
2 Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Am J Hum Genet 2003 2.73
3 Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1). Hum Mol Genet 2002 2.41
4 Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. J Invest Dermatol 2004 1.95
5 Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation. J Invest Dermatol 2003 1.67
6 Patients with recessive dystrophic epidermolysis bullosa develop squamous-cell carcinoma regardless of type VII collagen expression. J Invest Dermatol 2007 1.57
7 Autoantibodies to extracellular matrix protein 1 in lichen sclerosus. Lancet 2003 1.39
8 Gauging NOTCH1 Activation in Cancer Using Immunohistochemistry. PLoS One 2013 1.32
9 RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome. Am J Hum Genet 2012 1.18
10 Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis. Am J Hum Genet 2008 1.10
11 Fibroblast-derived dermal matrix drives development of aggressive cutaneous squamous cell carcinoma in patients with recessive dystrophic epidermolysis bullosa. Cancer Res 2012 1.07
12 Alterations in desmosome size and number coincide with the loss of keratinocyte cohesion in skin with homozygous and heterozygous defects in the desmosomal protein plakophilin 1. J Invest Dermatol 2003 1.04
13 Wnt5a is strongly expressed at the leading edge in non-melanoma skin cancer, forming active gradients, while canonical Wnt signalling is repressed. PLoS One 2012 1.02
14 Increased invasive behaviour in cutaneous squamous cell carcinoma with loss of basement-membrane type VII collagen. J Cell Sci 2009 1.01
15 Mathematical modeling of cancer cell invasion of tissue: biological insight from mathematical analysis and computational simulation. J Math Biol 2010 1.00
16 Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility. Am J Hum Genet 2012 0.99
17 The design and optimization of RNA trans-splicing molecules for skin cancer therapy. Mol Oncol 2013 0.99
18 Positional cloning identifies a novel cyclophilin as a candidate amplified oncogene in 1q21. Oncogene 2002 0.95
19 Increased keratinocyte proliferation initiated through downregulation of desmoplakin by RNA interference. Exp Cell Res 2007 0.95
20 Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma. Am J Hum Genet 2013 0.94
21 Development of antigen-specific ELISA for circulating autoantibodies to extracellular matrix protein 1 in lichen sclerosus. J Clin Invest 2004 0.93
22 The use of non-nutritive sucking to decrease the physiologic pain response during neonatal circumcision: a randomized controlled trial. Am J Obstet Gynecol 2005 0.89
23 The molecular skin pathology of familial primary localized cutaneous amyloidosis. Exp Dermatol 2010 0.89
24 Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children. J Invest Dermatol 2010 0.85
25 Utility of gastrointestinal fluoroscopic studies in detecting stricture after neonatal necrotizing enterocolitis. J Pediatr Gastroenterol Nutr 2014 0.84
26 Isolation and culture of squamous cell carcinoma lines. Methods Mol Biol 2011 0.83
27 The DSPII splice variant is crucial for desmosome-mediated adhesion in HaCaT keratinocytes. J Cell Sci 2012 0.83
28 Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation. Am J Pathol 2009 0.82
29 Feeder layers: co-culture with nonneoplastic cells. Methods Mol Biol 2011 0.81
30 An investigation into the MMP1 gene promoter region polymorphism--1607 2G with recessive dystrophic epidermolysis bullosa disease severity in northeastern Mexican patients. Int J Dermatol 2014 0.79
31 Reduced expression of insulin-like growth factor-binding protein-3 (IGFBP-3) in Squamous cell carcinoma complicating recessive dystrophic epidermolysis bullosa. J Invest Dermatol 2004 0.79
32 Type VII collagen regulates expression of OATP1B3, promotes front-to-rear polarity and increases structural organisation in 3D spheroid cultures of RDEB tumour keratinocytes. J Cell Sci 2013 0.76
33 Spatial analysis in support of community health intervention strategies. AMIA Annu Symp Proc 2012 0.76
34 No evidence that human papillomavirus is responsible for the aggressive nature of recessive dystrophic epidermolysis bullosa-associated squamous cell carcinoma. J Invest Dermatol 2010 0.75
35 Rapid diagnosis of lipoid proteinosis using an anti-extracellular matrix protein 1 (ECM1) antibody. J Dermatol Sci 2004 0.75
36 Identification and characterization of DSPIa, a novel isoform of human desmoplakin. Cell Tissue Res 2010 0.75
37 Strategies to identify disease genes. Drugs Today (Barc) 2002 0.75