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    • Research Article7

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    • Original Article Clinical Research: Patient Outcomes
      Open Archive

      Classification of the Clinical Images for Benign and Malignant Cutaneous Tumors Using a Deep Learning Algorithm

      Journal of Investigative Dermatology
      Vol. 138Issue 7p1529–1538Published online: February 8, 2018
      • Seung Seog Han
      • Myoung Shin Kim
      • Woohyung Lim
      • Gyeong Hun Park
      • Ilwoo Park
      • Sung Eun Chang
      Cited in Scopus: 336
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        We tested the use of a deep learning algorithm to classify the clinical images of 12 skin diseases—basal cell carcinoma, squamous cell carcinoma, intraepithelial carcinoma, actinic keratosis, seborrheic keratosis, malignant melanoma, melanocytic nevus, lentigo, pyogenic granuloma, hemangioma, dermatofibroma, and wart. The convolutional neural network (Microsoft ResNet-152 model; Microsoft Research Asia, Beijing, China) was fine-tuned with images from the training portion of the Asan dataset, MED-NODE dataset, and atlas site images (19,398 images in total).
        Classification of the Clinical Images for Benign and Malignant Cutaneous Tumors Using a Deep Learning Algorithm
      • Original Article Epidemiology
        Open Archive

        Incidence, Mortality, and Trends of Nonmelanoma Skin Cancer in Germany

        Journal of Investigative Dermatology
        Vol. 137Issue 9p1860–1867Published online: May 6, 2017
        • Ulrike Leiter
        • Ulrike Keim
        • Thomas Eigentler
        • Alexander Katalinic
        • Bernd Holleczek
        • Peter Martus
        • and others
        Cited in Scopus: 109
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          Increasing incidence rates (IRs) of nonmelanoma skin cancer (NMSC) in white populations have been described worldwide. Cancer registry data from the Saarland and Schleswig-Holstein federal states were used to analyze incidence and mortality trends in Germany. Age-standardized rates were compared with crude rates to assess disease burden. Joinpoint regression models were used to estimate annual percentage changes and 95% confidence intervals, allowing us to assess temporal trends between 1970 and 2012.
          Incidence, Mortality, and Trends of Nonmelanoma Skin Cancer in Germany
        • Original Article Epidemiology
          Open Archive

          Cigarette Smoking and the Risks of Basal Cell Carcinoma and Squamous Cell Carcinoma

          Journal of Investigative Dermatology
          Vol. 137Issue 8p1700–1708Published online: April 14, 2017
          • Jean Claude Dusingize
          • Catherine M. Olsen
          • Nirmala P. Pandeya
          • Padmini Subramaniam
          • Bridie S. Thompson
          • Rachel E. Neale
          • and others
          Cited in Scopus: 42
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            Sunlight is the principal environmental risk factor for keratinocyte cancers, but other carcinogens have also been implicated, including tobacco smoke. Findings have been conflicting, however. We investigated associations between cigarette smoking and incidence of basal cell carcinoma (BCC) or squamous cell carcinoma (SCC) in QSkin, a prospective study of skin cancer (N = 43,794). Smoking history was self-reported at baseline; newly diagnosed BCCs and SCCs were ascertained through data linkage and verified by histopathology reports.
            Cigarette Smoking and the Risks of Basal Cell Carcinoma and Squamous Cell Carcinoma
          • Original Article Clinical Research
            Open Archive

            Surgery Versus 5% Imiquimod for Nodular and Superficial Basal Cell Carcinoma: 5-Year Results of the SINS Randomized Controlled Trial

            Journal of Investigative Dermatology
            Vol. 137Issue 3p614–619Published online: December 5, 2016
            • Hywel C. Williams
            • Fiona Bath-Hextall
            • Mara Ozolins
            • Sarah J. Armstrong
            • Graham B. Colver
            • William Perkins
            • and others
            Cited in Scopus: 84
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              We previously reported modest clinical 3-year benefit for topical imiquimod compared with surgery for superficial or nodular basal cell carcinoma at low-risk sites in our noninferiority randomized controlled SINS trial. Here we report 5-year data. Participants were randomized to imiquimod 5% cream once daily (superficial basal cell carcinoma, 6 weeks; nodular basal cell carcinoma, 12 weeks) or excisional surgery (4-mm margin). The primary outcome was clinical absence of initial failure or signs of recurrence at the 3-year dermatology review.
              Surgery Versus 5% Imiquimod for Nodular and Superficial Basal Cell Carcinoma: 5-Year Results of the SINS Randomized Controlled Trial
            • Original Article Tumor Biology
              Open Archive

              MicroRNA-203 Inversely Correlates with Differentiation Grade, Targets c-MYC, and Functions as a Tumor Suppressor in cSCC

              Journal of Investigative Dermatology
              Vol. 136Issue 12p2485–2494Published online: July 21, 2016
              • Warangkana Lohcharoenkal
              • Masako Harada
              • Jakob Lovén
              • Florian Meisgen
              • Ning Xu Landén
              • Lingyun Zhang
              • and others
              Cited in Scopus: 32
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                Cutaneous squamous cell carcinoma (cSCC) is the second most common cancer and a leading cause of cancer mortality among solid organ transplant recipients. MicroRNAs (miR) are short RNAs that regulate gene expression and cellular functions. Here, we show a negative correlation between miR-203 expression and the differentiation grade of cSCC. Functionally, miR-203 suppressed cell proliferation, cell motility, and the angiogenesis-inducing capacity of cSCC cells in vitro and reduced xenograft tumor volume and angiogenesis in vivo.
                MicroRNA-203 Inversely Correlates with Differentiation Grade, Targets c-MYC, and Functions as a Tumor Suppressor in cSCC
              • Original Article Epidemiology
                Open Archive

                Prevalence of Skin Cancer and Related Skin Tumors in High-Risk Kidney and Liver Transplant Recipients in Queensland, Australia

                Journal of Investigative Dermatology
                Vol. 136Issue 7p1382–1386Published online: March 8, 2016
                • Michelle R. Iannacone
                • Sudipta Sinnya
                • Nirmala Pandeya
                • Nikky Isbel
                • Scott Campbell
                • Jonathan Fawcett
                • and others
                Cited in Scopus: 34
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                  The increased skin cancer incidence in organ transplant recipients is well-known, but the skin cancer burden at any one time is unknown. Our objective was to estimate the period prevalence of untreated skin malignancy and actinic keratoses in high-risk kidney and liver transplant recipients and to assess associated factors. Organ transplant recipients underwent full skin examinations by dermatologically trained physicians. The proportion of examined organ transplant recipients with histopathologically confirmed skin cancer in the 3-month baseline period was estimated.
                • Original Article Genetics
                  Open Archive

                  Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma

                  Journal of Investigative Dermatology
                  Vol. 136Issue 5p930–937Published online: January 29, 2016
                  • Maryam M. Asgari
                  • Wei Wang
                  • Nilah M. Ioannidis
                  • Jacqueline Itnyre
                  • Thomas Hoffmann
                  • Eric Jorgenson
                  • and others
                  Cited in Scopus: 70
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                    We report a genome-wide association study of cutaneous squamous cell carcinoma conducted among non-Hispanic white members of the Kaiser Permanente Northern California health care system. The study includes a genome-wide screen of 61,457 members (6,891 cases and 54,566 controls) genotyped on the Affymetrix Axiom European array and a replication phase involving an independent set of 6,410 additional members (810 cases and 5,600 controls). Combined analysis of screening and replication phases identified 10 loci containing single-nucleotide polymorphisms (SNPs) with P-values < 5 × 10−8.
                    Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma
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