Genome-wide analysis of constitutional DNA methylation in familial melanoma

Por Salgado, Catarina, Gruis, Nelleke, Heijmans, Bastiaan T., Oosting, Jan, van Doorn, Remco
Publicado no Clin Epigenetics (2020)

Genome‐wide characterization of 5‐hydoxymethylcytosine in melanoma reveals major differences with nevus

Por Salgado, Catarina, Oosting, Jan, Janssen, Bart, Kumar, Rajiv, Gruis, Nelleke, van Doorn, Remco
Publicado no Genes Chromosomes Cancer (2020)

Reply to Comment on “Improving clinical diagnosis of early-stage cutaneous melanoma based on Raman spectroscopy”

Por Santos, Inês P., Caspers, Peter J., van Doorn, Remco, Koljenović, Senada, Puppels, Gerwin J.
Publicado no Br J Cancer (2019)

Remission of psoriasis during treatment with sorafenib

Por van Kester, Marloes S., Luelmo, Saskia A.C., Vermeer, Maarten H., Blank, Christian, van Doorn, Remco
Publicado no JAAD Case Rep (2018)

Interplay between TERT promoter mutations and methylation culminates in chromatin accessibility and TERT expression

Por Salgado, Catarina, Roelse, Celine, Nell, Rogier, Gruis, Nelleke, van Doorn, Remco, van der Velden, Pieter
Publicado no PLoS One (2020)

Antagonistic TSC22D1 variants control BRAF(E600)-induced senescence

Por Hömig-Hölzel, Cornelia, van Doorn, Remco, Vogel, Celia, Germann, Markus, Cecchini, Marco G, Verdegaal, Els, Peeper, Daniel S
Publicado em 2011

HOXA1 drives melanoma tumor growth and metastasis and elicits an invasion gene expression signature that prognosticates clinical outcome

Por Wardwell-Ozgo, Joanna, Dogruluk, Turgut, Gifford, Armel, Zhang, Yiqun, Heffernan, Timothy P., van Doorn, Remco, Creighton, Chad J., Chin, Lynda, Scott, Kenneth L.
Publicado em 2013

Corresponding anaplastic lymphoma kinase–tropomyosin 3 (ALK-TPM3) fusion in a patient with a primary cutaneous anaplastic large-cell lymphoma and a Spitz nevus

Por Melchers, Rutger C., Willemze, Rein, van Doorn, Remco, Jansen, Patty M., Cleven, Arjen H.G., Solleveld, Nienke, Vermeer, Maarten H., Quint, Koen D.
Publicado no JAAD Case Rep (2019)

Exon skipping of TGFβRI affects signalling and ECM expression in hypertrophic scar-derived fibroblasts

Por Raktoe, Rajiv S, Rietveld, Marion H, Out-Luiting, Jacoba J, Kruithof-de Julio, Marianna, van Zuijlen, Paul PM, van Doorn, Remco, Ghalbzouri, Abdoelwaheb El
Publicado no Scars Burn Heal (2020)

Genome-Wide Analysis of Gene and Protein Expression of Dysplastic Naevus Cells

Por Gao, Linda, van Nieuwpoort, Frans A., Out-Luiting, Jacoba J., Hensbergen, Paul J., de Snoo, Femke A., Bergman, Wilma, van Doorn, Remco, Gruis, Nelleke A.
Publicado em 2012

Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non‐CDKN2A/CDK4 melanoma families

Por Potjer, Thomas P., Bollen, Sander, Grimbergen, Anneliese J.E.M., van Doorn, Remco, Gruis, Nelleke A., van Asperen, Christi J., Hes, Frederik J., van der Stoep, Nienke
Publicado no Int J Cancer (2019)

Disseminated Cutaneous Mycobacterium chelonae Infection in a Patient With Acute Myeloid Leukemia

Por Roukens, Anna Helena, Mendels, Elodie J., Verbeet, Nicolette L., von dem Borne, Peter A., Nicolae-Cristea, Alina R., Bentvelsen, Robbert G., van Doorn, Remco, de Boer, Mark G.
Publicado no Open Forum Infect Dis (2014)

Improving clinical diagnosis of early-stage cutaneous melanoma based on Raman spectroscopy

Por P. Santos, Inês, van Doorn, Remco, Caspers, Peter J., Bakker Schut, Tom C., Barroso, Elisa M., Nijsten, Tamar E. C., Noordhoek Hegt, Vincent, Koljenović, Senada, Puppels, Gerwin J.
Publicado no Br J Cancer (2018)

Efficacy of novel immunotherapy regimens in patients with metastatic melanoma with germline CDKN2A mutations

Por Helgadottir, Hildur, Ghiorzo, Paola, van Doorn, Remco, Puig, Susana, Levin, Max, Kefford, Richard, Lauss, Martin, Queirolo, Paola, Pastorino, Lorenza, Kapiteijn, Ellen, Potrony, Miriam, Carrera, Cristina, Olsson, Håkan, Höiom, Veronica, Jönsson, Göran
Publicado no J Med Genet (2020)

miRNA expression profiling of mycosis fungoides

Por van Kester, Marloes S., Ballabio, Erica, Benner, Marchina F., Chen, Xiao H., Saunders, Nigel J., van der Fits, Leslie, van Doorn, Remco, Vermeer, Maarten H., Willemze, Rein, Tensen, Cornelis P., Lawrie, Charles H.
Publicado no Mol Oncol (2011)

Genomic analysis and clinical management of adolescent cutaneous melanoma

Por Rabbie, Roy, Rashid, Mamunur, Arance, Ana M., Sánchez, Marcelo, Tell‐Marti, Gemma, Potrony, Miriam, Conill, Carles, van Doorn, Remco, Dentro, Stefan, Gruis, Nelleke A., Corrie, Pippa, Iyer, Vivek, Robles‐Espinoza, Carla Daniela, Puig‐Butille, Joan A., Puig, Susana, Adams, David J.
Publicado no Pigment Cell Melanoma Res (2017)

Germline TERT promoter mutations are rare in familial melanoma

Por Harland, Mark, Petljak, Mia, Robles-Espinoza, Carla Daniela, Ding, Zhihao, Gruis, Nelleke A., van Doorn, Remco, Pooley, Karen A., Dunning, Alison M., Aoude, Lauren G., Wadt, Karin A. W., Gerdes, Anne-Marie, Brown, Kevin M., Hayward, Nicholas K., Newton-Bishop, Julia A., Adams, David J., Bishop, D. Timothy
Publicado no Fam Cancer (2015)

Pro-invasion metastasis drivers in early stage melanoma are oncogenes

Por Scott, Kenneth L., Nogueira, Cristina, Heffernan, Timothy P., van Doorn, Remco, Dhakal, Sabin, Hanna, Jason A., Min, Chengyin, Jaskelioff, Mariela, Xiao, Yonghong, Wu, Chang-Jiun, Cameron, Lisa A., Perry, Samuel R., Zeid, Rhamy, Feinberg, Tamar, Kim, Minjung, Woude, George Vande, Granter, Scott R., Bosenberg, Marcus, Chu, Gerald C., DePinho, Ronald A., Rimm, David L., Chin, Lynda
Publicado em 2011

Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study

Por Davies, John R, Randerson-Moor, Juliette, Kukalizch, Kairen, Harland, Mark, Kumar, Rajiv, Madhusudan, Srinivasan, Nagore, Eduardo, Hansson, Johan, Höiom, Veronica, Ghiorzo, Paola, Gruis, Nelleke A, Kanetsky, Peter A, Wendt, Judith, Pjanova, Dace, Puig, Susana, Saiag, Philippe, Schadendorf, Dirk, Soufir, Nadem, Okamoto, Ichiro, Affleck, Paul, García-Casado, Zaida, Ogbah, Zighereda, Ozola, Aija, Queirolo, Paola, Sucker, Antje, Barrett, Jennifer H, van Doorn, Remco, Bishop, D Timothy, Newton-Bishop, Julia
Publicado em 2012

Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines

Por Chau, Cindy, van Doorn, Remco, van Poppelen, Natasha M., van der Stoep, Nienke, Mensenkamp, Arjen R., Sijmons, Rolf H., van Paassen, Barbara W., van den Ouweland, Ans M. W., Naus, Nicole C., van der Hout, Annemieke H., Potjer, Thomas P., Bleeker, Fonnet E., Wevers, Marijke R., van Hest, Liselotte P., Jongmans, Marjolijn C. J., Marinkovic, Marina, Bleeker, Jaco C., Jager, Martine J., Luyten, Gregorius P. M., Nielsen, Maartje
Publicado no Cancers (Basel) (2019)