Dislocation density assessment via X-ray GaN rocking curve scans von Booker, I., Rahimzadeh Khoshroo, L., Woitok, J. F., Kaganer, V., Mauder, C., Behmenburg, H., Gruis, J., Heuken, M., Kalisch, H., Jansen, R. H.

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Quaternary nitride heterostructure field effect transistors von Rahimzadeh Khoshroo, L., Ketteniss, N., Mauder, C., Behmenburg, H., Woitok, J. F., Booker, I., Gruis, J., Heuken, M., Vescan, A., Kalisch, H., Jansen, R. H.

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Epitaxy and characterisation of AlInGaN heterostructures for HEMT application von Khoshroo, L. Rahimzadeh, Mauder, C., Behmenburg, H., Woitok, J., Zander, W., Gruis, J., Reuters, B., Schubert, J., Vescan, A., Heuken, M., Kalisch, H., Jansen, R. H.

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Method for making turkey bacon von GRUIS DAVID J

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MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: a pooled analysis from the M-SKIP project von Tagliabue, Elena, Gandini, Sara, Bellocco, Rino, Maisonneuve, Patrick, Newton-Bishop, Julia, Polsky, David, Lazovich, DeAnn, Kanetsky, Peter A, Ghiorzo, Paola, Gruis, Nelleke A, Landi, Maria Teresa, Menin, Chiara, Fargnoli, Maria Concetta, García-Borrón, Jose Carlos, Han, Jiali, Little, Julian, Sera, Francesco, Raimondi, Sara

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Storage protein accumulation in the absence of the vacuolar processing enzyme family of cysteine proteases von Gruis, D, Schulze, J, Jung, R

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GNAQ and GNA11 mutations and downstream YAP activation in choroidal nevi von Vader, M J C, Madigan, M C, Versluis, M, Suleiman, H M, Gezgin, G, Gruis, N A, Out-Luiting, J J, Bergman, W, Verdijk, R M, Jager, M J, van der Velden, P A

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POT1 loss-of-function variants predispose to familial melanoma von Robles-Espinoza, Carla Daniela, Harland, Mark, Ramsay, Andrew J, Aoude, Lauren G, Quesada, Víctor, Ding, Zhihao, Pooley, Karen A, Pritchard, Antonia L, Tiffen, Jessamy C, Petljak, Mia, Palmer, Jane M, Symmons, Judith, Johansson, Peter, Stark, Mitchell S, Gartside, Michael G, Snowden, Helen, Montgomery, Grant W, Martin, Nicholas G, Liu, Jimmy Z, Choi, Jiyeon, Makowski, Matthew, Brown, Kevin M, Dunning, Alison M, Keane, Thomas M, López-Otín, Carlos, Gruis, Nelleke A, Hayward, Nicholas K, Bishop, D Timothy, Newton-Bishop, Julia A, Adams, David J

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Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non‐CDKN2A/CDK4 melanoma families von Potjer, Thomas P., Bollen, Sander, Grimbergen, Anneliese J.E.M., Doorn, Remco, Gruis, Nelleke A., Asperen, Christi J., Hes, Frederik J., Stoep, Nienke

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Magnetic Resonance Imaging Surveillance Detects Early-Stage Pancreatic Cancer in Carriers of a p16-Leiden Mutation von Vasen, Hans F.A, Wasser, Martin, van Mil, Anneke, Tollenaar, Rob A, Konstantinovski, Marja, Gruis, Nelleke A, Bergman, Wilma, Hes, Frederik J, Hommes, Daniel W, Offerhaus, G. Johan A, Morreau, Hans, Bonsing, Bert A, de Vos tot Nederveen Cappel, Wouter H

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Activation of the MAPK pathway is a common event in uveal melanomas although it rarely occurs through mutation of BRAF or RAS von Zuidervaart, W, van Nieuwpoort, F, Stark, M, Dijkman, R, Packer, L, Borgstein, A-M, Pavey, S, van der Velden, P, Out, C, Jager, M J, Hayward, N K, Gruis, N A

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Promoter CpG Island Hypermethylation in Dysplastic Nevus and Melanoma: CLDN11 as an Epigenetic Biomarker for Malignancy von Gao, Linda, van den Hurk, Karin, Moerkerk, Peter T.M., Goeman, Jelle J., Beck, Samuel, Gruis, Nelleke A., van den Oord, Joost J., Winnepenninckx, Véronique J., van Engeland, Manon, van Doorn, Remco

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Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls von Chang, Yu-mei, Barrett, Jennifer H, Bishop, D Timothy, Armstrong, Bruce K, Bataille, Veronique, Bergman, Wilma, Berwick, Marianne, Bracci, Paige M, Elwood, J Mark, Ernstoff, Marc S, Gallagher, Richard P, Green, Adèle C, Gruis, Nelleke A, Holly, Elizabeth A, Ingvar, Christian, Kanetsky, Peter A, Karagas, Margaret R, Lee, Tim K, Le Marchand, Loïc, Mackie, Rona M, Olsson, Håkan, Østerlind, Anne, Rebbeck, Timothy R, Sasieni, Peter, Siskind, Victor, Swerdlow, Anthony J, Titus-Ernstoff, Linda, Zens, Michael S, Newton-Bishop, Julia A

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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma von Aoude, Lauren G, Pritchard, Antonia L, Robles-Espinoza, Carla Daniela, Wadt, Karin, Harland, Mark, Choi, Jiyeon, Gartside, Michael, Quesada, Víctor, Johansson, Peter, Palmer, Jane M, Ramsay, Andrew J, Zhang, Xijun, Jones, Kristine, Symmons, Judith, Holland, Elizabeth A, Schmid, Helen, Bonazzi, Vanessa, Woods, Susan, Dutton-Regester, Ken, Stark, Mitchell S, Snowden, Helen, van Doorn, Remco, Montgomery, Grant W, Martin, Nicholas G, Keane, Thomas M, López-Otín, Carlos, Gerdes, Anne-Marie, Olsson, Håkan, Ingvar, Christian, Borg, Ake, Gruis, Nelleke A, Trent, Jeffrey M, Jönsson, Göran, Bishop, D Timothy, Mann, Graham J, Newton-Bishop, Julia A, Brown, Kevin M, Adams, David J, Hayward, Nicholas K

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CM-Score : A validated scoring system to predict CDKN2A germline mutations in melanoma families from Northern Europe von Potjer, Thomas P., Helgadottir, Hildur, Leenheer, Mirjam, Van Der Stoep, Nienke, Gruis, Nelleke A., Höiom, Veronica, Olsson, Håkan, Van Doorn, Remco, Vasen, Hans F.A., Van Asperen, Christi J., Dekkers, Olaf M., Hes, Frederik J.

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A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types von Kamb, Alexander, Gruis, Nelleke A., Weaver-Feldhaus, Jane, Liu, Qingyun, Harshman, Keith, Tavtigian, Sean V., Stockert, Elisabeth, Day, Rufus S., Johnson, Bruce E., Skolnick, Mark H.

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Loss of Wild-Type CDKN2A Is an Early Event in the Development of Melanoma in FAMMM Syndrome von Christodoulou, Eirini, Nell, Rogier J., Verdijk, Rob M., Gruis, Nelleke A., van der Velden, Pieter A., van Doorn, Remco

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MC1R variants in relation to naevi in melanoma cases and controls: a pooled analysis from the M‐SKIP project von Stefanaki, I., Stratigos, A.J., Kypreou, K.P., Evangelou, E., Gandini, S., Maisonneuve, P., Polsky, D., Lazovich, D., Newton‐Bishop, J., Kanetsky, P.A., Puig, S., Gruis, N.A., Ghiorzo, P., Pellegrini, C., De Nicolo, A., Ribas, G., Guida, G., Garcia‐Borron, J.C., Fargnoli, M.C., Nan, H., Landi, M.T., Little, J., Sera, F., Raimondi, S.

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Melanocortin-1 Receptor Gene Variants Determine the Risk of Nonmelanoma Skin Cancer Independently of Fair Skin and Red Hair von Bastiaens, Maarten T., Huurne, Jeannet A. C. ter, Kielich, Christine, Gruis, Nelleke A., Westendorp, Rudi G.J., Vermeer, Bert Jan, Bavinck, Jan Nico Bouwes

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Increased Risk of Cancer Other Than Melanoma in CDKN2A Founder Mutation (p16-Leiden)-Positive Melanoma Families von DE SNOO, Femke A, BISHOP, D. Timothy, WILLEMZE, Rein, BREUNING, Martijn H, GRUIS, Nelleke A, BERGMAN, Wilma, VAN LEEUWEN, Inge, VAN DER DRIFT, Clasine, VAN NIEUWPOORT, Frans A, OUT-LUITING, Coby J, VASEN, Hans F, TER HUURNE, Jeanet A. C, FRANTS, Rune R

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