Assessing a single SNP located at TERT/CLPTM1L multi-cancer risk region as a genetic modifier for risk of pancreatic cancer and melanoma in Dutch CDKN2A mutation carriers

por Christodoulou, E., Visser, M., Potjer, T. P., van der Stoep, N., Rodríguez-Girondo, M., van Doorn, R., Gruis, N.
Publicado 2019

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 2019

Application of a Serum Protein Signature for Pancreatic Cancer to Separate Cases from Controls in a Pancreatic Surveillance Cohort()()

por Potjer, Thomas P., Mertens, Bart J., Nicolardi, Simone, van der Burgt, Yuri E. M, Bonsing, Bert. A., Mesker, Wilma E., Tollenaar, Rob A. E. M, Vasen, Hans F. A
Publicado 2016

Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma

por Potjer, Thomas P, van der Grinten, Tara W J, Lakeman, Inge M M, Bollen, Sander H, Rodríguez-Girondo, Mar, Iles, Mark M, Barrett, Jennifer H, Kiemeney, Lambertus A, Gruis, Nelleke A, van Asperen, Christi J, van der Stoep, Nienke
Publicado 2021

Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants

por Overbeek, Kasper A, Rodríguez-Girondo, Mar DM, Wagner, Anja, van der Stoep, Nienke, van den Akker, Peter C, Oosterwijk, Jan C, van Os, Theo A, van der Kolk, Lizet E, Vasen, Hans F A, Hes, Frederik J, Cahen, Djuna L, Bruno, Marco J, Potjer, Thomas P
Publicado 2021

Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case–control study

por Potjer, Thomas P, van der Stoep, Nienke, Houwing-Duistermaat, Jeanine J, Konings, Ingrid C A W, Aalfs, Cora M, van den Akker, Peter C, Ausems, Margreet G, Dommering, Charlotte J, van der Kolk, Lizet E, Maiburg, Merel C, Spruijt, Liesbeth, Wagner, Anja, Vasen, Hans F A, Hes, Frederik J
Publicado 2015

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 2019