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Rigshospitalet - a part of Copenhagen University Hospital
  1. 2021
  2. Published

    Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel

    Byrjalsen, A., Diets, I. J., Bakhuizen, J., Hansen, T. V. O., Schmiegelow, K., Gerdes, A-M., Stoltze, U., Kuiper, R. P., Merks, J. H. M., Wadt, K. & Jongmans, M., Oct 2021, In: Familial Cancer. 20, 4, p. 279-287 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group

    SIOPE Host Genome Working Group, Oct 2021, In: Familial Cancer. 20, 4, p. 337-348 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published
  5. Published

    Genomforskningsprojekt påviser TP53-mutation hos en pige med rabdomyosarkom

    Behrendt-Møller, I., Stoltze, U., Hjalgrim, L. L., Hansen, T. V. O., Schmiegelow, K. & Wadt, K., 9 Aug 2021, In: Ugeskrift for Laeger. 183, 32

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

    Seppälä, T. T., Dominguez-Valentin, M., Crosbie, E. J., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Hovig, E., Nielsen, M., Sijmons, R. H., Bertario, L., Bonanni, B., Tibiletti, M. G., Cavestro, G. M., Mints, M., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C. A., Green, K., Lalloo, F., Hill, J., Schmiegel, W., Vangala, D., Perne, C., Strauß, H-G., Tecklenburg, J., Holinski-Feder, E., Steinke-Lange, V., Mecklin, J-P., Plazzer, J-P., Pineda, M., Navarro, M., Vida, J. B., Kariv, R., Rosner, G., Piñero, T. A., Pavicic, W., Kalfayan, P., Ten Broeke, S. W., Jenkins, M. A., Sunde, L., Bernstein, I., Burn, J., Greenblatt, M., de Vos Tot Nederveen Cappel, W. H., Della Valle, A., Lopez-Koestner, F., Alvarez, K., Büttner, R., Görgens, H., Morak, M., Holzapfel, S., Hüneburg, R., von Knebel Doeberitz, M., Loeffler, M., Redler, S., Weitz, J., Pylvänäinen, K., Renkonen-Sinisalo, L., Lepistö, A., Hopper, J. L., Win, A. K., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Therkildsen, C., Wadt, K. A. W., Mourits, M. J. E., Ketabi, Z., Denton, O. G., Rødland, E. A., Vasen, H., Neffa, F., Esperon, P., Tjandra, D., Möslein, G., Rokkones, E., Sampson, J. R., Evans, D. G. & Møller, P., 1 May 2021, In: European journal of cancer (Oxford, England : 1990). 148, p. 124-133 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li-Fraumeni syndrome

    Winter, G., Kirschner-Schwabe, R., Groeneveld-Krentz, S., Escherich, G., Möricke, A., von Stackelberg, A., Stanulla, M., Bailey, S., Richter, L., Steinemann, D., Ripperger, T., Escudero, A., Farah, R., Lohi, O., Wadt, K., Jongmans, M., van Engelen, N., Eckert, C. & Kratz, C. P., May 2021, In: Leukemia. 35, 5, p. 1475-1479 5 p.

    Research output: Contribution to journalLetterResearchpeer-review

  8. Published

    Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families

    Lacson, J. C. A., Zamani, S. A., Froes, L. A. R., Mitra, N., Qian, L., Doyle, S. H., Azizi, E., Balestrini, C., Bishop, D. T., Bruno, W., Carlos-Ortega, B., Cuellar, F., Cust, A. E., Elder, D. E., Gerdes, A-M., Ghiorzo, P., Grazziotin, T. C., Gruis, N. A., Hansson, J., Hočevar, M., Höiom, V., Holland, E. A., Ingvar, C., Landman, G., Larre-Borges, A., Mann, G. J., Molgo, M., Moredo, L. F., Olsson, H., Out-Luiting, J. J., Perić, B., Pjanova, D., Puig, S., Salas-Alanis, J., Schmid, H., Wadt, K. A. W., Newton-Bishop, J. A., Kanetsky, P. A. & GenoMEL Study Group, 23 Apr 2021, In: BMC PUBLIC HEALTH. 21, 1, 692.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. 2020
  10. Published

    Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes

    Byrjalsen, A., Hansen, T. V. O., Stoltze, U. K., Mehrjouy, M. M., Barnkob, N. M., Hjalgrim, L. L., Mathiasen, R., Lautrup, C. K., Gregersen, P. A., Hasle, H., Wehner, P. S., Tuckuviene, R., Sackett, P. W., Laspiur, A. O., Rossing, M., Marvig, R. L., Tommerup, N., Olsen, T. E., Scheie, D., Gupta, R., Gerdes, A-M., Schmiegelow, K. & Wadt, K., 17 Dec 2020, In: Plos Genetics. 16, 12, p. e1009231 e1009231.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    The molecular profile of mucosal melanoma

    Mikkelsen, L. H., Maag, E., Andersen, M. K., Kruhøffer, M., Larsen, A-C., Melchior, L. C., Toft, P. B., von Buchwald, C., Wadt, K. & Heegaard, S., Dec 2020, In: Melanoma Research. 30, 6, p. 533-542 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients

    Djursby, M., Madsen, M. B., Frederiksen, J. H., Berchtold, L. A., Therkildsen, C., Willemoe, G. L., Hasselby, J. P., Wikman, F., Okkels, H., Skytte, A-B., Nilbert, M., Wadt, K., Gerdes, A-M. & van Overeem Hansen, T., 24 Sep 2020, In: Frontiers in genetics. 11, p. 566266 566266.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

    Dominguez-Valentin, M., Sampson, J. R., Seppälä, T. T., Ten Broeke, S. W., Plazzer, J-P., Nakken, S., Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos Tot Nederveen Cappel, W. H., Sijmons, R. H., Bertario, L., Tibiletti, M. G., Cavestro, G. M., Lindblom, A., Della Valle, A., Lopez-Köstner, F., Gluck, N., Katz, L. H., Heinimann, K., Vaccaro, C. A., Büttner, R., Görgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Hüneburg, R., Knebel Doeberitz, M. V., Loeffler, M., Rahner, N., Schackert, H. K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvänäinen, K., Renkonen-Sinisalo, L., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Wadt, K., Therkildsen, C., Okkels, H., Ketabi, Z., Moreira, L., Sánchez, A., Serra-Burriel, M., Pineda, M., Navarro, M., Blanco, I., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Denton, O. G., Frayling, I. M., Rødland, E. A., Vasen, H., Mints, M., Neffa, F., Esperon, P., Alvarez, K., Kariv, R., Rosner, G., Pinero, T. A., Gonzalez, M. L., Kalfayan, P., Tjandra, D., Winship, I. M., Macrae, F., Möslein, G., Mecklin, J-P., Nielsen, M. & Møller, P., Sep 2020, In: Genetics in medicine : official journal of the American College of Medical Genetics. 22, 9, p. 1569 1 p.

    Research output: Contribution to journalComment/debateResearchpeer-review

  14. Published

    Guideline: Udredning og opfølgning for arvelige polyposesyndromer

    Jelsig, A. M., Karstensen, J. G., Lautrup, C., Rønlund, K., Wadt, K., Sunde, L., Jespersen, N. F. K., Thorlacius-Ussing, O., Ketabi, Z. & Qvist, N., 5 Aug 2020

    Research output: Other contributionCommunication

  15. Published

    Whole genome landscapes of uveal melanoma show an ultraviolet radiation signature in iris tumours

    Johansson, P. A., Brooks, K., Newell, F., Palmer, J. M., Wilmott, J. S., Pritchard, A. L., Broit, N., Wood, S., Carlino, M. S., Leonard, C., Koufariotis, L. T., Nathan, V., Beasley, A. B., Howlie, M., Dawson, R., Rizos, H., Schmidt, C. W., Long, G. V., Hamilton, H., Kiilgaard, J. F., Isaacs, T., Gray, E. S., Rolfe, O. J., Park, J. J., Stark, A., Mann, G. J., Scolyer, R. A., Pearson, J. V., van Baren, N., Waddell, N., Wadt, K. W., McGrath, L. A., Warrier, S. K., Glasson, W. & Hayward, N. K., 15 May 2020, In: Nature Communications. 11, 1, p. 2408 2408.

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. Published

    Variability in Medullary Thyroid Carcinoma in RET L790F Carriers: A Case Comparison Study of Index Patients

    Mathiesen, J. S., Nielsen, S. G., Rasmussen, Å. K., Kiss, K., Wadt, K., Hermann, A. P., Nielsen, M. F., Larsen, S. R., Brusgaard, K., Frederiksen, A. L., Godballe, C. & Rossing, M., 28 Apr 2020, In: Frontiers in Endocrinology. 11, p. 251 251.

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published
  18. Published

    A shared somatic translocation involving CUX1 in monozygotic twins as an early driver of AMKL in Down syndrome

    Bache, I., Wadt, K., Mehrjouy, M. M., Rossing, M., Østrup, O., Byrjalsen, A., Tommerup, N., Metzner, M., Vyas, P., Schmiegelow, K., Lausen, B. & Andersen, M. K., 3 Mar 2020, In: Blood Cancer Journal. 10, 3, p. 27

    Research output: Contribution to journalLetterResearchpeer-review

  19. Published

    Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

    Dominguez-Valentin, M., Sampson, J. R., Seppälä, T. T., Ten Broeke, S. W., Plazzer, J-P., Nakken, S., Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos Tot Nederveen Cappel, W. H., Sijmons, R. H., Bertario, L., Tibiletti, M. G., Cavestro, G. M., Lindblom, A., Della Valle, A., Lopez-Köstner, F., Gluck, N., Katz, L. H., Heinimann, K., Vaccaro, C. A., Büttner, R., Görgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Hüneburg, R., Knebel Doeberitz, M. V., Loeffler, M., Rahner, N., Schackert, H. K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvänäinen, K., Renkonen-Sinisalo, L., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Wadt, K., Therkildsen, C., Okkels, H., Ketabi, Z., Moreira, L., Sánchez, A., Serra-Burriel, M., Pineda, M., Navarro, M., Blanco, I., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Denton, O. G., Frayling, I. M., Rødland, E. A., Vasen, H., Mints, M., Neffa, F., Esperon, P., Alvarez, K., Kariv, R., Rosner, G., Pinero, T. A., Gonzalez, M. L., Kalfayan, P., Tjandra, D., Winship, I. M., Macrae, F., Möslein, G., Mecklin, J-P., Nielsen, M. & Møller, P., Jan 2020, In: Genetics in medicine : official journal of the American College of Medical Genetics. 22, 1, p. 15-25 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. 2019
  21. Published

    Germline variants in oculocutaneous albinism genes and predisposition to familial cutaneous melanoma

    Nathan, V., Johansson, P. A., Palmer, J. M., Howlie, M., Hamilton, H. R., Wadt, K., Jönsson, G., Brooks, K. M., Pritchard, A. L. & Hayward, N. K., Nov 2019, In: Pigment Cell & Melanoma Research. 32, 6, p. 854-863 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  22. Published

    Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma

    Johansson, P. A., Nathan, V., Bourke, L. M., Palmer, J. M., Zhang, T., Symmons, J., Howlie, M., Patch, A-M., Read, J., Holland, E. A., Schmid, H., Warrier, S., Glasson, W., Höiom, V., Wadt, K., Jönsson, G., Olsson, H., Ingvar, C., Mann, G., Brown, K. M., Hayward, N. K. & Pritchard, A. L., Oct 2019, In: Melanoma Research. 29, 5, p. 483-490 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. Published

    Global microRNA profiling of metastatic conjunctival melanoma

    Mikkelsen, L. H., Andersen, M. K., Andreasen, S., Larsen, A-C., Tan, Q., Toft, P. B., Wadt, K. & Heegaard, S., Oct 2019, In: Melanoma Research. 29, 5, p. 465-473 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT

    GenoMEL Study Group, 1 Aug 2019, In: Journal of the American Academy of Dermatology. 81, 2, p. 386-394 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    The genetic evolution of metastatic uveal melanoma

    Shain, A. H., Bagger, M. M., Yu, R., Chang, D., Liu, S., Vemula, S., Weier, J. F., Wadt, K., Heegaard, S., Bastian, B. C. & Kiilgaard, J. F., Jul 2019, In: Nature Genetics. 51, 7, p. 1123-1130 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. Published

    Exploring the hereditary background of renal cancer in Denmark

    Christensen, M. B., Wadt, K., Jensen, U. B., Lautrup, C. K., Bojesen, A., Krogh, L. N., Overeem Hansen, T. V. & Gerdes, A-M., 1 Apr 2019, In: PLoS One. 14, 4, p. e0215725 e0215725.

    Research output: Contribution to journalJournal articleResearchpeer-review

  27. Published
  28. Published

    A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis

    Altaraihi, M., Gerdes, A-M. & Wadt, K., 2019, In: Genome Research. 6, 1, p. 46 46.

    Research output: Contribution to journalJournal articleResearchpeer-review

  29. Published
  30. Published

    Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome

    Askaner, G., Lei, U., Bertelsen, B., Venzo, A. & Wadt, K., 2019, In: Case Reports in Genetics. 2019, p. 9650184

    Research output: Contribution to journalJournal articleResearchpeer-review

  31. 2018
  32. Published

    Pediatric cancer families' participation in whole-genome sequencing research in Denmark: Parent perspectives

    Byrjalsen, A., Stoltze, U., Wadt, K., Hjalgrim, L. L., Gerdes, A-M., Schmiegelow, K. & Wahlberg, A., Nov 2018, In: European Journal of Cancer Care. 27, 6, p. e12877

    Research output: Contribution to journalJournal articleResearchpeer-review

  33. Published

    En familie med nedarvet DICER1-mutation

    Altaraihi, M., Pedersen, J., Rossing, M., Gerdes, A-M. & Wadt, K., 18 Jun 2018, In: Ugeskrift for Laeger. 180, 24, p. V01180063

    Research output: Contribution to journalJournal articleResearchpeer-review

  34. Published

    Kræftdisponerende mutationer er hyppige hos børn og unge med kræft

    Stoltze, U. K., Byrjalsen, A., Hjalgrim, L. L., Wahlberg, A., Gupta, R., Gerdes, A-M., Wadt, K. & Schmiegelow, K., 23 Apr 2018, In: Ugeskrift for Laeger. 180, 17, p. V07170566

    Research output: Contribution to journalJournal articleResearchpeer-review

  35. Published

    Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark

    Stoltze, U., Skytte, A-B., Roed, H., Hasle, H., Ejlertsen, B., Overeem Hansen, T. V., Schmiegelow, K., Gerdes, A-M. & Wadt, K., 2018, In: P L o S One. 13, 1, p. e0190050

    Research output: Contribution to journalJournal articleResearchpeer-review

  36. Published

    Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide

    Walpole, S., Pritchard, A. L., Cebulla, C. M., Pilarski, R., Stautberg, M., Davidorf, F. H., de la Fouchardière, A., Cabaret, O., Golmard, L., Stoppa-Lyonnet, D., Garfield, E., Njauw, C-N., Cheung, M., Turunen, J. A., Repo, P., Järvinen, R-S., van Doorn, R., Jager, M. J., Luyten, G. P. M., Marinkovic, M., Chau, C., Potrony, M., Höiom, V., Helgadottir, H., Pastorino, L., Bruno, W., Andreotti, V., Dalmasso, B., Ciccarese, G., Queirolo, P., Mastracci, L., Wadt, K., Kiilgaard, J. F., Speicher, M. R., van Poppelen, N., Kilic, E., Al-Jamal, R. T., Dianzani, I., Betti, M., Bergmann, C., Santagata, S., Dahiya, S., Taibjee, S., Burke, J., Poplawski, N., O'Shea, S. J., Newton-Bishop, J., Adlard, J., Adams, D. J., Lane, A-M., Kim, I., Klebe, S., Racher, H., Harbour, J. W., Nickerson, M. L., Murali, R., Palmer, J. M., Howlie, M., Symmons, J., Hamilton, H., Warrier, S., Glasson, W., Johansson, P., Robles-Espinoza, C. D., Ossio, R., de Klein, A., Puig, S., Ghiorzo, P., Nielsen, M., Kivelä, T. T., Tsao, H., Testa, J. R., Gerami, P., Stern, M-H., Paillerets, B. B., Abdel-Rahman, M. H. & Hayward, N. K., 2018, In: Journal of the National Cancer Institute. 110, 12, p. 1328-1341 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  37. Published
  38. 2017
  39. Published

    Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families

    Taylor, N. J., Mitra, N., Goldstein, A. M., Tucker, M. A., Avril, M-F., Azizi, E., Bergman, W., Bishop, D. T., Bressac-de Paillerets, B., Bruno, W., Calista, D., Cannon-Albright, L. A., Cuellar, F., Cust, A. E., Demenais, F., Elder, D. E., Gerdes, A-M., Ghiorzo, P., Grazziotin, T. C., Hansson, J., Harland, M., Hayward, N. K., Hocevar, M., Höiom, V., Ingvar, C., Landi, M. T., Landman, G., Larre-Borges, A., Leachman, S. A., Mann, G. J., Nagore, E., Olsson, H., Palmer, J. M., Perić, B., Pjanova, D., Pritchard, A., Puig, S., van der Stoep, N., Wadt, K. A. W., Whitaker, L., Yang, X. R., Newton Bishop, J. A., Gruis, N. A., Kanetsky, P. A. & GenoMEL Study Group, Dec 2017, In: The Journal of investigative dermatology. 137, 12, p. 2606-2612 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  40. Published
  41. 2016
  42. Published

    Deep sequencing of uveal melanoma identifies a recurrent mutation in PLCB4

    Johansson, P., Aoude, L. G., Wadt, K., Glasson, W. J., Warrier, S. K., Hewitt, A. W., Kiilgaard, J. F., Heegaard, S., Isaacs, T., Franchina, M., Ingvar, C., Vermeulen, T., Whitehead, K. J., Schmidt, C. W., Palmer, J. M., Symmons, J., Gerdes, A-M., Jönsson, G. & Hayward, N. K., 14 Dec 2016, In: Oncotarget. 7, 4, p. 4624-31

    Research output: Contribution to journalJournal articleResearchpeer-review

  43. Published

    Phenotypic and histopathological tumor characteristics according to CDKN2A mutation status among affected members of melanoma families

    Taylor, N. J., Handorf, E. A., Mitra, N., Avril, M-F., Azizi, E., Bergman, W., Bianchi-Scarrà, G., Bishop, D. T., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L. A., Cuellar, F., Cust, A. E., Demenais, F., Elder, D. E., Friedman, E., Gerdes, A-M., Ghiorzo, P., Goldstein, A. M., Grazziotin, T. C., Hansson, J., Hayward, N. K., Hocevar, M., Höiom, V., Holland, E. A., Ingvar, C., Landi, M. T., Landman, G., Larre-Borges, A., Leachman, S. A., Mann, G. J., Nagore, E., Olsson, H., Palmer, J., Perić, B., Pjanova, D., Puig, S., Schmid, H., van der Stoep, N., Tucker, M. A., Wadt, K. A. W., Whitaker, L., Yang, X. R., Newton Bishop, J. A., Gruis, N. A., Kanetsky, P. A. & GenoMEL Consortium, 28 Jan 2016, In: The Journal of investigative dermatology. 136, 5, p. 1066–1069

    Research output: Contribution to journalJournal articleResearchpeer-review

  44. Published

    Germline TERT promoter mutations are rare in familial melanoma

    Harland, M., Petljak, M., Robles-Espinoza, C. D., Ding, Z., Gruis, N. A., van Doorn, R., Pooley, K. A., Dunning, A. M., Aoude, L. G., Wadt, K. A. W., Gerdes, A-M., Brown, K. M., Hayward, N. K., Newton-Bishop, J. A., Adams, D. J. & Bishop, D. T., 2016, In: Familial Cancer. 15, 1, p. 139-40

    Research output: Contribution to journalJournal articleResearchpeer-review

  45. 2015
  46. Published

    High accuracy of family history of melanoma in Danish melanoma cases

    Wadt, K. A. W., Drzewiecki, K. T. & Gerdes, A-M., Dec 2015, In: Familial Cancer. 14, 4, p. 609-13 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  47. Published

    POLE mutations in families predisposed to cutaneous melanoma

    Aoude, L. G., Heitzer, E., Johansson, P., Gartside, M., Wadt, K., Pritchard, A. L., Palmer, J. M., Symmons, J., Gerdes, A-M., Montgomery, G. W., Martin, N. G., Tomlinson, I., Kearsey, S. & Hayward, N. K., Dec 2015, In: Familial Cancer. 14, 4, p. 621-8 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  48. Published

    Melanoma genetics

    Read, J., Wadt, K. A. W. & Hayward, N. K., 3 Sep 2015, In: Journal of Medical Genetics. 53, 1, p. 1-14

    Research output: Contribution to journalJournal articleResearchpeer-review

  49. Published

    Germline RAD51B truncating mutation in a family with cutaneous melanoma

    Wadt, K. A. W., Aoude, L. G., Golmard, L., Hansen, T. V. O., Sastre-Garau, X., Hayward, N. K. & Gerdes, A-M., Jun 2015, In: Familial Cancer. 14, 2, p. 337-40 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  50. Published

    Genetics of familial melanoma: 20 years after CDKN2A

    Aoude, L. G., Wadt, K. A. W., Pritchard, A. L. & Hayward, N. K., Mar 2015, In: Pigment Cell & Melanoma Research. 28, 2, p. 148-60 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  51. Published

    Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma

    Aoude, L. G., Pritchard, A. L., Robles-Espinoza, C. D., Wadt, K., Harland, M., Choi, J., Gartside, M., Quesada, V., Johansson, P., Palmer, J. M., Ramsay, A. J., Zhang, X., Jones, K., Symmons, J., Holland, E. A., Schmid, H., Bonazzi, V., Woods, S., Dutton-Regester, K., Stark, M. S., Snowden, H., van Doorn, R., Montgomery, G. W., Martin, N. G., Keane, T. M., López-Otín, C., Gerdes, A-M., Olsson, H., Ingvar, C., Borg, A., Gruis, N. A., Trent, J. M., Jönsson, G., Bishop, D. T., Mann, G. J., Newton-Bishop, J. A., Brown, K. M., Adams, D. J. & Hayward, N. K., Feb 2015, In: National Cancer Institute. Journal (Online). 107, 2, p. dju408

    Research output: Contribution to journalJournal articleResearchpeer-review

  52. Published

    A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma

    Wadt, K. A. W., Aoude, L. G., Johansson, P., Solinas, A., Pritchard, A., Crainic, O., Andersen, M. T., Kiilgaard, J. F., Heegaard, S., Sunde, L., Federspiel, B., Madore, J., Thompson, J. F., McCarthy, S. W., Goodwin, A., Tsao, H., Jönsson, G., Busam, K., Gupta, R., Trent, J. M., Gerdes, A-M., Brown, K. M., Scolyer, R. A. & Hayward, N. K., 2015, In: Clinical Genetics. 88, 3, p. 267-72

    Research output: Contribution to journalJournal articleResearchpeer-review

  53. Published

    Molecular characterization of melanoma cases in denmark suspected of genetic predisposition

    Wadt, K. A. W., Aoude, L. G., Krogh, L., Sunde, L., Bojesen, A., Grønskov, K., Wartacz, N., Ek, J., Andersen, M. T., Andersen, M. K., Borg, Å., Heegaard, S., Kiilgaard, J. F., Hansen, T. V. O., Klein, K., Jönsson, G., Drzewiecki, K. T., Dunø, M., Hayward, N. K. & Gerdes, A-M., 2015, In: P L o S One. 10, 3, p. e0122662

    Research output: Contribution to journalJournal articleResearchpeer-review

  54. Published

    Molecular genetic characterisation of high-risk melanoma cases in Denmark

    Wadt, K., 2015, 138 p.

    Research output: Book/ReportPh.D. thesisResearch

  55. 2014
  56. Published

    CDKN2A-mutation hos en familie med arveligt malignt melanom

    Djursby, M., Wadt, K., Lorentzen, H., Borg, A., Gerdes, A-M. & Krogh, L., 29 Sep 2014, In: Ugeskrift for læger [online]. 176, 40

    Research output: Contribution to journalJournal articleResearchpeer-review

  57. Published
  58. 2013
  59. Published

    A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers

    Aoude, L. G., Wadt, K., Bojesen, A., Crüger, D. G., Borg, A., Trent, J. M., Brown, K. M., Gerdes, A-M., Jönsson, G. & Hayward, N. K., 2013, In: P L o S One. 8, 8, p. e72144

    Research output: Contribution to journalJournal articleResearchpeer-review

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