Karin Anna Wallentin Wadt

Karin Anna Wallentin Wadt

Clinical Associate Professor

Member of:

  • Clinical Genetics


Publication year:
All
31 - 40 out of 55Page size: 10
  1. 2021
  2. Published

    Danish guidelines for management of non-APC-associated hereditary polyposis syndromes

    Jelsig, A. M., Karstensen, John Gásdal, Jespersen, N., Ketabi, Z., Lautrup, C., Rønlund, K., Sunde, L., Wadt, Karin Anna Wallentin, Thorlacius-Ussing, O. & Qvist, N., 2021, In: Hereditary Cancer in Clinical Practice. 19, 9 p., 41.

    Research output: Contribution to journal › Review › Research › peer-review

  3. Published

    Novel Genetic Causes of Gastrointestinal Polyposis Syndromes

    Jelsig, A. M., Byrjalsen, A., Madsen, M. B., Kuhlmann, Tine Plato, Hansen, Thomas van Overeem, Wadt, Karin Anna Wallentin & Karstensen, John Gásdal, 2021, In: Application of Clinical Genetics. 14, p. 455-466 12 p.

    Research output: Contribution to journal › Review › Research › peer-review

  4. Published

    Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe

    extended ERN-GENTURIS Thematic Group 3, E. E. T. G. 3., 2021, In: European Journal of Medical Genetics. 64, 12, 7 p., 104350.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Prevalence of Pathogenic Germline DICER1 Variants in Young Individuals Thyroidectomised Due to Goitre – A National Danish Cohort

    Altaraihi, M., Hansen, T. V. O., Santoni Rugiu, Eric, Rossing, M., Rasmussen, Å. K., Gerdes, A. & Wadt, Karin Anna Wallentin, 2021, In: Frontiers in Endocrinology. 12, 7 p., 727970.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Published

    Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel

    Byrjalsen, A., Diets, I. J., Bakhuizen, J., Hansen, Thomas van Overeem, Schmiegelow, Kjeld, Gerdes, Anne-Marie Axø, Stoltze, U., Kuiper, R. P., Merks, J. H. M., Wadt, Karin Anna Wallentin & Jongmans, M., 2021, In: Familial Cancer. 20, 4, p. 279-287 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. Published

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

    Bakhuizen, J. J., Hanson, H., van der Tuin, K., Lalloo, F., Tischkowitz, M., Wadt, Karin Anna Wallentin, Jongmans, M. C. J., SIOPE Host Genome Working Group, S. H. G. W. G., CanGene-CanVar Clinical Guideline Working Group, C. C. G. W. G. & Expert Network Members, E. N. M., 2021, In: Familial Cancer. 20, 4, p. 337-348 12 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. 2020
  9. Published

    A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families

    Djursby, M., Wadt, Karin Anna Wallentin, Frederiksen, J. H., Madsen, M. B., Berchtold, L. A., Hasselby, Jane Preuss, Willemoe, G. L., Hansen, T. V. O. & Gerdes, Anne-Marie Axø, 2020, In: Hereditary Cancer in Clinical Practice. 18, 1, 8.

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. Published

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

    Bache, Iben, Wadt, Karin Anna Wallentin, Mehrjouy, M. M., Rossing, M., Østrup, O., Byrjalsen, A., Tommerup, Niels, Metzner, M., Vyas, P., Schmiegelow, Kjeld, Lausen, B. & Andersen, M. K., 2020, In: Blood Cancer Journal. 10, 3, 4 p., 27.

    Research output: Contribution to journal › Letter › Research › peer-review

  11. 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. & 68 others, 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, Karin Anna Wallentin, 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., 2020, In: Genetics in Medicine. 22, 1, p. 15-25 11 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  12. Published

    Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high frequency 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. & 3 others, Gerdes, Anne-Marie Axø, Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 2020, In: PLOS Genetics. 16, 12, e1009231.

    Research output: Contribution to journal › Journal article › Research › peer-review

Previous 1 2 3 4 5 6 Next

ID: 212547613