Home
Hildegunn Høberg Vetti's picture

Hildegunn Høberg Vetti

PhD Candidate
  • E-mailHildegunn.Vetti@uib.no
  • Visitor Address
    Haukeland universitetssykehus, Laboratoriebygget
  • Postal Address
    Postboks 7804
    5020 Bergen
Academic article
  • Grolleman, Judith E.; de Voer, Richarda M.; Elsayed, Fadwa A.; Nielsen, Maartje; Weren, Robbert D.A.; Palles, Claire; Ligtenberg, Marjolijn J.L.; Vos, Janet R.; ten Broeke, Sanne W.; de Miranda, Noel F.C.C.; Kuiper, Renske A.; Kamping, Eveline J.; Jansen, Erik A.M.; Vink-Börger, M. Elisa; Popp, Isabell; Lang, Alois; Spier, Isabel; Hüneburg, Robert; James, Paul A.; Li, Na; Staninova, Marija; Lindsay, Helen; Cockburn, David; Spasic-Boskovic, Olivera; Clendenning, Mark; Sweet, Kevin; Capellá, Gabriel; Sjursen, Wenche; Vetti, Hildegunn Høberg; Jongmans, Marjolijn C.; Neveling, Kornelia; van Kessel, Ad Geurts; Morreau, Hans; Hes, Frederik J.; Sijmons, Rolf H.; Schackert, Hans K.; Ruiz-Ponte, Clara; Dymerska, Dagmara; Lubiñski, Jan; Rivera, Barbara; Foulkes, William D.; Tomlinson, Ian P.; Valle, Laura; Buchanan, Daniel D.; Kenwrick, Sue; Adlard, Julian; Dimovski, Aleksandar J.; Campbell, Ian G.; Aretz, Stefan; Schindler, Detlev; van Wezel, Tom; Hoogerbrugge, Nicoline; Kuiper, Roland P. 2019. Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype. Cancer Cell. 256-266.e5.
  • Lønning, Per Eystein; Berge, Elisabet Ognedal; Bjørnslett, Merete Pauline; Minsaas, Laura; Chrisanthar, Ranjan; Vetti, Hildegunn Høberg; Dulary, Cécile; Busato, Florence; Bjørneklett, Silje; Eriksen, Christine; Kopperud, Reidun Kristin; Axcrona, Ulrika; Davidson, Ben; Bjørge, Line; Evans, D. Gareth; Howell, Anthony; Salvesen, Helga; Janszky, Imre; Hveem, Kristian; Romundstad, Pål Richard; Vatten, Lars Johan; Tost, Jörg; Dørum, Anne; Knappskog, Stian. 2018. White blood cell BRCA1 promoter methylation status and ovarian cancer risk. Annals of Internal Medicine. 326-334.
  • Høberg-Vetti, Hildegunn ; Eide, Geir Egil; Siglen, Elen; Listøl, Wenche; Haavind, Marianne Tveit; Hoogerbrugge, Nicoline; Bjorvatn, Cathrine. 2018. Cancer-related distress in unselected women with newly diagnosed breast or ovarian cancer undergoing BRCA1/2 testing without pretest genetic counseling. Acta Oncologica. 175-181.
  • Vogelaar, Ingrid P.; van der Post, Rachel S.; van Krieken, J. Han J.M.; Spruijt, Liesbeth; van Zelst-Stams, Wendy A.G.; Kets, C. Marleen; Lubinski, Jan; Jakubowska, Anna; Teodorczyk, Urszula; Aalfs, Cora M.; Van Hest, Liselotte P.; Pinheiro, Hugo; Oliveira, Carla; Jhangiani, Shalini N.; Muzny, Donna M.; Gibbs, Richard A.; Lupski, James R.; De Ligt, Joep; Vissers, Lisenka E.L.M.; Hoischen, Alexander; Gilissen, Christian; Van De Vorst, Maartje; Goeman, Jelle J.; Schackert, Hans K.; Ranzani, Guglielmina N.; Molinaro, Valeria; García, Encarna B. Gómez; Hes, Frederik J.; Holinski-Feder, Elke; Genuardi, Maurizio; Ausems, Margreet G.E.M.; Sijmons, Rolf H.; Wagner, Anja; Van Der Kolk, Lizet E.; Bjørnevoll, Inga; Vetti, Hildegunn Høberg; Van Kessel, Ad Geurts; Kuiper, Roland P.; Ligtenberg, Marjolijn J.L.; Hoogerbrugge, Nicoline. 2017. Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing. European Journal of Human Genetics. 1246-1252.
  • Neveling, Kornelia; Mensenkamp, Arjen R.; Derks, Ronny; Kwint, Michael; Ouchene, Hicham; Steehouwer, Marloes; Lier, Bart Van; Bosgoed, Ermanno; Rikken, Alwin; Tychon, Marloes; Zafeiropoulou, Dimitra; Castelein, Steven; Hehir-Kwa, Jayne; Thung, Djie Tjwan; Hofste, Tom; Lelieveld, Stefan H.; Bertens, Stijn M.M.; Adan, Ivo B.J.F.; Eijkelenboom, Astrid; Tops, Bastiaan B.; Yntema, Helger; Stokowy, Tomasz; Knappskog, Per; Vetti, Hildegunn Høberg; Steen, Vidar Martin; Boyle, Evan; Martin, Beth; Ligtenberg, Marjolijn J.L.; Shendure, Jay; Nelen, Marcel R.; Hoischen, Alexander. 2017. BRCA testing by single-molecule molecular inversion probes. Clinical Chemistry. 503-512.
  • Listøl, Wenche; Vetti, Hildegunn Høberg; Eide, Geir Egil; Bjorvatn, Cathrine. 2017. Anxiety and depression symptoms among women attending group-based patient education courses for hereditary breast and ovarian cancer. Hereditary Cancer in Clinical Practice. 1-9.
  • Augestad, Mirjam Tonheim; Vetti, Hildegunn Høberg; Bjorvatn, Cathrine; Sekse, Ragnhild Johanne Tveit. 2016. Identifying needs: a qualitative study of women’s experiences regarding rapid genetic testing for hereditary breast and ovarian cancer in the DNA BONus Study. Journal of Genetic Counseling. 182-189.
  • Vetti, Hildegunn Høberg; Bjorvatn, Cathrine; Fiane, Bent; Aas, Turid; Woie, Kathrine; Espelid, Helge; Eikesdal, Hans Petter; Listøl, Wenche; Haavind, Marianne Tveit; Knappskog, Per; Rusken, Tone; Haukanes, Bjørn Ivar; Steen, Vidar Martin; Hoogerbrugge, Nicoline. 2016. BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study. European Journal of Human Genetics. 881-888.
  • Hagen, Anne Irene; Mæhle, Lovise Olaug; Vedå, Nina; Vetti, Hildegunn Høberg; Stormorken, Astrid T.; Ludvigsen, Trond; Guntvedt, Bente; Isern, Anne Elisabeth Fløystad; Schlichting, Ellen; Kleppe, Geir; Bofin, Anna M.; Gullestad, Hans Petter; Møller, Pål. 2014. Risk reducing mastectomy, breast reconstruction and patient satisfaction in Norwegian BRCA1/2 mutation carriers. Breast. 38-43.
  • Puntervoll, Hanne Eknes; Yang, Xiaohong R.; Vetti, Hildegunn Høberg; Bachmann, Ingeborg M.; Avril, Marie Françoise; Benfodda, Meriem; Catricala, Caterina; Dalle, Stéphane; Duval-Modeste, Anne B.; Ghiorzo, Paola; Grammatico, Paola; Harland, Mark; Hayward, Nicholas K.; Hu, Hui-Han; Jouary, Thomas; Martin-Denavit, Tanguy; Ozola, Aija; Palmer, Jane M.; Pastorino, Lorenza; Pjanova, Dace; Soufir, Nadem; Steine, Solrun; Stratigos, Alexander J.; Thomas, Luc; Tinat, Julie; Tsao, Hensin; Veinalde, Rūta; Tucker, Margaret A.; Bressac-de Paillerets, Brigitte B.D.; Newton-Bishop, Julia A.; Goldstein, Alisa M.; Akslen, Lars A.; Molven, Anders. 2013. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants. Journal of Medical Genetics. 264-U82.
  • Vetti, Hildegunn Høberg; Molven, Anders; Eliassen, Aud Katrin; Steen, Vidar Martin. 2010. Er formakogenetisk CYP2D6-testing nyttig? Tidsskrift for Den norske legeforening. 2224-2228.
  • Vetti, Hildegunn Høberg; Molven, Anders; Eliassen, Aud Katrin; Steen, Vidar Martin. 2010. Er farmakogenetisk CYP2D6-testing nyttig? Tidsskrift for Den norske legeforening. 2224-2228.
  • Allerston, Charles K.; Vetti, Hildegunn Høberg; Houge, Gunnar; Phillips, Ian R.; Shephard, Elizabeth A. 2009. A novel mutation in the flavin-containing monooxygenase 3 gene (FMO3) of a Norwegian family causes trimethylaminuria. Molecular Genetics and Metabolism. 198-202.
Popular scientific article
  • Sjursen, Wenche; Vetti, Hildegunn Høberg. 2019. NTHL1-mutasjoner gir ikke bare polypose. Best Practice Gastroenterology. 18-20.
Poster
  • Augesatd Tonheim, Mirjam; Vetti, Hildegunn Høberg; Bjorvatn, Cathrine; Sekse, Ragnhild Johanne Tveit. 2016. Genetic testing at the time of diagnosis - Women's experiences when offered genetic testing immidiately after receiving a diagnosis of breast- or ovarian cancer. .

More information in national current research information system (CRIStin)