Small RNA expression from viruses, bacteria and human miRNAs in colon cancer tissue and its association with microsatellite instability and tumor location von Mjelle, Robin, Sjursen, Wenche, Thommesen, Liv, Sætrom, Pål, Hofsli, Eva

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Detecting copy number variation in next generation sequencing data from diagnostic gene panels von Singh, Ashish Kumar, Olsen, Maren Fridtjofsen, Lavik, Liss Anne Solberg, Vold, Trine, Drablos, Finn, Sjursen, Wenche

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Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer von Singh, Ashish Kumar, Talseth-Palmer, Bente, McPhillips, Mary, Lavik, Liss Anne Solberg, Xavier, Alexandre, Drablos, Finn, Sjursen, Wenche

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Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing von Singh, Ashish Kumar, Talseth-Palmer, Bente, Xavier, Alexandre, Scott, Rodney J, Drabløs, Finn, Sjursen, Wenche

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MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome von Wiik, Mariann Unhjem, Negline, Mia, Beisvåg, Vidar, Clapham, Matthew, Holliday, Elizabeth, Dueñas, Nuria, Brunet, Joan, Pineda, Marta, Bonifaci, Nuria, Aretz, Stefan, Klinkhammer, Hannah, Spier, Isabel, Perne, Claudia, Mayr, Andreas, Valle, Laura, Lubinski, Jan, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.

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Identification of metastasis-associated microRNAs in serum from rectal cancer patients von Mjelle, Robin, Sellæg, Kjersti, Sætrom, Pål, Thommesen, Liv, Sjursen, Wenche, Hofsli, Eva

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The Prognostic Value of Methylation Signatures and NF2 Mutations in Atypical Meningiomas von Meta, Rahmina, Boldt, Henning B., Kristensen, Bjarne W., Sahm, Felix, Sjursen, Wenche, Torp, Sverre H.

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sMETASeq: Combined Profiling of Microbiota and Host Small RNAs von Mjelle, Robin, Aass, Kristin Roseth, Sjursen, Wenche, Hofsli, Eva, Sætrom, Pål

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PMS2 mutation spectra in Norway and risk of cancer for carriers of pathogenic variants von Sjursen, Wenche, Hyldebrandt, Hanne K, Lavik, Liss Anne S, Haukanes, Bjørn Ivar, Ariansen, Sarah, Briskemyr, Siri, Sylvander, Anna E, Haavind, Marianne T, Olsen, Maren F, Røyset, Elin S, Vetti, Hildegunn, Stormorken, Astrid, Grindedal, Eli Marie

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Comprehensive mismatch repair gene panel identifies variants in patients with Lynch‐like syndrome von Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth‐Palmer, Bente A.

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Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations von Sjursen, Wenche, McPhillips, Mary, Scott, Rodney J., Talseth‐Palmer, Bente A.

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Update on genetic predisposition to colorectal cancer and polyposis von Valle, Laura, de Voer, Richarda M., Goldberg, Yael, Sjursen, Wenche, Försti, Asta, Ruiz-Ponte, Clara, Caldés, Trinidad, Garré, Pilar, Olsen, Maren F., Nordling, Margareta, Castellvi-Bel, Sergi, Hemminki, Kari

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Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype von 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, Høberg-Vetti, Hildegunn, Jongmans, Marjolijn C., Neveling, Kornelia, Geurts van Kessel, Ad, Morreau, Hans, Hes, Frederik J., Sijmons, Rolf H., Schackert, Hans K., Ruiz-Ponte, Clara, Dymerska, Dagmara, Lubinski, 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.

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No association between non-bullous skin reactions from lamotrigine and heterozygosity of UGT1A4 genetic variants 2(P24T) or 3(L48V) in Norwegian patients von Shirzadi, Maryam, Reimers, Arne, Helde, Grethe, Sjursen, Wenche, Brodtkorb, Eylert

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Small RNA sequencing of colorectal cancer to reveal differences in microRNA expression between normal and tumor tissue von Mjelle, Robin, Sjursen, Wenche, Thommesen, Liv, Hofsli, Eva

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A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing von Bjørnstad, Pål Marius, Aaløkken, Ragnhild, Åsheim, June, Sundaram, Arvind Y M, Felde, Caroline N, Østby, G Henriette, Dalland, Marianne, Sjursen, Wenche, Carrizosa, Christian, Vigeland, Magnus D, Sorte, Hanne S, Sheng, Ying, Ariansen, Sarah L, Grindedal, Eli Marie, Gilfillan, Gregor D

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Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing von Bjørnstad, Pål Marius, Aaløkken, Ragnhild, Åsheim, June, Sundaram, Arvind Y M, Felde, Caroline N, Østby, G Henriette, Dalland, Marianne, Sjursen, Wenche, Carrizosa, Christian, Vigeland, Magnus D, Sorte, Hanne S, Sheng, Ying, Ariansen, Sarah L, Grindedal, Eli Marie, Gilfillan, Gregor D

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Characterization of POLE c.1373A > T p.(Tyr458Phe), causing high cancer risk von Rocque, Mariève J., Leipart, Vilde, Kumar Singh, Ashish, Mur, Pilar, Olsen, Maren F., Engebretsen, Lars F., Martin-Ramos, Edgar, Aligué, Rosa, Sætrom, Pål, Valle, Laura, Drabløs, Finn, Otterlei, Marit, Sjursen, Wenche

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Use of multigene‐panel identifies pathogenic variants in several CRC‐predisposing genes in patients previously tested for Lynch Syndrome von Hansen, Maren F., Johansen, Jostein, Sylvander, Anna E., Bjørnevoll, Inga, Talseth‐Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche

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Comparison of the ABC and ACMG systems for variant classification von Houge, Gunnar, Bratland, Eirik, Aukrust, Ingvild, Tveten, Kristian, Žukauskaitė, Gabrielė, Sansovic, Ivona, Brea-Fernández, Alejandro J, Mayer, Karin, Paakkola, Teija, McKenna, Caoimhe, Wright, William, Markovic, Milica Keckarevic, Lildballe, Dorte L, Konecny, Michal, Smol, Thomas, Alhopuro, Pia, Gouttenoire, Estelle Arnaud, Obeid, Katharina, Todorova, Albena, Jankovic, Milena, Lubieniecka, Joanna M, Stojiljkovic, Maja, Buisine, Marie-Pierre, Haukanes, Bjørn Ivar, Lorans, Marie, Roomere, Hanno, Petit, François M, Haanpää, Maria K, Beneteau, Claire, Pérez, Belén, Plaseska-Karanfilska, Dijana, Rath, Matthias, Fuhrmann, Nico, Ferreira, Bibiana I, Stephanou, Coralea, Sjursen, Wenche, Maver, Aleš, Rouzier, Cécile, Chirita-Emandi, Adela, Gonçalves, João, Kuek, Wei Cheng David, Broly, Martin, Haer-Wigman, Lonneke, Thong, Meow-Keong, Tae, Sok-Kun, Hyblova, Michaela, den Dunnen, Johan T, Laner, Andreas

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