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2020
1 Mjelle, Robin; Aass, Kristin Roseth; Sjursen, Wenche; Hofsli, Eva; Sætrom, Pål.
sMETASeq: combined profiling of microbiota and host small RNAs. iScience 2020
NTNU Untitled
 
2019
2 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..
Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype. Cancer Cell 2019 ;Volum 35.(2) s. 256-266.e5
HAUKELAND NTNU STO Untitled
 
3 Mjelle, Robin; Sjursen, Wenche; Thommesen, Liv; Sætrom, Pål; Hofsli, Eva.
Small RNA expression from viruses, bacteria and human miRNAs in colon cancer tissue and its association with microsatellite instability and tumor location. BMC Cancer 2019 ;Volum 19.(1) s. 1-12
NTNU STO Untitled
 
4 Sjursen, Wenche; Vetti, Hildegunn Høberg.
NTHL1-mutasjoner gir ikke bare polypose. Best Practice Gastroenterology 2019 ;Volum November.(28) s. 18-20
HAUKELAND NTNU Untitled
 
5 Steinsbekk, Kristin Solum; Kjøbli, Eli; Kristiansen, Kine H; Prestvik, Wenche Slettahjell; Sjursen, Wenche; Bjørnevoll, Inga; Sæther, Mari; Olsen, Maren Fridtjofsen.
Høykapasitetsanalyser innen medisinsk genetikk; Nye tider – Nye kunnskapsbehov! SAMGen: Studentaktiv undervisning innen medisinsk bruk av genomsekvensering.. NSHG Fagmøte 2019; 2019-11-06 - 2019-11-07
STO NTNU Untitled
 
6 Suerink, Manon; Rodriguez-Girondo, Mar; van der Klift, Heleen M.; Colas, Chrystelle; Brugieres, Laurence; Lavoine, Noémie; Jongmans, Marjolijn; Munar, Gabriel Capellá; Evans, D. Gareth; Farrell, Michael P.; Genuardi, Maurizio; Goldberg, Yael; Gomez-Garcia, Encarna; Heinimann, Karl; Hoell, Jessica I.; Aretz, Stefan; Jasperson, Kory W.; Kedar, Inbal; Modi, Mitul B.; Nikolaev, Sergey; van Os, Theo A.M.; Ripperger, Tim; Rueda, Daniel; Senter, Leigha; Sjursen, Wenche; Sunde, Lone; Therkildsen, Christina; Tibiletti, Maria G.; Trainer, Alison H.; Vos, Yvonne J.; Wagner, Anja; Winship, Ingrid; Wimmer, Katharina; Zimmermann, Stefanie Y.; Vasen, Hans F.; van Asperen, Christi J.; Houwing-Duistermaat, Jeanine J.; ten Broeke, Sanne W.; Nielsen, Maartje.
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome. Genetics in Medicine 2019 ;Volum 21.(12) s. 1-7
NTNU STO Untitled
 
7 Valle, Laura; de Voer, Richarda M.; Goldberg, Yael; Sjursen, Wenche; Försti, Asta; Ruiz-Ponte, Clara; Caldés, Trinidad; Garré, Pilar; Olsen, Maren Fridtjofsen; Nordling, Margareta; Castellví-Bel, Sergi; Hemminki, Kari.
Update on genetic predisposition to colorectal cancer and polyposis. Molecular Aspects of Medicine 2019 s. 1-17
NTNU STO Untitled
 
8 Xavier, Alexandre; Olsen, Maren Fridtjofsen; Lavik, Liss Ane; Johansen, Jostein; Singh, Ashish Kumar; Sjursen, Wenche; Scott, Rodney J.; Talseth-Palmer, Bente Anita.
Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome. Molecular Genetics & Genomic Medicine 2019 ;Volum 7.(8) s. e850-
HMR NTNU STO Untitled
 
2017
9 Hansen, Maren; Johansen, Jostein; Sylvander, Anna Elisabeth; Bjørnevoll, Inga; Talseth-Palmer, Bente Anita; Lavik, Liss Ane; Xavier, Alexandre; Engebretsen, Lars Fredri; Scott, Rodney; Drabløs, Finn Sverre; Sjursen, Wenche.
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. Clinical Genetics 2017 ;Volum 92.(4) s. 405-414
HMR NTNU STO Untitled
 
10 Mjelle, Robin; Sellæg, Kjersti; Sætrom, Pål; Thommesen, Liv; Sjursen, Wenche; Hofsli, Eva.
Identification of metastasis-associated microRNAs in serum from rectal cancer patients. OncoTarget 2017 ;Volum 8.(52) s. 90077-90089
NTNU STO Untitled
 
2016
11 Shirzadi, Maryam; Reimers, Arne; Helde, Grethe; Sjursen, Wenche; Brodtkorb, Eylert.
No association between non-bullous skin reactions from lamotrigine and heterozygosity of UGT1A4 genetic variants *2(P24T) or *3(L48V). 12th European Congress on Epilepsy; 2016-09-11 - 2016-09-20
NTNU Untitled
 
12 Shirzadi, Maryam; Reimers, Arne; Helde, Grethe; Sjursen, Wenche; Brodtkorb, Eylert.
No association between non-bullous skin reactions from lamotrigine and heterozygosity of UGT1A4 genetic variants *2(P24T) or *3(L48V) in Norwegian patients. Seizure 2016 ;Volum 45. s. 169-171
NTNU STO Untitled
 
13 Sjursen, Wenche; McPhillips, Mary; Scott, Rodney J.; Talseth-Palmer, Bente.
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations. Molecular Genetics & Genomic Medicine 2016 ;Volum 4.(2) s. 223-231
HMR NTNU STO Untitled
 
14 Talseth-Palmer, Bente; Bauer, Denis; Sjursen, Wenche; Evans, Tiffany-Jane; McPhillips, Mary; Proietto, Anthony; Otten, Geoffrey; Spigelman, Allan D.; Scott, Rodney J..
Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families. Cancer Medicine 2016 ;Volum 5.(5) s. 929-941
NTNU STO Untitled
 
2015
15 Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål; Sandvik, Arne Kristian; Drabløs, Finn; Sjursen, Wenche.
A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine. Familial Cancer 2015 ;Volum 14.(3) s. 437-448
NTNU STO Untitled
 
16 Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål; Sandvik, Arne Kristian; Drabløs, Finn; Sjursen, Wenche.
A novel POLE variant, identified by exome sequencing, causes colorectal- and extra-colonic cancers. Familial Cancer 2015 ;Volum 14.(1) s. 44-44
NTNU STO Untitled
 
17 Hansen, Maren Fridtjofsen; Sjursen, Wenche.
En ny POLE-mutasjon som årsak til økt risiko i en familie med høy forekomst av tykk- og endetarmskreft. Bestpractice Onkologi/Hematologi 2015 ;Volum 21.(August) s. 15-17
NTNU Untitled
 
18 Svaasand, Eva Kathrine; Engebretsen, Lars Fredri; Ludvigsen, Trond; Brechan, Wenche; Sjursen, Wenche.
A Novel Deep Intronic Mutation Introducing a Cryptic Exon Causing Neurofibromatosis Type 1 in a Family with Highly Variable Phenotypes: A Case Study. Hereditary Genetics: Current Research 2015 ;Volum 4.(3) s. -
HAUKELAND NTNU STO Untitled
 
2014
19 Drabløs, Finn; Sjursen, Wenche.
A medical research infrastructure. COST Action BM1206 Meeting; 2014-03-12 - 2014-03-12
NTNU Untitled
 
20 Grindedal, Eli Marie; Aarset, Harald; Bjørnevoll, Inga; Røyset, Elin Synnøve; Mæhle, Lovise Olaug; Stormorken, Astrid T.; Heramb, Cecilie; Medvik, Heidi; Møller, Pål; Sjursen, Wenche.
The Norwegian PMS2 founder mutation c.989-1G>T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry. Hereditary Cancer in Clinical Practice 2014 ;Volum 12.(1)
NTNU OUS STO Untitled
 
21 Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål; Sandvik, Arne Kristian; Drabløs, Finn; Sjursen, Wenche.
Using exome sequencing for identification of high-risk genetic variants in a family predisposed for colorectal cancer. COST Action BM1206 Meeting; 2014-09-04 - 2014-09-04
NTNU STO Untitled
 
22 Hansen, Maren Fridtjofsen; Neckmann, Ulrike; Lavik, Liss Anne; Vold, Trine; Gilde, Bodil; Toft, Ragnhild Karlgård; Sjursen, Wenche.
A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes. Molecular Genetics & Genomic Medicine 2014
NTNU STO Untitled
 
23 Hansen, Maren Fridtjofsen; Steinsbekk, Kristin Solum; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Sjursen, Wenche; Drabløs, Finn.
Using exome sequencing for identification of high-risk genetic variants in a family predisposed for colorectal cancer. Translational genomics in biomedicine; 2014-03-13 - 2014-03-14
NTNU STO Untitled
 
24 Reimers, Arne; Sjursen, Wenche; Helde, Grethe; Brodtkorb, Eylert.
Frequencies of UGT1A4*2 (P24T) and *3 (L48V) and their effects on serum concentrations of lamotrigine. European journal of drug metabolism and pharmacokinetics 2014
NTNU STO Untitled
 
2013
25 Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Gilde, Bodil; Vold, Trine; Neckmann, Ulrike; Bye, Kristin; Sjursen, Wenche.
A Massive Parallel Sequencing Workflow for Routine Clinical Diagnostics of Lynch Syndrome. InSiGHT 2013; 2013-08-28 - 2013-08-31
NTNU STO Untitled
 
26 Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Gilde, Bodil; Vold, Trine; Neckmann, Ulrike; Bye, Kristin; Sjursen, Wenche.
Massive parallel sequencing in Molecular Diagnostics: Universal Tailed Amplicon Sequencing of Lynch Syndrome genes. European Human Genetics Conference 2013; 2013-06-08 - 2013-06-11
NTNU STO Untitled
 
27 Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Vold, Trine; Neckmann, Ulrike; Gilde, Bodil; Sjursen, Wenche.
Høykapasitetsekvensering møter humangenetikk: Amplicon Sekvensering av Lynch Syndrom Gener. Årlig seminar innen molekylærmedisin; 2013-01-23
NTNU STO Untitled
 
28 Hofsli, Eva; Sjursen, Wenche; Prestvik, Wenche S; Johansen, Jostein; Rye, Morten Beck; Tranø, Gerd; Wasmuth, Hans; Hatlevoll, Ingunn; Thommesen, Liv.
Identification of serum microRNA profiles in colon cancer. British Journal of Cancer 2013 ;Volum 108.(8) s. 1712-1719
NTNU STO Untitled
 
29 Sjursen, Wenche; Halvorsen, Henrik; Hofsli, Eva; Bachke, Siri; Berge, Åsa; Engebretsen, Lars Fredri; Falkmer, Sture Emil; Falkmer, Ursula; Varhaug, Jan Erik.
Mutation screening in a Norwegian cohort with pheochromocytoma. Familial Cancer 2013 ;Volum 12.(3) Suppl. Ja s. 529-535
HAUKELAND NTNU STO UiB Untitled
 
2012
30 Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Vold, Trine; Neckmann, Ulrike; Gilde, Bodil; Sjursen, Wenche.
From Sanger- to High-Throughput Sequencing in Molecular Diagnostics: Universal Tailed Amplicon Sequencing of Lynch Synrome Genes. Fagmøte i medisinsk genetikk; 2012-11-28 - 2012-11-29
NTNU STO Untitled
 
2011
31 Jühlen, Ramona.
Colorectal Cancer in Norway; Identification of Hereditary and Non-Hereditary Subtypes - Establishment of Tissue Microarray for Molecular-Genetic Subclassification of Colorectal Cancer. Trondheim: LBK - DMF - NTNU 2011 81 s.
NTNU Untitled
 
32 Tranø, Gerd; Wasmuth, Hans; Sjursen, Wenche; Vatten, Lars Johan.
Patient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: A Norwegian population-based study. Scandinavian Journal of Gastroenterology 2011 ;Volum 46.(10) s. 1236-1242
HNT NTNU STO Untitled
 
2010
33 Sjursen, Wenche; Haukanes, Bjørn Ivar; Grindedal, Eli Marie; Aarset, Harald; Stormorken, Astrid T.; Engebretsen, Lars Fredri; Jonsrud, Christoffer; Bjørnevoll, Inga; Andresen, Per Arne; Ariansen, Sarah Louise; Lavik, Liss Anne Solberg; Gilde, Bodil; Lothe, Inger M Bowitz; Mæhle, Lovise Olaug; Møller, Pål.
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers. Journal of Medical Genetics 2010 ;Volum 47.(9) s. 579-585
HAUKELAND NTNU OUS STO UNN Untitled
 
34 Tessem, May-Britt; Selnæs, Kirsten Margrete; Sjursen, Wenche; Tranø, Gerd; Giskeødegård, Guro F.; Bathen, Tone Frost; Gribbestad, Ingrid S; Hofsli, Eva.
Discrimination of Patients with Microsatellite Instability Colon Cancer using H-1 HR MAS MR Spectroscopy and Chemometric Analysis. Journal of Proteome Research 2010 ;Volum 9.(7) s. 3664-3670
HNT NTNU STO Untitled
 
35 Tranø, Gerd; Sjursen, Wenche; Wasmuth, Hans; Hofsli, Eva; Vatten, Lars Johan.
Performance of clinical guidelines compared with molecular tumour screening methods in identifying possible Lynch syndrome among colorectal cancer patients: a Norwegian population-based study. British Journal of Cancer 2010 ;Volum 102.(3) s. 482-488
HNT NTNU STO Untitled
 
2009
36 Tranø, G; Wasmuth, HH; Sjursen, Wenche; Hofsli, E; Vatten, Lars Johan.
Awareness of heredity in colorectal cancer patients is insufficient among clinicians: a Norwegian population-based study. Colorectal Disease 2009 ;Volum 11.(5) s. 456-461
NTNU SI STO Untitled
 
37 Sjursen, Wenche; Bjørnevoll, Inga; Engebretsen, Lars; Fjelland, Kristine; Halvorsen, Tore Bøhmer; Myrvold, Helge Elliot.
A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts. Familial Cancer 2009 ;Volum 8.(3) s. 179-186
HAUKELAND NTNU STO Untitled
 
38 Tessem, May-Britt; Selnæs, Kirsten Margrete; Sjursen, Wenche; Tranø, Gerd; Gribbestad, Ingrid S; Hofsli, Eva.
Characterization and evaluation of metabolic biomarkers for human colon adenocarcinomas by 1H HR MAS. International Society for Magnetic Resonance in Medicine (ISMRM) annual meeting; 2009-04-18 - 2009-04-24
NTNU Untitled
 
2002
39 Svaasand, Eva; Sjursen, Wenche; Eftedal, Ingrid; Prestvik, Wenche Slettahjell.
Detection of numerical chromosomal abnormalities by fluorescent microsatellite analysis. Biokjemisk kontaktmøte 2002; 2002-01-17 - 2002-01-20
NTNU STO Untitled
 
40 Gilde, B; Sjursen, Wenche.
Molecular diagnosis of hereditary non-polyposis colorectal cancer (HNPCC). 38. Biokjemiske kontaktmøte Functinal genomics - the mosaics of life; 2002-01-17 - 2002-01-20
NTNU Untitled
 
41 Prestvik, Wenche S.; Sjursen, Wenche; Svaasand, Eva K; Eftedal, Ingrid.
Diagnostikk av numeriske kromosomavvik ved hjelp av fluorescerende mikrosatelitt-analyser. Bioingeniøren 2002 (10) s. 4-7
NTNU Untitled
 
42 Prestvik, Wenche Slettahjell; Sjursen, Wenche; Svaasand, Eva; Eftedal, Ingrid.
Diagnostikk av numeriske kromosomavvik ved hjelp av fluorescerende mikrosatelitt-analyser Detection of numerical abnormalities by fluorescent microsatellite analysis. Bioingeniøren 2002 (10) s. 4-7
NTNU STO Untitled
 
43 Svaasand, Eva K; Sjursen, Wenche; Eftedal, Ingrid; Prestvik, Wenche S..
Detection of numerical chromosomal abnormalities by fluorescent microsatellite analysis. Biokjemisk kontaktmøte 2002; 2002-01-17 - 2002-01-20
NTNU Untitled
 
2000
44 Sjursen, Wenche; Brekke, Ole Lars; Johansen, Berit.
Secretory and cytosolic phospholipase A2 regulate the long term cytokine induced eicosanoid production in human keratinocytes. Cytokine 2000 ;Volum 12. s. 1189-1194
NTNU Untitled
 
45 Sjursen, Wenche; Brekke, Ole Lars; Johansen, Berit.
Secretory and cytosolic phospholipase A2 regulate the long term cytokine induced eicosanoid production in human keratinocytes. Cytokine 2000 ;Volum 12. s. 1189-1194
NTNU Untitled
 
1998
46 Johansen, Berit; Lægreid, Astrid; Sjursen, Wenche; Thommesen, Liv; Anthonsen, Marit Walbye.
A role for both secretory and cytosolic phospholipase A2 in TNF mediated nuclear translocation of NFkB and ICAM expression in keratinocytes?. NBS Kontaktmøte 98; 1998
NTNU Untitled
 
47 Johansen, Berit; Lægreid, Astrid; Sjursen, Wenche; Thommesen, Liv; Anthonsen, Marit Walbye.
A role of both secretory and cytosolic phospholipase A2 in TNF mediated nuclear translocation of NFkB and ICAM expression in keratinocytes?. NBS Kontaktmøte 98; 1998
NTNU Untitled
 
48 Thommesen, Liv; Sjursen, Wenche; Gåsvik, Kathrine; Hanssen, Wenche; Brekke, Ole-Lars; Skattebøl, Lars; Holmeide, Anne Kristin; Espevik, Terje; Johansen, Berit; Lægreid, Astrid.
Selective inhibitors of cytosolic or secretory phospholipase A2 block TNF-induced activation of transcription factor nuclear factor-kappa B and expression of ICAM-1. Journal of Immunology 1998 s. 3421-3430
NTNU UiO Untitled
 
1997
49 Frøyland, Livar; Madsen, Lise; Sjursen, W.; Garras, Alexis; Lie, Ø.; Songstad, Jon; Rustan, A. C.; Berge, Rolf Kristian.
Effect of 3-thia fatty acids on the lipid composition of rat liver, lipoproteins, and heart. Journal of Lipid Research 1997 ;Volum 38. s. 1522-1534
UiB Untitled
 
50 Frøyland, Livar; Madsen, Lise; Sjursen, Wenche; Garras, Alexis; Lie, Øyvind; Songstad, Jon; Rustan, Arild C.; berge, Rolf K..
Effects of 3-thia fatty acids on the lipid composition of rat liver, lipoproteins, and heart. Journal of Lipid Research 1997 ;Volum 38. s. 1522-1534
NTNU Untitled
 
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