Wenche Sjursen - Dept Lab Med Childrens & Womens Hlth, NTNU

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论文共 53 篇作者统计合作学者相似作者

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PMS2 Mutation Spectra in Norway and Risk of Cancer for Carriers of Pathogenic Variants

Wenche Sjursen,Hanne K. Hyldebrandt,Liss Anne S. Lavik,Bjørn Ivar Haukanes,Sarah Ariansen,Siri Briskemyr,Anna E. Sylvander, Marianne T. Haavind,Maren F. Olsen, Elin S. Røyset, Hildegunn Vetti,Astrid Stormorken,Eli Marie Grindedal

Hereditary Cancer in Clinical Practiceno. 1 (2024): 1-8

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Comparison of the ABC and ACMG Systems for Variant Classification

Gunnar Houge,Eirik Bratland,Ingvild Aukrust,Kristian Tveten,Gabriele Zukauskaite,Ivona Sansovic,Alejandro J. Brea-Fernandez,Karin Mayer, Teija Paakkola,Caoimhe McKenna, William Wright,Milica Keckarevic Markovic,Dorte L. Lildballe,Michal Konecny,Thomas Smol,Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid,Albena Todorova,Milena Jankovic, Joanna M. Lubieniecka,Maja Stojiljkovic,Marie-Pierre Buisine,Bjorn Ivar Haukanes, Marie Lorans,Hanno Roomere,Francois M. Petit,Maria K. Haanpaa,Claire Beneteau,Belen Perez,Dijana Plaseska-Karanfilska, Matthias Rath,Nico Fuhrmann,Bibiana I. Ferreira,Coralea Stephanou,Wenche Sjursen,Ales Maver,Cecile Rouzier,Adela Chirita-Emandi,Joao Goncalves, Wei Cheng David Kuek,Martin Broly,Lonneke Haer-Wigman,Meow-Keong Thong,Sok-Kun Tae,Michaela Hyblova,Johan T. den Dunnen,Andreas Laner

European Journal of Human Geneticsno. 7 (2024): 858-863

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P19.15.B TERT PROMOTOR MUTATIONS IN ATYPICAL MENINGIOMAS

R Meta, H Dai,W Sjursen, S Torp

Neuro-Oncologyno. Supplement_5 (2024)

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TERT PROMOTOR MUTATIONS IN ATYPICAL MENINGIOMAS

R. Meta, H. Dai,W. Sjursen, S. Torp

NEURO-ONCOLOGY (2024): V114-V115

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Mosaic Gorlin Syndrome with Ophthalmological Developmental Defects and a Mosaic SMO Variant

Cecilie Rustad,Wenche Sjursen,Josephine Prener Holtan, Anvor Rossow,Charlotte von der Lippe, Kristin Halvorsen Hortemo

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 405-405

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An Insertion in the MSH2 Gene Detected by Bionano Optical Mapping and Confirmed by Nanopore Sequencing in a Family with Suspected Lynch Syndrome

Ragnhild Margethe Aalokken,June Asheim,Marianne Dalland,Eli Marie Grindedal,Arvind Y. M. Sundaram,Pal Marius Bjornstad,Wenche Sjursen, Gregor Gilfillian

EUROPEAN JOURNAL OF HUMAN GENETICS（2023）

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MTHFR C677T and A1298C Polymorphism’s Effect on Risk of Colorectal Cancer in Lynch Syndrome

Mariann Unhjem Wiik, Mia Negline,Vidar Beisvåg,Matthew Clapham,Elizabeth Holliday,Nuria Dueñas,Joan Brunet,Marta Pineda,Nuria Bonifaci,Stefan Aretz,Hannah Klinkhammer,Isabel Spier,Claudia Perne,Andreas Mayr,Laura Valle,Jan Lubinski,Wenche Sjursen,Rodney J. Scott,Bente A. Talseth-Palmer

springernature（2023）

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Functional Analyses of Rare Germline Missense BRCA1 Variants Located Within and Outside Protein Domains with Known Functions

Henrikke Nilsen Hovland,Eunice Kabanyana Mchaina,Hildegunn Hoberg-Vetti,Sarah Louise Ariansen,Wenche Sjursen,Marijke Van Ghelue,Bjorn Ivar Haukanes,Per Morten Knappskog,Ingvild Aukrust,Elisabet Ognedal

Genes（2023）

引用3浏览0WOS引用

Merlin expression in human meningiomas - An immunohistochemical study

S. Torp, R. Meta,S. Tollefsen, I. Vestrheim,W. Sjursen

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGYno. 6 (2023): 565-565

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Detecting disease-causing genetic variants in 48 patients with familial colorectal cancer by using whole exome sequencing

Ashish Kumar Singh,Bente Talseth-Palmer,Alexandre Xavier,Rodney J. Scott,Finn Drablos,Wenche Sjursen

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 247-247

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