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2019
Mark EPCAM mutation update : Variants associated with congenital tufting enteropathy and Lynch syndrome
Pathak, Sagar J. ; Mueller, James L. ; Okamoto, Kevin ; Das, Barun ; Hertecant, Jozef ; Greenhalgh, Lynn ; Cole, Trevor ; Pinsk, Vered ; Yerushalmi, Baruch and Gurkan, Odul E. , et al. (2019) In Human Mutation 40(2). p.142-161
- Contribution to journal › Article
Mark Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predisposition
Lindberg, Lars J. ; Wegen-Haitsma, Wia ; Ladelund, Steen ; Smith-Hansen, Lars ; Therkildsen, Christina ^LU ; Bernstein, Inge and Nilbert, Mef ^LU (2019) In Familial Cancer 18(2). p.183-191
- Contribution to journal › Article
Mark Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes
Brandão, Rita D. ; Mensaert, Klaas ; López-Perolio, Irene ; Tserpelis, Demis ; Xenakis, Markos ; Lattimore, Vanessa ; Walker, Logan C. ; Kvist, Anders ^LU ; Vega, Ana and Gutiérrez-Enríquez, Sara , et al. (2019) In International Journal of Cancer 145(2). p.401-414
- Contribution to journal › Article
2018
Mark A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families 11 Medical and Health Sciences 1112 Oncology and Carcinogenesis 11 Medical and Health Sciences 1117 Public Health and Health Services
Karimi, Masoud ; Von Salomé, Jenny ; Aravidis, Christos ; Silander, Gustav ; Askmalm, Marie Stenmark ^LU ; Henriksson, Isabelle ; Gebre-Medhin, Samuel ^LU ; Frödin, Jan Erik ; Björck, Erik and Lagerstedt-Robinson, Kristina , et al. (2018) In Hereditary Cancer in Clinical Practice 16(1).
- Contribution to journal › Article
Mark Molecular subtype classification of urothelial carcinoma in Lynch syndrome
Therkildsen, Christina ^LU ; Eriksson, Pontus ^LU ; Höglund, Mattias ^LU ; Jönsson, Mats ^LU ; Sjödahl, Gottfrid ^LU ; Nilbert, Mef ^LU and Liedberg, Fredrik ^LU (2018) In Molecular Oncology 12(8). p.1286-1295
- Contribution to journal › Article
2017
Mark Differential expression of CK20, β-catenin, and MUC2/5AC/6 in Lynch syndrome and familial colorectal cancer type X
Haraldsson, Stefan ; Klarskov, Louise ; Nilbert, Mef ^LU ; Bernstein, Inge ; Bonde, Jesper and Holck, Susanne (2017) In BMC Clinical Pathology 17(1).
- Contribution to journal › Article
Mark Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
Rohlin, Anna ^LU ; Rambech, Eva ^LU ; Kvist, Anders ^LU ; Törngren, Therese ^LU ; Eiengård, Frida ; Lundstam, Ulf ; Zagoras, Theofanis ; Gebre-Medhin, Samuel ^LU ; Borg, Åke ^LU and Björk, Jan , et al. (2017) In Familial Cancer 16(2). p.195-203
- Contribution to journal › Article
2016
Mark Renal cell cancer linked to Lynch syndrome : Increased incidence and loss of mismatch repair protein expression
Therkildsen, Christina ^LU ; Joost, Patrick ^LU ; Lindberg, Lars Joachim ; Ladelund, Steen ; Smith-Hansen, Lars and Nilbert, Mef ^LU (2016) In International Journal of Urology 23(6). p.528-529
- Contribution to journal › Article
Mark Update on hereditary colorectal cancer
Da Silva, Felipe Carneiro ; Wernhoff, Patrik ^LU ; Dominguez-Barrera, Constantino and Dominguez-Valentin, Mev (2016) In Anticancer research 36(9). p.4399-4406
- Contribution to journal › Scientific review
Mark MLH1 Ile219Val polymorphism in argentinean families with suspected lynch syndrome
Dominguez-Valentin, Mev ; Wernhoff, Patrik ^LU ; Cajal, Andrea R. ; Kalfayan, Pablo G. ; Piñero, Tamara A. ; Gonzalez, Maria L. ; Ferro, Alejandra ; Sammartino, Ines ; Causada Calo, Natalia S. and Vaccaro, Carlos A. (2016) In Frontiers in Oncology 6(AUG).
- Contribution to journal › Article

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