Genetic modifiers of cancer risk in Lynch syndrome: a review

द्वारा Talseth-Palmer, Bente A., Wijnen, Juul T., Grice, Desma M., Scott, Rodney J.
प्रकाशित 2013

8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome

द्वारा Talseth-Palmer, Bente A, Scott, Rodney J, Vasen, Hans F A, Wijnen, Juul T
प्रकाशित 2012

The Risk of Extra-colonic, Extra-endometrial Cancer in the Lynch Syndrome

द्वारा Watson, Patrice, Vasen, Hans F.A., Mecklin, Jukka-Pekka, Bernstein, Inge, Aarnio, Markku, Järvinen, Heikki J., Myrhøj, Torben, Sunde, Lone, Wijnen, Juul T., Lynch, Henry T.
प्रकाशित 2008

Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses

द्वारा van der Klift, Heleen M, Jansen, Anne M L, van der Steenstraten, Niki, Bik, Elsa C, Tops, Carli M J, Devilee, Peter, Wijnen, Juul T
में प्रकाशित Mol Genet Genomic Med (2015)

Conventional and Tissue Microarray Immunohistochemical Expression Analysis of Mismatch Repair in Hereditary Colorectal Tumors

द्वारा Hendriks, Yvonne, Franken, Patrick, Dierssen, Jan Willem, de Leeuw, Wiljo, Wijnen, Juul, Dreef, Enno, Tops, Carli, Breuning, Martijn, Bröcker-Vriends, Annette, Vasen, Hans, Fodde, Riccardo, Morreau, Hans
प्रकाशित 2003

Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome

द्वारा Bellido, Fernando, Guinó, Elisabet, Jagmohan-Changur, Shantie, Seguí, Nuria, Pineda, Marta, Navarro, Matilde, Lázaro, Conxi, Blanco, Ignacio, Vasen, Hans FA, Moreno, Victor, Capellá, Gabriel, Wijnen, Juul T, Valle, Laura
प्रकाशित 2013

Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer

द्वारा Crobach, Stijn, Jansen, Anne M. L., Ligtenberg, Marjolein J. L., Koopmans, Marije, Nielsen, Maartje, Hes, Frederik J., Wijnen, Juul T., Dinjens, Winand N. M., van Wezel, Tom, Morreau, Hans
में प्रकाशित Fam Cancer (2017)

RNA analysis of cancer predisposing genes in formalin-fixed paraffin-embedded tissue determines aberrant splicing

द्वारा Jansen, Anne ML, van der Klift, Heleen M, Roos, Marieke AE, van Eendenburg, Jaap DH, Tops, Carli MJ, Wijnen, Juul T, Hes, Frederik J, Morreau, Hans, van Wezel, Tom
में प्रकाशित Eur J Hum Genet (2018)

The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material

द्वारा Jansen, Anne M. L., Tops, Carli M. J., Ruano, Dina, van Eijk, Ronald, Wijnen, Juul T., ten Broeke, Sanne, Nielsen, Maartje, Hes, Frederik J., van Wezel, Tom, Morreau, Hans
में प्रकाशित Eur J Hum Genet (2019)

Exome Sequencing of Germline DNA from Non-BRCA1/2 Familial Breast Cancer Cases Selected on the Basis of aCGH Tumor Profiling

द्वारा Hilbers, Florentine S., Meijers, Caro M., Laros, Jeroen F. J., van Galen, Michiel, Hoogerbrugge, Nicoline, Vasen, Hans F. A., Nederlof, Petra M., Wijnen, Juul T., van Asperen, Christi J., Devilee, Peter
प्रकाशित 2013

A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer

द्वारा Middeldorp, Anneke, Jagmohan-Changur, Shantie, Helmer, Quinta, van der Klift, Heleen M, Tops, Carli MJ, Vasen, Hans FA, Devilee, Peter, Morreau, Hans, Houwing-Duistermaat, Jeanine J, Wijnen, Juul T, van Wezel, Tom
प्रकाशित 2007

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients

द्वारा Talseth-Palmer, Bente A, Wijnen, Juul T, Andreassen, Eva K, Barker, Daniel, Jagmohan-Changur, Shantie, Tops, Carli M, Meldrum, Cliff, Spigelman, Allan, Hes, Frederik J, Van Wezel, Tom, Vasen, Hans FA, Scott, Rodney J
प्रकाशित 2013

Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers

द्वारा Jansen, Anne ML, van Wezel, Tom, van den Akker, Brendy EWM, Ventayol Garcia, Marina, Ruano, Dina, Tops, Carli MJ, Wagner, Anja, Letteboer, Tom GW, Gómez-García, Encarna B, Devilee, Peter, Wijnen, Juul T, Hes, Frederik J, Morreau, Hans
में प्रकाशित Eur J Hum Genet (2016)

A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants

द्वारा Wiik, Mariann Unhjem, Evans, Tiffany-Jane, Belhadj, Sami, Bolton, Katherine A., Dymerska, Dagmara, Jagmohan-Changur, Shantie, Capellá, Gabriel, Kurzawski, Grzegorz, Wijnen, Juul T., Valle, Laura, Vasen, Hans F. A., Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A.
में प्रकाशित Sci Rep (2021)

Macrophages inhibit human osteosarcoma cell growth after activation with the bacterial cell wall derivative liposomal muramyl tripeptide in combination with interferon-γ

द्वारा Pahl, Jens HW, Kwappenberg, Kitty MC, Varypataki, Eleni M, Santos, Susy J, Kuijjer, Marieke L, Mohamed, Susan, Wijnen, Juul T, van Tol, Maarten JD, Cleton-Jansen, Anne-Marie, Egeler, R Maarten, Jiskoot, Wim, Lankester, Arjan C, Schilham, Marco W
प्रकाशित 2014

Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer

द्वारा Elsayed, Fadwa A, Kets, C Marleen, Ruano, Dina, van den Akker, Brendy, Mensenkamp, Arjen R, Schrumpf, Melanie, Nielsen, Maartje, Wijnen, Juul T, Tops, Carli M, Ligtenberg, Marjolijn J, Vasen, Hans FA, Hes, Frederik J, Morreau, Hans, van Wezel, Tom
में प्रकाशित Eur J Hum Genet (2015)

MUTYH gene variants and breast cancer in a Dutch case–control study

द्वारा Out, Astrid A., Wasielewski, Marijke, Huijts, Petra E. A., van Minderhout, Ivonne J. H. M., Houwing-Duistermaat, Jeanine J., Tops, Carli M. J., Nielsen, Maartje, Seynaeve, Caroline, Wijnen, Juul T., Breuning, Martijn H., van Asperen, Christi J., Schutte, Mieke, Hes, Frederik J., Devilee, Peter
प्रकाशित 2012

Cancer occurrence during follow-up of the CAPP2 study -aspirin use for up to four years significantly reduces Lynch syndrome cancers for up to several years after completion of the...

द्वारा Burn, John, Mathers, John C, Gerdes, Anne-Marie, Bisgaard, MarieLuise, Evans, Gareth, Eccles, Diana, Lindblom, Annika, Macrae, Findlay, Maher, Eamonn R, Mecklin, Jukka-Pekka, Moslein, Gabriela, Olschwang, Sylviane, Ramesar, Raj, Vasen, Hans FA, Wijnen, Juul, Barker, Gail, Elliott, Faye, Lynch, Henry, Bishop, D Tim
प्रकाशित 2010

Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry

द्वारा Vasen, Hans F. A., Velthuizen, Mary E., Kleibeuker, Jan H., Menko, Fred H., Nagengast, Fokke M., Cats, Annemieke, van der Meulen-de Jong, Andrea E., Breuning, Martijn H., Roukema, Anne J., van Leeuwen-Cornelisse, Inge, de Vos tot Nederveen Cappel, Wouter H., Wijnen, Juul T.
में प्रकाशित Fam Cancer (2016)

Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome – a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts

द्वारा Talseth-Palmer, Bente A, Wijnen, Juul T, Brenne, Ingvild S, Jagmohan-Changur, Shantie, Ashton, Katie A, Tops, Carli M, Evans, Tiffany-Jane, McPhillips, Mary, Groombridge, Claire, Suchy, Janina, Kurzawski, Grzegorz, Spigelman, Allan, Møller, Pål, Morreau, Hans M, Van Wezel, Tom, Lubinski, Jan, Vasen, Hans FA, Scott, Rodney J
प्रकाशित 2012