Dominguez-Valentin M - Search Results

1

Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum.

Dominguez-Valentin M, Sampson JR, Møller P, Seppälä TT; PLSD Collaborators. Dominguez-Valentin M, et al. Int J Cancer. 2021 Jan 15;148(2):512-513. doi: 10.1002/ijc.33214. Epub 2020 Jul 30. Int J Cancer. 2021. PMID: 32783184 Free article. No abstract available.

2

Gain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer.

Therkildsen C, Jönsson G, Dominguez-Valentin M, Nissen A, Rambech E, Halvarsson B, Bernstein I, Borg K, Nilbert M. Therkildsen C, et al. Eur J Cancer. 2013 Apr;49(6):1226-35. doi: 10.1016/j.ejca.2012.11.011. Epub 2012 Dec 11. Eur J Cancer. 2013. PMID: 23245329

3

Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.

Dominguez-Valentin M, Therkildsen C, Veerla S, Jönsson M, Bernstein I, Borg A, Nilbert M. Dominguez-Valentin M, et al. PLoS One. 2013 Aug 12;8(8):e71755. doi: 10.1371/journal.pone.0071755. eCollection 2013. PLoS One. 2013. PMID: 23951239 Free PMC article.

4

Mutation spectrum in South American Lynch syndrome families.

Dominguez-Valentin M, Nilbert M, Wernhoff P, López-Köstner F, Vaccaro C, Sarroca C, Palmero EI, Giraldo A, Ashton-Prolla P, Alvarez K, Ferro A, Neffa F, Caris J, Carraro DM, Rossi BM. Dominguez-Valentin M, et al. Hered Cancer Clin Pract. 2013 Dec 18;11(1):18. doi: 10.1186/1897-4287-11-18. Hered Cancer Clin Pract. 2013. PMID: 24344984 Free PMC article.

5

Familial colorectal cancer type X: genetic profiles and phenotypic features.

Dominguez-Valentin M, Therkildsen C, Da Silva S, Nilbert M. Dominguez-Valentin M, et al. Mod Pathol. 2015 Jan;28(1):30-6. doi: 10.1038/modpathol.2014.49. Epub 2014 Apr 18. Mod Pathol. 2015. PMID: 24743215 Free article. Review.

6

Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome.

Jönsson JM, Bartuma K, Dominguez-Valentin M, Harbst K, Ketabi Z, Malander S, Jönsson M, Carneiro A, Måsbäck A, Jönsson G, Nilbert M. Jönsson JM, et al. Fam Cancer. 2014 Dec;13(4):537-45. doi: 10.1007/s10689-014-9728-1. Fam Cancer. 2014. PMID: 24848881 Free PMC article.

7

Urinary Tract Cancer in Lynch Syndrome; Increased Risk in Carriers of MSH2 Mutations.

Joost P, Therkildsen C, Dominguez-Valentin M, Jönsson M, Nilbert M. Joost P, et al. Urology. 2015 Dec;86(6):1212-7. doi: 10.1016/j.urology.2015.08.018. Epub 2015 Sep 15. Urology. 2015. PMID: 26385421

8

Frequent mismatch-repair defects link prostate cancer to Lynch syndrome.

Dominguez-Valentin M, Joost P, Therkildsen C, Jonsson M, Rambech E, Nilbert M. Dominguez-Valentin M, et al. BMC Urol. 2016 Mar 24;16:15. doi: 10.1186/s12894-016-0130-1. BMC Urol. 2016. PMID: 27013479 Free PMC article.

9

MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.

Dominguez-Valentin M, Wernhoff P, Cajal AR, Kalfayan PG, Piñero TA, Gonzalez ML, Ferro A, Sammartino I, Causada Calo NS, Vaccaro CA. Dominguez-Valentin M, et al. Front Oncol. 2016 Aug 24;6:189. doi: 10.3389/fonc.2016.00189. eCollection 2016. Front Oncol. 2016. PMID: 27606285 Free PMC article. No abstract available.

10

Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.

Dominguez-Valentin M, Nakken S, Tubeuf H, Vodak D, Ekstrøm PO, Nissen AM, Morak M, Holinski-Feder E, Martins A, Møller P, Hovig E. Dominguez-Valentin M, et al. Fam Cancer. 2018 Jan;17(1):141-153. doi: 10.1007/s10689-017-0011-0. Fam Cancer. 2018. PMID: 28608266

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