Publications:

Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs7607076

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

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Inversion of exons 1-7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population.

Familial Cancer

Rhees, Jennifer J; Arnold, Mildred M; Boland, C Richard CR

Publication Date: 2014-06

Variant appearance in text: rs7607076

PubMed Link: 24114314

Variant Present in the following documents:

• Main text

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DNA repair gene variants are associated with an increased risk of myelodysplastic syndromes in a Czech population.

Journal Of Hematology & Oncology

Belickova, Monika M; Merkerova, Michaela Dostalova MD; Stara, Eliska E; Vesela, Jitka J; Sponerova, Dana D; Mikulenkova, Dana D; Brdicka, Radim R; Neuwirtova, Radana R; Jonasova, Anna A; Cermak, Jaroslav J

Publication Date: 2013-01-22

Variant appearance in text: rs7607076

PubMed Link: 23339595

Variant Present in the following documents:

• Main text
• 1756-8722-6-9.pdf

View BVdb publication page