Kovac M - Search Results

1

Detection of APC germ line mosaicism in patients with de novo familial adenomatous polyposis: a plea for the protein truncation test.

Necker J, Kovac M, Attenhofer M, Reichlin B, Heinimann K. Necker J, et al. Among authors: kovac m. J Med Genet. 2011 Aug;48(8):526-9. doi: 10.1136/jmg.2011.089474. Epub 2011 Jun 7. J Med Genet. 2011. PMID: 21653199

2

Germline RET variants underlie a subset of paediatric osteosarcoma.

Kovac M, Woolley C, Ribi S, Blattmann C, Roth E, Morini M, Kovacova M, Ameline B, Kulozik A, Bielack S, Hartmann W, Ballinger ML, Thomas DM, Tomlinson I, Nathrath M, Heinimann K, Baumhoer D. Kovac M, et al. J Med Genet. 2021 Jan;58(1):20-24. doi: 10.1136/jmedgenet-2019-106734. Epub 2020 Mar 16. J Med Genet. 2021. PMID: 32179705

3

High-resolution breakpoint analysis provides evidence for the sequence-directed nature of genome rearrangements in hereditary disorders.

Kovac MB, Kovacova M, Bachraty H, Bachrata K, Piscuoglio S, Hutter P, Ilencikova D, Bartosova Z, Tomlinson I, Roethlisberger B, Heinimann K. Kovac MB, et al. Hum Mutat. 2015 Feb;36(2):250-9. doi: 10.1002/humu.22734. Hum Mutat. 2015. PMID: 25418510

4

Familial colorectal cancer: eleven years of data from a registry program in Switzerland.

Kovac M, Laczko E, Haider R, Jiricny J, Mueller H, Heinimann K, Marra G. Kovac M, et al. Fam Cancer. 2011 Sep;10(3):605-16. doi: 10.1007/s10689-011-9458-6. Fam Cancer. 2011. PMID: 21671081 Free article.

5

3'-UTR poly(T/U) tract deletions and altered expression of EWSR1 are a hallmark of mismatch repair-deficient cancers.

Kishore S, Piscuoglio S, Kovac MB, Gylling A, Wenzel F, Trapani F, Altermatt HJ, Mele V, Marra G, Peltomäki P, Terracciano L, Zavolan M, Heinimann K. Kishore S, et al. Among authors: kovac mb. Cancer Res. 2014 Jan 1;74(1):224-34. doi: 10.1158/0008-5472.CAN-13-2100. Epub 2013 Oct 24. Cancer Res. 2014. PMID: 24158095

6

Evidence for breast cancer as an integral part of Lynch syndrome.

Buerki N, Gautier L, Kovac M, Marra G, Buser M, Mueller H, Heinimann K. Buerki N, et al. Among authors: kovac m. Genes Chromosomes Cancer. 2012 Jan;51(1):83-91. doi: 10.1002/gcc.20935. Epub 2011 Oct 27. Genes Chromosomes Cancer. 2012. PMID: 22034109

7

SH2D4A is frequently downregulated in hepatocellular carcinoma and cirrhotic nodules.

Quagliata L, Andreozzi M, Kovac M, Tornillo L, Makowska Z, Moretti F, Heim MH, Heinimann K, Piscuoglio S, Terracciano LM. Quagliata L, et al. Among authors: kovac m. Eur J Cancer. 2014 Mar;50(4):731-8. doi: 10.1016/j.ejca.2013.11.018. Epub 2013 Dec 3. Eur J Cancer. 2014. PMID: 24315626

8

Combined analysis of specific KRAS mutation, BRAF and microsatellite instability identifies prognostic subgroups of sporadic and hereditary colorectal cancer.

Zlobec I, Kovac M, Erzberger P, Molinari F, Bihl MP, Rufle A, Foerster A, Frattini M, Terracciano L, Heinimann K, Lugli A. Zlobec I, et al. Among authors: kovac m. Int J Cancer. 2010 Dec 1;127(11):2569-75. doi: 10.1002/ijc.25265. Int J Cancer. 2010. PMID: 20162668

9

Target gene mutational pattern in Lynch syndrome colorectal carcinomas according to tumour location and germline mutation.

Pinheiro M, Pinto C, Peixoto A, Veiga I, Lopes P, Henrique R, Baldaia H, Carneiro F, Seruca R, Tomlinson I, Kovac M, Heinimann K, Teixeira MR. Pinheiro M, et al. Among authors: kovac m. Br J Cancer. 2015 Aug 11;113(4):686-92. doi: 10.1038/bjc.2015.281. Epub 2015 Aug 6. Br J Cancer. 2015. PMID: 26247575 Free PMC article.

10

Convergent Evolution of Copy Number Alterations in Multi-Centric Hepatocellular Carcinoma.

Lackner C, Quagliata L, Cross W, Ribi S, Heinimann K, Paradiso V, Quintavalle C, Kovacova M, Baumhoer D, Piscuoglio S, Terracciano L, Kovac M. Lackner C, et al. Among authors: kovac m. Sci Rep. 2019 Mar 14;9(1):4611. doi: 10.1038/s41598-019-40843-9. Sci Rep. 2019. PMID: 30872650 Free PMC article.

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