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  • 2020
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Author

  • Bettina Meier
Article

Analysis of mutational signatures in C. elegans: Implications for cancer genome analysis

Meier, B., Volkova, N. V., Gerstung, M. & Gartner, A., 28 Aug 2020, In : DNA Repair. 95, 11 p., 102957.

Research output: Contribution to journalArticle

C. elegans whole genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiency.

Meier, B., Cooke, S. L., Weiss, J., Bailly, A. P., Alexandrov, L. B., Marshall, J., Raine, K., Maddison, M., Anderson, E., Stratton, M. R., Gartner, A. & Campbell, P. J., 2014, In : Genome Research. 24, p. 1624-1636 14 p.

Research output: Contribution to journalArticle

Open Access
87 Citations (Scopus)

Combinatorial regulation of meiotic holliday junction resolution in C. elegans by HIM-6 (BLM) helicase, SLX-4, and the SLX-1, MUS-81 and XPF-1 nucleases

Agostinho, A., Meier, B., Sonneville, R., Jagut, M., Woglar, A., Blow, J., Jantsch, V. & Gartner, A., 18 Jul 2013, In : PLoS Genetics. 9, 7, e1003591.

Research output: Contribution to journalArticle

55 Citations (Scopus)

Having a direct look: analysis of DNA damage and repair mechanisms by next generation sequencing

Meier, B. & Gartner, A., 15 Nov 2014, In : Experimental Cell Research. 329, 1, p. 35-41 7 p.

Research output: Contribution to journalArticle

Open Access
File
5 Citations (Scopus)
162 Downloads (Pure)

Mutational signatures are jointly shaped by DNA damage and repair

Volkova, N. V., Meier, B., González-Huici, V., Bertolini, S., Gonzalez, S., Vöhringer, H., Abascal, F., Martincorena, I., Campbell, P. J., Gartner, A. & Gerstung, M., 1 May 2020, In : Nature Communications. 11, p. 1-15 15 p., 2169.

Research output: Contribution to journalArticle

Open Access
File
6 Citations (Scopus)
26 Downloads (Pure)
Open Access
File
13 Citations (Scopus)
297 Downloads (Pure)
Letter

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Shlien, A., Campbell, B. B., De Borja, R., Alexandrov, L. B., Merico, D., Wedge, D., Van Loo, P., Tarpey, P. S., Coupland, P., Behjati, S., Pollett, A., Lipman, T., Heidari, A., Deshmukh, S., Avitzur, N., Meier, B., Gerstung, M., Hong, Y., Merino, D. M., Ramakrishna, M. & 31 others, Remke, M., Arnold, R., Panigrahi, G. B., Thakkar, N. P., Hodel, K. P., Henninger, E. E., Göksenin, A. Y., Bakry, D., Charames, G. S., Druker, H., Lerner-Ellis, J., Mistry, M., Dvir, R., Grant, R., Elhasid, R., Farah, R., Taylor, G. P., Nathan, P. C., Alexander, S., Ben-Shachar, S., Ling, S. C., Gallinger, S., Constantini, S., Dirks, P., Huang, A., Scherer, S. W., Grundy, R. G., Durno, C., Aronson, M., Gartner, A. & for the Biallelic Mismatch Repair Deficiency Consortium, 2 Feb 2015, In : Nature Genetics. 47, 3, p. 257-262 6 p.

Research output: Contribution to journalLetter

184 Citations (Scopus)