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Germline variant affecting p53β isoforms predisposes to familial cancer.
Schubert SA, Ruano D, Joruiz SM, Stroosma J, Glavak N, Montali A, Pinto LM, Rodríguez-Girondo M, Barge-Schaapveld DQCM, Nielsen M, van Nesselrooij BPM, Mensenkamp AR, van Leerdam ME, Sharp TH, Morreau H, Bourdon JC, de Miranda NFCC, van Wezel T. Schubert SA, et al. Nat Commun. 2024 Sep 18;15(1):8208. doi: 10.1038/s41467-024-52551-8. Nat Commun. 2024. PMID: 39294166 Free PMC article.
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
Schubert SA, Ruano D, Elsayed FA, Boot A, Crobach S, Sarasqueta AF, Wolffenbuttel B, van der Klauw MM, Oosting J, Tops CM, van Eijk R, Vasen HF, Vossen RH, Nielsen M, Castellví-Bel S, Ruiz-Ponte C, Tomlinson I, Dunlop MG, Vodicka P, Wijnen JT, Hes FJ, Morreau H, de Miranda NF, Sijmons RH, van Wezel T. Schubert SA, et al. Br J Cancer. 2017 Sep 5;117(6):1215-1223. doi: 10.1038/bjc.2017.240. Epub 2017 Jul 25. Br J Cancer. 2017. PMID: 28742792 Free PMC article.
The missing heritability of familial colorectal cancer.
Schubert SA, Morreau H, de Miranda NFCC, van Wezel T. Schubert SA, et al. Mutagenesis. 2020 Jul 11;35(3):221-231. doi: 10.1093/mutage/gez027. Mutagenesis. 2020. PMID: 31605533 Free PMC article. Review.
Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer.
Schubert SA, Ruano D, Tiersma Y, Drost M, de Wind N, Nielsen M, van Hest LP, Morreau H, de Miranda NFCC, van Wezel T. Schubert SA, et al. Genes Chromosomes Cancer. 2020 Jul 2;59(12):697-701. doi: 10.1002/gcc.22883. Online ahead of print. Genes Chromosomes Cancer. 2020. PMID: 32615015 Free PMC article.
Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome.
Golubicki M, Bonjoch L, Acuña-Ochoa JG, Díaz-Gay M, Muñoz J, Cuatrecasas M, Ocaña T, Iseas S, Mendez G, Cisterna D, Schubert SA, Nielsen M, van Wezel T, Goldberg Y, Pikarsky E, Robbio J, Roca E, Castells A, Balaguer F, Antelo M, Castellví-Bel S. Golubicki M, et al. Among authors: schubert sa. JCI Insight. 2020 Sep 17;5(18):e140698. doi: 10.1172/jci.insight.140698. JCI Insight. 2020. PMID: 32841224 Free PMC article.
Germline NPAT inactivating variants as cause of hereditary colorectal cancer.
Terradas M, Schubert SA, Viana-Errasti J, Ruano D, Aiza G, Nielsen M, Marciel P, Tops CM, Parra G, Morreau H, Torrents D, van Leerdam ME, Capellá G, de Miranda NFCC, Valle L, van Wezel T. Terradas M, et al. Among authors: schubert sa. Eur J Hum Genet. 2024 Jul;32(7):871-875. doi: 10.1038/s41431-024-01625-8. Epub 2024 May 22. Eur J Hum Genet. 2024. PMID: 38778081
Divergent WNT signaling and drug sensitivity profiles within hepatoblastoma tumors and organoids.
Kluiver TA, Lu Y, Schubert SA, Kraaier LJ, Ringnalda F, Lijnzaad P, DeMartino J, Megchelenbrink WL, Amo-Addae V, Eising S, de Faria FW, Münter D, van de Wetering M, Kerl K, Duiker E, van den Heuvel MC, de Meijer VE, de Kleine RH, Molenaar JJ, Margaritis T, Stunnenberg HG, de Krijger RR, Zsiros J, Clevers H, Peng WC. Kluiver TA, et al. Among authors: schubert sa. Nat Commun. 2024 Nov 20;15(1):8576. doi: 10.1038/s41467-024-52757-w. Nat Commun. 2024. PMID: 39567475 Free PMC article.
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
Schubert SA, Ruano D, Elsayed FA, Boot A, Crobach S, Sarasqueta AF, Wolffenbuttel B, van der Klauw MM, Oosting J, Tops CM, van Eijk R, Vasen HF, Vossen RH, Nielsen M, Castellví-Bel S, Ruiz-Ponte C, Tomlinson I, Dunlop MG, Vodicka P, Wijnen JT, Hes FJ, Morreau H, de Miranda NF, Sijmons RH, van Wezel T. Schubert SA, et al. Br J Cancer. 2018 Jan;118(2):e4. doi: 10.1038/bjc.2017.380. Epub 2017 Oct 12. Br J Cancer. 2018. PMID: 29361631 Free PMC article. No abstract available.
26 results