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MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies.
Ripperger T, Hofmann W, Koch JC, Shirneshan K, Haase D, Wulf G, Issing PR, Karnebogen M, Schmidt G, Auber B, Schlegelberger B, Illig T, Zirn B, Steinemann D. Ripperger T, et al. Among authors: schmidt g. Haematologica. 2018 Feb;103(2):e55-e58. doi: 10.3324/haematol.2017.178723. Epub 2017 Nov 2. Haematologica. 2018. PMID: 29097497 Free PMC article. No abstract available.
Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
Penkert J, Schmidt G, Hofmann W, Schubert S, Schieck M, Auber B, Ripperger T, Hackmann K, Sturm M, Prokisch H, Hille-Betz U, Mark D, Illig T, Schlegelberger B, Steinemann D. Penkert J, et al. Among authors: schmidt g. Breast Cancer Res. 2018 Aug 7;20(1):87. doi: 10.1186/s13058-018-1011-1. Breast Cancer Res. 2018. PMID: 30086788 Free PMC article.
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants.
Schubert S, van Luttikhuizen JL, Auber B, Schmidt G, Hofmann W, Penkert J, Davenport CF, Hille-Betz U, Wendeburg L, Bublitz J, Tauscher M, Hackmann K, Schröck E, Scholz C, Wallaschek H, Schlegelberger B, Illig T, Steinemann D. Schubert S, et al. Among authors: schmidt g. Int J Cancer. 2019 Jun 1;144(11):2683-2694. doi: 10.1002/ijc.31992. Epub 2019 Jan 11. Int J Cancer. 2019. PMID: 30426508 Free article.
From a variant of unknown significance to pathogenic: Reclassification of a large novel duplication in BRCA2 by high-throughput sequencing.
van Luttikhuizen JL, Bublitz J, Schubert S, Schmidt G, Hofmann W, Morlot S, Buurman R, Auber B, Schlegelberger B, Steinemann D. van Luttikhuizen JL, et al. Among authors: schmidt g. Mol Genet Genomic Med. 2020 Sep;8(9):e1045. doi: 10.1002/mgg3.1045. Epub 2019 Nov 13. Mol Genet Genomic Med. 2020. PMID: 31724318 Free PMC article.
Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotype.
Warnstorf D, Bawadi R, Schienke A, Strasser R, Schmidt G, Illig T, Tauscher M, Thol F, Heuser M, Steinemann D, Davenport C, Schlegelberger B, Behrens YL, Göhring G. Warnstorf D, et al. Among authors: schmidt g. Genes Chromosomes Cancer. 2021 Jun;60(6):452-457. doi: 10.1002/gcc.22938. Epub 2021 Feb 19. Genes Chromosomes Cancer. 2021. PMID: 33486841
A common ancestral DNMT3A-mutated preleukemic clone giving rise to AML and MDS in an adolescent girl.
Göhring G, Thomay K, Schmidt G, Ripperger T, Xu M, Wittner N, Chao MM, Baumann I, Niewisch M, Reinhardt D, Klingebiel T, Thol F, Schlegelberger B, Niemeyer CM. Göhring G, et al. Among authors: schmidt g. Leuk Lymphoma. 2017 Mar;58(3):718-721. doi: 10.1080/10428194.2016.1207765. Epub 2016 Nov 28. Leuk Lymphoma. 2017. PMID: 27892742 No abstract available.
2,624 results