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Page 1
A holistic approach to maximise diagnostic output in trio exome sequencing.
Front Pediatr. 2023 May 19;11:1183891. doi: 10.3389/fped.2023.1183891. eCollection 2023.
Front Pediatr. 2023.
PMID: 37274821
Free PMC article.
12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature.
Heldt F, Wallaschek H, Ripperger T, Morlot S, Illig T, Eggermann T, Schlegelberger B, Scholz C, Steinemann D.
Heldt F, et al. Among authors: wallaschek h.
Eur J Med Genet. 2018 Aug;61(8):421-427. doi: 10.1016/j.ejmg.2018.02.010. Epub 2018 Mar 1.
Eur J Med Genet. 2018.
PMID: 29501611
Review.
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MiR-129-5p exerts Wnt signaling-dependent tumor-suppressive functions in hepatocellular carcinoma by directly targeting hepatoma-derived growth factor HDGF.
Huge N, Reinkens T, Buurman R, Sandbothe M, Bergmann A, Wallaschek H, Vajen B, Stalke A, Decker M, Eilers M, Schäffer V, Dittrich-Breiholz O, Gürlevik E, Kühnel F, Schlegelberger B, Illig T, Skawran B.
Huge N, et al. Among authors: wallaschek h.
Cancer Cell Int. 2022 May 16;22(1):192. doi: 10.1186/s12935-022-02582-2.
Cancer Cell Int. 2022.
PMID: 35578240
Free PMC article.
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Plasma Metabolome Signature Indicative of BRCA1 Germline Status Independent of Cancer Incidence.
Penkert J, Märtens A, Seifert M, Auber B, Derlin K, Hille-Betz U, Hörmann P, Klopp N, Prokein J, Schlicker L, Wacker F, Wallaschek H, Schlegelberger B, Hiller K, Ripperger T, Illig T.
Penkert J, et al. Among authors: wallaschek h.
Front Oncol. 2021 Apr 7;11:627217. doi: 10.3389/fonc.2021.627217. eCollection 2021.
Front Oncol. 2021.
PMID: 33898308
Free PMC article.
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Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1.
Castle AMR, Salian S, Bassan H, Sofrin-Drucker E, Cusmai R, Herman KC, Heron D, Keren B, Johnstone DL, Mears W, Morlot S, Nguyen TTM, Rock R, Stolerman E, Russo J, Burns WB, Jones JR, Serpieri V, Wallaschek H, Zanni G, Dyment DA, Campeau PM.
Castle AMR, et al. Among authors: wallaschek h.
Neurol Genet. 2021 Oct 21;7(6):e631. doi: 10.1212/NXG.0000000000000631. eCollection 2021 Dec.
Neurol Genet. 2021.
PMID: 34703884
Free PMC article.
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Psychological Distress and Coping Ability of Women at High Risk of Hereditary Breast and Ovarian Cancer before Undergoing Genetic Counseling-An Exploratory Study from Germany.
Vajen B, Rosset M, Wallaschek H, Baumann E, Schlegelberger B.
Vajen B, et al. Among authors: wallaschek h.
Int J Environ Res Public Health. 2021 Apr 19;18(8):4338. doi: 10.3390/ijerph18084338.
Int J Environ Res Public Health. 2021.
PMID: 33921890
Free PMC article.
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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: wallaschek h.
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.
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