Kamu erişimi zorunlu olan makaleler - Albrecht Stenzinger, MDDaha fazla bilgi edinin
Hiçbir yerde sunulmuyor: 39
İncele
NRG1 Fusions in KRAS Wild-Type Pancreatic Cancer
C Heining, P Horak, S Uhrig, PL Codo, B Klink, B Hutter, M Fröhlich, ...
Cancer discovery 8 (9), 1087-1095, 2018
Zorunlu olanlar: Helmholtz Association, Federal Ministry of Education and Research, Germany
İncele
Comprehensive genomic and transcriptomic analysis for guiding therapeutic decisions in patients with rare cancers
P Horak, C Heining, S Kreutzfeldt, B Hutter, A Mock, J Hüllein, M Fröhlich, ...
Cancer discovery 11 (11), 2780-2795, 2021
Zorunlu olanlar: Helmholtz Association
İncele
Size matters: dissecting key parameters for panel‐based tumor mutational burden analysis
I Buchhalter, E Rempel, V Endris, M Allgäuer, O Neumann, AL Volckmar, ...
International journal of cancer 144 (4), 848-858, 2019
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real‐life analysis of three larger gene panels
V Endris, I Buchhalter, M Allgäuer, E Rempel, A Lier, AL Volckmar, ...
International journal of cancer 144 (9), 2303-2312, 2019
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Variant classification in precision oncology
J Leichsenring, P Horak, S Kreutzfeldt, C Heining, P Christopoulos, ...
International Journal of Cancer 145 (11), 2996-3010, 2019
Zorunlu olanlar: Helmholtz Association
İncele
Identification of a highly lethal V3+TP53+ subset in ALK+ lung adenocarcinoma
P Christopoulos, M Kirchner, F Bozorgmehr, V Endris, M Elsayed, ...
International Journal of Cancer 144 (1), 190-199, 2019
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Cancer beyond organ and tissue specificity: next‐generation‐sequencing gene mutation data reveal complex genetic similarities across major cancers
D Heim, J Budczies, A Stenzinger, D Treue, P Hufnagl, C Denkert, ...
International journal of cancer 135 (10), 2362-2369, 2014
Zorunlu olanlar: Human Frontier Science Program
İncele
Mutational diversity and therapy response in breast cancer: a sequencing analysis in the neoadjuvant GeparSepto trial
S Loibl, D Treue, J Budczies, K Weber, A Stenzinger, WD Schmitt, ...
Clinical Cancer Research 25 (13), 3986-3995, 2019
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Mutation patterns in genes encoding interferon signaling and antigen presentation: A pan‐cancer survey with implications for the use of immune checkpoint inhibitors
J Budczies, M Bockmayr, F Klauschen, V Endris, S Fröhling, ...
Genes, Chromosomes and Cancer 56 (8), 651-659, 2017
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Copy number changes of clinically actionable genes in melanoma, non‐small cell lung cancer and colorectal cancer—A survey across 822 routine diagnostic cases
N Pfarr, R Penzel, F Klauschen, D Heim, R Brandt, D Kazdal, ...
Genes, Chromosomes and Cancer 55 (11), 821-833, 2016
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Fully automatic deep learning in bi-institutional prostate magnetic resonance imaging: effects of cohort size and heterogeneity
N Netzer, C Weißer, P Schelb, X Wang, X Qin, M Görtz, V Schütz, ...
Investigative radiology 56 (12), 799-808, 2021
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Risk stratification of EGFR+ lung cancer diagnosed with panel-based next-generation sequencing
P Christopoulos, M Kirchner, J Roeper, F Saalfeld, M Janning, ...
Lung cancer 148, 105-112, 2020
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Trailblazing precision medicine in Europe: A joint view by Genomic Medicine Sweden and the Centers for Personalized Medicine, ZPM, in Germany
A Stenzinger, A Edsjö, C Ploeger, M Friedman, S Fröhling, V Wirta, ...
Seminars in cancer biology 84, 242-254, 2022
Zorunlu olanlar: Vinnova, Sweden
İncele
RSPO2 gene rearrangement: a powerful driver of β-catenin activation in liver tumours
T Longerich, V Endris, O Neumann, E Rempel, M Kirchner, Z Abadi, ...
Gut 68 (7), 1287-1296, 2019
Zorunlu olanlar: German Research Foundation, Federal Ministry of Education and Research, Germany
İncele
Quantifying potential confounders of panel-based tumor mutational burden (TMB) measurement
J Budczies, D Kazdal, M Allgäuer, P Christopoulos, E Rempel, N Pfarr, ...
Lung Cancer 142, 114-119, 2020
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
KIT-dependent and KIT-independent genomic heterogeneity of resistance in gastrointestinal stromal tumors—TORC1/2 inhibition as salvage strategy
T Mühlenberg, J Ketzer, MC Heinrich, S Grunewald, A Marino-Enriquez, ...
Molecular cancer therapeutics 18 (11), 1985-1996, 2019
Zorunlu olanlar: US Department of Veterans Affairs
İncele
Targeted next‐generation sequencing enables reliable detection of HER2 (ERBB2) status in breast cancer and provides ancillary information of clinical relevance
N Pfarr, R Penzel, V Endris, C Lier, C Flechtenmacher, AL Volckmar, ...
Genes, Chromosomes and Cancer 56 (4), 255-265, 2017
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Validating comprehensive next-generation sequencing results for precision oncology: the NCT/DKTK molecularly aided stratification for tumor eradication research experience
A Lier, R Penzel, C Heining, P Horak, M Fröhlich, S Uhrig, J Budczies, ...
JCO Precision Oncology 2, 1-13, 2018
Zorunlu olanlar: Helmholtz Association
İncele
Global DNA methylation reflects spatial heterogeneity and molecular evolution of lung adenocarcinomas
S Dietz, A Lifshitz, D Kazdal, A Harms, V Endris, H Winter, A Stenzinger, ...
International journal of cancer 144 (5), 1061-1072, 2019
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
İncele
Combined immunohistochemistry after mass spectrometry imaging for superior spatial information
K Kriegsmann, R Longuespée, M Hundemer, C Zgorzelski, R Casadonte, ...
PROTEOMICS–Clinical Applications 13 (1), 1800035, 2019
Zorunlu olanlar: Federal Ministry of Education and Research, Germany
Yayıncılık ve maddi kaynak bilgileri otomatik olarak bir bilgisayar programı tarafından belirlenmektedir