Detalhe da pesquisa
1.
Deep Learning-Enabled Diagnosis of Liver Adenocarcinoma.
Gastroenterology
; 165(5): 1262-1275, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37562657
2.
Accurate and efficient detection of gene fusions from RNA sequencing data.
Genome Res
; 31(3): 448-460, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33441414
3.
Profound tumor response to combined CTLA-4 and PD-1 inhibition in systemic fourth line therapy observed in a patient with hepatocellular carcinoma harboring SETD2 and LRP1B mutations.
Z Gastroenterol
; 61(1): 71-75, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36379463
4.
Prognostic impact of copy number alterations and tumor mutational burden in carcinoma of unknown primary.
Genes Chromosomes Cancer
; 61(9): 551-560, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35430765
5.
Assigning evidence to actionability: An introduction to variant interpretation in precision cancer medicine.
Genes Chromosomes Cancer
; 61(6): 303-313, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34331337
6.
Integrative analysis reveals early and distinct genetic and epigenetic changes in intraductal papillary and tubulopapillary cholangiocarcinogenesis.
Gut
; 71(2): 391-401, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33468537
7.
Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing.
Br J Cancer
; 127(8): 1540-1549, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35871236
8.
KRAS/GNAS-testing by highly sensitive deep targeted next generation sequencing improves the endoscopic ultrasound-guided workup of suspected mucinous neoplasms of the pancreas.
Genes Chromosomes Cancer
; 60(7): 489-497, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33686791
9.
[Variant interpretation in molecular pathology and oncology : An introduction]. / Varianteninterpretation in der molekularen Pathologie und Onkologie : Eine Einführung.
Pathologe
; 42(4): 369-379, 2021 Jul.
Artigo
em Alemão
| MEDLINE | ID: mdl-33938987
10.
Immuno-oncology gene expression profiling of formalin-fixed and paraffin-embedded clear cell renal cell carcinoma: Performance comparison of the NanoString nCounter technology with targeted RNA sequencing.
Genes Chromosomes Cancer
; 59(7): 406-416, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32212351
11.
Integrated clinicomolecular characterization identifies RAS activation and CDKN2A deletion as independent adverse prognostic factors in cancer of unknown primary.
Int J Cancer
; 146(11): 3053-3064, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31970771
12.
Nuclear pore component Nup98 is a potential tumor suppressor and regulates posttranscriptional expression of select p53 target genes.
Mol Cell
; 48(5): 799-810, 2012 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23102701
13.
Next generation sequencing of the cellular and liquid fraction of pancreatic cyst fluid supports discrimination of IPMN from pseudocysts and reveals cases with multiple mutated driver clones: First findings from the prospective ZYSTEUS biomarker study.
Genes Chromosomes Cancer
; 58(1): 3-11, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30230086
14.
RSPO2 gene rearrangement: a powerful driver of ß-catenin activation in liver tumours.
Gut
; 68(7): 1287-1296, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30901310
15.
Comparative genetic profiling aids diagnosis and clinical decision making in challenging cases of CUP syndrome.
Int J Cancer
; 145(11): 2963-2973, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30963573
16.
Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real-life analysis of three larger gene panels.
Int J Cancer
; 144(9): 2303-2312, 2019 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30446996
17.
Size matters: Dissecting key parameters for panel-based tumor mutational burden analysis.
Int J Cancer
; 144(4): 848-858, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30238975
18.
Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: Analysis of the first 3,000 Heidelberg cases.
Int J Cancer
; 145(3): 649-661, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30653256
19.
Variant classification in precision oncology.
Int J Cancer
; 145(11): 2996-3010, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31008532
20.
Erratum zu: Varianteninterpretation in dermolekularen Pathologie und Onkologie.
Pathologe
; 42(6): 602, 2021 Nov.
Artigo
em Alemão
| MEDLINE | ID: mdl-34605937