Detalhe da pesquisa
1.
Knowledge bases and software support for variant interpretation in precision oncology.
Brief Bioinform
; 22(6)2021 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33971666
2.
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
3.
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
4.
RREB1-MKL2 fusion in a spindle cell sinonasal sarcoma: biphenotypic sinonasal sarcoma or ectomesenchymal chondromyxoid tumor in an unusual site?
Genes Chromosomes Cancer
; 60(8): 565-570, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33715240
5.
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
6.
Genomic Characterization of Cholangiocarcinoma in Primary Sclerosing Cholangitis Reveals Therapeutic Opportunities.
Hepatology
; 72(4): 1253-1266, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31925805
7.
[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
8.
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
9.
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
10.
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
11.
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
12.
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
13.
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
14.
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
15.
Variant classification in precision oncology.
Int J Cancer
; 145(11): 2996-3010, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31008532
16.
The BRCA2 mutation status shapes the immune phenotype of prostate cancer.
Cancer Immunol Immunother
; 68(10): 1621-1633, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31549213
17.
A field guide for cancer diagnostics using cell-free DNA: From principles to practice and clinical applications.
Genes Chromosomes Cancer
; 57(3): 123-139, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29205637
18.
Targeted deep sequencing of effusion cytology samples is feasible, informs spatiotemporal tumor evolution, and has clinical and diagnostic utility.
Genes Chromosomes Cancer
; 57(2): 70-79, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29044880
19.
Knowledge bases and software support for variant interpretation in precision oncology.
Brief Bioinform
; 22(6)2021 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34125166
20.
Relevance of polymorphisms in MC4R and BDNF in short normal stature.
BMC Pediatr
; 18(1): 278, 2018 08 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-30134862