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European Journal of Cancer (Oxford, England : 1990)
|
August 6, 2023
Tumour mutational burden and survival with molecularly matched therapy
Till de Bortoli, Manuela Benary, Peter Horak, et al.
Journal of the American Medical Informatics Association : JAMIA
|
April 20, 2023
Creation of a structured molecular genomics report for Germany as a local adaption of HL7's Genomic Reporting Implementation Guide
Caroline Stellmach, Julian Sass, Bernd Auber, et al.
The Oncologist
|
April 22, 2026
Liquid biopsy-based detection of acquired MET resistance enables sequential targeted therapy in MET fusion-positive NSCLC
Stanislav Rosnev, Katharina Klein, Lukas Heukamp, et al.
BMC Medicine
|
October 24, 2022
Feasibility and outcome of reproducible clinical interpretation of high-dimensional molecular data: a comparison of two molecular tumor boards
Damian T Rieke, Till de Bortoli, Peter Horak, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 27, 2020
Support of a molecular tumour board by an evidence-based decision management system for precision oncology
Mario Lamping, Manuela Benary, Serge Leyvraz, et al.
The Oncologist
|
June 17, 2024
A diagnostic challenge of KIT p.V559D and BRAF p.G469A mutations in a paragastric mass
Stefan Habringer, Jana Ihlow, Karsten Kleo, et al.
Nature Cancer
|
June 28, 2024
The proteogenomic landscape of multiple myeloma reveals insights into disease biology and therapeutic opportunities
Evelyn Ramberger, Valeriia Sapozhnikova, Yuen Lam Dora Ng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 1, 2022
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)
Peter Horak, Malachi Griffith, Arpad M Danos, et al.
European Journal of Cancer (Oxford, England : 1990)
|
September 18, 2024
Benchmarking whole exome sequencing in the German network for personalized medicine
Michael Menzel, Mihaela Martis-Thiele, Hannah Goldschmid, et al.
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Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
European Journal of Cancer (Oxford, England : 1990)
|
August 6, 2023
Tumour mutational burden and survival with molecularly matched therapy
Till de Bortoli, Manuela Benary, Peter Horak, et al.
Journal of the American Medical Informatics Association : JAMIA
|
April 20, 2023
Creation of a structured molecular genomics report for Germany as a local adaption of HL7's Genomic Reporting Implementation Guide
Caroline Stellmach, Julian Sass, Bernd Auber, et al.
The Oncologist
|
April 22, 2026
Liquid biopsy-based detection of acquired MET resistance enables sequential targeted therapy in MET fusion-positive NSCLC
Stanislav Rosnev, Katharina Klein, Lukas Heukamp, et al.
BMC Medicine
|
October 24, 2022
Feasibility and outcome of reproducible clinical interpretation of high-dimensional molecular data: a comparison of two molecular tumor boards
Damian T Rieke, Till de Bortoli, Peter Horak, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 27, 2020
Support of a molecular tumour board by an evidence-based decision management system for precision oncology
Mario Lamping, Manuela Benary, Serge Leyvraz, et al.
The Oncologist
|
June 17, 2024
A diagnostic challenge of KIT p.V559D and BRAF p.G469A mutations in a paragastric mass
Stefan Habringer, Jana Ihlow, Karsten Kleo, et al.
Nature Cancer
|
June 28, 2024
The proteogenomic landscape of multiple myeloma reveals insights into disease biology and therapeutic opportunities
Evelyn Ramberger, Valeriia Sapozhnikova, Yuen Lam Dora Ng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 1, 2022
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)
Peter Horak, Malachi Griffith, Arpad M Danos, et al.
European Journal of Cancer (Oxford, England : 1990)
|
September 18, 2024
Benchmarking whole exome sequencing in the German network for personalized medicine
Michael Menzel, Mihaela Martis-Thiele, Hannah Goldschmid, et al.
Page
of 2