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Molecular and Cellular Probes
|
May 17, 2015
Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies
Stephan Waldmüller, Christopher Schroeder, Marc Sturm, et al.
Molecular Genetics & Genomic Medicine
|
February 10, 2023
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome
Dennis Witt, Ulrike Faust, Gertrud Strobl-Wildemann, et al.
Pigment Cell & Melanoma Research
|
June 4, 2026
Copy Number Analysis in Congenital Nevi: Concordance and Diagnostic Limitations of aCGH, sWGS, and Methylation Sequencing
Anton Karelin, Ines B Brecht, Michaela Pogoda, et al.
Cancers
|
August 23, 2020
Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients
Franz J Hilke, Tobias Sinnberg, Axel Gschwind, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2014
Genome-wide UPD screening in patients with intellectual disability
Christopher Schroeder, Arif Bülent Ekici, Ute Moog, et al.
Frontiers in Oncology
|
April 22, 2025
Case Report: FGFR2 inhibitor resistance via <i>PIK3CA</i> and <i>CDKN2A/B</i> in an intrahepatic cholangiocarcinoma patient with <i>FGFR2-SH3GLB1</i> fusion
Nadja Ballin, Alexander Ott, Olga Seibel-Kelemen, et al.
Journal of Cancer Research and Clinical Oncology
|
February 22, 2022
TMB and BRAF mutation status are independent predictive factors in high-risk melanoma patients with adjuvant anti-PD-1 therapy
Julia Eckardt, Christopher Schroeder, Peter Martus, et al.
Biology
|
December 30, 2025
Multi-Omics Tumor Immunogenicity Score Predicts Immunotherapy Outcome and Survival
Axel Gschwind, Nadja Ballin, Alexander Ott, et al.
Cell Death & Disease
|
May 17, 2023
ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways-lessons from breast cancer patients
Juliane Sachsenweger, Rebecca Jansche, Tatjana Merk, et al.
NPJ Genomic Medicine
|
March 15, 2024
Genomes in clinical care
Olaf Riess, Marc Sturm, Benita Menden, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 78) with videos related to
Sort By:
Page
of 8
Molecular and Cellular Probes
|
May 17, 2015
Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies
Stephan Waldmüller, Christopher Schroeder, Marc Sturm, et al.
Molecular Genetics & Genomic Medicine
|
February 10, 2023
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome
Dennis Witt, Ulrike Faust, Gertrud Strobl-Wildemann, et al.
Pigment Cell & Melanoma Research
|
June 4, 2026
Copy Number Analysis in Congenital Nevi: Concordance and Diagnostic Limitations of aCGH, sWGS, and Methylation Sequencing
Anton Karelin, Ines B Brecht, Michaela Pogoda, et al.
Cancers
|
August 23, 2020
Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients
Franz J Hilke, Tobias Sinnberg, Axel Gschwind, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2014
Genome-wide UPD screening in patients with intellectual disability
Christopher Schroeder, Arif Bülent Ekici, Ute Moog, et al.
Frontiers in Oncology
|
April 22, 2025
Case Report: FGFR2 inhibitor resistance via <i>PIK3CA</i> and <i>CDKN2A/B</i> in an intrahepatic cholangiocarcinoma patient with <i>FGFR2-SH3GLB1</i> fusion
Nadja Ballin, Alexander Ott, Olga Seibel-Kelemen, et al.
Journal of Cancer Research and Clinical Oncology
|
February 22, 2022
TMB and BRAF mutation status are independent predictive factors in high-risk melanoma patients with adjuvant anti-PD-1 therapy
Julia Eckardt, Christopher Schroeder, Peter Martus, et al.
Biology
|
December 30, 2025
Multi-Omics Tumor Immunogenicity Score Predicts Immunotherapy Outcome and Survival
Axel Gschwind, Nadja Ballin, Alexander Ott, et al.
Cell Death & Disease
|
May 17, 2023
ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways-lessons from breast cancer patients
Juliane Sachsenweger, Rebecca Jansche, Tatjana Merk, et al.
NPJ Genomic Medicine
|
March 15, 2024
Genomes in clinical care
Olaf Riess, Marc Sturm, Benita Menden, et al.
Page
of 8