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Stephan Ossowski

Showing results (91-100 of 155) with videos related to

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British Journal of Cancer|April 9, 2026
Genetic landscape of stage II melanoma identifies CBL as a new driver gene and prognostic biomarkerElena Sophia Lindner, Jakob Admard, German Demidov, 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 GuideCaroline Stellmach, Julian Sass, Bernd Auber, et al.
Nature Genetics|August 30, 2011
Whole-genome sequencing of multiple Arabidopsis thaliana populationsJun Cao, Korbinian Schneeberger, Stephan Ossowski, et al.
Cancers|December 24, 2021
Characterization of Genetic Heterogeneity in Recurrent Metastases of Renal Cell CarcinomaCarolin Sauter-Meyerhoff, Regina Bohnert, Pascale Mazzola, et al.
The Journal of Investigative Dermatology|April 4, 2016
Identification of Gene Mutations and Fusion Genes in Patients with Sézary SyndromeAparna Prasad, Raquel Rabionet, Blanca Espinet, et al.
Cell|December 4, 2014
Species-wide genetic incompatibility analysis identifies immune genes as hot spots of deleterious epistasisEunyoung Chae, Kirsten Bomblies, Sang-Tae Kim, et al.
Neurology. Genetics|December 13, 2021
Transcript-Specific Loss-of-Function Variants in <i>VPS16</i> Are Enriched in Patients With DystoniaJoohyun Park, Annemarie Reilaender, Jan N Petry-Schmelzer, et al.
Lung Cancer (Amsterdam, Netherlands)|October 23, 2025
Distinct genomic profile of pediatric lung carcinoma: High frequency of ALK fusions and TP53 mutations compared to adultsMichael Abele, Anton Karelin, Michaela Pogoda, et al.
NAR Genomics and Bioinformatics|September 13, 2021
CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graphChengyao Peng, Simon Dieck, Alexander Schmid, et al.
Scientific Reports|March 16, 2019
Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic ArthritisRaquel Rabionet, Agustín Remesal, Anna Mensa-Vilaró, et al.
Pageof 16

Showing results (91-100 of 155) with videos related to

Sort By:
Pageof 16
British Journal of Cancer|April 9, 2026
Genetic landscape of stage II melanoma identifies CBL as a new driver gene and prognostic biomarkerElena Sophia Lindner, Jakob Admard, German Demidov, 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 GuideCaroline Stellmach, Julian Sass, Bernd Auber, et al.
Nature Genetics|August 30, 2011
Whole-genome sequencing of multiple Arabidopsis thaliana populationsJun Cao, Korbinian Schneeberger, Stephan Ossowski, et al.
Cancers|December 24, 2021
Characterization of Genetic Heterogeneity in Recurrent Metastases of Renal Cell CarcinomaCarolin Sauter-Meyerhoff, Regina Bohnert, Pascale Mazzola, et al.
The Journal of Investigative Dermatology|April 4, 2016
Identification of Gene Mutations and Fusion Genes in Patients with Sézary SyndromeAparna Prasad, Raquel Rabionet, Blanca Espinet, et al.
Cell|December 4, 2014
Species-wide genetic incompatibility analysis identifies immune genes as hot spots of deleterious epistasisEunyoung Chae, Kirsten Bomblies, Sang-Tae Kim, et al.
Neurology. Genetics|December 13, 2021
Transcript-Specific Loss-of-Function Variants in <i>VPS16</i> Are Enriched in Patients With DystoniaJoohyun Park, Annemarie Reilaender, Jan N Petry-Schmelzer, et al.
Lung Cancer (Amsterdam, Netherlands)|October 23, 2025
Distinct genomic profile of pediatric lung carcinoma: High frequency of ALK fusions and TP53 mutations compared to adultsMichael Abele, Anton Karelin, Michaela Pogoda, et al.
NAR Genomics and Bioinformatics|September 13, 2021
CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graphChengyao Peng, Simon Dieck, Alexander Schmid, et al.
Scientific Reports|March 16, 2019
Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic ArthritisRaquel Rabionet, Agustín Remesal, Anna Mensa-Vilaró, et al.
Pageof 16