المؤلفون: Steffen Hirsch, Caroline Hutter, Bianca Goemans, Kristian W. Pajtler, David Reuss, Gabriele Calaminus, Gnana Prakash Balasubramanian, Nicola Dikow, C. Michel Zwaan, Arndt Borkhardt, David T.W. Jones, Birgit Burkhardt, Matthias Schwab, Ingrid Øra, Ines B. Brecht, Uta Dirksen, Christian Sutter, Kathrin Schramm, Roman Tremmel, Bernarda Kazanowska, Peter Lichter, M. Scheer, Gudrun Fleischhack, André O. von Bueren, Mirjam Blattner-Johnson, David Capper, Felix Sahm, Simone Fulda, Natalie Jäger, Nicolas U. Gerber, Olaf Witt, Jan-Henning Klusmann, Irene Schmid, Petra Fiesel, Matthias Fischer, Roland Meisel, Stefan M. Pfister, Michaela Nathrath, Cornelis M. van Tilburg, Angelika Eggert, Sebastian Stark, Christof M. Kramm, Elke Pfaff, Kerstin Grund, Arend von Stackelberg, Andrej Lissat, Peter Vorwerk, Petra Ketteler, Angelika Freitag, Olli Lohi, Michael T. Meister, Ruth Witt, Norbert Graf, Annette Kopp-Schneider, Pascal D. Johann, Dominik T. Schneider, Karin P.S. Langenberg, Simone Hettmer, Dirk Reinhardt, Antonis Kattamis, Andreas E. Kulozik, Andreas von Deimling, Jan J. Molenaar, Wilhelm Wößmann, Maria Filippidou, Stephan Tippelt, Frank Westermann, Stephan Wolf, Michael C. Frühwald, Barbara C. Jones, Ewa Koscielniak, Till Milde, Stefanie Hecker-Nolting, Dietrich von Schweinitz

المساهمون: Pediatrics, Tampere University, Department of Paediatrics, BioMediTech

المصدر: Cancer Discovery, 11(11), 2764-2779. American Association for Cancer Research Inc.
Cancer discovery, Vol. 11, No 11 (2021) pp. 2764-2779

مصطلحات موضوعية: Prioritization, medicine.medical_specialty, Treatment response, 3122 Cancers, Medizin, MEDLINE, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, 3123 Gynaecology and paediatrics, Internal medicine, Neoplasms, medicine, Humans, Prospective Studies, Registries, Medical diagnosis, Precision Medicine, Child, 030304 developmental biology, 0303 health sciences, ddc:618, business.industry, Cancer, medicine.disease, Confidence interval, Progression-Free Survival, ddc, 3. Good health, Oncology, Precision oncology, 030220 oncology & carcinogenesis, Molecular targets, 3111 Biomedicine, business

وصف الملف: application/pdf; fulltext

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3aa2e6219234f552ef0d4f152d58341
https://pubmed.ncbi.nlm.nih.gov/34725088

المؤلفون: Roman Tremmel, Kathrin Klein, Saskia Biskup, Tim Scheurenbrand, Elke Schaeffeler, Ulrich M. Zanger, S. Fehr, Stefan Winter, Matthias Schwab, Florian Battke

المصدر: Human Genetics

مصطلحات موضوعية: Genetic Markers, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system diseases, DNA Copy Number Variations, Computational biology, Biology, Correlation, 03 medical and health sciences, Exon, mental disorders, Exome Sequencing, Genetics, Humans, Copy-number variation, Exome, Gene, Genetics (clinical), 030304 developmental biology, Retrospective Studies, 0303 health sciences, 030305 genetics & heredity, Computational Biology, High-Throughput Nucleotide Sequencing, Human genetics, 3. Good health, Liver, Genetic marker, Pharmacogenetics, Pharmacogenomics

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb48b313c29c11ca18404cbeb9224fa4
https://pubmed.ncbi.nlm.nih.gov/31786673

المؤلفون: Kathrin Klein, Roman Tremmel, Stefan Winter, Sarah Fehr, Florian Battke, Tim Scheurenbrand, Elke Schaeffeler, Saskia Biskup, Matthias Schwab, Ulrich M. Zanger

المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 10 (2019)

مصطلحات موضوعية: lcsh:QH426-470, Biology, DNA sequencing, 03 medical and health sciences, 0302 clinical medicine, Genotype, Genetics, Coding region, Indel, Gene, Genetics (clinical), 030304 developmental biology, Original Research, next generation sequencing, pharmacogenomics, 0303 health sciences, Intron, rare variants, 3. Good health, Minor allele frequency, lcsh:Genetics, genomic DNA, ADME, eQTL analysis, 030220 oncology & carcinogenesis, Molecular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86568e793f6c4b9717e85eadc291864e
http://europepmc.org/articles/PMC6365429

المؤلفون: Debora S. Marks, Charlotta P I Schärfe, Roman Tremmel, Matthias Schwab, Oliver Kohlbacher

المصدر: Genome Medicine
Genome Medicine, Vol 9, Iss 1, Pp 1-15 (2017)

مصطلحات موضوعية: 0301 basic medicine, Drug, Exome sequence analysis, Drug-Related Side Effects and Adverse Reactions, Pharmacogenomic Variants, lcsh:QH426-470, media_common.quotation_subject, Population, lcsh:Medicine, Biology, Bioinformatics, Efficacy, 03 medical and health sciences, 0302 clinical medicine, Bioinformatics analysis, Mutation Rate, Pharmacokinetics, Genetic variation, Genetics, Humans, Quantitative Biology - Genomics, Genetic variability, Adverse effect, education, Gene, Molecular Biology, Genetics (clinical), Exome sequencing, 030304 developmental biology, media_common, Genomics (q-bio.GN), 0303 health sciences, education.field_of_study, Genome, Human, Research, lcsh:R, Human genetics, 3. Good health, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, FOS: Biological sciences, Pharmacogenomics, Molecular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::babef81becda05909090c789729097ad