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1دورية أكاديمية
المؤلفون: Marija Gjorgjievska, Sanja Mehandziska, Aleksandra Stajkovska, Slavica Pecioska-Dokuzovska, Anica Dimovska, Idriz Durmish, Sara Ismail, Teodora Pavlovska, Antonija Stojchevska, Haris Amedi, Jasna Andonova, Marija Nikolovska, Sara Velickovikj, Zan Mitrev, Ivan Kungulovski, Goran Kungulovski
المصدر: Frontiers in Genetics, Vol 13 (2022)
مصطلحات موضوعية: COVID-19, co-infection, omicron, next-generation sequencing, SARS- CoV2, Genetics, QH426-470
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Sanja Mehandziska, Aleksandra Stajkovska, Margarita Stavrevska, Kristina Jakovleva, Marija Janevska, Rodney Rosalia, Ivan Kungulovski, Zan Mitrev, Goran Kungulovski
المصدر: Frontiers in Genetics, Vol 11 (2020)
مصطلحات موضوعية: exome, genome, personalized medicine, precision genomics, clinical practice, implementation, Genetics, QH426-470
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Aleksandra Stajkovska, Sanja Mehandziska, Rodney Rosalia, Margarita Stavrevska, Marija Janevska, Martina Markovska, Ivan Kungulovski, Zan Mitrev, Goran Kungulovski
المصدر: Frontiers in Genetics, Vol 10 (2019)
مصطلحات موضوعية: next-generation sequencing, North Macedonia, hereditary cancer syndromes, Lynch syndrome, TP53, MLH1, Genetics, QH426-470
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Aleksandra Stajkovska, Sanja Mehandziska, Margarita Stavrevska, Kristina Jakovleva, Natasha Nikchevska, Zan Mitrev, Ivan Kungulovski, Gjorgje Zafiroski, Velibor Tasic, Goran Kungulovski
المصدر: Frontiers in Genetics, Vol 9 (2018)
مصطلحات موضوعية: next-generation sequencing, exome sequencing, case report, multicentric carpotarsal osteolysis syndrome, Balkan, Genetics, QH426-470
وصف الملف: electronic resource
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المؤلفون: Aleksandra Stajkovska, Kristina Jakovleva, Ivan Kungulovski, Marija Janevska, Zan Mitrev, Margarita Stavrevska, Sanja Mehandziska, Rodney A. Rosalia, Goran Kungulovski
المصدر: Frontiers in Genetics, Vol 11 (2020)
Frontiers in Geneticsمصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, Computer science, Genomics, Computational biology, 03 medical and health sciences, 0302 clinical medicine, precision genomics, Genetics, implementation, Exome, genome, Genetics (clinical), Selection (genetic algorithm), Protocol (science), business.industry, personalized medicine, Brief Research Report, Risk factor (computing), Pipeline (software), clinical practice, lcsh:Genetics, 030104 developmental biology, Workflow, 030220 oncology & carcinogenesis, Molecular Medicine, Personalized medicine, business, exome
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9913c75190e608878ea1779506b67d96
https://www.frontiersin.org/article/10.3389/fgene.2020.00619/full -
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المؤلفون: Rodney A. Rosalia, Ivan Kungulovski, Martina Markovska, Marija Janevska, Zan Mitrev, Aleksandra Stajkovska, Goran Kungulovski, Sanja Mehandziska
مصطلحات موضوعية: medicine.medical_treatment, medicine, Cancer, Immunotherapy, Computational biology, Biology, Gene deletion, Mutually exclusive events, medicine.disease, Chromatin
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5163edb017c4265bedf2c4efe2eef6b9
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7
المؤلفون: Sanja Mehandziska, Rodney A. Rosalia, Ivan Kungulovski, Margarita Stavrevska, Martina Markovska, Marija Janevska, Aleksandra Stajkovska, Zan Mitrev, Goran Kungulovski
المصدر: Frontiers in Genetics, Vol 10 (2019)
Frontiers in Geneticsمصطلحات موضوعية: 0301 basic medicine, North Macedonia, lcsh:QH426-470, Biology, medicine.disease_cause, MLH1, Germline, Frameshift mutation, 03 medical and health sciences, 0302 clinical medicine, medicine, Genetics, Missense mutation, case report, TP53, Gene, Genetics (clinical), hereditary cancer syndromes, Mutation, medicine.disease, Lynch syndrome, lcsh:Genetics, 030104 developmental biology, Li–Fraumeni syndrome, 030220 oncology & carcinogenesis, Molecular Medicine, next-generation sequencing, Li-Fraumeni
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21f19f5de4dbaeceb498456908e402e2
https://www.frontiersin.org/article/10.3389/fgene.2019.00952/full -
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المؤلفون: Margarita Stavrevska, Gjorgje Zafiroski, Zan Mitrev, Kristina Jakovleva, Ivan Kungulovski, Sanja Mehandziska, Velibor Tasic, Aleksandra Stajkovska, Goran Kungulovski, Natasha Nikchevska
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 9 (2018)مصطلحات موضوعية: 0301 basic medicine, Proband, Osteolysis, lcsh:QH426-470, 030105 genetics & heredity, Bioinformatics, Asymptomatic, DNA sequencing, Nephropathy, 03 medical and health sciences, Skeletal disorder, Balkan, medicine, Genetics, case report, Genetics (clinical), Exome sequencing, business.industry, multicentric carpotarsal osteolysis syndrome, medicine.disease, lcsh:Genetics, 030104 developmental biology, MAFB, Molecular Medicine, next-generation sequencing, medicine.symptom, business, exome sequencing
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e016bccaffe0a7cc5ab066f61c15bc
http://europepmc.org/articles/PMC5895704