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G Jonasson

Showing results (121-130 of 150) with videos related to

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International Journal of Cancer|September 9, 2010
High constant incidence rates of second primary cancers of the head and neck: a pooled analysis of 13 cancer registriesCristina Bosetti, Ghislaine Scelo, Shu-Chun Chuang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 6, 2020
Assessing thyroid cancer risk using polygenic risk scoresSandya Liyanarachchi, Julius Gudmundsson, Egil Ferkingstad, et al.
Blood|May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderlyFlorian Zink, Simon N Stacey, Gudmundur L Norddahl, et al.
Scientific Reports|February 17, 2026
A meta-analysis identifies driver genes and characterizes the molecular epidemiology of colorectal cancerSigurgeir Olafsson, Thorri Thorarinsson, Sigurjon A Gudjonsson, et al.
British Journal of Cancer|September 17, 2020
Breast cancer survival in Nordic BRCA2 mutation carriers-unconventional association with oestrogen receptor statusElinborg J Olafsdottir, Ake Borg, Maj-Britt Jensen, et al.
Nature Communications|May 4, 2017
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L Frankel, et al.
British Journal of Cancer|August 18, 2023
Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosisMagnus I Magnusson, Bjarni A Agnarsson, Jon G Jonasson, et al.
Nature|May 7, 2013
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traitsUnnur Styrkarsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Journal of Cellular and Molecular Medicine|October 17, 2018
Identification of Lynch syndrome risk variants in the Romanian populationPaul D Iordache, Dana Mates, Bjarni Gunnarsson, et al.
Nature Communications|February 5, 2022
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome geneGudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
Pageof 15

Showing results (121-130 of 150) with videos related to

Sort By:
Pageof 15
International Journal of Cancer|September 9, 2010
High constant incidence rates of second primary cancers of the head and neck: a pooled analysis of 13 cancer registriesCristina Bosetti, Ghislaine Scelo, Shu-Chun Chuang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 6, 2020
Assessing thyroid cancer risk using polygenic risk scoresSandya Liyanarachchi, Julius Gudmundsson, Egil Ferkingstad, et al.
Blood|May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderlyFlorian Zink, Simon N Stacey, Gudmundur L Norddahl, et al.
Scientific Reports|February 17, 2026
A meta-analysis identifies driver genes and characterizes the molecular epidemiology of colorectal cancerSigurgeir Olafsson, Thorri Thorarinsson, Sigurjon A Gudjonsson, et al.
British Journal of Cancer|September 17, 2020
Breast cancer survival in Nordic BRCA2 mutation carriers-unconventional association with oestrogen receptor statusElinborg J Olafsdottir, Ake Borg, Maj-Britt Jensen, et al.
Nature Communications|May 4, 2017
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L Frankel, et al.
British Journal of Cancer|August 18, 2023
Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosisMagnus I Magnusson, Bjarni A Agnarsson, Jon G Jonasson, et al.
Nature|May 7, 2013
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traitsUnnur Styrkarsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Journal of Cellular and Molecular Medicine|October 17, 2018
Identification of Lynch syndrome risk variants in the Romanian populationPaul D Iordache, Dana Mates, Bjarni Gunnarsson, et al.
Nature Communications|February 5, 2022
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome geneGudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
Pageof 15