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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 registries
Cristina 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 scores
Sandya Liyanarachchi, Julius Gudmundsson, Egil Ferkingstad, et al.
Blood
|
May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly
Florian 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 cancer
Sigurgeir 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 status
Elinborg 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 PMS2
Sigurdis 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 diagnosis
Magnus 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 traits
Unnur 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 population
Paul 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 gene
Gudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 150) with videos related to
Sort By:
Page
of 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 registries
Cristina 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 scores
Sandya Liyanarachchi, Julius Gudmundsson, Egil Ferkingstad, et al.
Blood
|
May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly
Florian 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 cancer
Sigurgeir 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 status
Elinborg 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 PMS2
Sigurdis 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 diagnosis
Magnus 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 traits
Unnur 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 population
Paul 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 gene
Gudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
Page
of 15