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Blood Advances
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May 21, 2020
Search for multiple myeloma risk factors using Mendelian randomization
Molly Went, Alex J Cornish, Philip J Law, et al.
Genome Medicine
|
August 25, 2025
Replication-associated mechanisms contribute to an increased CpG > TpG mutation burden in mismatch repair-deficient cancers
Joseph C Ward, Ignacio Soriano, Steve Thorn, et al.
Nature Genetics
|
February 13, 2026
Comprehensive repertoire of the chromosomal alteration and mutational signatures across 16 cancer types
Andrew Everall, Avraam Tapinos, Aliah Hawari, et al.
Research Square
|
December 18, 2023
Whole genome sequencing refines stratification and therapy of patients with clear cell renal cell carcinoma
Richard Houlston, Richard Culliford, Sam Lawrence, et al.
Nature Communications
|
June 23, 2016
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer
Daniel Chubb, Peter Broderick, Sara E Dobbins, et al.
Molecular Cancer Research : MCR
|
January 21, 2026
Contrasting features of papillary and chromophobe renal cell carcinoma revealed by whole genome sequencing
Richard Culliford, Charlie Mills, Daniel Chubb, et al.
Nature Communications
|
July 15, 2024
Whole genome sequencing refines stratification and therapy of patients with clear cell renal cell carcinoma
Richard Culliford, Samuel E D Lawrence, Charlie Mills, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2015
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Ben Kinnersley, Yoichiro Kamatani, Marianne Labussière, et al.
Scientific Reports
|
December 3, 2015
Quantifying the heritability of glioma using genome-wide complex trait analysis
Ben Kinnersley, Jonathan S Mitchell, Konstantinos Gousias, et al.
Journal of the National Cancer Institute
|
April 29, 2014
Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis
Ben Kinnersley, Stephan Buch, Sergi Castellví-Bel, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 62) with videos related to
Sort By:
Page
of 7
Blood Advances
|
May 21, 2020
Search for multiple myeloma risk factors using Mendelian randomization
Molly Went, Alex J Cornish, Philip J Law, et al.
Genome Medicine
|
August 25, 2025
Replication-associated mechanisms contribute to an increased CpG > TpG mutation burden in mismatch repair-deficient cancers
Joseph C Ward, Ignacio Soriano, Steve Thorn, et al.
Nature Genetics
|
February 13, 2026
Comprehensive repertoire of the chromosomal alteration and mutational signatures across 16 cancer types
Andrew Everall, Avraam Tapinos, Aliah Hawari, et al.
Research Square
|
December 18, 2023
Whole genome sequencing refines stratification and therapy of patients with clear cell renal cell carcinoma
Richard Houlston, Richard Culliford, Sam Lawrence, et al.
Nature Communications
|
June 23, 2016
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer
Daniel Chubb, Peter Broderick, Sara E Dobbins, et al.
Molecular Cancer Research : MCR
|
January 21, 2026
Contrasting features of papillary and chromophobe renal cell carcinoma revealed by whole genome sequencing
Richard Culliford, Charlie Mills, Daniel Chubb, et al.
Nature Communications
|
July 15, 2024
Whole genome sequencing refines stratification and therapy of patients with clear cell renal cell carcinoma
Richard Culliford, Samuel E D Lawrence, Charlie Mills, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2015
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Ben Kinnersley, Yoichiro Kamatani, Marianne Labussière, et al.
Scientific Reports
|
December 3, 2015
Quantifying the heritability of glioma using genome-wide complex trait analysis
Ben Kinnersley, Jonathan S Mitchell, Konstantinos Gousias, et al.
Journal of the National Cancer Institute
|
April 29, 2014
Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis
Ben Kinnersley, Stephan Buch, Sergi Castellví-Bel, et al.
Page
of 7