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Aung Ko Win

Showing results (121-130 of 135) with videos related to

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Nature Communications|May 16, 2019
Association analyses identify 31 new risk loci for colorectal cancer susceptibilityPhilip J Law, Maria Timofeeva, Ceres Fernandez-Rozadilla, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2020
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 25, 2019
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Journal of Clinical Medicine|July 2, 2021
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in <i>MLH1</i> and <i>MSH2</i>: A Prospective Lynch Syndrome Database StudyMev Dominguez-Valentin, John-Paul Plazzer, Julian R Sampson, et al.
Scientific Reports|December 2, 2015
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1Timothy H T Cheng, Deborah Thompson, Jodie Painter, et al.
American Journal of Human Genetics|August 8, 2020
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer RiskMinta Thomas, Lori C Sakoda, Michael Hoffmeister, et al.
American Journal of Human Genetics|March 5, 2021
Response to Li and HopperMinta Thomas, Lori C Sakoda, Michael Hoffmeister, et al.
Eclinicalmedicine|May 14, 2023
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome databaseMev Dominguez-Valentin, Saskia Haupt, Toni T Seppälä, et al.
Gastroenterology|December 24, 2019
Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset CancerAlexi N Archambault, Yu-Ru Su, Jihyoun Jeon, et al.
Hereditary Cancer in Clinical Practice|October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumPål Møller, Toni Seppälä, James G Dowty, et al.
Pageof 14

Showing results (121-130 of 135) with videos related to

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Pageof 14
Nature Communications|May 16, 2019
Association analyses identify 31 new risk loci for colorectal cancer susceptibilityPhilip J Law, Maria Timofeeva, Ceres Fernandez-Rozadilla, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2020
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 25, 2019
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Journal of Clinical Medicine|July 2, 2021
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in <i>MLH1</i> and <i>MSH2</i>: A Prospective Lynch Syndrome Database StudyMev Dominguez-Valentin, John-Paul Plazzer, Julian R Sampson, et al.
Scientific Reports|December 2, 2015
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1Timothy H T Cheng, Deborah Thompson, Jodie Painter, et al.
American Journal of Human Genetics|August 8, 2020
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer RiskMinta Thomas, Lori C Sakoda, Michael Hoffmeister, et al.
American Journal of Human Genetics|March 5, 2021
Response to Li and HopperMinta Thomas, Lori C Sakoda, Michael Hoffmeister, et al.
Eclinicalmedicine|May 14, 2023
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome databaseMev Dominguez-Valentin, Saskia Haupt, Toni T Seppälä, et al.
Gastroenterology|December 24, 2019
Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset CancerAlexi N Archambault, Yu-Ru Su, Jihyoun Jeon, et al.
Hereditary Cancer in Clinical Practice|October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumPål Møller, Toni Seppälä, James G Dowty, et al.
Pageof 14