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Markus Loeffler

Showing results (301-310 of 329) with videos related to

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European Journal of Cancer (Oxford, England : 1990)|March 20, 2021
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportToni T Seppälä, Mev Dominguez-Valentin, Emma J Crosbie, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2020
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportMev Dominguez-Valentin, Emma J Crosbie, Christoph Engel, 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.
Nature Communications|September 28, 2018
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volumeDina Vojinovic, Hieab H Adams, Xueqiu Jian, et al.
Nature Communications|September 23, 2020
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adultsEdith Hofer, Gennady V Roshchupkin, Hieab H H Adams, et al.
Nature Genetics|September 3, 2021
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expressionUrmo Võsa, Annique Claringbould, Harm-Jan Westra, 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.
European Journal of Epidemiology|October 19, 2022
Framework and baseline examination of the German National Cohort (NAKO)Annette Peters, , Annette Peters, et al.
Pageof 33

Showing results (301-310 of 329) with videos related to

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Pageof 33
European Journal of Cancer (Oxford, England : 1990)|March 20, 2021
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportToni T Seppälä, Mev Dominguez-Valentin, Emma J Crosbie, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2020
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportMev Dominguez-Valentin, Emma J Crosbie, Christoph Engel, 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.
Nature Communications|September 28, 2018
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volumeDina Vojinovic, Hieab H Adams, Xueqiu Jian, et al.
Nature Communications|September 23, 2020
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adultsEdith Hofer, Gennady V Roshchupkin, Hieab H H Adams, et al.
Nature Genetics|September 3, 2021
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expressionUrmo Võsa, Annique Claringbould, Harm-Jan Westra, 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.
European Journal of Epidemiology|October 19, 2022
Framework and baseline examination of the German National Cohort (NAKO)Annette Peters, , Annette Peters, et al.
Pageof 33