Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez–Valentin, Steven Gallinger, Inge Bernstein et al.|Genetics in Medicine|2019Cited by 666
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database StudyMev Dominguez–Valentin, Wolff Schmiegel, John‐Paul Plazzer et al.|Journal of Clinical Medicine|2021Cited by 20
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, Steven Gallinger, Julian R. Sampson et al.|Genetics in Medicine|2020Cited by 12
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (vol 22, pg 15, 2020)Mev Dominguez–Valentin, Steven Gallinger, Julian R. Sampson et al.|Genetics in Medicine|2020Cited by 0
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database StudyMev Dominguez–Valentin, Jürgen Weitz, John‐Paul Plazzer et al.|Kölner Universitäts PublikationsServer (Universität zu Köln)|2021Cited by 0