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Wiener Klinische Wochenschrift|May 20, 2026
[Antihyperglycemic treatment of type 2 diabetes mellitus (Update 2026)]Martin Clodi, Heidemarie Abrahamian, Felix Aberer, et al.Hereditary Cancer in Clinical Practice|March 13, 2019
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportToni T Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, et al.The Lancet. Oncology|December 15, 2010
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort studyMarlies J E Kempers, Roland P Kuiper, Charlotte W Ockeloen, et al.The Lancet. Oncology|November 27, 2022
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk SyndromesJosé Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, et al.Journal of Behavioral Addictions|February 13, 2025
Motives for pornography use and women's sexual wellbeing: Insights from a 42-country studyAteret Gewirtz-Meydan, Hagit Feder, Léna Nagy, et al.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|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.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 MLH1 and MSH2: A Prospective Lynch Syndrome Database StudyMev Dominguez-Valentin, John-Paul Plazzer, Julian R Sampson, et al.Pageof 224