P. Kalfayan

发表

From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America

P. Møller, E. Hovig, P. Ashton-Prolla, 2018, International journal of cancer.

Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database

B. Bonanni, P. Møller, E. Hovig, 2020, Journal of clinical medicine.

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2021, European journal of cancer.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2019, Genetics in Medicine.

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2020, Genetics in Medicine.

A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries.

P. Møller, E. Hovig, J. C. Bazo-Alvarez, 2019, European journal of cancer.

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2020, Genetics in Medicine.

Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

Aung Ko Win, M. Kloor, B. Bonanni, 2022, Hereditary Cancer in Clinical Practice.

Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort

C. Vaccaro, Fabiana Alejandra Ferro, M. Dominguez-Valentin, 2017, Familial Cancer.

No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2021, Journal of clinical medicine.

A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America

P. Møller, E. Hovig, R. Reis, 2017, BMC Cancer.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2019, Genetics in Medicine.

Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort

Mev Dominguez-Valentin, C. Vaccaro, María Laura González, 2018, Familial Cancer.

Evaluation of MLH1 variants of unclear significance

R. Reis, I. Hinrichsen, G. Plotz, 2018, Genes, chromosomes & cancer.

MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome

C. Vaccaro, M. Dominguez-Valentin, P. Wernhoff, 2016, Front. Oncol..

Hereditary Renal Cell Carcinoma: Is Age an Independent Criterion for Genetic Testing? A Large Cohort from a Latin America Referral Center

P. Kalfayan, A. Jurado, V. de Miguel, 2023, Journal of kidney cancer and VHL.

Lynch syndrome in South America: past, present and future

J. Church, H. Lynch, F. López-Kostner, 2016, Familial Cancer.