Florencia Neffa

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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.

Novel large deletion in an atypical Peutz-Jeghers patient

N. Artagaveytia, G. Ardao, Florencia Neffa, 2017 .

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.

Germline Mutations in PALB 2 , BRCA 1 , and RAD 51 C , Which Regulate DNA Recombination Repair , in Patients With Gastric Cancer

C. Yau, N. Hu, A. Goldstein, 2017 .

Genetic and epigenetic characteristics of patients with colorectal cancer from Uruguay.

Florencia Neffa, P. Esperón, Carolina Vergara, 2022, Pathology, research and practice.

Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer.

C. Yau, N. Hu, A. Goldstein, 2017, Gastroenterology.

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.

Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study.

Katherine M. Tucker, Aung Ko Win, Swati G. Patel, 2021, The Lancet. Oncology.

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.

Mutation spectrum in South American Lynch syndrome families

P. Ashton-Prolla, D. Carraro, M. Nilbert, 2013, Hereditary cancer in clinical practice.

Evaluation of MLH1 variants of unclear significance

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

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

M. Kloor, P. Møller, E. Hovig, 2019, Hereditary Cancer in Clinical Practice.

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 database

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2023, EClinicalMedicine.

Aalborg Universitet Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by overdiagnosis ; A prospective Lynch syndrome database report

M. Kloor, P. Møller, E. Hovig, 2019 .

Aggressive mutation in a familial adenomatous polyposis syndrome family: when phenotype guides clinical surveillance.

Florencia Neffa, P. Esperón, A. Della Valle, 2018, Journal of gastrointestinal oncology.

Lynch syndrome in South America: past, present and future

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