ESPERON, PATRICIA; NEFFA, FLORENCIA; PAVICIC, WALTER HERNÁN; DOMINGUEZ-VALENTIN, MEV

A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin America

FAMILIAL CANCER; Lugar: Berlin; Año: 2024

DOMINGUEZ-VALENTIN, MEV; HAUPT, SASKIA; SEPPÄLÄ, TONI T.; SAMPSON, JULIAN R.; SUNDE, LONE; BERNSTEIN, INGE; JENKINS, MARK A.; ENGEL, CHRISTOPH; ARETZ, STEFAN; NIELSEN, MAARTJE; CAPELLA, GABRIEL; BALAGUER, FRANCESC; EVANS, DAFYDD GARETH; BURN, JOHN; HOLINSKI-FEDER, ELKE; BERTARIO, LUCIO; BONANNI, BERNARDO; LINDBLOM, ANNIKA; LEVI, ZOHAR; MACRAE, FINLAY; WINSHIP, INGRID; PLAZZER, JOHN-PAUL; SIJMONS, ROLF; LAGHI, LUIGI; DELLA VALLE, ADRIANA; HEINIMANN, KARL; D?BNIAK, TADEUSZ; FRUSCIO, ROBERT; LOPEZ-KOESTNER, FRANCISCO; ALVAREZ-VALENZUELA, KARIN; KATZ, LIOR H.; LAISH, IDO; VAINER, ELEZ; VACCARO, CARLOS; CARRARO, DIRCE MARIA; MONAHAN, KEVIN; HALF, ELIZABETH; STAKELUM, AINE; WINTER, DES; KENNELLY, RORY; GLUCK, NATHAN; SHETH, HARSH; ABU-FREHA, NAIM; GREENBLATT, MARC; ROSSI, BENEDITO MAURO; BOHORQUEZ, MABEL; CAVESTRO, GIULIA MARTINA; LINO-SILVA, LEONARDO S.; HORISBERGER, KAROLINE; TIBILETTI, MARIA GRAZIA; NASCIMENTO, IVANA DO; THOMAS, HUW; ROSSI, NORMA TERESA; APOLINÁRIO DA SILVA, LEANDRO; ZARÁND, ATTILA; RUIZ-BAÑOBRE

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

eClinicalMedicine; Año: 2023 vol. 58

BRUNNER, MAURICIO; MULLEN, LUCAS; JAUK, FEDERICO; OLIVER, JAVIER; CAYOL, FEDERICO; MINATA, JOSÉ; HERRERA, VICTOR; PAVICIC, WALTER; LUNA, DANIEL; RISK, MARCELO; GARCIA RIVELLO, HERNAN; BENITEZ, SONIA

Automatic Integration of Clinical and Genetic Data Using cBioPortal

Studies in Health Technology and Informatics; Año: 2022 vol. 290 p. 799 - 803

OLKINUORA, ALISA PETRIINA; MAYORDOMO, ANDREA CONSTANZA; KAUPPINEN, ANNI KATARIINA; CERLIANI, MARÍA BELÉN; CORAGLIO, MARIANA; COLLIA, ÁVILA KARINA; GUTIÉRREZ, ALEJANDRO; ALVAREZ, KARIN; CASSANA, ALESSANDRA; LOPÉZ-KÖSTNER, FRANCISCO; JAUK, FEDERICO; GARCÍA-RIVELLO, HERNÁN; RISTIMÄKI, ARI; KOSKENVUO, LAURA; LEPISTÖ, ANNA; NIEMINEN, TAINA TUULIKKI; VACCARO, CARLOS ALBERTO; PAVICIC, WALTER HERNÁN; PELTOMÄKI, PÄIVI

Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents

Frontiers in Oncology; Año: 2022 vol. 12

MOLLER PAL; SEPPÄLÄ TT; VACCARO, CARLOS A.; PAVICIC WH; THE EUROPEAN HEREDITARY TUMOUR GROUP

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

HEREDITARY CANCER IN CLINICAL PRACTICE; Lugar: Londres; Año: 2022

VACCARO, CARLOS ALBERTO; SOAREZ, JULIETA; DOMINGUEZ-VALENTIN, MEV; PAVICIC, WALTER HERNÁN

Editorial: Advances in genetics and molecular diagnosis in colorectal, stomach, and pancreatic cancer

Frontiers in Oncology; Año: 2022 vol. 12

SEPPÄLÄ TT; DOMINGUEZ-VALENTIN, MEV; VACCARO, CARLOS ALBERTO; PIÑERO, TAMARA ALEJANDRA; PAVICIC WH; GARETH EVANS D; MOLLER PAL

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

EUROPEAN JOURNAL OF CANCER; Lugar: Amsterdam; Año: 2021

CERLIANI MB; MAYORDOMO AC; SANCHEZ DOVA AC; SOAREZ JN; FUHR ETCHEVERRY J; PIÑERO, TAMARA ALEJANDRA; CAJAL, ANDREA ROMINA; JAUK VITALI F; GARCIA RIVELLO H; VACCARO, CARLOS ALBERTO; RICHARD SM; BRAVI CM; PAVICIC WH

Maternal ancestry and hematological cancer risk: case?control study in an Argentinean population

PERSONALIZED MEDICINE; Lugar: Londres; Año: 2021

DOMINGUEZ-VALENTIN, MEV; PLAZZER, JOHN-PAUL; LOPEZ-KOSTNER, FRANCISCO; ALVAREZ, KARIN; VACCARO, CARLOS A.; PIÑERO, TAMARA ALEJANDRA; PAVICIC, WALTER HERNÁN; KALFAYAN, PABLO; PELTOMÄKI, PÄIVI; MØLLER, PÅL

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

Journal of Clinical Medicine; Año: 2021 vol. 10

PIÑERO, TAMARA ALEJANDRA; SOUKARIEH, OMAR; ROLAIN, MARION; ALVAREZ, KARIN; LÓPEZ-KÖSTNER, FRANCISCO; TORREZAN, GIOVANA TARDIN; CARRARO, DIRCE MARIA; DE OLIVEIRA NASCIMENTO, IVANA LUCIA; BOMFIM, THAÍS FERREIRA; MACHADO-LOPES, TAÍSA MANUELA BONFIM; FREITAS, JULIANA CÔRTES; TORALLES, MARIA BETÂNIA; SANDES, KIYOKO ABE; ROSSI, BENEDITO MAURO; JUNIOR, SAMUEL AGUIAR; MEIRA, JOANNA; DOMINGUEZ-VALENTIN, MEV; MØLLER, PÅL; VACCARO, CARLOS ALBERTO; MARTINS, ALEXANDRA; PAVICIC, WALTER HERNÁN

MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing

FAMILIAL CANCER; Lugar: Berlin; Año: 2020

VENTURA, C.; ZAPPIA, C.D.; LASAGNA, M.; PAVICIC, W.; RICHARD, S.; BOLZAN, A.D.; MONCZOR, F.; NÚÑEZ, M.; COCCA, C.

Effects of the pesticide chlorpyrifos on breast cancer disease. Implication of epigenetic mechanisms

JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY; Año: 2019 vol. 186 p. 96 - 104

GONZÁLEZ, MARÍA LAURA; CAUSADA-CALO, NATALIA; SANTINO, JUAN PABLO; DOMINGUEZ-VALENTIN, MEV; FERRO, FABIANA ALEJANDRA; SAMMARTINO, INÉS; KALFAYAN, PABLO GERMÁN; VERZURA, MARIA ALICIA; PIÑERO, TAMARA ALEJANDRA; CAJAL, ANDREA ROMINA; PAVICIC, WALTER; VACCARO, CARLOS

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

FAMILIAL CANCER; Lugar: Berlin; Año: 2018 vol. 17 p. 395 - 402

CERLIANI MB; PAVICIC W.; GILI JA; KLEIN G; SABA S; RICHARD S.M.

Cigarette smoking, dietary habits and genetic polymorphisms in GSTT1, GSTM1 and CYP1A1 metabolic genes: A case-control study in oncohematological diseases

World Journal of Clinical Oncology; Año: 2016 vol. 7

NIEMINEN T.; PAVICIC W.; PORKKA NOORA; KANKAINEN MATTI; JÄRVINEN HEIKKI J.; LEPISTÖ ANNA; PELTOMÄKI P.

Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis

Oncotarget; Lugar: Nueva York; Año: 2016

CERLIANI MB; GILI JA; PAVICIC WH; KLEIN G; SABA S; RICHARD SM

Association between PER3 length polymorphism and onco-hematological diseases and its influence on patients functionality

Advances in Modern Oncology Research; Año: 2015 vol. 1 p. 132 - 140

JOENSUU E.; NIEMINEN T.; LOTSARI J.; PAVICIC W.; W. M. ABDEL-RAHMAN; PELTOMÄKI P.

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

GENES, CHROMOSOMES & CANCER.; Lugar: New York; Año: 2015 vol. 54 p. 776 - 787

PAVICIC W.; NIEMINEN T.; GYLLING A; PURSIHEIMO JP; LAIHO A; GYENESEI A; JÄRVINEN HJ; PELTOMÄKI P.

Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

GENES, CHROMOSOMES & CANCER.; Lugar: New York; Año: 2014 vol. 53 p. 857 - 864

PAVICIC, W.; JOENSUU EI.; NIEMINEN T.; PELTOMÄKI P.

LINE-1 hypomethylation in familial and sporadic cancer

JOURNAL OF MOLECULAR MEDICINE (BERLIN, GERMANY); Lugar: Berlin; Año: 2012 vol. 90 p. 827 - 835

PAVICIC W.; PERKIÖ E.; KAUR S.; PELTOMÄKI P.

Altered Methylation at MicroRNA-Associated CpG Islands in Hereditary and Sporadic Carcinomas: MS-MLPA-Based Approach

MOLECULAR MEDICINE; Año: 2011 p. 726 - 735

PAVICIC W.; RICHARD SM.

Correlation analysis between mtDNA 4977-bp deletion and ageing

MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS; Año: 2009 p. 99 - 102

PAVICIC W.; LAGUENS M.; RICHARD S.M.

Analysis Association between Mitochondrial Genome Instability and Xenobiotic Metabolizing Genes in Human Breast Cancer

MOLECULAR MEDICINE; Año: 2009 p. 160 - 165

NÉSTOR O. BIANCHI; SILVINA M. RICHARD; WALTER PAVICIC

Y chromosome instability in testicular cancer

MUTATION RESEARCH. REVIEWS IN MUTATION RESEARCH; Año: 2006 vol. 612 p. 172 - 188

BIANCHI, N.O.; RICHARD, SILVINA M.; PAVICIC, W.

Inestabilidad del cromosoma Y en el cáncer testicular.

REVISTA ARGENTINA DE ENDOCRINOLOGIA Y METABOLISMO; Año: 2006 vol. 43 p. 194 - 214

S.M. RICHARD; BIANCHI N. O.; BIANCHI M. S.; PELTOMÄKI P.; LOTHE R. A.; PAVICIC W.

Ethnic variation in the prevalence of AZF deletions in testicular cancer.

MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS; Año: 2004 vol. 554 p. 45 - 51