Publications by authors named "John-Paul Plazzer"

18Publications

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

Genet Med 2020 Sep;22(9):1569

Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41436-020-0892-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462742PMC
September 2020

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

Authors:
Adriana Della Valle Benedito Mauro Rossi Edenir Inêz Palmero Marina Antelo Carlos Alberto Vaccaro Francisco López-Kostner Karin Alvarez Marcia Cruz-Correa Luisina Inés Bruno Nora Manoukian Forones Jorge Andres Rugeles Mindiola José Buleje Florencia Spirandelli Mabel Bohorquez Alicia Maria Cock-Rada Yasser Sullcahuaman Ivana Nascimento Kiyoko Abe-Sandes Leonardo S Lino-Silva Florencia Petracchi Alejandra Mampel Yeni Rodriguez Norma Teresa Rossi Claudio Benavides Yañez Cladelis Rubio Tirzah Braz Petta-Lajus Elizabeth Lemos Silveira-Lucas Geiner Jiménez Carlos Mario Muñeton Peña Carlos Reyes-Silva María de la Luz Ayala-Madrigal Julio Sánchez Del Monte Richard Quispe Alcides Recalde Florencia Neffa Carlos Sarroca Henrique de Campos Reis Galvão Mariano Golubicki Tamara A Piñero Pablo G Kalfayan Fabiana Alejandra Ferro Maria Laura Gonzalez Julyann Pérez-Mayoral Celia Aparecida Marques Pimenta Sandra Patricia Bello Uyaban Ana Protzel Guiliana Chávez Milagros Dueñas María Luisa Guevara Gil Enrique Spirandelli Sergio Chialina Magdalena Echeverry Luis José Palacios Fuenmayor Mariela Torres Thais F Bonfim Palma Nadia Cambados Héritas Claudia Martin Alfonso Suárez Michael Vallejo Ana Rafaela de Souza Timoteo Carlos Afanador Ayala Gabriela Jaramillo-Koupermann Jesús Arturo Hernández-Sandoval Angélica Hernandez Guerrero Constantino Dominguez-Barrera Juan Carlos Bazo-Alvarez Patrik Wernhoff John-Paul Plazzer Yesilda Balavarca Eivind Hovig Pål Møller Mev Dominguez-Valentin

Eur J Cancer 2019 09 20;119:112-121. Epub 2019 Aug 20.

Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejca.2019.07.017DOI Listing
September 2019

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

Genet Med 2020 01 24;22(1):15-25. Epub 2019 Jul 24.

Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41436-019-0596-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371626PMC
January 2020

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.

Hered Cancer Clin Pract 2019 28;17. Epub 2019 Feb 28.

4Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital, Olso, Norway.

View Article

Download full-text PDF

Source
https://hccpjournal.biomedcentral.com/articles/10.1186/s1305
Publisher Site
http://dx.doi.org/10.1186/s13053-019-0106-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394091PMC
February 2019

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

Int J Cancer 2019 07 5;145(2):318-326. Epub 2018 Dec 5.

Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ijc.31920
Publisher Site
http://dx.doi.org/10.1002/ijc.31920DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587543PMC
July 2019

An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.

Fam Cancer 2018 07;17(3):421-427

The University of Melbourne, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10689-017-0037-3DOI Listing
July 2018

Harmonizing the interpretation of genetic variants across the world: the Malaysian experience.

BMC Res Notes 2016 Feb 26;9:125. Epub 2016 Feb 26.

Department of Pediatric, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, Kubang Kerian, 16150, Kota Bharu, Kelantan, Malaysia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s13104-015-1798-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768322PMC
February 2016

DNA variant databases: current state and future directions.

Methods Mol Biol 2014 ;1168:263-73

Department of Colorectal Medicine and Genetics, Royal Melbourne Hospital, RMH, Grattan Street, Parkville, VIC, 3050, Australia,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-1-4939-0847-9_15DOI Listing
January 2015

Annotating the biomedical literature for the human variome.

Database (Oxford) 2013 12;2013:bat019. Epub 2013 Apr 12.

National ICT Australia (NICTA), Victoria Research Laboratory, Level 2, Building 193, The University of Melbourne, Parkville VIC 3010, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/database/bat019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3676157PMC
June 2013

Reporting of Genetic Variants by Diagnostic Laboratories and other Centres.

Clin Biochem Rev 2012 Feb;33(1):21-4

Curator, International Society for Gastrointestinal Hereditary Tumours (InSiGHT), The Royal Melbourne Hospital, Parkville, Vic., Australia;

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284340PMC
February 2012