Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift

por Møller, Pål, Dominguez-Valentin, Mev, Rødland, Einar Andreas, Hovig, Eivind
Publicado 2019

Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11...

por Møller, Pål, Dominguez-Valentin, Mev, Rødland, Einar Andreas, Hovig, Eivind
Publicado 2020

Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD)

por Seppälä, Toni T., Dominguez-Valentin, Mev, Sampson, Julian R., Møller, Pål
Publicado 2020

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

por Vaccaro, Carlos Alberto, Soarez, Julieta, Dominguez-Valentin, Mev, Pavicic, Walter Hernán
Publicado 2022

Challenges to Bringing Personalized Medicine to a Low-Resource Setting in Peru

por Solis, Nelly, Zavaleta, Elizabeth, Wernhoff, Patrik, Dominguez-Barrera, Constantino, Dominguez-Valentin, Mev
Publicado 2021

Frequent mismatch-repair defects link prostate cancer to Lynch syndrome

por Dominguez-Valentin, Mev, Joost, Patrick, Therkildsen, Christina, Jonsson, Mats, Rambech, Eva, Nilbert, Mef
Publicado 2016

Distinct Gene Expression Signatures in Lynch Syndrome and Familial Colorectal Cancer Type X

por Dominguez-Valentin, Mev, Therkildsen, Christina, Veerla, Srinivas, Jönsson, Mats, Bernstein, Inge, Borg, Åke, Nilbert, Mef
Publicado 2013

The first three reported cases of Sporothrix brasiliensis cat-transmitted sporotrichosis outside South America

por Barnacle, James R., Chow, Yimmy J., Borman, Andrew M., Wyllie, Steven, Dominguez, Valentin, Russell, Katherine, Roberts, Helen, Armstrong-James, Darius, Whittington, Ashley M.
Publicado 2022

Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein

por Dominguez-Valentin, Mev, Drost, Mark, Therkildsen, Christina, Rambech, Eva, Ehrencrona, Hans, Angleys, Maria, Lau Hansen, Thomas, de Wind, Niels, Nilbert, Mef, Juel Rasmussen, Lene
Publicado 2014

Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome

por Jönsson, Jenny-Maria, Bartuma, Katarina, Dominguez-Valentin, Mev, Harbst, Katja, Ketabi, Zohreh, Malander, Susanne, Jönsson, Mats, Carneiro, Ana, Måsbäck, Anna, Jönsson, Göran, Nilbert, Mef
Publicado 2014

Key Roles for MYC, KIT and RET signaling in secondary angiosarcomas

por Styring, E, Seinen, J, Dominguez-Valentin, M, Domanski, H A, Jönsson, M, von Steyern, F V, Hoekstra, H J, Suurmeijer, A J H, Nilbert, M
Publicado 2014

Molecular Subtyping of Serous Ovarian Tumors Reveals Multiple Connections to Intrinsic Breast Cancer Subtypes

por Jönsson, Jenny-Maria, Johansson, Ida, Dominguez-Valentin, Mev, Kimbung, Siker, Jönsson, Mats, Bonde, Jesper Hansen, Kannisto, Päivi, Måsbäck, Anna, Malander, Susanne, Nilbert, Mef, Hedenfalk, Ingrid
Publicado 2014

Increased infiltration and tolerised antigen-specific CD8(+) T(EM) cells in tumor but not peripheral blood have no impact on survival of HCMV(+) glioblastoma patients

por Bahador, M., Gras Navarro, A., Rahman, M.A., Dominguez-Valentin, M., Sarowar, S., Ulvestad, E., Njølstad, G., Lie, S.A., Kristoffersen, E.K., Bratland, E., Chekenya, M.
Publicado 2017

Identification of genetic variants for clinical management of familial colorectal tumors

por Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Martins, Alexandra, Møller, Pål, Hovig, Eivind
Publicado 2018

A Breast Cancer Polygenic Risk Score Is Feasible for Risk Stratification in the Norwegian Population

por Akdeniz, Bayram Cevdet, Mattingsdal, Morten, Dominguez-Valentin, Mev, Frei, Oleksandr, Shadrin, Alexey, Puustusmaa, Mikk, Saar, Regina, Sõber, Siim, Møller, Pål, Andreassen, Ole A., Padrik, Peeter, Hovig, Eivind
Publicado 2023

MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome

por Dominguez-Valentin, Mev, Wernhoff, Patrik, Cajal, Andrea R., Kalfayan, Pablo G., Piñero, Tamara A., Gonzalez, Maria L., Ferro, Alejandra, Sammartino, Ines, Causada Calo, Natalia S., Vaccaro, Carlos A.
Publicado 2016

Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds

por Dominguez-Valentin, Mev, Evans, D. Gareth R., Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Martins, Alexandra, Møller, Pål, Hovig, Eivind
Publicado 2018

Spectrum and Frequency of Tumors, Cancer Risk and Survival in Chilean Families with Lynch Syndrome: Experience of the Implementation of a Registry

por Álvarez, Karin, Orellana, Paulina, De la Fuente, Marjorie, Canales, Tamara, Pinto, Eliana, Heine, Claudio, Solar, Benjamín, Hurtado, Claudia, Møller, Pål, Kronberg, Udo, Zarate, Alejandro José, Dominguez-Valentin, Mev, López-Köstner, Francisco
Publicado 2020

Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing

por Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Holth, Arild, Capella, Gabriel, Davidson, Ben, Evans, D. Gareth, Martins, Alexandra, Møller, Pål, Hovig, Eivind
Publicado 2019

Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas...

por Hodan, Rachel, Rodgers‐Fouche, Linda, Arora, Sanjeevani, Dominguez‐Valentin, Mev, Kanth, Priyanka, Katona, Bryson W., Mraz, Kathryn A., Roberts, Maegan E., Vilar, Eduardo, Soto‐Azghani, Cynthia M., Brand, Randall E, Esplin, Edward D., Perez, Kimberly
Publicado 2022