Mariona Terradas

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 19

Top Venues

European journal of human genetics : EJHG

Scientific reports

Human mutation

Molecular cancer research : MCR

Institut d'Investigació Biomédica de Bellvitge

Universitat Autònoma de Barcelona (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Institut d'Investigació Biomédica de Bellvitge Dec 01 2019

Spain

AECC funded researcher :: Hereditary Cancer Program

Institut d'Investigacio Biomedica de Bellvitge May 02 2017 - Nov 30 2019

Spain

Postdoc :: Hereditary Cancer

Universitat Autònoma de Barcelona Facultat de Biociències Oct 01 2012 - Apr 30 2017

Spain

Postdoc :: Cell Biology, Animal Physiology and Immunology

Universitat Autònoma de Barcelona Facultat de Biociències Sep 15 2011 - Sep 14 2012

Spain

Postdoc with teaching duties :: Animal Biology, Vegetal Biology and Ecology

Universitat Autònoma de Barcelona Facultat de Biociències Oct 01 2006 - May 09 2011

Spain

PhD student :: Cell Biology, Animal Physiology and Immunology

Education History

Universitat Autònoma de Barcelona

Spain

PHD :: Cell Biology

Publications

Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Maria A Andrianova, Vladimir B Seplyarskiy, Mariona Terradas, Ana Beatriz Sanchez-Heras, Pilar Mur, José Luís Soto, Gemma Aiza, Emma Borràs, Fyodor A Kondrashov, Alexey S Kondrashov, Georgii A Bazykin, Laura Valle
Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells. European journal of human genetics : EJHG 32 (7) (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Maria A Andrianova, Vladimir B Seplyarskiy, Mariona Terradas, Ana Beatriz Sanchez-Heras, Pilar Mur, José Luís Soto, Gemma Aiza, Emma Borràs, Fyodor A Kondrashov, Alexey S Kondrashov, Georgii A Bazykin, Laura Valle
Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells. European journal of human genetics : EJHG 32 (7) (2024)
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, Dina Ruano, Gemma Aiza, Maartje Nielsen, Paula Marciel, Carli M Tops, Genís Parra, Hans Morreau, David Torrents, Monique E van Leerdam, Gabriel Capellá Munar, Noel F C C de Miranda, Laura Valle, J Tom van Wezel
Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European journal of human genetics : EJHG 32 (7) (2024)
Maria A Andrianova, Vladimir B Seplyarskiy, Mariona Terradas, Ana Beatriz Sanchez-Heras, Pilar Mur, José Luís Soto, Gemma Aiza, Emma Borràs, Fyodor A Kondrashov, Alexey S Kondrashov, Georgii A Bazykin, Laura Valle
Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells. European journal of human genetics : EJHG 32 (7) (2024)
Maria A Andrianova, Vladimir B Seplyarskiy, Mariona Terradas, Ana Beatriz Sanchez-Heras, Pilar Mur, José Luís Soto, Gemma Aiza, Emma Borràs, Fyodor A Kondrashov, Alexey S Kondrashov, Georgii A Bazykin, Laura Valle
Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells. European journal of human genetics : EJHG 32 (7) (2024)
Maria A Andrianova, Vladimir B Seplyarskiy, Mariona Terradas, Ana Beatriz Sanchez-Heras, Pilar Mur, José Luís Soto, Gemma Aiza, Emma Borràs, Fyodor A Kondrashov, Alexey S Kondrashov, Georgii A Bazykin, Laura Valle
Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells. European journal of human genetics : EJHG (2024)
Isabel Quintana, Pilar Mur, Mariona Terradas, Sandra García-Mulero, Gemma Aiza, Matilde Navarro, Virginia Piñol, Joan Brunet, Victor Moreno, Vicente Martín, Gabriel Capellá, Laura Valle
Potential Involvement of NSD1 , KRT24 and ACACA in the Genetic Predisposition to Colorectal Cancer. Cancers 14 (3) (2022)
Lourdes González-Bermúdez, Anna Genescà, Mariona Terradas, Marta Martín
Role of H4K16 acetylation in 53BP1 recruitment to double-strand break sites in in vitro aged cells. Biogerontology 23 (4) (2022)
Maria Daca-Alvarez, Isabel Quintana, Mariona Terradas, Pilar Mur, Francesc Balaguer, Laura Valle
The Inherited and Familial Component of Early-Onset Colorectal Cancer. Cells 10 (3) (2021)
Sami Belhadj, Mariona Terradas, Pau M Muñoz-Torres, Gemma Aiza, Matilde Navarro, Gabriel Capellá Munar, Laura Valle
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review. Human mutation 41 (9) (2020)
Mariona Terradas, Pilar Mur, Sami Belhadj, Emma Roisin Woodward, George Joseph Burghel, Pau M Muñoz-Torres, Isabel Quintana, Matilde Navarro, Joan Brunet, Conxi Lazaro Garcia, Marta Pineda, Victor Moreno, Gabriel Capellá Munar, Dafydd Gareth Evans, Laura Valle
TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut 70 (6) (2020)
Joan Repullés, Teresa Anglada, David Soler, Juan Carlos Ramírez, Anna Genescà, Mariona Terradas
Radiation-Induced Malignant Transformation of Preneoplastic and Normal Breast Primary Epithelial Cells. Molecular cancer research : MCR 17 (4) (2019)
Sami Belhadj, Isabel Quintana, Pilar Mur, Pau M Munoz-Torres, Maria Henar Alonso, Matilde Navarro, Mariona Terradas, Virginia Piñol, Joan Brunet, Victor Moreno, Conxi Lázaro, Gabriel Capellá, Laura Valle
NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas. Scientific reports 9 (1) (2019)
Lourdes González-Bermúdez, Teresa Anglada, Anna Genescà, Marta Martín, Mariona Terradas
Identification of reference genes for RT-qPCR data normalisation in aging studies. Scientific reports 9 (1) (2019)
Mariona Terradas, Pau M Muñoz-Torres, Sami Belhadj, Gemma Aiza, Matilde Navarro, Joan Brunet, Gabriel Capellá Munar, Laura Valle
Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1- and MSH3-associated polyposes. Human mutation 40 (11) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Mariona Terradas