Laura Valle

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2014-2024
Publications (10 Years): 38

Top Topics

Endometrial Cancer

Dna Methylation

Top Venues

European journal of human genetics : EJHG

Cancer research communications

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

Publications

Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring co-occurring POLE exonuclease and non-exonuclease domain mutations and their impact on tumor mutagenicity. Cancer research communications (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)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (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)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (2024)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (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)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (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)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring co-occurring POLE exonuclease and non-exonuclease domain mutations and their impact on tumor mutagenicity. Cancer research communications (2024)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (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)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (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)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (2024)
Shreya M Shah, Elena V Demidova, Salena Ringenbach, Bulat Faezov, Mark D Andrake, Arjun Gandhi, Pilar Mur, Julen Viana-Errasti, Joanne Xiu, Jeffrey Swensen, Laura Valle, Roland L Dunbrack, Michael J Hall, Sanjeevani Arora
Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer research communications 4 (1) (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)
Laura Valle, Lior H Katz, Andrew Latchford, Pilar Mur, Victor Moreno, Ian M Frayling, Brandie H Leach, Gabriel Capellá Munar, null null
Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on APC I1307K and cancer risk. Journal of medical genetics (2023)
Mariona Terradas, Noemi Gonzalez-Abuin, Sandra García-Mulero, Julen Viana-Errasti, Gemma Aiza, Josep M Piulats, Joan Brunet, Gabriel Capellá Munar, Laura Valle
MBD4-associated neoplasia syndrome: screening of cases with suggestive phenotypes. European journal of human genetics : EJHG (2023)
Pilar Mur, Julen Viana-Errasti, Sandra García-Mulero, Lorena Magraner-Pardo, Inés G Muñoz, Tirso Pons, Gabriel Capellá, Marta Pineda, Lidia Feliubadaló, Laura Valle
Recommendations for the classification of germline variants in the exonuclease domain of POLE and POLD1. Genome medicine 15 (1) (2023)
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)
Pilar Mur, Lorena Magraner-Pardo, Sandra García-Mulero, Anna Díez-Villanueva, Jesús Del Valle, Elsa Ezquerro, Conxi Lazaro Garcia, Gabriel Capellá Munar, Victor Moreno, Rebeca Sanz-Pamplona, Tirso Pons, Laura Valle
Solving the enigma of POLD1 p.V295M as a potential cause of increased cancer risk. European journal of human genetics : EJHG (2021)
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)
Pilar Mur, Nuria Bonifaci, Anna Díez-Villanueva, Elisabet Munté, Maria Henar Alonso, Mireia Obón-Santacana, Gemma Aiza, Matilde Navarro, Virginia Piñol, Joan Brunet, Ian Tomlinson, Gabriel Capellá, Victor Moreno, Laura Valle
Non-Lynch Familial and Early-Onset Colorectal Cancer Explained by Accumulation of Low-Risk Genetic Variants. Cancers 13 (15) (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, Gabriel Capellá, Laura Valle
Dominantly Inherited Hereditary Nonpolyposis Colorectal Cancer Not Caused by MMR Genes. Journal of clinical medicine 9 (6) (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)
Pilar Mur, Sandra García-Mulero, Jesús Del Valle, Lorena Magraner-Pardo, August Vidal, Marta Pineda, Giacomo Cinnirella, Edgar Martín-Ramos, Tirso Pons, Adriana López-Doriga, Sami Belhadj, Lidia Feliubadaló, Pau M Munoz-Torres, Matilde Navarro, Elia Grau, Esther Darder, Gemma Llort, Judit Sanz, Teresa Ramón Y Cajal, Judith Balmana, Joan Brunet, Victor Moreno, Josep M Piulats, Xavier Matías-Guiu, Rebeca Sanz-Pamplona, Rosa Aligué, Gabriel Capellá, Conxi Lázaro, Laura Valle
Role of POLE and POLD1 in familial cancer. Genetics in medicine : official journal of the American College of Medical Genetics 22 (12) (2020)
Pilar Mur, Claire Palles, Ian P M Tomlinson, Laura Valle
Reply to: "Development of an MSI-positive colon tumor with aberrant DNA methylation in a PPAP patient". Journal of human genetics 65 (6) (2019)
Laura Valle, Eduardo Vilar, Sean V Tavtigian, Elena M Stoffel
Genetic predisposition to colorectal cancer: syndromes, genes, classification of genetic variants and implications for precision medicine. The Journal of pathology 247 (5) (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)
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)
Isabel Quintana, Raquel Mejías-Luque, Mariona Terradas, Matilde Navarro, Virginia Piñol, Pilar Mur, Sami Belhadj, Elia Grau, Esther Darder, Ares Solanes, Joan Brunet, Gabriel Capellá, Markus Gerhard, Laura Valle
Evidence suggests that germline RNF43 mutations are a rare cause of serrated polyposis. Gut 67 (12) (2018)
Pilar Mur, Richarda M De Voer, Rubén Olivera-Salguero, Sandra Rodríguez-Perales, Tirso Pons, Fernando Setién, Gemma Aiza, Rafael Valdés-Mas, Angelo Bertini, Marta Pineda, Lilian Vreede, Matilde Navarro, Silvia Iglesias, Sara González, Joan Brunet, Alfonso Valencia, Manel Esteller, Conxi Lázaro, Geert J P L Kops, Miguel Urioste, Xose S Puente, Gabriel Capellá, Laura Valle
Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis. Molecular cancer 17 (1) (2018)
Pilar Mur, Ann-Sofie Jemth, Luka Bevc, Nuno Amaral, Matilde Navarro, Rafael Valdés-Mas, Tirso Pons, Gemma Aiza, Miguel Urioste, Alfonso Valencia, Conxi Lazaro Garcia, Victor Moreno, Xose S Puente, Pål Stenmark, Ulrika Warpman-Berglund, Gabriel Capellá Munar, Thomas Helleday, Laura Valle
Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis. Human mutation 39 (9) (2018)
Nuria Seguí, Matilde Navarro, Marta Pineda, Nicole Köger, Fernando Bellido, Sara González, Olga Campos, Silvia Iglesias, Rafael Valdés-Mas, Adriana López-Doriga, Marta Gut, Ignacio Blanco, Conxi Lázaro, Gabriel Capellá, Xose S Puente, Guido Plotz, Laura Valle
Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype. Gut 64 (2) (2014)