Laura Valle

3.8k total citations
61 papers, 1.5k citations indexed

About

Laura Valle is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Cancer Research. According to data from OpenAlex, Laura Valle has authored 61 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Pathology and Forensic Medicine, 29 papers in Molecular Biology and 25 papers in Cancer Research. Recurrent topics in Laura Valle's work include Genetic factors in colorectal cancer (44 papers), Cancer Genomics and Diagnostics (23 papers) and DNA Repair Mechanisms (10 papers). Laura Valle is often cited by papers focused on Genetic factors in colorectal cancer (44 papers), Cancer Genomics and Diagnostics (23 papers) and DNA Repair Mechanisms (10 papers). Laura Valle collaborates with scholars based in Spain, United States and Netherlands. Laura Valle's co-authors include Miguel Urioste, Gabriel Capellá, Elena M. Stoffel, Eduardo Vilar, Sean V. Tavtigian, Javier Benı́tez, Mariona Terradas, Matilde Navarro, Anthony A. Gaspari and Rephael Zeltser and has published in prestigious journals such as Science, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Laura Valle

60 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Laura Valle Spain 19 881 632 576 488 333 61 1.5k
Sara González Spain 18 865 1.0× 714 1.1× 1.2k 2.0× 538 1.1× 328 1.0× 47 1.9k
Swen Weßendorf Germany 19 665 0.8× 624 1.0× 521 0.9× 299 0.6× 325 1.0× 31 1.6k
Clyde Bailey United States 10 702 0.8× 645 1.0× 425 0.7× 302 0.6× 206 0.6× 35 1.3k
Marjo van Puijenbroek Netherlands 22 878 1.0× 814 1.3× 359 0.6× 479 1.0× 210 0.6× 33 1.4k
Raihanatou Diallo Germany 22 554 0.6× 784 1.2× 846 1.5× 828 1.7× 424 1.3× 47 2.2k
Shuichi Nakatsuru Japan 10 897 1.0× 698 1.1× 846 1.5× 367 0.8× 206 0.6× 10 1.7k
Marianne Tijssen Netherlands 25 347 0.4× 371 0.6× 705 1.2× 352 0.7× 157 0.5× 40 1.3k
Carsten Schwäenen Germany 19 420 0.5× 377 0.6× 663 1.2× 362 0.7× 347 1.0× 25 1.4k
Gunn Iren Meling Norway 21 709 0.8× 796 1.3× 868 1.5× 525 1.1× 130 0.4× 26 1.6k
Nils Rahner Germany 17 658 0.7× 445 0.7× 310 0.5× 331 0.7× 230 0.7× 35 1.0k

Countries citing papers authored by Laura Valle

Since Specialization
Citations

This map shows the geographic impact of Laura Valle's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Laura Valle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura Valle more than expected).

Fields of papers citing papers by Laura Valle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laura Valle. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Laura Valle. The network helps show where Laura Valle may publish in the future.

Co-authorship network of co-authors of Laura Valle

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Valle. A scholar is included among the top collaborators of Laura Valle based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Laura Valle. Laura Valle is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Terradas, Mariona, Pilar Mur, Chiara Maria Lavinia Löffler, et al.. (2025). Constitutional epimutations in LTBP4, a component of the TGF-β signaling, and in BRCA1, as potential drivers of early-onset colorectal cancer. Clinical Epigenetics. 17(1). 183–183. 1 indexed citations
2.
Rofes, Paula, Mireia Menéndez, Àlex Teulé, et al.. (2025). TP53 germline testing and hereditary cancer: how somatic events and clinical criteria affect variant detection rate. Genome Medicine. 17(1). 3–3. 1 indexed citations
3.
Seplyarskiy, Vladimir B., Mariona Terradas, Pilar Mur, et al.. (2024). 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. 32(7). 837–845. 5 indexed citations
4.
Andrake, Mark, Pilar Mur, Joanne Xiu, et al.. (2024). Exploring Co-occurring POLE Exonuclease and Non-exonuclease Domain Mutations and Their Impact on Tumor Mutagenicity. Cancer Research Communications. 4(1). 213–225. 6 indexed citations
5.
Terradas, Mariona, Dina Ruano, Gemma Aiza, et al.. (2024). Germline NPAT inactivating variants as cause of hereditary colorectal cancer. European Journal of Human Genetics. 32(7). 871–875. 2 indexed citations
6.
Valle, Laura, Lior H. Katz, Andrew Latchford, et al.. (2023). Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on APC I1307K and cancer risk. Journal of Medical Genetics. 60(11). 1035–1043. 12 indexed citations
7.
Beisvåg, Vidar, Elizabeth Holliday, Joan Brunet, et al.. (2023). MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome. Scientific Reports. 13(1). 18783–18783. 3 indexed citations
8.
Mur, Pilar, Mariona Terradas, Sandra García‐Mulero, et al.. (2022). Potential Involvement of NSD1, KRT24 and ACACA in the Genetic Predisposition to Colorectal Cancer. Cancers. 14(3). 699–699. 2 indexed citations
9.
Mur, Pilar, Núria Bonifaci, Anna Díez-Villanueva, et al.. (2021). Non-Lynch Familial and Early-Onset Colorectal Cancer Explained by Accumulation of Low-Risk Genetic Variants. Cancers. 13(15). 3857–3857. 5 indexed citations
10.
Daca-Álvarez, María, et al.. (2021). The Inherited and Familial Component of Early-Onset Colorectal Cancer. Cells. 10(3). 710–710. 56 indexed citations
11.
Fernández–Rozadilla, Ceres, Jorge Amigo, José Cameselle‐Teijeiro, et al.. (2021). Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer. Scientific Reports. 11(1). 11135–11135. 7 indexed citations
12.
Terradas, Mariona, Pilar Mur, Sami Belhadj, et al.. (2020). TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut. 70(6). 1139–1146. 11 indexed citations
13.
Valle, Laura, Richarda M. de Voer, Yael Goldberg, et al.. (2019). Update on genetic predisposition to colorectal cancer and polyposis. Molecular Aspects of Medicine. 69. 10–26. 116 indexed citations
14.
Belhadj, Sami, Pilar Mur, M. Henar Alonso, et al.. (2019). NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas. Scientific Reports. 9(1). 9020–9020. 18 indexed citations
15.
Mur, Pilar, Ann‐Sofie Jemth, Nuno Amaral, et al.. (2018). Germline variation in the oxidative DNA repair genesNUDT1andOGG1is not associated with hereditary colorectal cancer or polyposis. Human Mutation. 39(9). 1214–1225. 5 indexed citations
16.
Sanz‐Pamplona, Rebeca, Adriana López‐Doriga, Laia Paré, et al.. (2015). Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer. Clinical Cancer Research. 21(20). 4709–4718. 44 indexed citations
17.
Bellido, Fernando, Elisabet Guinó, Shantie Jagmohan–Changur, et al.. (2012). Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome. European Journal of Human Genetics. 21(5). 511–516. 17 indexed citations
18.
Zeng, Qinghua, Yanfei Xu, Maureen Sadim, et al.. (2009). Tgfbr1 Haploinsufficiency Is a Potent Modifier of Colorectal Cancer Development. Cancer Research. 69(2). 678–686. 45 indexed citations
19.
Valle, Laura, Sandya Liyanarachchi, Heather Hampel, et al.. (2008). Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal Cancer. Science. 321(5894). 1361–1365. 107 indexed citations
20.
Valle, Laura, et al.. (2007). MLH1 germline epimutations in selected patients with early‐onset non‐polyposis colorectal cancer. Clinical Genetics. 71(3). 232–237. 48 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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