Pedro Pinto

1.2k total citations
31 papers, 433 citations indexed

About

Pedro Pinto is a scholar working on Molecular Biology, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Pedro Pinto has authored 31 papers receiving a total of 433 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Cancer Research and 11 papers in Pathology and Forensic Medicine. Recurrent topics in Pedro Pinto's work include Cancer Genomics and Diagnostics (14 papers), Genetic factors in colorectal cancer (10 papers) and BRCA gene mutations in cancer (9 papers). Pedro Pinto is often cited by papers focused on Cancer Genomics and Diagnostics (14 papers), Genetic factors in colorectal cancer (10 papers) and BRCA gene mutations in cancer (9 papers). Pedro Pinto collaborates with scholars based in Portugal, United Kingdom and Chile. Pedro Pinto's co-authors include Ana Peixoto, Manuel R. Teixeira, Carla Pinto, Manuela Pinheiro, Catarina Santos, Patrícia Rocha, Rui Henrique, Sofia Maia, Paula Paulo and Isabel Veiga and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and PLoS Genetics.

In The Last Decade

Pedro Pinto

29 papers receiving 431 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Pedro Pinto Portugal	15	210	155	152	135	131	31	433
Wojciech Kluźniak Poland	12	202 1.0×	150 1.0×	161 1.1×	297 2.2×	130 1.0×	26	482
Mark Barnes United Kingdom	6	198 0.9×	201 1.3×	67 0.4×	62 0.5×	51 0.4×	7	306
Adrien Briaux France	11	146 0.7×	85 0.5×	111 0.7×	69 0.5×	78 0.6×	17	304
Giona Turri Italy	6	101 0.5×	134 0.9×	161 1.1×	62 0.5×	102 0.8×	10	331
Rachel T. Klein United States	10	204 1.0×	205 1.3×	140 0.9×	354 2.6×	299 2.3×	15	600
Petra Zemánková Czechia	10	149 0.7×	97 0.6×	106 0.7×	117 0.9×	72 0.5×	23	308
Vida Stegel Slovenia	11	143 0.7×	87 0.6×	75 0.5×	135 1.0×	56 0.4×	36	334
Helena Rodrigues Portugal	6	205 1.0×	165 1.1×	147 1.0×	100 0.7×	89 0.7×	13	336
Javier del Rey Spain	10	103 0.5×	84 0.5×	61 0.4×	96 0.7×	89 0.7×	24	302
Matthew Egyud United States	8	156 0.7×	163 1.1×	66 0.4×	51 0.4×	30 0.2×	11	326

Countries citing papers authored by Pedro Pinto

Since Specialization

Citations

This map shows the geographic impact of Pedro Pinto'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 Pedro Pinto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pedro Pinto more than expected).

Fields of papers citing papers by Pedro Pinto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pedro Pinto. 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 Pedro Pinto. The network helps show where Pedro Pinto may publish in the future.

Co-authorship network of co-authors of Pedro Pinto

This figure shows the co-authorship network connecting the top 25 collaborators of Pedro Pinto. A scholar is included among the top collaborators of Pedro Pinto 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 Pedro Pinto. Pedro Pinto is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Pinto, Carla, Pedro Pinto, Manuela Pinheiro, et al.. (2023). Frequency of CDH1, CTNNA1 and CTNND1 Germline Variants in Families with Diffuse and Mixed Gastric Cancer. Cancers. 15(17). 4313–4313. 2 indexed citations

Silva, Fernanda, Ana Peixoto, Pedro Pinto, et al.. (2022). Establishment and characterization of a novel ovarian high-grade serous carcinoma cell line—IPO43. Cancer Cell International. 22(1). 175–175. 2 indexed citations

Pinheiro, Manuela, Ana Peixoto, Patrícia Rocha, et al.. (2022). KRAS and NRAS mutational analysis in plasma ctDNA from patients with metastatic colorectal cancer by real-time PCR and digital PCR. International Journal of Colorectal Disease. 37(4). 895–905. 5 indexed citations

Maia, Luís, et al.. (2021). Acute variceal bleeding and out-of-hours endoscopy: Evaluation of an emergency care setting according to Baveno VI guidelines adherence. Digestive and Liver Disease. 53(10). 1320–1326. 4 indexed citations

Barbosa, Ana Paula Fernandes, Pedro Pinto, Ana Peixoto, et al.. (2021). Next Generation Sequencing of Tumor and Matched Plasma Samples: Identification of Somatic Variants in ctDNA From Ovarian Cancer Patients. Frontiers in Oncology. 11. 754094–754094. 6 indexed citations

Pinto, Carla, Joana Vieira, Ana Peixoto, et al.. (2020). The role of TP53 pathogenic variants in early-onset HER2-positive breast cancer. Familial Cancer. 20(3). 173–180. 4 indexed citations

Pinheiro, Manuela, Ana Peixoto, Catarina Santos, et al.. (2020). Pathogenicity reclassification of two BRCA1/BRCA2 exonic duplications after identification of genomic breakpoints and tandem orientation. Cancer Genetics. 248-249. 18–24. 2 indexed citations

Barbosa, Ana Paula Fernandes, Ana Peixoto, Pedro Pinto, Manuela Pinheiro, & Manuel R. Teixeira. (2018). Potential clinical applications of circulating cell-free DNA in ovarian cancer patients. Expert Reviews in Molecular Medicine. 20. e6–e6. 19 indexed citations

Paulo, Paula, Sofia Maia, Carla Pinto, et al.. (2018). Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer. PLoS Genetics. 14(4). e1007355–e1007355. 45 indexed citations

10.

Paulo, Paula, Pedro Pinto, Ana Peixoto, et al.. (2017). Validation of a Next-Generation Sequencing Pipeline for the Molecular Diagnosis of Multiple Inherited Cancer Predisposing Syndromes. Journal of Molecular Diagnostics. 19(4). 502–513. 11 indexed citations

11.

Cabreira, Verónica, Carla Pinto, Manuela Pinheiro, et al.. (2016). Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression. Familial Cancer. 16(1). 73–81. 3 indexed citations

12.

Pinto, Pedro, Ana Peixoto, Catarina Santos, et al.. (2016). Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas. PLoS ONE. 11(8). e0161438–e0161438. 17 indexed citations

13.

Maia, Sofia, Marta Cardoso, Paula Paulo, et al.. (2015). The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer. Familial Cancer. 15(1). 111–121. 18 indexed citations

14.

Maia, Sofia, Marta Cardoso, Pedro Pinto, et al.. (2015). Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients. PLoS ONE. 10(7). e0132728–e0132728. 32 indexed citations

15.

Pinto, Carla, Manuela Pinheiro, Ana Peixoto, et al.. (2015). Co-occurrence of nonsense mutations in MSH6 and MSH2 in Lynch syndrome families evidencing that not all truncating mutations are equal. Journal of Human Genetics. 61(2). 151–156. 7 indexed citations

16.

Hartley, Taila, Luca Cavallone, Nelly Sabbaghian, et al.. (2014). Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada. Hereditary Cancer in Clinical Practice. 12(1). 19–19. 18 indexed citations

17.

Santos, Catarina, Ana Peixoto, Patrícia Rocha, et al.. (2014). Pathogenicity Evaluation of BRCA1 and BRCA2 Unclassified Variants Identified in Portuguese Breast/Ovarian Cancer Families. Journal of Molecular Diagnostics. 16(3). 324–334. 17 indexed citations

18.

Peixoto, Ana, Manuela Pinheiro, Catarina Santos, et al.. (2012). Genomic characterization of two large Alu-mediated rearrangements of the BRCA1 gene. Journal of Human Genetics. 58(2). 78–83. 25 indexed citations

19.

Pinto, Pedro, Patrícia Rocha, Isabel Veiga, et al.. (2011). Comparison of methodologies for KRAS mutation detection in metastatic colorectal cancer. Cancer Genetics. 204(8). 439–446. 34 indexed citations

20.

Pinto, Pedro, Conceição Nogueira, & João Manuel de Oliveira. (2010). Debates feministas sobre pornografia heteronormativa: estéticas e ideologias da sexualização Feminist debates on heteronormative pornography: aesthetics and ideologies of sexualization. SHILAP Revista de lepidopterología. 2 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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