Manuela Pinheiro

1.3k citations

52 papers · 761 indexed · h-index 19

Co-authors: Manuel R. Teixeira Ana Peixoto Carla Pinto Catarina Santos Pedro Pinto Rui Henrique Isabel Veiga Patrícia Rocha
Topics: Cancer Genomics and Diagnostics (20 papers)Genetic factors in colorectal cancer (17 papers)BRCA gene mutations in cancer (12 papers)
Cited by: Cancer Research Pathology and Forensic Medicine Oncology
Journals: PLoS ONE JNCI Journal of the National Cancer Institute British Journal of Cancer
Partner nations: Portugal United Kingdom United States

In The Last Decade

Manuela Pinheiro

51 papers receiving 757 citations

Peers

Countries citing papers authored by Manuela Pinheiro

Since Specialization

Citations

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

Fields of papers citing papers by Manuela Pinheiro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Pinheiro

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	The role of TP53 pathogenic variants in early-onset HER2-positive breast cancer 2020 ·Familial Cancer ·(unknown),Carla Pinto,Joana Vieira,Ana Peixoto,Pedro Pinto,Manuela Pinheiro,Catarina Santos,(unknown),Susana Lisboa,(unknown),João Silva,Conceição Leal,(unknown),Paula Lopes,(unknown),Ana Berta Sousa,Manuel R. Teixeira	4
2	Potential clinical applications of circulating cell-free DNA in ovarian cancer patients 2018 ·Expert Reviews in Molecular Medicine ·Ana Paula Fernandes Barbosa,Ana Peixoto,Pedro Pinto,Manuela Pinheiro,Manuel R. Teixeira	19
3	Ovarian metastasis from uveal melanoma with MLH1/PMS2 protein loss in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence? 2016 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·João Lobo,Carla Pinto,(unknown),Manuela Pinheiro,José R. Vizcaíno,Esther Oliva,Manuel R. Teixeira,Cármen Jerónimo,Carla Bartosch	9
4	Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression 2016 ·Familial Cancer ·Verónica Cabreira,Carla Pinto,Manuela Pinheiro,Paula Lopes,Ana Peixoto,Catarina Santos,Isabel Veiga,Patrícia Rocha,Pedro Pinto,Rui Henrique,Manuel R. Teixeira	3
5	Target gene mutational pattern in Lynch syndrome colorectal carcinomas according to tumour location and germline mutation 2015 ·British Journal of Cancer ·Manuela Pinheiro,Carla Pinto,Ana Peixoto,Isabel Veiga,Paula Lopes,Rui Henrique,(unknown),Fátima Carneiro,Raquel Seruca,Ian Tomlinson,Michal Kováč,Karl Heinimann,Manuel R. Teixeira	25
6	The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer 2015 ·Familial Cancer ·Sofia Maia,Marta Cardoso,Paula Paulo,Manuela Pinheiro,Pedro Pinto,Catarina Santos,Carla Pinto,Ana Peixoto,Rui Henrique,Manuel R. Teixeira	18
7	Re: Role of the Oxidative DNA Damage Repair Gene OGG1 in Colorectal Tumorigenesis 2014 ·JNCI Journal of the National Cancer Institute ·Ben Kinnersley,Stephan Buch,Sergi Castellvı́-Bel,Susan M. Farrington,Asta Försti,Jochen Hampe,Kari Hemminki,Robert M.W. Hofstra,(unknown),Claire Palles,Manuela Pinheiro,Clara Ruíz-Ponte,Clemens Schafmayer,Manuel R. Teixeira,Helga Westers,Tom van Wezel,D. Timothy Bishop,Ian Tomlinson,Malcolm G. Dunlop,Richard S. Houlston	9
8	The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families 2012 ·Clinical Genetics ·Manuela Pinheiro,Carla Pinto,Ana Peixoto,Isabel Veiga,Bárbara Mesquita,Rui Henrique,Paula Lopes,(unknown),Maria Fragoso,(unknown),(unknown),(unknown),Elisabeth Mangold,Carlos Vaccaro,D. Gareth Evans,Susan M. Farrington,(unknown),(unknown)	11
9	Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion 2012 ·BMC Cancer ·(unknown),Ingrid Petroni Ewald,(unknown),Manuela Pinheiro,Ana Peixoto,(unknown),Dirce Maria Carraro,Manuel R. Teixeira,Patrícia Ashton‐Prolla,Maria Isabel Achatz,Carla Rosenberg,Ana Cristina Victorino Krepischi	13
10	Acute megakaryoblastic leukemia with a four‐way variant translocation originating the RBM15–MKL1 fusion gene 2011 ·Pediatric Blood & Cancer ·Lurdes Torres,Susana Lisboa,Joana Vieira,Nuno Cerveira,Joana Santos,Manuela Pinheiro,Cecília Correia,Susana Bizarro,(unknown),Manuel R. Teixeira	11
11	Promoter methylation and large intragenic rearrangements of DPYD are not implicated in severe toxicity to 5-fluorouracil-based chemotherapy in gastrointestinal cancer patients 2010 ·BMC Cancer ·(unknown),Joäo Carvalho,Manuela Pinheiro,Vera L. Costa,Ângelo Rodrigues,Paula C. Dias,Isabel Veiga,Manuela Machado,Manuel R. Teixeira,Rui Henrique,Cármen Jerónimo	21
12	Chromosome copy number changes carry prognostic information independent of KIT/PDGFRA point mutations in gastrointestinal stromal tumors 2010 ·BMC Medicine ·(unknown),Isabel Veiga,Franclim R. Ribeiro,Joana Vieira,Carla Pinto,Manuela Pinheiro,Bárbara Mesquita,Catarina Santos,Marta Soares,José Dinis,Lúcio Lara Santos,Paula Lopes,(unknown),Carlos Lopes,Manuel R. Teixeira	13
13	Coexistence of alternative MLL–SEPT9 fusion transcripts in an acute myeloid leukemia with t(11;17)(q23;q25) 2010 ·Cancer Genetics and Cytogenetics ·Joana Santos,Nuno Cerveira,Cecília Correia,Susana Lisboa,Manuela Pinheiro,Lurdes Torres,Susana Bizarro,Joana Vieira,Luísa Viterbo,José Mariz,Manuel R. Teixeira	10
14	Feasibility of differential diagnosis of kidney tumors by comparative genomic hybridization of fine needle aspiration biopsies 2010 ·Genes Chromosomes and Cancer ·Joana Vieira,Rui Henrique,Franclim R. Ribeiro,João D. Barros‐Silva,Ana Peixoto,Catarina Santos,Manuela Pinheiro,Vera L. Costa,(unknown),Jorge Oliveira,Cármen Jerónimo,Manuel R. Teixeira	30
15	TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset 2009 ·Familial Cancer ·Carla Pinto,Isabel Veiga,Manuela Pinheiro,Ana Peixoto,(unknown),José Manuel Lopes,Rui Manuel Reis,Carla Oliveíra,(unknown),Lúcia Roque,Fernando Regateiro,Luı́s Cirnes,Robert M.W. Hofstra,Raquel Seruca,Sérgio Castedo,Manuel R. Teixeira	12
16	Hereditary gastrointestinal stromal tumors sharing the KIT Exon 17 germline mutation p.Asp820Tyr develop through different cytogenetic progression pathways 2009 ·Genes Chromosomes and Cancer ·Isabel Veiga,(unknown),Joana Vieira,Carla Pinto,Manuela Pinheiro,Lurdes Torres,Marta Soares,Lúcio Lara Santos,(unknown),(unknown),(unknown),José Dinis,Carlos Lopes,Manuel R. Teixeira	15
17	Haplotype and quantitative transcript analyses of Portuguese breast/ovarian cancer families with the BRCA1 R71G founder mutation of Galician origin 2009 ·Familial Cancer ·Catarina Santos,Ana Peixoto,Patrícia Rocha,Ana Vega,(unknown),Nuno Cerveira,Susana Bizarro,Manuela Pinheiro,Deolinda Pereira,Helena Rodrigues,Fernando Castro,Rui Henrique,Manuel R. Teixeira	8
18	Molecular characterization of the MLL-SEPT6 fusion gene in acute myeloid leukemia: identification of novel fusion transcripts and cloning of genomic breakpoint junctions 2008 ·Haematologica ·Nuno Cerveira,Francesca Micci,Joana Santos,Manuela Pinheiro,Cecília Correia,Susana Lisboa,Susana Bizarro,Lucília Norton,Anders Glomstein,Arne Åsberg,Sverre Heim,Manuel R. Teixeira	13
19	The c.156_157insAlu BRCA2 rearrangement accounts for more than one-fourth of deleterious BRCA mutations in northern/central Portugal 2008 ·Breast Cancer Research and Treatment ·Ana Peixoto,Catarina Santos,Patrícia Rocha,Manuela Pinheiro,(unknown),Deolinda Pereira,Helena Rodrigues,Fernando Castro,(unknown),Leonor Gusmão,António Amorim,Manuel R. Teixeira	41
20	MSH6 germline mutations in early-onset colorectal cancer patients without family history of the disease 2006 ·British Journal of Cancer ·Carla Pinto,Isabel Veiga,Manuela Pinheiro,Bárbara Mesquita,Cármen Jerónimo,(unknown),Maria Fragoso,Lúcio Lara Santos,Luís Moreira‐Dias,(unknown),Carlos Lopes,Sérgio Castedo,Manuel R. Teixeira	15

About Manuela Pinheiro

Manuela Pinheiro is a scholar working on Cancer Research, Pathology and Forensic Medicine and Oncology, having authored 52 papers that have together received 761 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (20 papers), Genetic factors in colorectal cancer (17 papers) and BRCA gene mutations in cancer (12 papers). The work is most often cited by research in Cancer Research (286 citations), Pathology and Forensic Medicine (269 citations) and Oncology (279 citations). Manuela Pinheiro has collaborated with scholars based in Portugal, United Kingdom and United States. Frequent co-authors include Manuel R. Teixeira, Ana Peixoto, Carla Pinto, Catarina Santos, Pedro Pinto, Rui Henrique, Isabel Veiga, Patrícia Rocha, Paula Lopes and Cármen Jerónimo. Their work appears in journals such as PLoS ONE, JNCI Journal of the National Cancer Institute and British Journal of Cancer.

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.

Explore authors with similar magnitude of impact