Marbin Pineda

3.3k total citations
31 papers, 1.7k citations indexed

About

Marbin Pineda is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Marbin Pineda has authored 31 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Cancer Research and 8 papers in Genetics. Recurrent topics in Marbin Pineda's work include BRCA gene mutations in cancer (6 papers), MicroRNA in disease regulation (5 papers) and RNA modifications and cancer (5 papers). Marbin Pineda is often cited by papers focused on BRCA gene mutations in cancer (6 papers), MicroRNA in disease regulation (5 papers) and RNA modifications and cancer (5 papers). Marbin Pineda collaborates with scholars based in United States, France and Poland. Marbin Pineda's co-authors include Paul S. Meltzer, Robert L. Walker, Sven Bilke, Yuelin J. Zhu, Sean Davis, Ogan D. Abaan, Lee J. Helman, Joshua J. Waterfall, J. Keith Killian and Princy Francis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Marbin Pineda

31 papers receiving 1.7k citations

Peers

Marbin Pineda
Comparison fields: 5 of 90
  • Molecular Biology 965
  • Cancer Research 445
  • Oncology 396
  • Pulmonary and Respiratory Medicine 328
  • Pathology and Forensic Medicine 224
E. Lin United States
Christopher C. Porter United States
Kerstin A. David Germany
Stefan Bentink United States
Mark L. Levitt United States
Larissa V. Furtado United States
Maria Monne Italy
Stephen J. Murphy United States
Alberto Gallardo Spain
Donavan T. Cheng United States
E. Lin United States View profile →
Citations per field, relative to Marbin Pineda
Marbin Pineda · 1×
Citations per year, relative to Marbin Pineda
Marbin Pineda · 1×

Countries citing papers authored by Marbin Pineda

Since Specialization
Citations

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

Fields of papers citing papers by Marbin Pineda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marbin Pineda

This figure shows the co-authorship network connecting the top 25 collaborators of Marbin Pineda. A scholar is included among the top collaborators of Marbin Pineda 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 Marbin Pineda. Marbin Pineda 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
# Title Journal Authors Indexed citations
1 Whole Genome Sequencing of Newly Established Pancreatic Cancer Lines Identifies Novel Somatic Mutation (c.2587G>A) in Axon Guidance Receptor Plexin A1 as Enhancer of Proliferation and Invasion PLoS ONE Rebecca Sorber, Yaroslav Teper et al. 22
2 NUP98–PHF23 Is a Chromatin-Modifying Oncoprotein That Causes a Wide Array of Leukemias Sensitive to Inhibition of PHD Histone Reader Function Cancer Discovery Sheryl M. Gough, Fan Lee et al. 59
3 Characterization of Fibroblast Growth Factor Receptor 1 in Small-Cell Lung Cancer Journal of Thoracic Oncology Anish Thomas, Jih‐Hsiang Lee et al. 26
4 A mutant p53/let-7i-axis-regulated gene network drives cell migration, invasion and metastasis Oncogene Megha Subramanian, P. Francis et al. 70
5 The Exomes of the NCI-60 Panel: A Genomic Resource for Cancer Biology and Systems Pharmacology Cancer Research Ogan D. Abaan, Eric C. Polley et al. 204
6 High prevalence of MAP2K1 mutations in variant and IGHV4-34–expressing hairy-cell leukemias Nature Genetics Joshua J. Waterfall, Evgeny Arons et al. 180
7 Massively-parallel sequencing of genes on a single chromosome: a comparison of solution hybrid selection and flow sorting BMC Genomics Jamie K. Teer, Jennifer J. Johnston et al. 4
8 Immunohistochemical Loss of Succinate Dehydrogenase Subunit A (SDHA) in Gastrointestinal Stromal Tumors (GISTs) Signals SDHA Germline Mutation The American Journal of Surgical Pathology Markku Miettinen, Jonathan Keith Killian et al. 128
9 Oncogenic ETS fusions deregulate E2F3 target genes in Ewing sarcoma and prostate cancer Genome Research Sven Bilke, Raphaela Schwentner et al. 80
10 Abstract 1113: Role of the microRNA-23∼27∼24 clusters in osteosarcoma Cancer Research Princy Francis, So Young Moon et al. 1
11 Inhibition of Polo-like kinase 1 prevents the growth of metastatic breast cancer cells in the brain Clinical & Experimental Metastasis Yongzhen Qian, Emily Hua et al. 33
12 Genome-Wide Identification of PAX3-FKHR Binding Sites in Rhabdomyosarcoma Reveals Candidate Target Genes Important for Development and Cancer Cancer Research Liang Cao, Yunkai Yu et al. 174
13 Expression and Mutational Status of c-kit in Thymic Epithelial Tumors Journal of Thoracic Oncology Iacopo Petrini, Paolo Andrea Zucali et al. 55
14 Thyroid Nodules, Polymorphic Variants in DNA Repair andRET-Related Genes, and Interaction with Ionizing Radiation Exposure from Nuclear Tests in Kazakhstan Radiation Research Alice J. Sigurdson, Charles E. Land et al. 37
15 The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies BMC Genetics Lutécia H. Mateus Pereira, Marbin Pineda et al. 6
16 Polymorphisms in DNA repair genes, ionizing radiation exposure and risk of breast cancer in U.S. Radiologic technologists International Journal of Cancer Parveen Bhatti, Jeffery P. Struewing et al. 46
17 TheATMmissense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer Human Mutation Montserrat García‐Closas, Marbin Pineda et al. 49
18 Skewed X chromosome inactivation and early-onset breast cancer Journal of Medical Genetics Jeffery P. Struewing, Marbin Pineda et al. 11
19 Mutational analysis of theBRCA1-interacting genesZNF350/ZBRK1andBRIP1/BACH1amongBRCA1andBRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals Human Mutation Joni L. Rutter, Alice J. Sigurdson et al. 46
20 High transdominant RevM10 protein levels are required to inhibit HIV-1 replication in cell lines and primary T cells: implication for gene therapy of AIDS Gene Therapy Ivan Plavec, Manju Agarwal et al. 64

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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