Pawan Pandoh

4.5k total citations
23 papers, 584 citations indexed

About

Pawan Pandoh is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Pawan Pandoh has authored 23 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 8 papers in Cancer Research and 6 papers in Genetics. Recurrent topics in Pawan Pandoh's work include Genomics and Phylogenetic Studies (12 papers), Molecular Biology Techniques and Applications (7 papers) and RNA modifications and cancer (5 papers). Pawan Pandoh is often cited by papers focused on Genomics and Phylogenetic Studies (12 papers), Molecular Biology Techniques and Applications (7 papers) and RNA modifications and cancer (5 papers). Pawan Pandoh collaborates with scholars based in Canada, Switzerland and Hong Kong. Pawan Pandoh's co-authors include Steven J.M. Jones, Yongjun Zhao, Richard A. Moore, Shaun D. Jackman, İnanç Birol, Jöerg Bohlmann, Marco A. Marra, Martin Hirst, Heather Kirk and Simon K. Chan and has published in prestigious journals such as Nucleic Acids Research, Blood and PLoS ONE.

In The Last Decade

Pawan Pandoh

21 papers receiving 582 citations

Peers

Pawan Pandoh
Pawan Pandoh
Citations per year, relative to Pawan Pandoh Pawan Pandoh (= 1×) peers Yaron S.N. Butterfield

Countries citing papers authored by Pawan Pandoh

Since Specialization
Citations

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

Fields of papers citing papers by Pawan Pandoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pawan Pandoh

This figure shows the co-authorship network connecting the top 25 collaborators of Pawan Pandoh. A scholar is included among the top collaborators of Pawan Pandoh 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 Pawan Pandoh. Pawan Pandoh 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.
Haile, Simon, Richard Corbett, Kieran O’Neill, et al.. (2024). Adaptable and comprehensive approaches for long-read nanopore sequencing of polyadenylated and non-polyadenylated RNAs. Frontiers in Genetics. 15. 1466338–1466338.
2.
Coombe, Lauren, Kristina Gagalova, René L. Warren, et al.. (2023). Assembly and annotation of the black spruce genome provide insights on spruce phylogeny and evolution of stress response. G3 Genes Genomes Genetics. 14(1). 4 indexed citations
3.
Xu, Jing, Pawan Pandoh, Richard Corbett, et al.. (2023). A High-throughput Pipeline for DNA/RNA/small RNA Purification from Tissue Samples for Sequencing. BioTechniques. 75(2). 47–55.
4.
Garant, Jean‐Michel, Kieran O’Neill, Pawan Pandoh, et al.. (2022). Genome-wide detection of imprinted differentially methylated regions using nanopore sequencing. eLife. 11. 26 indexed citations
5.
Garant, Jean‐Michel, Kieran O’Neill, Pawan Pandoh, et al.. (2021). Megabase-scale methylation phasing using nanopore long reads and NanoMethPhase. Genome biology. 22(1). 68–68. 42 indexed citations
6.
Christensen, Kris A., Éric Rondeau, Dionne Sakhrani, et al.. (2021). The pink salmon genome: Uncovering the genomic consequences of a two-year life cycle. PLoS ONE. 16(12). e0255752–e0255752. 16 indexed citations
7.
Jackman, Shaun D., Lauren Coombe, René L. Warren, et al.. (2020). Complete Mitochondrial Genome of a Gymnosperm, Sitka Spruce (Picea sitchensis), Indicates a Complex Physical Structure. Genome Biology and Evolution. 12(7). 1174–1179. 68 indexed citations
8.
Coope, Robin, Richard Corbett, Stephen Pleasance, et al.. (2020). Whole‐slide laser microdissection for tumour enrichment. The Journal of Pathology. 253(2). 225–233. 4 indexed citations
9.
Pandoh, Pawan, Richard Corbett, Helen McDonald, et al.. (2019). A High-Throughput Protocol for Isolating Cell-Free Circulating Tumor DNA from Peripheral Blood. BioTechniques. 66(2). 85–92. 12 indexed citations
10.
Berner, Daniel, Marius Roesti, Simon K. Chan, et al.. (2019). De Novo Sequencing, Assembly, and Annotation of Four Threespine Stickleback Genomes Based on Microfluidic Partitioned DNA Libraries. Genes. 10(6). 426–426. 9 indexed citations
11.
Haile, Simon, Richard Corbett, Karen Mungall, et al.. (2019). Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA. PLoS ONE. 14(10). e0224578–e0224578. 14 indexed citations
12.
Coombe, Lauren, Shaun D. Jackman, Kristina Gagalova, et al.. (2019). Complete Chloroplast Genome Sequence of an Engelmann Spruce ( Picea engelmannii , Genotype Se404-851) from Western Canada. Microbiology Resource Announcements. 8(24). 3 indexed citations
13.
Haile, Simon, Richard Corbett, Heather Kirk, et al.. (2018). Sources of erroneous sequences and artifact chimeric reads in next generation sequencing of genomic DNA from formalin-fixed paraffin-embedded samples. Nucleic Acids Research. 47(2). e12–e12. 44 indexed citations
14.
Taylor, Gregory A., Heather Kirk, Lauren Coombe, et al.. (2018). The Genome of the North American Brown Bear or Grizzly: Ursus arctos ssp. horribilis. Genes. 9(12). 598–598. 25 indexed citations
15.
Nguyen, Long, Maisam Makarem, Annaïck Carles, et al.. (2014). Clonal Analysis via Barcoding Reveals Diverse Growth and Differentiation of Transplanted Mouse and Human Mammary Stem Cells. Cell stem cell. 14(2). 253–263. 50 indexed citations
16.
Keeling, Christopher I., Macaire M. S. Yuen, Nancy Liao, et al.. (2013). Draft genome of the mountain pine beetle, Dendroctonus ponderosae Hopkins, a major forest pest. Genome biology. 14(3). R27–R27. 224 indexed citations
18.
Morrissy, A. Sorana, Yongjun Zhao, Allen Delaney, et al.. (2010). Digital Gene Expression by Tag Sequencing on the Illumina Genome Analyzer. Current Protocols in Human Genetics. 65(1). Unit 11.11.1–36. 16 indexed citations
19.
Morin, Ryan D., Yongjun Zhao, Anna‐Liisa Prabhu, et al.. (2010). Preparation and Analysis of MicroRNA Libraries Using the Illumina Massively Parallel Sequencing Technology. Methods in molecular biology. 650. 173–199. 9 indexed citations
20.
Vatcher, Greg, Duane E. Smailus, Martin Krzywinski, et al.. (2002). Resuspension of DNA Sequencing Reaction Products in Agarose Increases Sequence Quality on an Automated Sequencer. BioTechniques. 33(3). 532–538. 5 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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