Adam Frankish

48.5k citations
39 papers · 3.2k indexed · 1 hit paper · h-index 27

Impact in

    • Cancer-related molecular mechanisms research
    • MicroRNA in disease regulation
    • RNA modifications and cancer
    • RNA Research and Splicing
    • RNA and protein synthesis mechanisms
    • Genomics and Phylogenetic Studies
    • Genomics and Chromatin Dynamics
    • Circular RNAs in diseases

Papers in

    • RNA and protein synthesis mechanisms 23
    • Genomics and Phylogenetic Studies 22
    • RNA modifications and cancer 18
    • RNA Research and Splicing 9
    • Genomics and Chromatin Dynamics 6
    • Machine Learning in Bioinformatics 3
    • Molecular Biology Techniques and Applications 3
    • Cancer-related molecular mechanisms research 5

Adam Frankish

39 papers receiving 3.1k citations

Hit Papers

Towards a complete map of the human long non-coding RNA transcriptome 2018 · 431 citations
4312018202620202023100200300400

Peers

Adam Frankish
Comparison fields: 5 of 126
  • Cancer Research 1.1k
  • Molecular Biology 2.7k
  • Genetics 373
  • Endocrinology 56
  • Plant Science 295
Replace Debasish Raha with:
Debasish Raha United States
Christopher D. Armour United States
Sandro J. de Souza Brazil
Namshin Kim South Korea
Liana F. Lareau United States
San Ming Wang United States
Shunmin He China
Daniel R. Schoenberg United States
Christine Mayer Germany
Brian J. Raney United States
Adam Frankish relative to Debasish Raha United States Debasish Raha's profile →
Citations per field
00.5×1.5×1.9×
Debasish Raha · 1×
Citations per year

Countries citing papers authored by Adam Frankish

Since Specialization
Citations

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

Fields of papers citing papers by Adam Frankish

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Adam Frankish, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Adam Frankish Line = papers co-authored together Adam Frankish links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20251
2 202119
3 202028
4 201932
5
Towards a complete map of the human long non-coding RNA transcriptome
Hit paper breakdown →
2018431
6 2017165
7 201426
8 2014334
9 201342
10 201242
11 2012251
12 201122
13 2011101
14 20101
15 2010134
16 201081
17 2007164
18 200656
19 20051
20 200448

About Adam Frankish

Adam Frankish is a scholar working on Molecular Biology, Cancer Research, Genetics, Sensory Systems and Spectroscopy, having authored 39 papers that have together received 3.2k indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (23 papers), Genomics and Phylogenetic Studies (22 papers), RNA modifications and cancer (18 papers), RNA Research and Splicing (9 papers), Genomics and Chromatin Dynamics (6 papers), Cancer-related molecular mechanisms research (5 papers), Machine Learning in Bioinformatics (3 papers) and Molecular Biology Techniques and Applications (3 papers). The work is most often cited by research in Cancer Research (1.1k citations), Molecular Biology (2.7k citations), Genetics (373 citations), Endocrinology (56 citations) and Plant Science (295 citations). Adam Frankish has collaborated with scholars based in United Kingdom, United States and Spain. Frequent co-authors include Jennifer Harrow, Roderic Guigó, Julien Lagarde, Rory Johnson, Barbara Uszczyńska-Ratajczak, Mark Gerstein, Tim Hubbard, Alexandre Reymond, Mark Diekhans and Alfonso Valencia. Their work appears in journals such as Genome biology, Genome Research, BMC Genomics, Human Molecular Genetics and Molecular Biology and Evolution.

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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