Seth Berger

3.5k citations
44 papers · 1.8k · 1 hit paper · h-index 18

Impact in

Papers in

    • Hedgehog Signaling Pathway Studies 5
    • Genomics and Rare Diseases 7
    • Genomic variations and chromosomal abnormalities 6
    • Genetics and Neurodevelopmental Disorders 6

Seth Berger

41 papers receiving 1.8k citations

Hit Papers

ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments 2010 · 677 citations
6770+5+10Years since publication200400600

Peers

Seth Berger
Comparison fields: 5 of 125
  • Computational Theory and Mathematics 369
  • Pharmacology 168
  • Molecular Biology 1.2k
  • Cancer Research 158
  • Aging 14
Replace Juan Manuel Ramírez‐Anguita with:
Juan Manuel Ramírez‐Anguita Spain
Neil Benson United Kingdom
Mirra Chung United States
Lang Li United States
Amitabh Sharma United States
Alba Gutiérrez‐Sacristán United States
Álex Bravo Spain
Samik Ghosh Japan
Raymond Wu United States
Richard E. Higgs United States
Seth Berger relative to Juan Manuel Ramírez‐Anguita Spain Juan Manuel Ramírez‐Anguita's profile →
Citations per field
00.5×
Juan Manuel Ramírez‐Anguita · 1×
Citations per year

Countries citing papers authored by Seth Berger

Since Specialization
Citations

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

Fields of papers citing papers by Seth Berger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Seth Berger, 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 Seth Berger Line = papers co-authored together Seth Berger links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 44 papers — load more, or switch the sort, to bring in the rest.

#Work
1
ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments
Hit paper breakdown →
2010677
2 2009374
3 2007118
4 2010101
5 201098
6 200952
7 202131
8 202029
9 200926
10 201925
11 200821
12 200721
13 202120
14 202019
15 201819
16 201918
17 201718
18 201217
19 201716
20 202016

About Seth Berger

Seth Berger is a scholar working on Molecular Biology, Genetics, Physiology, Infectious Diseases and Hematology, having authored 44 papers that have together received 1.8k indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (9 papers), Parvovirus B19 Infection Studies (9 papers), Blood groups and transfusion (8 papers), Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Computational Drug Discovery Methods (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Hedgehog Signaling Pathway Studies (5 papers). The work is most often cited by research in Computational Theory and Mathematics (369 citations), Pharmacology (168 citations), Molecular Biology (1.2k citations), Cancer Research (158 citations) and Aging (14 citations). Seth Berger has collaborated with scholars based in United States, Switzerland and Saudi Arabia. Frequent co-authors include Ravi Iyengar, Avi Ma’ayan, Jayanth Krishnan, Huilei Xu, Amin R. Mazloom, Alexander Lachmann, Huda B. Al‐Kouatly, Maximilian Muenke, Paul Kruszka and Ariel F. Martinez. Their work appears in journals such as Genetics in Medicine, Bioinformatics, Prenatal Diagnosis, Human Mutation and The American Journal of Human Genetics.

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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