Eric Bartell

1.3k citations
8 papers · 618 · 1 hit paper · h-index 6

Impact in

  • Genetics top 10%
    • Genetic Associations and Epidemiology
    • Genetic Mapping and Diversity in Plants and Animals
    • Genetic and phenotypic traits in livestock
    • Genomics and Rare Diseases

Papers in

    • Genetic Associations and Epidemiology 4
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic Syndromes and Imprinting 1
    • RNA modifications and cancer 3
    • Wnt/β-catenin signaling in development and cancer 1

Eric Bartell

7 papers receiving 608 citations

Eric Bartell's Hit Papers

A saturated map of common genetic variants associated with human height 2022 · 456 citations
4560+1+2Years since publication100200300400

Peers

Eric Bartell
Comparison fields: 5 of 94
  • Genetics 331
  • Aging 10
  • Cancer Research 41
  • Molecular Biology 186
  • Pediatrics, Perinatology and Child Health 37
Replace Katri Pärna with:
Katri Pärna Estonia
Joshua D. Arias United States
Poornima Devineni United States
Tori L. Melendez United States
Paola Tesolin Italy
Divya Sri Priyanka Tallapragada India
Hyejin Lee South Korea
Shengchao A. Li United States
Xinyuan Zhang United States
Marielisa Graff United States
Eric Bartell relative to Katri Pärna Estonia Katri Pärna's profile →
Citations per field
00.5×2×3×4×4.5×
Katri Pärna · 1×
Citations per year

Countries citing papers authored by Eric Bartell

Since Specialization
Citations

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

Fields of papers citing papers by Eric Bartell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

8 of 8 papers shown
#Work
1
A saturated map of common genetic variants associated with human height
Hit paper breakdown →
2022456
2 201689
3 202032
4 202516
5 202414
6 202310
7 20201
8 20230

About Eric Bartell

Eric Bartell is a scholar working on Genetics, Molecular Biology, Cancer Research, Endocrinology, Diabetes and Metabolism and Pediatrics, Perinatology and Child Health, having authored 8 papers that have together received 618 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (4 papers), RNA modifications and cancer (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), interferon and immune responses (1 paper), Genetic Syndromes and Imprinting (1 paper), Wnt/β-catenin signaling in development and cancer (1 paper), Adipose Tissue and Metabolism (1 paper) and Birth, Development, and Health (1 paper). The work is most often cited by research in Genetics (331 citations), Aging (10 citations), Cancer Research (41 citations), Molecular Biology (186 citations) and Pediatrics, Perinatology and Child Health (37 citations). Eric Bartell has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Jiangchuan Ye, Gizem Rizki, David J. Milan, Elzo de Wit, Manolis Kellis, Laurie A. Boyer, Pim van der Harst, Vidya Subramanian, Robert W. Mills and Jordan S Leyton-Mange. Their work appears in journals such as Nature, Cell, Nature Medicine, Cell Genomics and Human Molecular 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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