Barbara E. Stranger

41.0k citations
72 papers · 7.6k indexed · 2 hit papers · h-index 36
  • Genetics top 0.2%
    • Genetic Associations and Epidemiology 31
    • Genomic variations and chromosomal abnormalities 12
    • Genetic Mapping and Diversity in Plants and Animals 10
    • Genomics and Chromatin Dynamics 13
    • Gene expression and cancer classification 11
    • Bioinformatics and Genomic Networks 7
    • RNA and protein synthesis mechanisms 6
    • Epigenetics and DNA Methylation 6
  • Immunology top 2%
  • Aging top 5%

Barbara E. Stranger

71 papers receiving 7.5k citations

Hit Papers

Population genomics of human gene expression78920072026201320194008001.2k

Peers

Barbara E. Stranger
Comparison fields: 5 of 157
  • Genetics 3.8k
  • Cancer Research 932
  • Molecular Biology 4.2k
  • Immunology 1.2k
  • Aging 59
Replace Kristin Ardlie with:
Kristin Ardlie United States
Joseph E. Powell Australia
Stephen B. Montgomery United States
Krishna M. Roskin United States
Nadine Binart France
Shrikant Mane United States
Olivier Delaneau Switzerland
John M. Greally United States
Tim Wiltshire United States
David R. Beier United States
Barbara E. Stranger relative to Kristin Ardlie United States Kristin Ardlie's profile →
Citations per field
00.5×1.5×2.2×
Kristin Ardlie · 1×
Citations per year

Countries citing papers authored by Barbara E. Stranger

Since Specialization
Citations

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

Fields of papers citing papers by Barbara E. Stranger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara E. Stranger. 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 Barbara E. Stranger. The network helps show where Barbara E. Stranger may publish in the future.

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20230
2 202318
3 202312
4 202014
5 201923
6 201914
7 20196
8 2019158
9 201831
10 2018179
11 20169
12 201520
13 201515
14 201415
15 201441
16 2013195
17 2009489
18 2007127
19 200636
20 200619

About Barbara E. Stranger

Barbara E. Stranger is a scholar working on Genetics, Molecular Biology and Aging, having authored 72 papers that have together received 7.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (31 papers), Genomics and Chromatin Dynamics (13 papers), Genomic variations and chromosomal abnormalities (12 papers), Gene expression and cancer classification (11 papers), Genetic Mapping and Diversity in Plants and Animals (10 papers), Bioinformatics and Genomic Networks (7 papers), RNA and protein synthesis mechanisms (6 papers) and Epigenetics and DNA Methylation (6 papers). The work is most often cited by research in Genetics (3.8k citations), Cancer Research (932 citations) and Molecular Biology (4.2k citations). Barbara E. Stranger has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Emmanouil T. Dermitzakis, Claude Beazley, Towfique Raj, Panos Deloukas, Catherine Ingle, Antigone S. Dimas, Stephen B. Montgomery, Simon Tavaré, Matthew S. Forrest and Christine Bird. Their work appears in journals such as PLoS Genetics, The American Journal of Human Genetics, Science, Human Molecular Genetics and Bioinformatics.

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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