Barbara E. Stranger

41.0k total citations · 2 hit papers
72 papers, 7.6k citations indexed

About

Barbara E. Stranger is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Barbara E. Stranger has authored 72 papers receiving a total of 7.6k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 46 papers in Molecular Biology and 10 papers in Immunology. Recurrent topics in Barbara E. Stranger's work include Genetic Associations and Epidemiology (31 papers), Genomics and Chromatin Dynamics (13 papers) and Genomic variations and chromosomal abnormalities (12 papers). Barbara E. Stranger is often cited by papers focused on Genetic Associations and Epidemiology (31 papers), Genomics and Chromatin Dynamics (13 papers) and Genomic variations and chromosomal abnormalities (12 papers). Barbara E. Stranger collaborates with scholars based in United States, United Kingdom and Germany. Barbara E. Stranger's 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 and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Barbara E. Stranger

71 papers receiving 7.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes

2007 1.3k citations Barbara E. Stranger, Catherine Ingle et al. Science profile →
Population genomics of human gene expression

2007 789 citations Barbara E. Stranger, Antigone S. Dimas et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Barbara E. Stranger United States	36	4.2k	3.8k	1.2k	932	570	72	7.6k
Alexander Hoischen Netherlands	46	3.9k 0.9×	4.0k 1.1×	1.0k 0.9×	940 1.0×	290 0.5×	142	8.2k
Sarah Hunt United Kingdom	28	3.9k 0.9×	4.1k 1.1×	678 0.6×	1.1k 1.1×	681 1.2×	55	8.2k
Stephen B. Montgomery United States	44	6.8k 1.6×	4.6k 1.2×	849 0.7×	1.5k 1.6×	494 0.9×	111	10.3k
Kristin Ardlie United States	37	4.4k 1.1×	4.1k 1.1×	1.5k 1.3×	906 1.0×	412 0.7×	71	9.7k
Jacek Majewski Canada	56	6.1k 1.5×	2.9k 0.8×	958 0.8×	1.1k 1.2×	323 0.6×	216	9.6k
Bryan Howie United States	15	2.6k 0.6×	4.5k 1.2×	925 0.8×	549 0.6×	415 0.7×	17	7.6k
Michele Cargill United States	19	2.9k 0.7×	3.2k 0.9×	1.3k 1.1×	354 0.4×	509 0.9×	23	6.6k
John M. Greally United States	53	6.8k 1.6×	2.3k 0.6×	615 0.5×	1.0k 1.1×	579 1.0×	196	9.1k
Tomi Pastinen Canada	39	3.5k 0.8×	1.9k 0.5×	795 0.7×	567 0.6×	289 0.5×	147	5.8k

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 of co-authors of Barbara E. Stranger

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara E. Stranger. A scholar is included among the top collaborators of Barbara E. Stranger 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 Barbara E. Stranger. Barbara E. Stranger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Huang, Yingbo, et al.. (2024). Sex differences in the molecular profile of adult diffuse glioma are shaped by IDH status and tumor microenvironment. Neuro-Oncology. 27(2). 430–444. 3 indexed citations

Khramtsova, Ekaterina, Stacey J. Winham, Lea K. Davis, Barbara E. Stranger, & Melissa A. Wilson. (2023). Toward a deeper understanding of gene-by-sex interaction models. Cell Genomics. 3(5). 100324–100324.

Khramtsova, Ekaterina, Melissa A. Wilson, Joanna Martin, et al.. (2023). Quality control and analytic best practices for testing genetic models of sex differences in large populations. Cell. 186(10). 2044–2061. 18 indexed citations

Skol, Andrew D., Segun Jung, Siquan Chen, et al.. (2020). Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes. eLife. 9. 26 indexed citations

Tilot, Amanda K., Ekaterina Khramtsova, Dan Liang, et al.. (2020). The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cerebral Cortex. 31(4). 1873–1887. 14 indexed citations

Hernandez, Wenndy, Keith Danahey, Xun Pei, et al.. (2019). Pharmacogenomic genotypes define genetic ancestry in patients and enable population-specific genomic implementation. The Pharmacogenomics Journal. 20(1). 126–135. 14 indexed citations

Applebaum, Mark A., Jason Karpus, Diana C. West-Szymanski, et al.. (2019). 5-Hydroxymethylcytosine Profiles in Circulating Cell-Free DNA Associate with Disease Burden in Children with Neuroblastoma. Clinical Cancer Research. 26(6). 1309–1317. 23 indexed citations

Khramtsova, Ekaterina, et al.. (2018). Sex differences in the genetic architecture of obsessive–compulsive disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 180(6). 351–364. 31 indexed citations

Khramtsova, Ekaterina, Lea K. Davis, & Barbara E. Stranger. (2018). The role of sex in the genomics of human complex traits. Nature Reviews Genetics. 20(3). 173–190. 179 indexed citations

10.

Khramtsova, Ekaterina & Barbara E. Stranger. (2016). Assocplots: a Python package for static and interactive visualization of multiple-group GWAS results. Bioinformatics. 33(3). 432–434. 9 indexed citations

11.

Sul, Jae Hoon, Towfique Raj, Simone de Jong, et al.. (2015). Accurate and Fast Multiple-Testing Correction in eQTL Studies. The American Journal of Human Genetics. 96(6). 857–868. 20 indexed citations

12.

Eisenhaure, Thomas, F. Ann Ran, Lucas D. Ward, et al.. (2014). Common Genetic Variants Modulate Pathogen-Sensing Responses in Human Dendritic Cells. Science. 343(6175). 1246980–1246980. 15 indexed citations

13.

Li, Qiyuan, Constance Chen, Siddhartha Kar, et al.. (2014). Expression QTL-based analyses reveal candidate causal genes and loci across five tumor types. Human Molecular Genetics. 23(19). 5294–5302. 41 indexed citations

14.

Hu, Xinli, Hyun Kim, Towfique Raj, et al.. (2014). Regulation of Gene Expression in Autoimmune Disease Loci and the Genetic Basis of Proliferation in CD4+ Effector Memory T Cells. PLoS Genetics. 10(6). e1004404–e1004404. 35 indexed citations

15.

Patsopoulos, Nikolaos A., Lisa F. Barcellos, Rogier Q. Hintzen, et al.. (2013). Fine-Mapping the Genetic Association of the Major Histocompatibility Complex in Multiple Sclerosis: HLA and Non-HLA Effects. PLoS Genetics. 9(11). e1003926–e1003926. 184 indexed citations

16.

Stranger, Barbara E. & Phillip L. De Jager. (2012). Coordinating GWAS results with gene expression in a systems immunologic paradigm in autoimmunity. Current Opinion in Immunology. 24(5). 544–551. 11 indexed citations

17.

Yang, Tsun-Po, Claude Beazley, Stephen B. Montgomery, et al.. (2010). Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies. Bioinformatics. 26(19). 2474–2476. 186 indexed citations

18.

Dimas, Antigone S., Samuel Deutsch, Barbara E. Stranger, et al.. (2009). Common Regulatory Variation Impacts Gene Expression in a Cell Type–Dependent Manner. Science. 325(5945). 1246–1250. 489 indexed citations

19.

Bird, Christine, Barbara E. Stranger, Daryl J. Thomas, et al.. (2007). Fast-evolving noncoding sequences in the human genome. Genome biology. 8(6). R118–R118. 127 indexed citations

20.

Bird, Christine, Barbara E. Stranger, & Emmanouil T. Dermitzakis. (2006). Functional variation and evolution of non-coding DNA. Current Opinion in Genetics & Development. 16(6). 559–564. 36 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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