Brendan Bulik‐Sullivan is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience.
According to data from OpenAlex, Brendan Bulik‐Sullivan has authored 14 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Brendan Bulik‐Sullivan's work include Genetic Associations and Epidemiology (6 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers) and Genetic and phenotypic traits in livestock (3 papers). Brendan Bulik‐Sullivan is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers) and Genetic and phenotypic traits in livestock (3 papers). Brendan Bulik‐Sullivan collaborates with scholars based in United States, United Kingdom and Australia. Brendan Bulik‐Sullivan's co-authors include Hilary K. Finucane, Po‐Ru Loh, Mark J. Daly, Benjamin M. Neale, Alkes L. Price, Stephan Ripke, Alkes L. Price, Jian Yang, Alexander Gusev and Verneri Anttila and has published in prestigious journals such as Nature Communications, Nature Genetics and Bioinformatics.
In The Last Decade
Brendan Bulik‐Sullivan
13 papers
receiving
6.6k citations
Hit Papers
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.
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
20152.5k citationsBrendan Bulik‐Sullivan, Po‐Ru Loh et al.Nature Geneticsprofile →
An atlas of genetic correlations across human diseases and traits
20152.2k citationsBrendan Bulik‐Sullivan, Hilary K. Finucane et al.Nature Geneticsprofile →
Efficient Bayesian mixed-model analysis increases association power in large cohorts
2015766 citationsPo‐Ru Loh, George Tucker et al.Nature Geneticsprofile →
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
2016406 citationsJie Zheng, A. Mesut Erzurumluoglu et al.Bioinformaticsprofile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
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Countries citing papers authored by Brendan Bulik‐Sullivan
Since
Specialization
Citations
This map shows the geographic impact of Brendan Bulik‐Sullivan'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 Brendan Bulik‐Sullivan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brendan Bulik‐Sullivan more than expected).
Fields of papers citing papers by Brendan Bulik‐Sullivan
This network shows the impact of papers produced by Brendan Bulik‐Sullivan. 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 Brendan Bulik‐Sullivan. The network helps show where Brendan Bulik‐Sullivan may publish in the future.
Co-authorship network of co-authors of Brendan Bulik‐Sullivan
This figure shows the co-authorship network connecting the top 25 collaborators of Brendan Bulik‐Sullivan.
A scholar is included among the top collaborators of Brendan Bulik‐Sullivan 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 Brendan Bulik‐Sullivan. Brendan Bulik‐Sullivan is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Zheng, Jie, A. Mesut Erzurumluoglu, Benjamin Elsworth, et al.. (2016). LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. Bioinformatics. 33(2). 272–279.406 indexed citations breakdown →
5.
Bulik‐Sullivan, Brendan. (2016). Genomic Analysis of Polygenic Traits. Digital Academic REpository of VU University Amsterdam (Vrije Universiteit Amsterdam).1 indexed citations
6.
Bulik‐Sullivan, Brendan, Po‐Ru Loh, Hilary K. Finucane, et al.. (2015). LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics. 47(3). 291–295.2510 indexed citations breakdown →
7.
Loh, Po‐Ru, George Tucker, Brendan Bulik‐Sullivan, et al.. (2015). Efficient Bayesian mixed-model analysis increases association power in large cohorts. Nature Genetics. 47(3). 284–290.766 indexed citations breakdown →
Bulik‐Sullivan, Brendan, Hilary K. Finucane, Verneri Anttila, et al.. (2015). An atlas of genetic correlations across human diseases and traits. Nature Genetics. 47(11). 1236–1241.2172 indexed citations breakdown →
11.
Day, Felix R., Brendan Bulik‐Sullivan, David A. Hinds, et al.. (2015). Genetic determinants of puberty timing in men and women: shared genetic aetiology between sexes and with health-related outcomes.1 indexed citations
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive
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incomplete records, variations in author disambiguation, differences in journal indexing, and
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