Jeffrey T. Leek

30.5k total citations · 5 hit papers
82 papers, 16.1k citations indexed

About

Jeffrey T. Leek is a scholar working on Molecular Biology, Artificial Intelligence and Genetics. According to data from OpenAlex, Jeffrey T. Leek has authored 82 papers receiving a total of 16.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 12 papers in Artificial Intelligence and 12 papers in Genetics. Recurrent topics in Jeffrey T. Leek's work include Gene expression and cancer classification (32 papers), Bioinformatics and Genomic Networks (16 papers) and Molecular Biology Techniques and Applications (12 papers). Jeffrey T. Leek is often cited by papers focused on Gene expression and cancer classification (32 papers), Bioinformatics and Genomic Networks (16 papers) and Molecular Biology Techniques and Applications (12 papers). Jeffrey T. Leek collaborates with scholars based in United States, United Kingdom and Mexico. Jeffrey T. Leek's co-authors include John D. Storey, Andrew E. Jaffe, Steven L. Salzberg, W. Evan Johnson, Daehwan Kim, Geo Pertea, Mihaela Pertea, Hilary S. Parker, Ben Langmead and Rafael A. Irizarry and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Jeffrey T. Leek

81 papers receiving 15.9k citations

Hit Papers

Transcript-level expressi... 2007 2026 2013 2019 2016 2012 2010 2007 2012 1000 2.0k 3.0k 4.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeffrey T. Leek United States 39 10.0k 2.5k 2.5k 1.7k 1.4k 82 16.1k
Sandrine Dudoit United States 50 11.4k 1.1× 1.6k 0.6× 2.2k 0.9× 790 0.5× 1.4k 1.0× 99 17.4k
Gilbert Chu United States 43 14.0k 1.4× 2.3k 0.9× 3.0k 1.2× 1.4k 0.8× 1.5k 1.1× 87 19.8k
Olga G. Troyanskaya United States 54 11.3k 1.1× 2.1k 0.8× 1.3k 0.5× 538 0.3× 802 0.6× 153 15.8k
John D. Storey United States 40 15.2k 1.5× 5.5k 2.2× 2.3k 0.9× 2.0k 1.2× 1.7k 1.2× 83 26.0k
W. Evan Johnson United States 35 8.9k 0.9× 1.8k 0.7× 2.5k 1.0× 425 0.2× 1.6k 1.1× 126 14.6k
Jean Yang Australia 52 8.2k 0.8× 1.2k 0.5× 1.6k 0.6× 661 0.4× 1.6k 1.1× 257 13.8k
Satoru Miyano Japan 58 10.5k 1.0× 1.3k 0.5× 2.7k 1.1× 850 0.5× 1.1k 0.8× 523 15.5k
Hongyu Zhao United States 77 11.6k 1.2× 6.4k 2.5× 1.5k 0.6× 3.2k 1.9× 1.4k 1.0× 746 25.1k
Michael Q. Zhang United States 68 18.2k 1.8× 2.4k 0.9× 2.9k 1.2× 1.7k 1.0× 1.3k 0.9× 226 21.6k
Benjamin M. Bolstad United States 8 7.7k 0.8× 1.3k 0.5× 2.0k 0.8× 886 0.5× 1.2k 0.8× 10 11.5k

Countries citing papers authored by Jeffrey T. Leek

Since Specialization
Citations

This map shows the geographic impact of Jeffrey T. Leek'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 Jeffrey T. Leek with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jeffrey T. Leek more than expected).

Fields of papers citing papers by Jeffrey T. Leek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey T. Leek. 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 Jeffrey T. Leek. The network helps show where Jeffrey T. Leek may publish in the future.

Co-authorship network of co-authors of Jeffrey T. Leek

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

All Works

20 of 20 papers shown
1.
Majumder, Mary A., et al.. (2024). Large-scale genotype prediction from RNA sequence data necessitates a new ethical and policy framework. Nature Genetics. 56(8). 1537–1540. 1 indexed citations
2.
Kammers, Kai, Margaret A. Taub, Benjamin A.T. Rodriguez, et al.. (2020). Transcriptional profile of platelets and iPSC-derived megakaryocytes from whole-genome and RNA sequencing. Blood. 137(7). 959–968. 13 indexed citations
3.
McCormick, Tyler H., et al.. (2020). Methods for correcting inference based on outcomes predicted by machine learning. Proceedings of the National Academy of Sciences. 117(48). 30266–30275. 32 indexed citations
4.
Ellis, Shannon, Leonardo Collado‐Torres, Andrew E. Jaffe, & Jeffrey T. Leek. (2018). Improving the value of public RNA-seq expression data by phenotype prediction. Nucleic Acids Research. 46(9). e54–e54. 23 indexed citations
5.
Boca, Simina M. & Jeffrey T. Leek. (2018). A direct approach to estimating false discovery rates conditional on covariates. PeerJ. 6. e6035–e6035. 53 indexed citations
6.
Jaffe, Andrew E., Richard E. Straub, Joo Heon Shin, et al.. (2018). Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis. Nature Neuroscience. 21(8). 1117–1125. 211 indexed citations
7.
Jaffe, Andrew E., Ran Tao, Alexis L. Norris, et al.. (2017). qSVA framework for RNA quality correction in differential expression analysis. Proceedings of the National Academy of Sciences. 114(27). 7130–7135. 59 indexed citations
8.
Nellore, Abhinav, Christopher Wilks, Kasper D. Hansen, Jeffrey T. Leek, & Ben Langmead. (2016). Rail-dbGaP: analyzing dbGaP-protected data in the cloud with Amazon Elastic MapReduce. Bioinformatics. 32(16). 2551–2553. 3 indexed citations
9.
Nellore, Abhinav, Leonardo Collado‐Torres, Andrew E. Jaffe, et al.. (2016). Rail-RNA: scalable analysis of RNA-seq splicing and coverage. Bioinformatics. 33(24). 4033–4040. 38 indexed citations
10.
Manimaran, Solaiappan, Kwame Okrah, Jeffrey T. Leek, et al.. (2016). BatchQC: interactive software for evaluating sample and batch effects in genomic data. Bioinformatics. 32(24). 3836–3838. 45 indexed citations
11.
Pertea, Mihaela, Daehwan Kim, Geo Pertea, Jeffrey T. Leek, & Steven L. Salzberg. (2016). Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown. Nature Protocols. 11(9). 1650–1667. 4416 indexed citations breakdown →
12.
Patil, Prasad, et al.. (2015). Test set bias affects reproducibility of gene signatures. Bioinformatics. 31(14). 2318–2323. 74 indexed citations
13.
Jager, Leah R. & Jeffrey T. Leek. (2013). An estimate of the science-wise false discovery rate and application to the top medical literature. Biostatistics. 15(1). 1–12. 109 indexed citations
14.
Parker, Hilary S. & Jeffrey T. Leek. (2012). The practical effect of batch on genomic prediction. Statistical Applications in Genetics and Molecular Biology. 11(3). Article 10–Article 10. 20 indexed citations
15.
Jaffe, Andrew E., Peter Murakami, Hwa-Jin Lee, et al.. (2012). Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies. International Journal of Epidemiology. 41(1). 200–209. 457 indexed citations breakdown →
16.
Leek, Jeffrey T. & John D. Storey. (2011). The Joint Null Criterion for Multiple Hypothesis Tests. Statistical Applications in Genetics and Molecular Biology. 10(1). 16 indexed citations
17.
Frazee, Alyssa C., Ben Langmead, & Jeffrey T. Leek. (2011). ReCount: A multi-experiment resource of analysis-ready RNA-seq gene count datasets. BMC Bioinformatics. 12(1). 449–449. 103 indexed citations
18.
Leek, Jeffrey T. & John D. Storey. (2008). A general framework for multiple testing dependence. Proceedings of the National Academy of Sciences. 105(48). 18718–18723. 237 indexed citations
19.
Storey, John D., James Y. Dai, & Jeffrey T. Leek. (2006). The optimal discovery procedure for large-scale significance testing, with applications to comparative microarray experiments. Biostatistics. 8(2). 414–432. 106 indexed citations
20.
Craig, Jamie E., et al.. (2002). Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease. Journal of Medical Genetics. 39. 47–48. 4 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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