Daniel Taliun

32.4k total citations
15 papers, 413 citations indexed

About

Daniel Taliun is a scholar working on Genetics, Molecular Biology and Artificial Intelligence. According to data from OpenAlex, Daniel Taliun has authored 15 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 1 paper in Artificial Intelligence. Recurrent topics in Daniel Taliun's work include Genetic Associations and Epidemiology (12 papers), Genetic Mapping and Diversity in Plants and Animals (8 papers) and Bioinformatics and Genomic Networks (3 papers). Daniel Taliun is often cited by papers focused on Genetic Associations and Epidemiology (12 papers), Genetic Mapping and Diversity in Plants and Animals (8 papers) and Bioinformatics and Genomic Networks (3 papers). Daniel Taliun collaborates with scholars based in United States, Italy and Austria. Daniel Taliun's co-authors include Peter VandeHaar, Gonçalo R. Abecasis, Michael Boehnke, Ryan Welch, Andrew P. Boughton, Matthew Flickinger, Cristian Pattaro, Claude Bhérer, J. Brent Richards and Katerina Trajanoska and has published in prestigious journals such as Nature, Nucleic Acids Research and Bioinformatics.

In The Last Decade

Daniel Taliun

13 papers receiving 411 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniel Taliun United States	9	220	145	44	41	30	15	413
Fang Xu China	12	146 0.7×	122 0.8×	20 0.5×	36 0.9×	27 0.9×	40	352
Sajjad Rafiq United Kingdom	12	195 0.9×	157 1.1×	73 1.7×	76 1.9×	82 2.7×	16	511
Ekta Rai India	14	190 0.9×	344 2.4×	61 1.4×	61 1.5×	26 0.9×	36	636
Laure Maneix United States	12	86 0.4×	162 1.1×	40 0.9×	48 1.2×	37 1.2×	24	353
Joseph Maranville United States	11	97 0.4×	166 1.1×	19 0.4×	75 1.8×	33 1.1×	20	412
Yoshifumi Ohnishi Japan	7	151 0.7×	179 1.2×	61 1.4×	43 1.0×	70 2.3×	13	459
Jessica Bonneau France	8	96 0.4×	88 0.6×	52 1.2×	24 0.6×	18 0.6×	10	314
Luisa Ronzoni Italy	13	78 0.4×	188 1.3×	86 2.0×	23 0.6×	22 0.7×	43	455
Mia Ståhle Finland	11	114 0.5×	82 0.6×	28 0.6×	20 0.5×	20 0.7×	25	495
Yoshiyuki Kinoshita Japan	10	170 0.8×	108 0.7×	19 0.4×	32 0.8×	88 2.9×	14	449

Countries citing papers authored by Daniel Taliun

Since Specialization

Citations

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

Fields of papers citing papers by Daniel Taliun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Taliun

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

All Works

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15 of 15 papers shown

Diaz-Papkovich, Alex, Guillaume Sillon, Daniela D’Agostino, et al.. (2025). Using the ancestral recombination graph to study the history of rare variants in founder populations. The American Journal of Human Genetics. 112(12). 2973–2981.

Bérubé, M.A., et al.. (2025). CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens. Nucleic Acids Research. 53(W1). W193–W202.

Forer, Lukas, Daniel Taliun, Jonathon LeFaive, et al.. (2024). Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers. Nucleic Acids Research. 52(W1). W70–W77. 4 indexed citations

Trajanoska, Katerina, Claude Bhérer, Daniel Taliun, et al.. (2023). From target discovery to clinical drug development with human genetics. Nature. 620(7975). 737–745. 81 indexed citations

Boughton, Andrew P., Ryan Welch, Matthew Flickinger, et al.. (2021). LocusZoom.js: interactive and embeddable visualization of genetic association study results. Bioinformatics. 37(18). 3017–3018. 135 indexed citations

Fritsche, Lars G., Snehal Patil, Lauren J. Beesley, et al.. (2020). Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. The American Journal of Human Genetics. 107(5). 815–836. 67 indexed citations

Wojcik, Genevieve L., Christian Fuchsberger, Daniel Taliun, et al.. (2018). Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. G3 Genes Genomes Genetics. 8(10). 3255–3267. 21 indexed citations

Quick, Corbin, Christian Fuchsberger, Daniel Taliun, et al.. (2018). emeraLD: rapid linkage disequilibrium estimation with massive datasets. Bioinformatics. 35(1). 164–166. 6 indexed citations

Taliun, Daniel, Sonia Chothani, Sebastian Schönherr, et al.. (2017). LASER server: ancestry tracing with genotypes or sequence reads. Bioinformatics. 33(13). 2056–2058. 23 indexed citations

10.

Rainer, Johannes, et al.. (2016). FamAgg: an R package to evaluate familial aggregation of traits in large pedigrees. Bioinformatics. 32(10). 1583–1585. 15 indexed citations

11.

Jobling, Mark A., et al.. (2015). On the use of dense SNP marker data for the identification of distant relative pairs. Theoretical Population Biology. 107. 14–25. 12 indexed citations

12.

Taliun, Daniel, Johann Gamper, Ulf Leser, & Cristian Pattaro. (2015). Fast Sampling-Based Whole-Genome Haplotype Block Recognition. IEEE/ACM Transactions on Computational Biology and Bioinformatics. 13(2). 315–325. 5 indexed citations

13.

Taliun, Daniel, Johann Gamper, & Cristian Pattaro. (2014). Efficient haplotype block recognition of very long and dense genetic sequences. BMC Bioinformatics. 15(1). 10–10. 30 indexed citations

14.

Volpato, Cláudia B., Alessandro De Grandi, Martin Gögele, et al.. (2011). Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27. Journal of Medical Genetics. 48(8). 549–556. 3 indexed citations

15.

Fuchsberger, Christian, Daniel Taliun, Peter P. Pramstaller, & Cristian Pattaro. (2011). GWAtoolbox: an R package for fast quality control and handling of genome-wide association studies meta-analysis data. Bioinformatics. 28(3). 444–445. 11 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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