Tanner Jensen

1.1k total citations
10 papers, 194 citations indexed

About

Tanner Jensen is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Tanner Jensen has authored 10 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Neurology and 3 papers in Genetics. Recurrent topics in Tanner Jensen's work include Genomics and Rare Diseases (3 papers), Single-cell and spatial transcriptomics (2 papers) and MicroRNA in disease regulation (2 papers). Tanner Jensen is often cited by papers focused on Genomics and Rare Diseases (3 papers), Single-cell and spatial transcriptomics (2 papers) and MicroRNA in disease regulation (2 papers). Tanner Jensen collaborates with scholars based in United States, France and Canada. Tanner Jensen's co-authors include John Denis Fryer, Jonathon Sens, Mark Ebbert, Owen A. Ross, Leonard Petrucelli, Minerva M. Carrasquillo, Dirk Keene, Paul K. Crane, Kuixi Zhu and Bin Zhang and has published in prestigious journals such as Genome Research, The American Journal of Human Genetics and Genome biology.

In The Last Decade

Tanner Jensen

10 papers receiving 192 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tanner Jensen United States	6	100	62	49	29	27	10	194
Shadi Shams United States	4	228 2.3×	58 0.9×	48 1.0×	22 0.8×	54 2.0×	7	292
James D. Cooper United Kingdom	7	219 2.2×	80 1.3×	21 0.4×	18 0.6×	55 2.0×	8	277
Ethan J. Armand United States	4	153 1.5×	22 0.4×	31 0.6×	25 0.9×	38 1.4×	4	208
Ximena Corso‐Díaz United States	9	200 2.0×	34 0.5×	19 0.4×	19 0.7×	24 0.9×	13	274
Frederik Ziebell Germany	4	190 1.9×	53 0.9×	13 0.3×	15 0.5×	24 0.9×	4	285
Christine Gran Neurauter Norway	9	280 2.8×	51 0.8×	17 0.3×	10 0.3×	40 1.5×	11	320
Christina Volsko United States	7	152 1.5×	25 0.4×	34 0.7×	34 1.2×	71 2.6×	8	245
Ada Ndoja United States	4	225 2.3×	25 0.4×	43 0.9×	32 1.1×	18 0.7×	6	286
Nataša Josipović Germany	9	308 3.1×	51 0.8×	17 0.3×	28 1.0×	44 1.6×	11	387
Shane A. Evans United States	6	237 2.4×	31 0.5×	23 0.5×	43 1.5×	38 1.4×	7	317

Countries citing papers authored by Tanner Jensen

Since Specialization

Citations

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

Fields of papers citing papers by Tanner Jensen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tanner Jensen

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

All Works

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10 of 10 papers shown

Jensen, Tanner, Bohan Ni, Chloe M. Reuter, et al.. (2025). Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease. Genome Research. 35(4). 914–928. 2 indexed citations

Chemparathy, Augustine, Yann Le Guen, Yi Zeng, et al.. (2024). A 3′UTR Insertion Is a Candidate Causal Variant at the TMEM106B Locus Associated With Increased Risk for FTLD-TDP. Neurology Genetics. 10(1). e200124–e200124. 5 indexed citations

Pan, Jie, Jaume Forés-Martos, Tanner Jensen, et al.. (2024). Deciphering glial contributions to CSF1R-related disorder via single-nuclear transcriptomic profiling: a case study. Acta Neuropathologica Communications. 12(1). 139–139. 2 indexed citations

Goddard, Pagé C., Tanner Jensen, Kevin S. Smith, et al.. (2024). Impact of genome build on RNA-seq interpretation and diagnostics. The American Journal of Human Genetics. 111(7). 1282–1300. 5 indexed citations

Jensen, Tanner, Jonathon Sens, Kuixi Zhu, et al.. (2022). Culture shock: microglial heterogeneity, activation, and disrupted single-cell microglial networks in vitro. Molecular Neurodegeneration. 17(1). 26–26. 49 indexed citations

Olney, Kimberly C., Praveen N. Pallegar, Tanner Jensen, et al.. (2022). Widespread choroid plexus contamination in sampling and profiling of brain tissue. Molecular Psychiatry. 27(3). 1839–1847. 13 indexed citations

Luke, Steven G. & Tanner Jensen. (2022). The effect of sudden-onset distractors on reading efficiency and comprehension. Quarterly Journal of Experimental Psychology. 76(5). 1195–1206. 2 indexed citations

Jensen, Tanner, et al.. (2020). Analysis of Identification Method for Bacterial Species and Antibiotic Resistance Genes Using Optical Data From DNA Oligomers. Frontiers in Microbiology. 11. 257–257. 7 indexed citations

Ebbert, Mark, Tanner Jensen, Karen Jansen‐West, et al.. (2019). Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight. Genome biology. 20(1). 97–97. 108 indexed citations

10.

Jensen, Tanner, et al.. (2018). The PepSeq Pipeline. 2. 139–144. 1 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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