David E. Bergstrom

1.3k total citations
22 papers, 825 citations indexed

About

David E. Bergstrom is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, David E. Bergstrom has authored 22 papers receiving a total of 825 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Sensory Systems. Recurrent topics in David E. Bergstrom's work include Genomics and Chromatin Dynamics (5 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (4 papers). David E. Bergstrom is often cited by papers focused on Genomics and Chromatin Dynamics (5 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (4 papers). David E. Bergstrom collaborates with scholars based in United States, Netherlands and Singapore. David E. Bergstrom's co-authors include Ronald K. Blackman, Eva M. Eicher, Chantal M. Longo-Guess, K. Albrecht, Maureen Young, Sherri M. Jones, John C. Schimenti, Rebecca A. Bergstrom, Robert J. Munroe and Leona H. Gagnon and has published in prestigious journals such as Journal of Clinical Investigation, Genes & Development and Blood.

In The Last Decade

David E. Bergstrom

21 papers receiving 816 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David E. Bergstrom United States 13 440 240 206 144 116 22 825
Michael Nefedov United States 6 977 2.2× 161 0.7× 358 1.7× 97 0.7× 35 0.3× 6 1.4k
Manousos Koutsourakis United Kingdom 3 924 2.1× 156 0.7× 324 1.6× 98 0.7× 33 0.3× 5 1.3k
Jean‐Pierre Desvignes France 17 603 1.4× 52 0.2× 324 1.6× 139 1.0× 13 0.1× 31 1.0k
Elaine Y.M. Wong United States 16 533 1.2× 44 0.2× 120 0.6× 40 0.3× 266 2.3× 23 908
Koko Urase Japan 19 776 1.8× 88 0.4× 138 0.7× 68 0.5× 70 0.6× 26 1.0k
Heinz‐Dieter Gabriel Germany 9 841 1.9× 92 0.4× 129 0.6× 77 0.5× 88 0.8× 10 1.1k
Dawn E. Watkins‐Chow United States 17 648 1.5× 60 0.3× 237 1.2× 164 1.1× 26 0.2× 37 1.1k
Roger Ferreira Canada 15 897 2.0× 121 0.5× 104 0.5× 70 0.5× 35 0.3× 16 1.2k
Haigen Huang United States 15 561 1.3× 80 0.3× 216 1.0× 46 0.3× 14 0.1× 23 825
Eleen Y. Shum United States 13 981 2.2× 49 0.2× 129 0.6× 32 0.2× 176 1.5× 16 1.2k

Countries citing papers authored by David E. Bergstrom

Since Specialization
Citations

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

Fields of papers citing papers by David E. Bergstrom

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David E. Bergstrom. 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 David E. Bergstrom. The network helps show where David E. Bergstrom may publish in the future.

Co-authorship network of co-authors of David E. Bergstrom

This figure shows the co-authorship network connecting the top 25 collaborators of David E. Bergstrom. A scholar is included among the top collaborators of David E. Bergstrom 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 David E. Bergstrom. David E. Bergstrom 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.
Krishnan, Vaidehi, King Pan Ng, Chuqi Wang, et al.. (2024). The BIM deletion polymorphism potentiates the survival of leukemia stem and progenitor cells and impairs response to targeted therapies. Leukemia. 39(1). 134–143.
2.
Loberg, Matthew A., Rebecca K. Bell, Leslie O. Goodwin, et al.. (2019). Sequentially inducible mouse models reveal that Npm1 mutation causes malignant transformation of Dnmt3a-mutant clonal hematopoiesis. Leukemia. 33(7). 1635–1649. 77 indexed citations
3.
Cheng, Kai, Leslie O. Goodwin, Judith L. Morgan, et al.. (2018). Viable Mice with Extensive Gene Humanization (25-kbp) Created Using Embryonic Stem Cell/Blastocyst and CRISPR/Zygote Injection Approaches. Scientific Reports. 8(1). 15028–15028. 11 indexed citations
4.
Loberg, Matthew A., Rebecca K. Bell, Timothy M. Stearns, et al.. (2018). Mutation in DNA Methyltransferase DNMT3A Confers Enhanced Self-Renewal Capacity Onto Multipotent Progenitor Cells and Predisposes to Acute Myeloid Leukemia (AML). Blood. 132(Supplement 1). 2569–2569. 1 indexed citations
5.
Vijayakumar, Sarath, Teresa E. Lever, Xing Zhao, et al.. (2015). Vestibular dysfunction, altered macular structure and trait localization in A/J inbred mice. Mammalian Genome. 26(3-4). 154–172. 12 indexed citations
6.
Palmer, Kristina, Heather Fairfield, Mohamed G. Hassan, et al.. (2015). Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology. Developmental Biology. 415(2). 216–227. 27 indexed citations
7.
Pratt, C. Herbert, Christopher J. Potter, Heather Fairfield, et al.. (2015). Dsprul: A spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome. Experimental and Molecular Pathology. 98(2). 164–172. 10 indexed citations
8.
Flaherty, John P., et al.. (2010). Molecular characterization of an allelic series of mutations in the mouse Nox3 gene. Mammalian Genome. 22(3-4). 156–169. 11 indexed citations
9.
Flaherty, John P., et al.. (2010). Generation of a conditional null allele of NADPH oxidase activator 1 (NOXA1). genesis. 48(9). 568–575. 10 indexed citations
10.
Nakano, Yoko, Chantal M. Longo-Guess, David E. Bergstrom, et al.. (2008). Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice. Journal of Clinical Investigation. 118(3). 1176–85. 90 indexed citations
11.
Longo-Guess, Chantal M., Leona H. Gagnon, David E. Bergstrom, & Kenneth R. Johnson. (2007). A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9. Hearing Research. 234(1-2). 21–28. 42 indexed citations
12.
Bergstrom, Rebecca A., Francesca Pasutto, Philipp Wabnitz, et al.. (2004). Vestibular defects in head-tilt mice result from mutations inNox3, encoding an NADPH oxidase. Genes & Development. 18(5). 486–491. 213 indexed citations
13.
Bergstrom, David E., Rebecca A. Bergstrom, Robert J. Munroe, et al.. (2003). Overlapping deletions spanning the proximal two-thirds of the mouse t complex. Mammalian Genome. 14(12). 817–829. 12 indexed citations
14.
Bergstrom, David E., Maureen Young, K. Albrecht, & Eva M. Eicher. (2000). Related function of mouse SOX3, SOX9, and SRY HMG domains assayed by male sex determination. genesis. 28(34). 111–124. 2 indexed citations
15.
Bergstrom, David E., Maureen Young, K. Albrecht, & Eva M. Eicher. (2000). Related function of mouse SOX3, SOX9, and SRY HMG domains assayed by male sex determination. genesis. 28(3-4). 111–124. 84 indexed citations
16.
Bergstrom, David E., Leona H. Gagnon, & Eva M. Eicher. (1999). Genetic and Physical Mapping of the Dreher Locus on Mouse Chromosome 1. Genomics. 59(3). 291–299. 15 indexed citations
17.
Bergstrom, David E., et al.. (1998). The Mouse Y Chromosome: Enrichment, Sizing, and Cloning by Bivariate Flow Cytometry. Genomics. 48(3). 304–313. 8 indexed citations
18.
Bergstrom, David E., et al.. (1997). An expanded collection of mouse Y Chromosome RDA clones. Mammalian Genome. 8(7). 510–512. 13 indexed citations
19.
Bergstrom, David E., et al.. (1996). Promoter specificity mediates the independent regulation of neighboring genes.. Genes & Development. 10(10). 1260–1270. 94 indexed citations
20.
Bergstrom, David E., et al.. (1995). Regulatory autonomy and molecular characterization of the Drosophila out at first gene.. Genetics. 139(3). 1331–1346. 26 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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