Bernard A. Hauser

1.9k total citations
32 papers, 1.5k citations indexed

About

Bernard A. Hauser is a scholar working on Molecular Biology, Plant Science and Bioengineering. According to data from OpenAlex, Bernard A. Hauser has authored 32 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 23 papers in Plant Science and 4 papers in Bioengineering. Recurrent topics in Bernard A. Hauser's work include Plant Molecular Biology Research (15 papers), Photosynthetic Processes and Mechanisms (13 papers) and Plant Reproductive Biology (11 papers). Bernard A. Hauser is often cited by papers focused on Plant Molecular Biology Research (15 papers), Photosynthetic Processes and Mechanisms (13 papers) and Plant Reproductive Biology (11 papers). Bernard A. Hauser collaborates with scholars based in United States, Colombia and Switzerland. Bernard A. Hauser's co-authors include Charles S. Gasser, Jean Broadhvest, Kelian Sun, Robert J. Meister, Kimberly Hunt, Kay Schneitz, Julie Villanueva, Lee H. Pratt, David G Oppenheimer and Sung Ok Park and has published in prestigious journals such as Genes & Development, SHILAP Revista de lepidopterología and Development.

In The Last Decade

Bernard A. Hauser

31 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernard A. Hauser United States 21 1.3k 1.1k 191 56 25 32 1.5k
Jim Mattsson Canada 18 2.2k 1.7× 1.9k 1.7× 112 0.6× 45 0.8× 18 0.7× 32 2.4k
Jo Putterill New Zealand 15 1.3k 1.0× 1.1k 1.0× 91 0.5× 77 1.4× 17 0.7× 19 1.6k
Daniel I. Păcurar Sweden 10 1.8k 1.4× 1.2k 1.1× 91 0.5× 46 0.8× 46 1.8× 15 1.9k
Emmanuel Gendreau France 14 1.4k 1.1× 952 0.9× 96 0.5× 31 0.6× 25 1.0× 16 1.6k
Javier Agustí Spain 21 2.2k 1.7× 1.3k 1.2× 449 2.4× 46 0.8× 33 1.3× 37 2.3k
Chin‐Mei Lee United States 12 1.6k 1.2× 903 0.8× 113 0.6× 51 0.9× 25 1.0× 26 1.8k
Luiz Gustavo Guedes Corrêa Germany 8 1.1k 0.9× 879 0.8× 79 0.4× 65 1.2× 24 1.0× 8 1.4k
Annakaisa Elo Finland 14 1.1k 0.9× 1.1k 1.1× 60 0.3× 52 0.9× 32 1.3× 15 1.4k
Candela Cuesta Spain 17 893 0.7× 554 0.5× 112 0.6× 53 0.9× 30 1.2× 33 1.0k
Reyes Benlloch Spain 16 1.5k 1.2× 1.2k 1.1× 129 0.7× 80 1.4× 64 2.6× 21 1.7k

Countries citing papers authored by Bernard A. Hauser

Since Specialization
Citations

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

Fields of papers citing papers by Bernard A. Hauser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernard A. Hauser. 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 Bernard A. Hauser. The network helps show where Bernard A. Hauser may publish in the future.

Co-authorship network of co-authors of Bernard A. Hauser

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard A. Hauser. A scholar is included among the top collaborators of Bernard A. Hauser 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 Bernard A. Hauser. Bernard A. Hauser 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.
Zhang, Zheng‐Zhi, Evgeny V. Mavrodiev, Matthew A. Gitzendanner, et al.. (2025). Development of an efficient CRISPR-mediated genome editing platform in the diploid-polyploid model system Tragopogon (Asteraceae). Journal of Experimental Botany. 76(22). 6700–6713. 1 indexed citations
2.
Wang, Yaying, et al.. (2023). During Water Stress, Fertility Modulated by ROS Scavengers Abundant in Arabidopsis Pistils. Plants. 12(11). 2182–2182. 4 indexed citations
3.
Yang, Bing, et al.. (2023). Developing a CRISPR System in Nongenetic Model Polyploids. Methods in molecular biology. 2545. 475–490. 1 indexed citations
4.
Mavrodiev, Evgeny V., Riqing Li, Zheng‐Zhi Zhang, et al.. (2018). Application of CRISPR/Cas9 to Tragopogon (Asteraceae), an evolutionary model for the study of polyploidy. Molecular Ecology Resources. 18(6). 1427–1443. 30 indexed citations
5.
Vanegas, Diana, et al.. (2017). Microprofiling real time nitric oxide flux for field studies using a stratified nanohybrid carbon–metal electrode. Analytical Methods. 9(42). 6061–6072. 5 indexed citations
6.
Guo, Jianjun, Jue Fan, Bernard A. Hauser, & Seung Y. Rhee. (2015). Target Enrichment Improves Mapping of Complex Traits by Deep Sequencing. G3 Genes Genomes Genetics. 6(1). 67–77. 12 indexed citations
7.
Wang, Yaying, et al.. (2014). The APX4 locus regulates seed vigor and seedling growth in Arabidopsis thaliana. Planta. 239(4). 909–919. 29 indexed citations
8.
Taguchi, Masashige, et al.. (2013). Emerging technologies for non-invasive quantification of physiological oxygen transport in plants. Planta. 238(3). 599–614. 10 indexed citations
9.
He, Yan, Li‐Qun Chen, Yuan Zhou, et al.. (2010). Functional characterization of Arabidopsis thaliana isopropylmalate dehydrogenases reveals their important roles in gametophyte development. New Phytologist. 189(1). 160–175. 33 indexed citations
10.
Hill, Theresa, Debra J. Skinner, Anat Izhaki, et al.. (2006). ABERRANT TESTA SHAPE encodes a KANADI family member, linking polarity determination to separation and growth of Arabidopsis ovule integuments. The Plant Journal. 46(3). 522–531. 112 indexed citations
11.
Buzgo, Matyas, et al.. (2006). Perianth Development in the Basal Monocot Triglochin Maritima (Juncaginaceae). Aliso. 22(1). 107–125. 16 indexed citations
12.
Kim, Sangtae, Jin Koh, Hong Mā, et al.. (2005). Sequence and Expression Studies of A‐, B‐, and E‐Class MADS‐Box Homologues in Eupomatia (Eupomatiaceae): Support for the Bracteate Origin of the Calyptra. International Journal of Plant Sciences. 166(2). 185–198. 50 indexed citations
13.
Hauser, Bernard A., Kelian Sun, David G Oppenheimer, & Tammy L. Sage. (2005). Changes in mitochondrial membrane potential and accumulation of reactive oxygen species precede ultrastructural changes during ovule abortion. Planta. 223(3). 492–499. 37 indexed citations
14.
Sun, Kelian, Yuehua Cui, & Bernard A. Hauser. (2005). Environmental stress alters genes expression and induces ovule abortion: reactive oxygen species appear as ovules commit to abort. Planta. 222(4). 632–642. 37 indexed citations
15.
Park, Sung Ok, et al.. (2004). The phenotype ofArabidopsisovule mutants mimics the morphology of primitive seed plants. Proceedings of the Royal Society B Biological Sciences. 271(1536). 311–316. 15 indexed citations
16.
Villanueva, Julie, Jean Broadhvest, Bernard A. Hauser, et al.. (1999). INNER NO OUTER regulates abaxial- adaxial patterning in Arabidopsis ovules. Genes & Development. 13(23). 3160–3169. 264 indexed citations
17.
Hauser, Bernard A., Marie-Michèle Cordonnier-Pratt, & Lee H. Pratt. (1998). Temporal and photoregulated expression of five tomato phytochrome genes. The Plant Journal. 14(4). 431–439. 28 indexed citations
18.
19.
Hauser, Bernard A., et al.. (1995). The phytochrome gene family in tomato includes a novel subfamily. Plant Molecular Biology. 29(6). 1143–1155. 71 indexed citations
20.
Pratt, L. H., M. M. Cordonnier-Pratt, Bernard A. Hauser, & Michel Caboche. (1995). Tomato contains two differentially expressed genes encoding B-type phytochromes, neither of which can be considered an ortholog of Arabidopsis phytochrome B. Planta. 197(1). 203–6. 35 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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