Mark D. Rose

13.3k total citations · 5 hit papers
96 papers, 11.7k citations indexed

About

Mark D. Rose is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Mark D. Rose has authored 96 papers receiving a total of 11.7k indexed citations (citations by other indexed papers that have themselves been cited), including 92 papers in Molecular Biology, 56 papers in Cell Biology and 7 papers in Plant Science. Recurrent topics in Mark D. Rose's work include Fungal and yeast genetics research (68 papers), Cellular transport and secretion (28 papers) and Microtubule and mitosis dynamics (28 papers). Mark D. Rose is often cited by papers focused on Fungal and yeast genetics research (68 papers), Cellular transport and secretion (28 papers) and Microtubule and mitosis dynamics (28 papers). Mark D. Rose collaborates with scholars based in United States, Japan and Germany. Mark D. Rose's co-authors include Fred Winston, David Botstein, Philip Hieter, Gerald R. Fink, Joseph P. Vogel, James H. Thomas, Peter Novick, Rita K. Miller, Alison E. Gammie and Dina P. Matheos and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Mark D. Rose

96 papers receiving 11.4k citations

Hit Papers

Methods in Yeast Genetics... 1987 2026 2000 2013 1990 1987 2000 1989 1992 500 1000 1.5k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Mark D. Rose 10.4k 5.1k 1.5k 752 580 96 11.7k
Akio Toh‐e 9.5k 0.9× 3.2k 0.6× 1.8k 1.2× 725 1.0× 639 1.1× 217 10.7k
Achim Wach 10.3k 1.0× 3.3k 0.7× 1.5k 1.0× 705 0.9× 712 1.2× 31 11.1k
Sergio Moreno 10.7k 1.0× 4.6k 0.9× 1.5k 1.0× 830 1.1× 464 0.8× 98 12.6k
Mark S. Longtine 9.2k 0.9× 3.7k 0.7× 1.3k 0.9× 373 0.5× 634 1.1× 61 11.0k
Gustav Ammerer 8.4k 0.8× 2.2k 0.4× 1.7k 1.1× 548 0.7× 537 0.9× 105 10.0k
R. Daniel Gietz 12.3k 1.2× 2.0k 0.4× 2.9k 1.9× 979 1.3× 1.4k 2.4× 44 14.5k
R Sikorski 8.1k 0.8× 2.3k 0.4× 1.0k 0.7× 523 0.7× 532 0.9× 18 8.8k
Arndt Brachat 7.5k 0.7× 2.4k 0.5× 1.0k 0.7× 390 0.5× 485 0.8× 20 8.2k
Peter Philippsen 17.4k 1.7× 5.0k 1.0× 3.7k 2.4× 1.1k 1.5× 1.3k 2.2× 102 19.0k
Vytas A. Bankaitis 7.3k 0.7× 5.6k 1.1× 1.0k 0.7× 837 1.1× 136 0.2× 159 9.6k

Countries citing papers authored by Mark D. Rose

Since Specialization
Citations

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

Fields of papers citing papers by Mark D. Rose

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark D. Rose. 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 Mark D. Rose. The network helps show where Mark D. Rose may publish in the future.

Co-authorship network of co-authors of Mark D. Rose

This figure shows the co-authorship network connecting the top 25 collaborators of Mark D. Rose. A scholar is included among the top collaborators of Mark D. Rose 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 Mark D. Rose. Mark D. Rose 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.
Rose, Mark D., et al.. (2018). Cell fusion in yeast is negatively regulated by components of the cell wall integrity pathway. Molecular Biology of the Cell. 30(4). 441–452. 7 indexed citations
2.
Rose, Mark D., et al.. (2013). ER-associated SNAREs and Sey1p mediate nuclear fusion at two distinct steps during yeast mating. Molecular Biology of the Cell. 24(24). 3896–3908. 15 indexed citations
3.
Shen, Steven S., et al.. (2009). Distinct Roles for Key Karyogamy Proteins during Yeast Nuclear Fusion. Molecular Biology of the Cell. 20(17). 3773–3782. 19 indexed citations
4.
Sheltzer, Jason M. & Mark D. Rose. (2009). The Class V Myosin Myo2p Is Required for Fus2p Transport and Actin Polarization during the Yeast Mating Response. Molecular Biology of the Cell. 20(12). 2909–2919. 21 indexed citations
5.
Rose, Mark D., et al.. (2009). Prm3p Is a Pheromone-induced Peripheral Nuclear Envelope Protein Required for Yeast Nuclear Fusion. Molecular Biology of the Cell. 20(9). 2438–2450. 19 indexed citations
6.
Clark, Sean W. & Mark D. Rose. (2005). Arp10p Is a Pointed-End-associated Component of Yeast Dynactin. Molecular Biology of the Cell. 17(2). 738–748. 14 indexed citations
7.
Clark, Sean W. & Mark D. Rose. (2005). Alanine Scanning of Arp1 Delineates a Putative Binding Site for Jnm1/Dynamitin and Nip100/p150Glued. Molecular Biology of the Cell. 16(9). 3999–4012. 9 indexed citations
8.
Kimata, Yukio, Yusuke Shimizu, Hiroshi Abe, et al.. (2003). Genetic Evidence for a Role of BiP/Kar2 That Regulates Ire1 in Response to Accumulation of Unfolded Proteins. Molecular Biology of the Cell. 14(6). 2559–2569. 172 indexed citations
9.
Kabani, Mehdi, Stephanie Kelley, Diana Montgomery, et al.. (2003). Dependence of Endoplasmic Reticulum-associated Degradation on the Peptide Binding Domain and Concentration of BiP. Molecular Biology of the Cell. 14(8). 3437–3448. 91 indexed citations
10.
Metodiev, Metodi V., Dina P. Matheos, Mark D. Rose, & David E. Stone. (2002). Regulation of MAPK Function by Direct Interaction with the Mating-Specific Gα in Yeast. Science. 296(5572). 1483–1486. 86 indexed citations
11.
Miller, Rita K., Soo-Chen Cheng, & Mark D. Rose. (2000). Bim1p/Yeb1p Mediates the Kar9p-dependent Cortical Attachment of Cytoplasmic Microtubules. Molecular Biology of the Cell. 11(9). 2949–2959. 131 indexed citations
12.
Gammie, Alison E., et al.. (1999). The Two Forms of Karyogamy Transcription Factor Kar4p Are Regulated by Differential Initiation of Transcription, Translation, and Protein Turnover. Molecular and Cellular Biology. 19(1). 817–825. 31 indexed citations
13.
Brizzio, Valeria, et al.. (1999). Genetic Interactions betweenKAR7/SEC71,KAR8/JEM1,KAR5, andKAR2during Nuclear Fusion inSaccharomyces cerevisiae. Molecular Biology of the Cell. 10(3). 609–626. 38 indexed citations
14.
Miller, Rita K., et al.. (1998). The Kinesin-related Proteins, Kip2p and Kip3p, Function Differently in Nuclear Migration in Yeast. Molecular Biology of the Cell. 9(8). 2051–2068. 120 indexed citations
15.
Gammie, Alison E., Valeria Brizzio, & Mark D. Rose. (1998). Distinct Morphological Phenotypes of Cell Fusion Mutants. Molecular Biology of the Cell. 9(6). 1395–1410. 86 indexed citations
16.
McClellan, Amie J., et al.. (1998). Specific Molecular Chaperone Interactions and an ATP-dependent Conformational Change Are Required during Posttranslational Protein Translocation into the Yeast ER. Molecular Biology of the Cell. 9(12). 3533–3545. 67 indexed citations
17.
Marsh, Lorraine & Mark D. Rose. (1997). 10 The Pathway of Cell and Nuclear Fusion during Mating in S. cerevisiae. Cold Spring Harbor Monograph Archive. 827–888. 4 indexed citations
18.
Kurihara, Laurie, et al.. (1996). Kar4p, a Karyogamy-Specific Component of the Yeast Pheromone Response Pathway. Molecular and Cellular Biology. 16(8). 3990–4002. 48 indexed citations
19.
Scidmore, Marci A., Heidi Okamura, & Mark D. Rose. (1993). Genetic interactions between KAR2 and SEC63, encoding eukaryotic homologues of DnaK and DnaJ in the endoplasmic reticulum.. Molecular Biology of the Cell. 4(11). 1145–1159. 117 indexed citations
20.
Rose, Mark D. & James R. Broach. (1991). [14] Cloning genes by complementation in yeast. Methods in enzymology on CD-ROM/Methods in enzymology. 194. 195–230. 243 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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