Robert S. Weiss

6.5k total citations
95 papers, 4.5k citations indexed

About

Robert S. Weiss is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Robert S. Weiss has authored 95 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 20 papers in Oncology and 13 papers in Genetics. Recurrent topics in Robert S. Weiss's work include DNA Repair Mechanisms (27 papers), CRISPR and Genetic Engineering (9 papers) and Cancer-related Molecular Pathways (9 papers). Robert S. Weiss is often cited by papers focused on DNA Repair Mechanisms (27 papers), CRISPR and Genetic Engineering (9 papers) and Cancer-related Molecular Pathways (9 papers). Robert S. Weiss collaborates with scholars based in United States, Spain and United Kingdom. Robert S. Weiss's co-authors include Ronald T. Javier, Siu Sylvia Lee, Marcus J. C. Long, Yimon Aye, Philip Leder, M Li, Gordon F. Streib, Colin Murray Parkes, Hening Lin and Yashira L. Negrón Abril and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Robert S. Weiss

92 papers receiving 4.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert S. Weiss United States 32 2.5k 1.1k 603 550 517 95 4.5k
Susanne Strand Germany 40 2.5k 1.0× 1.5k 1.4× 361 0.6× 664 1.2× 582 1.1× 134 6.7k
Sebastian Wagner Germany 32 5.2k 2.1× 1.3k 1.2× 969 1.6× 772 1.4× 384 0.7× 64 7.7k
Lynne S. Cox United Kingdom 31 2.3k 0.9× 914 0.8× 288 0.5× 385 0.7× 206 0.4× 62 3.7k
Marina Bibikova United States 37 9.2k 3.7× 655 0.6× 403 0.7× 1.2k 2.1× 2.6k 5.1× 87 11.3k
Mats Gullberg Sweden 21 4.0k 1.6× 566 0.5× 760 1.3× 343 0.6× 375 0.7× 47 6.4k
Mark D. Allen United Kingdom 38 2.8k 1.1× 662 0.6× 373 0.6× 115 0.2× 392 0.8× 100 5.1k
Jason G. Williams United States 45 3.7k 1.5× 517 0.5× 1.9k 3.1× 368 0.7× 527 1.0× 144 6.4k
Christopher V. Nicchitta United States 51 5.2k 2.1× 591 0.5× 1.7k 2.9× 307 0.6× 478 0.9× 110 6.9k
Patrick A. Grant United States 40 7.2k 2.9× 490 0.4× 301 0.5× 328 0.6× 681 1.3× 76 8.1k
Thomas M. Johnson United States 27 1.4k 0.6× 692 0.6× 131 0.2× 331 0.6× 159 0.3× 93 3.1k

Countries citing papers authored by Robert S. Weiss

Since Specialization
Citations

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

Fields of papers citing papers by Robert S. Weiss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert S. Weiss. 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 Robert S. Weiss. The network helps show where Robert S. Weiss may publish in the future.

Co-authorship network of co-authors of Robert S. Weiss

This figure shows the co-authorship network connecting the top 25 collaborators of Robert S. Weiss. A scholar is included among the top collaborators of Robert S. Weiss 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 Robert S. Weiss. Robert S. Weiss 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.
Constâncio, Vera, Isaac Braga, Joaquina Maurício, et al.. (2025). MicroRNA-371–373 cluster extracellular vesicle-based communication in testicular germ cell tumors. Cell Communication and Signaling. 23(1). 252–252.
2.
Latifkar, Arash, Fangyu Wang, Elena Panizza, et al.. (2022). IGF2BP2 promotes cancer progression by degrading the RNA transcript encoding a v-ATPase subunit. Proceedings of the National Academy of Sciences. 119(45). e2200477119–e2200477119. 21 indexed citations
3.
Kobayashi, Mutsumi, Misato Kobayashi, Junko Odajima, et al.. (2022). Expanding Homogeneous Culture of Human Primordial Germ Cell–Like Cells Maintaining Germline Features Without Serum or Feeder Layers. Obstetrical & Gynecological Survey. 77(5). 280–281.
4.
Greene, Kai Su, Michael J. Lukey, Xueying Wang, et al.. (2019). SIRT5 stabilizes mitochondrial glutaminase and supports breast cancer tumorigenesis. Proceedings of the National Academy of Sciences. 116(52). 26625–26632. 94 indexed citations
5.
Pierpont, Timothy M., Qiming Jin, Elizabeth S. Moore, et al.. (2017). Chemotherapy-Induced Depletion of OCT4-Positive Cancer Stem Cells in a Mouse Model of Malignant Testicular Cancer. Cell Reports. 21(7). 1896–1909. 43 indexed citations
6.
Sadhukhan, Sushabhan, Xiaojing Liu, Dongryeol Ryu, et al.. (2016). Metabolomics-assisted proteomics identifies succinylation and SIRT5 as important regulators of cardiac function. Proceedings of the National Academy of Sciences. 113(16). 4320–4325. 283 indexed citations
7.
Jing, Hui, Jing Hu, Bin He, et al.. (2016). A SIRT2-Selective Inhibitor Promotes c-Myc Oncoprotein Degradation and Exhibits Broad Anticancer Activity. Cancer Cell. 29(3). 297–310. 184 indexed citations
8.
Balmus, Gabriel, Pei Xin Lim, Alessandra Cassano, et al.. (2015). HUS1 regulates in vivo responses to genotoxic chemotherapies. Oncogene. 35(5). 662–669. 8 indexed citations
9.
Aye, Yimon, M Li, Marcus J. C. Long, & Robert S. Weiss. (2014). Ribonucleotide reductase and cancer: biological mechanisms and targeted therapies. Oncogene. 34(16). 2011–2021. 316 indexed citations
10.
Lim, Pei Xin, J. Kim Holloway, Rui Kan, et al.. (2013). Conditional Inactivation of the DNA Damage Response Gene Hus1 in Mouse Testis Reveals Separable Roles for Components of the RAD9-RAD1-HUS1 Complex in Meiotic Chromosome Maintenance. PLoS Genetics. 9(2). e1003320–e1003320. 42 indexed citations
11.
Vasileva, Ana, et al.. (2013). Clamping down on mammalian meiosis. Cell Cycle. 12(19). 3135–3334. 11 indexed citations
12.
Korte, F. Steven, Guy L. Odom, Jin Dai, et al.. (2012). Broad Transgenic, and Cardiac-Specific Viral Mediated, Over-Expression of Ribonucleotide Reductase Increases In Vivo Cardiac Contractility. Biophysical Journal. 102(3). 615a–615a. 1 indexed citations
13.
Selvaraj, Vimal, Atsushi Asano, Jennifer L. Page, et al.. (2010). Mice lacking FABP9/PERF15 develop sperm head abnormalities but are fertile. Developmental Biology. 348(2). 177–189. 35 indexed citations
14.
Ylikallio, Emil, Jennifer L. Page, Xia Xu, et al.. (2010). Ribonucleotide reductase is not limiting for mitochondrial DNA copy number in mice. Nucleic Acids Research. 38(22). 8208–8218. 25 indexed citations
15.
Xu, Xia, Jennifer L. Page, Jennifer A. Surtees, et al.. (2008). Broad Overexpression of Ribonucleotide Reductase Genes in Mice Specifically Induces Lung Neoplasms. Cancer Research. 68(8). 2652–2660. 75 indexed citations
16.
Zhu, Min & Robert S. Weiss. (2007). Increased Common Fragile Site Expression, Cell Proliferation Defects, and Apoptosis following Conditional Inactivation of MouseHus1in Primary Cultured Cells. Molecular Biology of the Cell. 18(3). 1044–1055. 29 indexed citations
17.
Chung, Sang‐Hyuk, et al.. (2007). Functionally distinct monomers and trimers produced by a viral oncoprotein. Oncogene. 27(10). 1412–1420. 14 indexed citations
18.
Latorre, Isabel, Michael H. Roh, Kristopher K. Frese, et al.. (2005). Viral oncoprotein-induced mislocalization of select PDZ proteins disrupts tight junctions and causes polarity defects in epithelial cells. Journal of Cell Science. 118(18). 4283–4293. 111 indexed citations
19.
Weiss, Robert S., Shuhei Matsuoka, Stephen J. Elledge, & Philip Leder. (2002). Hus1 Acts Upstream of Chk1 in a Mammalian DNA Damage Response Pathway. Current Biology. 12(1). 73–77. 77 indexed citations
20.
Weiss, Robert S., Corwin F. Kostrub, Tamar Enoch, & Philip Leder. (1999). Mouse Hus1, a Homolog of the Schizosaccharomyces pombe hus1+ Cell Cycle Checkpoint Gene. Genomics. 59(1). 32–39. 12 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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