David Schild

6.3k total citations
46 papers, 5.3k citations indexed

About

David Schild is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, David Schild has authored 46 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 12 papers in Oncology and 12 papers in Cancer Research. Recurrent topics in David Schild's work include DNA Repair Mechanisms (29 papers), Fungal and yeast genetics research (18 papers) and Carcinogens and Genotoxicity Assessment (12 papers). David Schild is often cited by papers focused on DNA Repair Mechanisms (29 papers), Fungal and yeast genetics research (18 papers) and Carcinogens and Genotoxicity Assessment (12 papers). David Schild collaborates with scholars based in United States, Norway and Hong Kong. David Schild's co-authors include Robert Mortimer, Larry H. Thompson, C. Rebecca Contopoulou, Claudia Wiese, Breck Byers, David J. Chen, Jonathan A. Kans, Minoru Takata, Seiji Tachiiri and Shunichi Takeda and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

David Schild

46 papers receiving 5.1k 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 Schild United States 36 4.9k 1.0k 846 762 642 46 5.3k
Lee Bardwell United States 36 4.8k 1.0× 383 0.4× 308 0.4× 731 1.0× 422 0.7× 68 5.3k
Małgorzata Z. Zdzienicka Netherlands 36 4.6k 0.9× 2.0k 1.9× 1.5k 1.7× 523 0.7× 790 1.2× 87 5.4k
A.A. van Zeeland Netherlands 48 7.0k 1.4× 1.1k 1.1× 2.6k 3.1× 842 1.1× 824 1.3× 146 7.9k
Michael Lisby Denmark 42 6.0k 1.2× 880 0.9× 696 0.8× 743 1.0× 586 0.9× 117 6.5k
Ted Weinert United States 27 6.9k 1.4× 1.7k 1.7× 1.1k 1.3× 875 1.1× 513 0.8× 47 7.6k
J. Martin Brown United States 21 2.1k 0.4× 589 0.6× 524 0.6× 255 0.3× 299 0.5× 33 3.1k
Noel F. Lowndes Ireland 36 4.6k 0.9× 1.1k 1.0× 835 1.0× 419 0.5× 336 0.5× 83 5.1k
Carrie Baker Brachmann United States 25 4.2k 0.9× 549 0.5× 209 0.2× 614 0.8× 248 0.4× 45 5.5k
Susan L. Forsburg United States 38 5.3k 1.1× 492 0.5× 304 0.4× 826 1.1× 421 0.7× 114 5.9k
Michael M. Seidman United States 48 6.0k 1.2× 998 1.0× 1.2k 1.4× 680 0.9× 888 1.4× 147 6.8k

Countries citing papers authored by David Schild

Since Specialization
Citations

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

Fields of papers citing papers by David Schild

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Schild

This figure shows the co-authorship network connecting the top 25 collaborators of David Schild. A scholar is included among the top collaborators of David Schild 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 Schild. David Schild 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.
Roy, Sunetra, Yue Chen, A.S. Arvai, et al.. (2023). RAD51C-XRCC3 structure and cancer patient mutations define DNA replication roles. Nature Communications. 14(1). 4445–4445. 23 indexed citations
2.
Parplys, Ann Christin, et al.. (2014). RAD51AP1 -deficiency in vertebrate cells impairs DNA replication. DNA repair. 24. 87–97. 23 indexed citations
3.
Dray, Eloïse, Weixing Zhao, Joseph San Filippo, et al.. (2012). Mechanistic Insights into RAD51-associated Protein 1 (RAD51AP1) Action in Homologous DNA Repair. Journal of Biological Chemistry. 287(15). 12343–12347. 36 indexed citations
4.
Dray, Eloïse, Weixing Zhao, Miaw-Sheue Tsai, et al.. (2011). RAD51-associated Protein 1 (RAD51AP1) Interacts with the Meiotic Recombinase DMC1 through a Conserved Motif. Journal of Biological Chemistry. 286(43). 37328–37334. 18 indexed citations
5.
Dray, Eloïse, Julia Etchin, Claudia Wiese, et al.. (2010). Enhancement of RAD51 recombinase activity by the tumor suppressor PALB2. Nature Structural & Molecular Biology. 17(10). 1255–1259. 128 indexed citations
6.
Schild, David & Claudia Wiese. (2009). Overexpression of RAD51 suppresses recombination defects: a possible mechanism to reverse genomic instability. Nucleic Acids Research. 38(4). 1061–1070. 79 indexed citations
7.
Kovalenko, Oleg, Claudia Wiese, & David Schild. (2006). RAD51AP2, a novel vertebrate- and meiotic-specific protein, shares a conserved RAD51-interacting C-terminal domain with RAD51AP1/PIR51. Nucleic Acids Research. 34(18). 5081–5092. 21 indexed citations
8.
Schild, David, et al.. (2004). Human Rad51C Deficiency Destabilizes XRCC3, Impairs Recombination, and Radiosensitizes S/G2-phase Cells. Journal of Biological Chemistry. 279(40). 42313–42320. 53 indexed citations
9.
Thompson, Larry H. & David Schild. (2001). Homologous recombinational repair of DNA ensures mammalian chromosome stability. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 477(1-2). 131–153. 343 indexed citations
10.
Sigurðsson, Stefán, Stephen Van Komen, Wendy Bussen, et al.. (2001). Mediator function of the human Rad51B–Rad51C complex in Rad51/RPA-catalyzed DNA strand exchange. Genes & Development. 15(24). 3308–3318. 188 indexed citations
11.
Thompson, Larry H. & David Schild. (1999). The contribution of homologous recombination in preserving genome integrity in mammalian cells. Biochimie. 81(1-2). 87–105. 114 indexed citations
12.
Liu, Nan, Jane E. Lamerdin, Robert S. Tebbs, et al.. (1998). XRCC2 and XRCC3, New Human Rad51-Family Members, Promote Chromosome Stability and Protect against DNA Cross-Links and Other Damages. Molecular Cell. 1(6). 783–793. 461 indexed citations
13.
14.
Schild, David, Robert Mortimer, Brian Glassner, Marian Carlson, & Brehon C. Laurent. (1992). Identification of RAD 16, a yeast excision repair gene homologous to the recombinational repair gene RAD 54 and to the SNF2 gene involved in transcriptioal activation. Yeast. 8(5). 385–395. 57 indexed citations
15.
Schild, David, et al.. (1991). Sequence of RAD54, a Saccharomyces cerevisiae gene involved in recombination and repair. Gene. 104(1). 103–106. 87 indexed citations
16.
17.
Schild, David, A J Brake, Michael Kiefer, D B Young, & P J Barr. (1990). Cloning of three human multifunctional de novo purine biosynthetic genes by functional complementation of yeast mutations.. Proceedings of the National Academy of Sciences. 87(8). 2916–2920. 101 indexed citations
18.
Mortimer, Robert, David Schild, C. Rebecca Contopoulou, & Jonathan A. Kans. (1989). Genetic map of Saccharomyces cerevisiae, edition 10. Yeast. 5(5). 321–403. 245 indexed citations
19.
Schild, David, J. R. Johnston, Caren Chang, & Robert Mortimer. (1984). Cloning and Mapping of Saccharomyces cerevisiae Photoreactivation Gene PHR1. Molecular and Cellular Biology. 4(9). 1864–1870. 9 indexed citations
20.
Mortimer, Robert & David Schild. (1981). Genetic Mapping in Saccharomyces cerevisiae. Cold Spring Harbor Monograph Archive. 11–26. 56 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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