Lisa D. McDaniel

2.4k total citations · 1 hit paper
33 papers, 1.8k citations indexed

About

Lisa D. McDaniel is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Lisa D. McDaniel has authored 33 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Plant Science. Recurrent topics in Lisa D. McDaniel's work include DNA Repair Mechanisms (18 papers), CRISPR and Genetic Engineering (10 papers) and Genomic variations and chromosomal abnormalities (4 papers). Lisa D. McDaniel is often cited by papers focused on DNA Repair Mechanisms (18 papers), CRISPR and Genetic Engineering (10 papers) and Genomic variations and chromosomal abnormalities (4 papers). Lisa D. McDaniel collaborates with scholars based in United States, United Kingdom and Canada. Lisa D. McDaniel's co-authors include Roger A. Schultz, Errol C. Friedberg, Srividya Subramanian, Quan‐Zhen Li, Edward K. Wakeland, Katalin Tus, Jinchun Zhou, Xin J. Zhou, Andrew Wang and Chaoying Liang and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Lisa D. McDaniel

33 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A Tlr7 translocation accelerates systemic autoimmunity in murine lupus

2006 505 citations Srividya Subramanian, Katalin Tus et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lisa D. McDaniel United States	16	1.2k	494	341	284	246	33	1.8k
G L Shen-Ong United States	19	1.2k 1.0×	417 0.8×	255 0.7×	279 1.0×	622 2.5×	27	1.9k
Teresita Díaz de Ståhl Sweden	23	810 0.7×	278 0.6×	318 0.9×	607 2.1×	201 0.8×	50	1.7k
A. Hagemeijer Netherlands	24	843 0.7×	272 0.6×	123 0.4×	340 1.2×	240 1.0×	53	1.9k
Mark J. Neveu United States	13	859 0.7×	400 0.8×	475 1.4×	179 0.6×	498 2.0×	13	1.7k
Tomohiko Taki Japan	36	2.4k 2.0×	328 0.7×	343 1.0×	303 1.1×	402 1.6×	127	3.7k
Gérard Goubin France	20	959 0.8×	201 0.4×	177 0.5×	208 0.7×	235 1.0×	41	1.4k
Daniel Zingg Switzerland	18	1.0k 0.8×	359 0.7×	257 0.8×	107 0.4×	473 1.9×	33	1.6k
E. Ogawa Japan	12	1.8k 1.5×	369 0.7×	306 0.9×	154 0.5×	620 2.5×	20	2.3k
Ian D. Dubé Canada	26	1.8k 1.5×	286 0.6×	157 0.5×	638 2.2×	391 1.6×	69	2.9k
J A Steitz United States	12	1.6k 1.3×	356 0.7×	338 1.0×	129 0.5×	617 2.5×	13	2.4k

Countries citing papers authored by Lisa D. McDaniel

Since Specialization

Citations

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

Fields of papers citing papers by Lisa D. McDaniel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa D. McDaniel

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa D. McDaniel. A scholar is included among the top collaborators of Lisa D. McDaniel 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 Lisa D. McDaniel. Lisa D. McDaniel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Rosenfeld, Jill A., Lisa D. McDaniel, Roger A. Schultz, et al.. (2014). Experience Using a Rapid Assay for Aneuploidy and Microdeletion/Microduplication Detection in over 2,900 Prenatal Specimens. Fetal Diagnosis and Therapy. 36(3). 231–241. 9 indexed citations

Kolquist, Kathryn A., Roger A. Schultz, Marilyn L. Slovak, et al.. (2011). Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis. Molecular Cytogenetics. 4(1). 25–25. 10 indexed citations

Chen, Yanping, et al.. (2010). Small scale genetic alterations contribute to increased mutability at the X-linked Hprt locus in vivo in Blm hypomorphic mice. DNA repair. 9(5). 551–557. 5 indexed citations

McDaniel, Lisa D., et al.. (2009). Polk mutant mice have a spontaneous mutator phenotype. DNA repair. 8(12). 1355–1362. 46 indexed citations

McDaniel, Lisa D. & Roger A. Schultz. (2008). XPF/ERCC4 and ERCC1: Their Products and Biological Roles. Advances in experimental medicine and biology. 637. 65–82. 14 indexed citations

Subramanian, Srividya, Katalin Tus, Quan‐Zhen Li, et al.. (2006). A Tlr7 translocation accelerates systemic autoimmunity in murine lupus. Proceedings of the National Academy of Sciences. 103(26). 9970–9975. 505 indexed citations breakdown →

Burr, Karen, et al.. (2006). Elevated mutation rates in the germline of Polκ mutant male mice. DNA repair. 5(7). 860–862. 21 indexed citations

McDaniel, Lisa D., Roger A. Schultz, & Errol C. Friedberg. (2006). TERF2-XPF: Caught in the middle; beginnings from the end. DNA repair. 5(7). 868–872. 4 indexed citations

McDaniel, Lisa D., et al.. (2006). A novel XPC pathogenic variant detected in archival material from a patient diagnosed with Xeroderma Pigmentosum: A case report and review of the genetic variants reported in XPC. DNA repair. 6(1). 100–114. 19 indexed citations

10.

McDaniel, Lisa D., et al.. (2006). Validation of XP-C pathogenic variations in archival material from a live XP patient. DNA repair. 6(1). 115–120. 2 indexed citations

11.

Fischhaber, Paula L., Lisa D. McDaniel, & Errol C. Friedberg. (2006). DNA Polymerases for Translesion DNA Synthesis: Enzyme Purification and Mouse Models for Studying Their Function. Methods in enzymology on CD-ROM/Methods in enzymology. 408. 355–378. 1 indexed citations

12.

McDaniel, Lisa D., Darrell J. Tomkins, Eric J. Stanbridge, et al.. (2005). Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells. The American Journal of Human Genetics. 77(1). 132–139. 5 indexed citations

13.

Porter, Paul C., et al.. (2005). Telomerase-immortalized human fibroblasts retain UV-induced mutagenesis and p53-mediated DNA damage responses. DNA repair. 5(1). 61–70. 8 indexed citations

14.

Nahari, Dorit, et al.. (2004). Mutations in the Trp53 gene of UV-irradiated Xpc mutant mice suggest a novel Xpc-dependent DNA repair process. DNA repair. 3(4). 379–386. 21 indexed citations

15.

Friedberg, Errol C., Lisa D. McDaniel, & Roger A. Schultz. (2003). The role of endogenous and exogenous DNA damage and mutagenesis. Current Opinion in Genetics & Development. 14(1). 5–10. 125 indexed citations

16.

McDaniel, Lisa D., Nicholas Chester, Mark L. Watson, et al.. (2003). Chromosome instability and tumor predisposition inversely correlate with BLM protein levels. DNA repair. 2(12). 1387–1404. 40 indexed citations

17.

Luo, Guangbin, Irma Μ. Santoro, Lisa D. McDaniel, et al.. (2000). Cancer predisposition caused by elevated mitotic recombination in Bloom mice. Nature Genetics. 26(4). 424–429. 319 indexed citations

18.

Giesler, Theresa L., et al.. (1997). Correction of the bloom syndrome cellular phenotypes. Somatic Cell and Molecular Genetics. 23(5). 303–312. 4 indexed citations

19.

McDaniel, Lisa D., Randy J. Legerski, Alan R. Lehmann, Errol C. Friedberg, & Roger A. Schultz. (1997). Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne syndrome patient using monoallelic mutation analysis in somatic cell hybrids. Human Mutation. 10(4). 317–321. 8 indexed citations

20.

Henning, Karla A., Lei Li, Narayan V. Iyer, et al.. (1995). The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH. Cell. 82(4). 555–564. 388 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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