Leslie Smith

3.3k total citations · 1 hit paper
24 papers, 2.5k citations indexed

About

Leslie Smith is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Leslie Smith has authored 24 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 6 papers in Cell Biology and 6 papers in Genetics. Recurrent topics in Leslie Smith's work include DNA Repair Mechanisms (10 papers), Genomics and Chromatin Dynamics (8 papers) and Microtubule and mitosis dynamics (5 papers). Leslie Smith is often cited by papers focused on DNA Repair Mechanisms (10 papers), Genomics and Chromatin Dynamics (8 papers) and Microtubule and mitosis dynamics (5 papers). Leslie Smith collaborates with scholars based in United States, Sweden and India. Leslie Smith's co-authors include Mathew J. Thayer, Roni J. Bollag, J. Russell Lipford, Sean M. Baker, Mary Kay Lescoe, Michael Kane, Christian Bronner, Magnus Nordenskj�ld, Richard D. Kolodner and R. Michael Liskay and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Leslie Smith

23 papers receiving 2.5k citations

Hit Papers

Mutation in the DNA mismatch repair gene homologue hMLH 1... 1994 2026 2004 2015 1994 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leslie Smith United States 18 1.4k 1.3k 951 920 476 24 2.5k
David Bicknell United Kingdom 12 408 0.3× 869 0.7× 409 0.4× 363 0.4× 337 0.7× 16 1.5k
Wai Yin Tsui China 10 721 0.5× 823 0.6× 825 0.9× 493 0.5× 322 0.7× 11 1.7k
Petra Platzer United States 17 384 0.3× 947 0.7× 584 0.6× 601 0.7× 299 0.6× 19 1.8k
Tiziana Venesio Italy 22 575 0.4× 815 0.6× 955 1.0× 640 0.7× 181 0.4× 68 1.8k
Zimu Zheng United States 6 397 0.3× 1.5k 1.2× 457 0.5× 251 0.3× 324 0.7× 6 2.0k
Marianne Tiainen Finland 19 406 0.3× 779 0.6× 483 0.5× 217 0.2× 226 0.5× 26 1.4k
Annie S.Y. Chan China 19 366 0.3× 1.1k 0.8× 581 0.6× 465 0.5× 184 0.4× 20 1.8k
Martin Janz Germany 23 597 0.4× 1.3k 1.0× 786 0.8× 400 0.4× 99 0.2× 47 2.5k
F Kasumi Japan 16 380 0.3× 686 0.5× 529 0.6× 530 0.6× 373 0.8× 53 1.4k
Laufey T. Ámundadóttir United States 21 174 0.1× 1.0k 0.8× 641 0.7× 287 0.3× 385 0.8× 47 1.7k

Countries citing papers authored by Leslie Smith

Since Specialization
Citations

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

Fields of papers citing papers by Leslie Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leslie Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Leslie Smith. A scholar is included among the top collaborators of Leslie Smith 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 Leslie Smith. Leslie Smith 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
2.
Smith, Leslie, et al.. (2024). The US FDA's proposed rule on laboratory-developed tests: Impacts on clinical laboratory testing. Practical Laboratory Medicine. 40. e00407–e00407. 2 indexed citations
3.
Donley, Nathan, Leslie Smith, & Mathew J. Thayer. (2015). ASAR15, A cis-Acting Locus that Controls Chromosome-Wide Replication Timing and Stability of Human Chromosome 15. PLoS Genetics. 11(1). e1004923–e1004923. 32 indexed citations
4.
Donley, Nathan, et al.. (2013). Asynchronous Replication, Mono-Allelic Expression, and Long Range Cis-Effects of ASAR6. PLoS Genetics. 9(4). e1003423–e1003423. 34 indexed citations
5.
Smith, Leslie & Mathew J. Thayer. (2012). Chromosome Replicating Timing Combined with Fluorescent <em>In situ</em> Hybridization. Journal of Visualized Experiments. e4400–e4400. 9 indexed citations
6.
Duncan, Andrew W., Amy E. Hanlon Newell, Leslie Smith, et al.. (2011). Frequent Aneuploidy Among Normal Human Hepatocytes. Gastroenterology. 142(1). 25–28. 146 indexed citations
7.
8.
Smith, Leslie, et al.. (2005). Engineering translocations with delayed replication: evidence for cis control of chromosome replication timing. Human Molecular Genetics. 14(19). 2813–2827. 34 indexed citations
9.
Smith, Leslie, et al.. (2004). Ionizing Radiation Induces Frequent Translocations with Delayed Replication and Condensation. Cancer Research. 64(22). 8231–8238. 31 indexed citations
10.
Denissenko, Mikhail F., Tatiana Koudriakova, Leslie Smith, et al.. (1998). The p53 codon 249 mutational hotspot in hepatocellular carcinoma is not related to selective formation or persistence of aflatoxin B1 adducts. Oncogene. 17(23). 3007–3014. 78 indexed citations
11.
Smith, Leslie, Lisa V. Goodrich, David A. Jacobson, et al.. (1998). Duplication of ATR inhibits MyoD, induces aneuploidy and eliminates radiation-induced G1 arrest. Nature Genetics. 19(1). 39–46. 68 indexed citations
12.
Johnson, Kenneth R., Leslie Smith, Dabney K. Johnson, et al.. (1996). Mapping of theARIXHomeodomain Gene to Mouse Chromosome 7 and Human Chromosome 11q13. Genomics. 33(3). 527–531. 7 indexed citations
13.
Schultz, Dennis W., M. Litt, Leslie Smith, Mathew J. Thayer, & Ken McCormack. (1996). Localization of Two Potassium Channel β Subunit Genes, KCNA1B and KCNA2B. Genomics. 31(3). 389–391. 18 indexed citations
14.
Whitney, Michael, Carol Reifsteck, Susan B. Olson, et al.. (1995). Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p. Nature Genetics. 11(3). 341–343. 113 indexed citations
15.
Bronner, Christian, Sean M. Baker, Paul T. Morrison, et al.. (1994). Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer. Nature. 368(6468). 258–261. 1605 indexed citations breakdown →
16.
Magenis, R.E., Leslie Smith, Joseph H. Nadeau, et al.. (1994). Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and human. Mammalian Genome. 5(8). 503–508. 62 indexed citations
17.
Grandy, David K., et al.. (1992). The human gene fro apurinic/apyrimidinic endonuclease (HAP1): sequence and localization to chromosome 14 band q12. Nucleic Acids Research. 20(15). 4097–4098. 16 indexed citations
18.
Sharma, Vikram, et al.. (1991). Dinucleotide repeat polymorphism at the D14S43 locus. Nucleic Acids Research. 19(7). 1722–1722. 20 indexed citations
19.
Weber, Bernhard H. F., Leland Allen, R. Ellen Magenis, et al.. (1991). Intrachromosomal location of the telomeric repeat (TTAGGG)n. Mammalian Genome. 1(4). 211–216. 28 indexed citations
20.
Sharma, Vikram, et al.. (1991). Dinucleotide repeat polymorphism at the D9S55 locus. Nucleic Acids Research. 19(14). 4023–4023. 10 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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