Michael Schertzer

1.8k total citations
25 papers, 1.3k citations indexed

About

Michael Schertzer is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Michael Schertzer has authored 25 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Physiology. Recurrent topics in Michael Schertzer's work include DNA Repair Mechanisms (8 papers), Telomeres, Telomerase, and Senescence (5 papers) and CRISPR and Genetic Engineering (4 papers). Michael Schertzer is often cited by papers focused on DNA Repair Mechanisms (8 papers), Telomeres, Telomerase, and Senescence (5 papers) and CRISPR and Genetic Engineering (4 papers). Michael Schertzer collaborates with scholars based in Canada, United States and France. Michael Schertzer's co-authors include Peter M. Lansdorp, Stephen Wood, Iris Cheung, Ann M. Rose, Catherine Blackwell, Robert Lanza, Gabriela M. Baerlocher, Vincent J. Cristofalo, Jennifer Sze Man Mak and Elizabeth A. Chavez and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Michael Schertzer

25 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael Schertzer Canada 15 994 320 305 162 157 25 1.3k
Nobuaki Kikyo United States 24 1.5k 1.5× 309 1.0× 123 0.4× 77 0.5× 276 1.8× 46 1.8k
Ma Wan United States 10 1.3k 1.3× 139 0.4× 564 1.8× 93 0.6× 33 0.2× 12 1.5k
Stuart P. Atkinson Spain 20 1.4k 1.4× 136 0.4× 267 0.9× 31 0.2× 137 0.9× 38 1.7k
Lioudmila V. Sharova United States 16 1.0k 1.0× 139 0.4× 121 0.4× 60 0.4× 86 0.5× 23 1.2k
Tae Ho Shin United States 13 1.2k 1.2× 97 0.3× 60 0.2× 112 0.7× 151 1.0× 13 1.4k
Mary Kay Francis United States 16 636 0.6× 179 0.6× 206 0.7× 20 0.1× 170 1.1× 18 1.1k
Louise Hyslop United Kingdom 11 1.0k 1.0× 132 0.4× 66 0.2× 65 0.4× 334 2.1× 17 1.4k
Niolette I. McGill United Kingdom 7 889 0.9× 501 1.6× 391 1.3× 324 2.0× 13 0.1× 7 1.4k
Marta Garcı́a-Cao Spain 9 1.3k 1.3× 123 0.4× 829 2.7× 164 1.0× 28 0.2× 11 1.7k
Patricia G. Wilson United States 20 872 0.9× 169 0.5× 50 0.2× 107 0.7× 65 0.4× 40 1.3k

Countries citing papers authored by Michael Schertzer

Since Specialization
Citations

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

Fields of papers citing papers by Michael Schertzer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Schertzer

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Schertzer. A scholar is included among the top collaborators of Michael Schertzer 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 Michael Schertzer. Michael Schertzer 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.
Smith, Rebecca, et al.. (2024). DNA damage–induced EMT controlled by the PARP-dependent chromatin remodeler ALC1 promotes DNA repair efficiency through RAD51 in tumor cells. Molecular Biology of the Cell. 35(12). ar151–ar151. 1 indexed citations
2.
Schertzer, Michael, et al.. (2023). Human RTEL1 Interacts with KPNB1 (Importin β) and NUP153 and Connects Nuclear Import to Nuclear Envelope Stability in S-Phase. Cells. 12(24). 2798–2798. 3 indexed citations
3.
Méndez-Bermúdez, Aarón, Serge Bauwens, Marie‐Josèphe Giraud‐Panis, et al.. (2018). Genome-wide Control of Heterochromatin Replication by the Telomere Capping Protein TRF2. Molecular Cell. 70(3). 449–461.e5. 44 indexed citations
4.
Schertzer, Michael, Karina Jouravleva, Mylène Perderiset, et al.. (2015). Human regulator of telomere elongation helicase 1 (RTEL1) is required for the nuclear and cytoplasmic trafficking of pre-U2 RNA. Nucleic Acids Research. 43(3). 1834–1847. 20 indexed citations
5.
Guen, Tangui Le, Fabien Touzot, Michael Schertzer, et al.. (2013). Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability. Human Molecular Genetics. 22(16). 3239–3249. 122 indexed citations
6.
Cheung, Iris, Michael Schertzer, Ann M. Rose, & Peter M. Lansdorp. (2002). Disruption of dog-1 in Caenorhabditis elegans triggers deletions upstream of guanine-rich DNA. Nature Genetics. 31(4). 405–409. 216 indexed citations
7.
Paznekas, William A., Kazuki Okajima, Michael Schertzer, Stephen Wood, & Ethylin Wang Jabs. (1999). Genomic Organization, Expression, and Chromosome Location of the Human SNAIL Gene (SNAI1) and a Related Processed Pseudogene (SNAI1P). Genomics. 62(1). 42–49. 47 indexed citations
8.
Cohen, Michael E., et al.. (1998). HumanSLUGGene Organization, Expression, and Chromosome Map Location on 8q. Genomics. 51(3). 468–471. 36 indexed citations
9.
Bruskiewich, Richard, Michael Schertzer, & Stephen Wood. (1997). A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus. Genome. 40(1). 77–83. 1 indexed citations
10.
Bruskiewich, Richard, Li Ma, Lucas Chan, et al.. (1996). Analysis of CA repeat polymorphisms places three human gene loci on the 8p linkage map. Cytogenetic and Genome Research. 73(4). 331–333. 5 indexed citations
11.
Schertzer, Michael, et al.. (1995). Identification of the human neuronal nicotinic cholinergic α2 receptor locus, (CHRNA2), within an 8p21 mapped locus, by sequence homology with rat DNA. Somatic Cell and Molecular Genetics. 21(2). 147–150. 9 indexed citations
12.
Wood, Stephen, et al.. (1995). Sequence identity locates CEBPD and FGFR1 to mapped human loci within proximal 8p. Cytogenetic and Genome Research. 70(3-4). 188–191. 10 indexed citations
13.
14.
Wood, Stephen, Michael Schertzer, Michael R. Hayden, & Yuanhong Ma. (1993). Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene. Human Genetics. 91(4). 312–6. 18 indexed citations
15.
Tomfohrde, James, Stephen Wood, Michael Schertzer, et al.. (1992). Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors. Genomics. 14(1). 144–152. 59 indexed citations
16.
Wood, Stephen & Michael Schertzer. (1992). Linkage mapping of the D8S133 locus to chromosome 8p using a highly informative, polymorphic, complex dinucleotide repeat. Genomics. 13(1). 232–232. 9 indexed citations
17.
Wood, Stephen, Michael Schertzer, Harry A. Drabkin, et al.. (1992). Characterization of a human chromosome 8 cosmid library constructed from flow-sorted chromosomes. Cytogenetic and Genome Research. 59(4). 243–247. 41 indexed citations
18.
Wood, Stephen & Michael Schertzer. (1992). A Polymorphic Complex Dinucleotide Repeat at the Telomeric D8S7 Locus. Human Heredity. 42(3). 149–152. 44 indexed citations
19.
Wood, Stephen & Michael Schertzer. (1991). Dinucleotide repeat polymorphism at the D8S135 locus on chromosome 8p. Nucleic Acids Research. 19(23). 6664–6664. 1 indexed citations
20.
Dill, F. J., et al.. (1987). Inverted tandem duplication generates a duplication deficiency of chromosome 8p. Clinical Genetics. 32(2). 109–113. 38 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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