L.M. Pertz

2.1k total citations · 2 hit papers
6 papers, 1.5k citations indexed

About

L.M. Pertz is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, L.M. Pertz has authored 6 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Plant Science. Recurrent topics in L.M. Pertz's work include Genomic variations and chromosomal abnormalities (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Genomics and Phylogenetic Studies (2 papers). L.M. Pertz is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Genomics and Phylogenetic Studies (2 papers). L.M. Pertz collaborates with scholars based in United States and Italy. L.M. Pertz's co-authors include Evan E. Eichler, Donna G. Albertson, Daniel Pinkel, Andrew J. Sharp, Jeffrey A. Bailey, Maynard V. Olson, Eric Haugen, Rajinder Kaul, Victoria Morrison and Eray Tüzün and has published in prestigious journals such as Nature Genetics, Genetics and The American Journal of Human Genetics.

In The Last Decade

L.M. Pertz

6 papers receiving 1.5k 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.

Fine-scale structural variation of the human genome

2005 742 citations Eray Tüzün, Andrew J. Sharp et al. Nature Genetics profile →
Segmental Duplications and Copy-Number Variation in the Human Genome

2005 678 citations Andrew J. Sharp, Devin P. Locke et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L.M. Pertz United States	5	1.2k	862	625	158	153	6	1.5k
Charlotte N. Henrichsen Switzerland	8	599 0.5×	493 0.6×	230 0.4×	77 0.5×	115 0.8×	9	877
Kristin Mrasek Germany	24	1.3k 1.1×	891 1.0×	842 1.3×	500 3.2×	115 0.8×	86	1.8k
Ercole Rao Germany	12	777 0.6×	763 0.9×	178 0.3×	46 0.3×	59 0.4×	19	1.1k
Claude‐Lise Richer Canada	15	397 0.3×	458 0.5×	194 0.3×	95 0.6×	81 0.5×	35	759
Jonathan Davies Canada	7	502 0.4×	1.5k 1.7×	102 0.2×	124 0.8×	215 1.4×	10	1.7k
Sandra R. Richardson Australia	16	273 0.2×	1.3k 1.5×	818 1.3×	41 0.3×	113 0.7×	23	1.5k
Kyle R. Upton Australia	11	296 0.2×	959 1.1×	663 1.1×	22 0.1×	122 0.8×	17	1.2k
Annelyse Mertz Germany	9	752 0.6×	663 0.8×	174 0.3×	53 0.3×	46 0.3×	9	947
Ayelet Rahat Israel	12	545 0.4×	1.0k 1.2×	167 0.3×	35 0.2×	55 0.4×	14	1.2k
Tahsin Stefan Barakat Netherlands	18	722 0.6×	1.3k 1.5×	112 0.2×	32 0.2×	207 1.4×	45	1.5k

Countries citing papers authored by L.M. Pertz

Since Specialization

Citations

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

Fields of papers citing papers by L.M. Pertz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L.M. Pertz. 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 L.M. Pertz. The network helps show where L.M. Pertz may publish in the future.

Co-authorship network of co-authors of L.M. Pertz

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Pertz, L.M., Gayle J. Pauer, E. Simpson, et al.. (2006). Mutation Screen in the COCH Gene in 190 Patients with Glaucoma. Investigative Ophthalmology & Visual Science. 47(13). 210–210. 2 indexed citations

2.

Pertz, L.M., et al.. (2006). Chromosome-wide, allele-specific analysis of the histone code on the human X chromosome. Human Molecular Genetics. 15(15). 2335–2347. 23 indexed citations

3.

Chadwick, Lisa H., L.M. Pertz, Karl W. Broman, Marisa S. Bartolomei, & Huntington F. Willard. (2006). Genetic Control of X Chromosome Inactivation in Mice: Definition of theXceCandidate Interval. Genetics. 173(4). 2103–2110. 46 indexed citations

4.

Sharp, Andrew J., Devin P. Locke, Sean McGrath, et al.. (2005). Segmental Duplications and Copy-Number Variation in the Human Genome. The American Journal of Human Genetics. 77(1). 78–88. 678 indexed citations breakdown →

5.

Tüzün, Eray, Andrew J. Sharp, Jeffrey A. Bailey, et al.. (2005). Fine-scale structural variation of the human genome. Nature Genetics. 37(7). 727–732. 742 indexed citations breakdown →

6.

Locke, Devin P., Zhaoshi Jiang, L.M. Pertz, et al.. (2004). Molecular evolution of the human chromosome 15 pericentromeric region. Cytogenetic and Genome Research. 108(1-3). 73–82. 18 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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