L.M. Pertz

2.1k citations
6 papers · 1.5k · 2 hit papers · h-index 5

Impact in

  • Genetics top 1%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Chromosomal and Genetic Variations

Papers in

    • Genomics and Phylogenetic Studies 2
    • Genomics and Chromatin Dynamics 1
    • Genomic variations and chromosomal abnormalities 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Genomics and Rare Diseases 1

L.M. Pertz

6 papers receiving 1.5k citations

L.M. Pertz's Hit Papers

Fine-scale structural variation of the human genome 2005 · 744 citations
7440+7+14Years since publication200400600

Peers

L.M. Pertz
Comparison fields: 5 of 70
  • Genetics 1.1k
  • Plant Science 530
  • Molecular Biology 744
  • Cancer Research 128
  • Pediatrics, Perinatology and Child Health 130
Replace Kristin Mrasek with:
Kristin Mrasek Germany
Ercole Rao Germany
Charlotte N. Henrichsen Switzerland
Jonathan Davies Canada
Davut Pehli̇van United States
Sandra R. Richardson Australia
M. Winkelmann Germany
Kyle R. Upton Australia
Giancarlo Bonora United States
Marten Jäger Germany
L.M. Pertz relative to Kristin Mrasek Germany Kristin Mrasek's profile →
Citations per field
00.5×1.5×
Kristin Mrasek · 1×
Citations per year

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-authors

The 25 scholars most cited alongside L.M. Pertz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with L.M. Pertz Line = papers co-authored together L.M. Pertz links everyone, so they are left out of the graph.

All Works

6 of 6 papers shown
#Work
1
Fine-scale structural variation of the human genome
Hit paper breakdown →
2005744
2
Segmental Duplications and Copy-Number Variation in the Human Genome
Hit paper breakdown →
2005682
3 200648
4 200623
5 200418
6
Mutation Screen in the COCH Gene in 190 Patients with Glaucoma
20062

About L.M. Pertz

L.M. Pertz is a scholar working on Molecular Biology, Genetics, Plant Science, Ophthalmology and Infectious Diseases, having authored 6 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Phylogenetic Studies (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Chromosomal and Genetic Variations (2 papers), Glaucoma and retinal disorders (1 paper), Intraocular Surgery and Lenses (1 paper), Genomics and Rare Diseases (1 paper) and Genomics and Chromatin Dynamics (1 paper). The work is most often cited by research in Genetics (1.1k citations), Plant Science (530 citations), Molecular Biology (744 citations), Cancer Research (128 citations) and Pediatrics, Perinatology and Child Health (130 citations). L.M. Pertz has collaborated with scholars based in United States and Italy. Frequent co-authors include Evan E. Eichler, Donna G. Albertson, Daniel Pinkel, Jeffrey A. Bailey, Andrew J. Sharp, Hillary S. Hayden, Victoria Morrison, Rajinder Kaul, Eray Tüzün and Maynard V. Olson. Their work appears in journals such as Cytogenetic and Genome Research, Investigative Ophthalmology & Visual Science, Nature Genetics, Human Molecular Genetics and Genetics.

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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