Elizabeth A. Ostermeyer

1.4k citations
10 papers · 1.2k · h-index 9

Impact in

  • Genetics top 5%
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Ovarian cancer diagnosis and treatment

Papers in

    • BRCA gene mutations in cancer 5
    • Genomic variations and chromosomal abnormalities 4
    • Cellular Mechanics and Interactions 3

Elizabeth A. Ostermeyer

10 papers receiving 1.2k citations

Peers

Elizabeth A. Ostermeyer
Comparison fields: 5 of 72
  • Genetics 696
  • Reproductive Medicine 101
  • Pathology and Forensic Medicine 199
  • Cancer Research 157
  • Molecular Biology 723
Replace Magdalena Ratajska with:
Magdalena Ratajska Poland
Sabine Pagès France
J M Parrington United Kingdom
Sandra Bonache Spain
Anneke Y. van der Veen Netherlands
Susan L. Slager United States
Britta Skawran Germany
Mireia Menéndez Spain
Antonis C. Antoniou United Kingdom
Therese Sandberg Sweden
Elizabeth A. Ostermeyer relative to Magdalena Ratajska Poland Magdalena Ratajska's profile →
Citations per field
00.5×1.5×1.8×
Magdalena Ratajska · 1×
Citations per year

Countries citing papers authored by Elizabeth A. Ostermeyer

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth A. Ostermeyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth A. Ostermeyer. 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 Elizabeth A. Ostermeyer. The network helps show where Elizabeth A. Ostermeyer may publish in the future.

Co-authors

The 25 scholars most cited alongside Elizabeth A. Ostermeyer, 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 Elizabeth A. Ostermeyer Line = papers co-authored together Elizabeth A. Ostermeyer links everyone, so they are left out of the graph.

All Works

10 of 10 papers shown
#Work
1 1994525
2 1997239
3
Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families.
1995158
4
Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden.
1996115
5
The search for BRCA1.
199449
6 199649
7 199542
8 199111
9 199010
10 19912

About Elizabeth A. Ostermeyer

Elizabeth A. Ostermeyer is a scholar working on Genetics, Cell Biology, Molecular Biology, Reproductive Medicine and Cancer Research, having authored 10 papers that have together received 1.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Glycosylation and Glycoproteins Research (3 papers), Cellular Mechanics and Interactions (3 papers), DNA Repair Mechanisms (2 papers), CRISPR and Genetic Engineering (1 paper), Cancer Genomics and Diagnostics (1 paper) and Ovarian cancer diagnosis and treatment (1 paper). The work is most often cited by research in Genetics (696 citations), Reproductive Medicine (101 citations), Pathology and Forensic Medicine (199 citations), Cancer Research (157 citations) and Molecular Biology (723 citations). Elizabeth A. Ostermeyer has collaborated with scholars based in United States, Sweden and Denmark. Frequent co-authors include Mary‐Claire King, Lori Sickels Friedman, Patrick J. Dowd, Sarah E. Rowell, Csilla I. Szabo, Eric D. Lynch, Ming K. Lee, Bjørn Tore Gjertsen, Hanlee P. Ji and Ketil Heimdal. Their work appears in journals such as Molecular and Cellular Biology, Genomics, Nature Genetics, The American Journal of Human Genetics and Developmental 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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