Peter C. Verlander

1.6k citations
18 papers · 921 · h-index 14

Impact in

Papers in

    • DNA Repair Mechanisms 10
    • CRISPR and Genetic Engineering 4
    • Genomic variations and chromosomal abnormalities 3

Peter C. Verlander

17 papers receiving 899 citations

Peers

Peter C. Verlander
Comparison fields: 5 of 69
  • Cancer Research 206
  • Molecular Biology 695
  • Genetics 255
  • Hematology 100
  • Oncology 132
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Jonathan P. Park United States
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J D Vassalli Switzerland
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Jason E. Farrar United States
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Citations per field
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Citations per year

Countries citing papers authored by Peter C. Verlander

Since Specialization
Citations

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

Fields of papers citing papers by Peter C. Verlander

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter C. Verlander. 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 Peter C. Verlander. The network helps show where Peter C. Verlander may publish in the future.

Co-authors

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

All Works

18 of 18 papers shown
#Work
1 2001158
2
Mutation analysis of the Fanconi anemia gene FACC.
1994107
3 199797
4 199795
5 200181
6 200271
7 200665
8 199550
9 199844
10 199935
11 199530
12 199728
13
A locus for Fanconi anemia on 16q determined by homozygosity mapping.
199624
14 199718
15 19979
16
Stem cells in dentistry and medicine: the dentist's role.
20115
17 19973
18 20051

About Peter C. Verlander

Peter C. Verlander is a scholar working on Molecular Biology, Genetics, Cancer Research, Pulmonary and Respiratory Medicine and Oncology, having authored 18 papers that have together received 921 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (10 papers), CRISPR and Genetic Engineering (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Carcinogens and Genotoxicity Assessment (3 papers), Acute Lymphoblastic Leukemia research (2 papers), Chromosomal and Genetic Variations (2 papers), Cancer Genomics and Diagnostics (2 papers) and Cancer-related Molecular Pathways (2 papers). The work is most often cited by research in Cancer Research (206 citations), Molecular Biology (695 citations), Genetics (255 citations), Hematology (100 citations) and Oncology (132 citations). Peter C. Verlander has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Arleen D. Auerbach, Sat Dev Batish, Orna Levran, John Gregory, Philip F. Giampietro, Alfred P. Gillio, Christopher G. Mathew, John E. Wagner, Cindy Eide and Betsy Hirsch. Their work appears in journals such as Proceedings of the National Academy of Sciences, Genomics, Blood, Journal of Clinical Laboratory Analysis and Clinical Cancer Research.

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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