Charité Ricker

2.0k citations
61 papers · 1.2k · h-index 18

Impact in

  • Genetics top 2%
    • BRCA gene mutations in cancer
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Cancer Genomics and Diagnostics

Papers in

Charité Ricker

57 papers receiving 1.1k citations

Peers

Charité Ricker
Comparison fields: 5 of 68
  • Genetics 770
  • Cancer Research 169
  • Pathology and Forensic Medicine 166
  • Oncology 182
  • Public Health, Environmental and Occupational Health 153
Replace Kristen M. Shannon with:
Kristen M. Shannon United States
Daniela Turchetti Italy
Joanne L. Johnson United States
Amanda Gammon United States
Bert van Geel Netherlands
Carina C. M. Bartels Netherlands
Eileen Dimond United States
Susan Randall Armel Canada
Leon C. Verhoog Netherlands
Lisa R. Susswein United States
Charité Ricker relative to Kristen M. Shannon United States Kristen M. Shannon's profile →
Citations per field
00.5×1.7×
Kristen M. Shannon · 1×
Citations per year

Countries citing papers authored by Charité Ricker

Since Specialization
Citations

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

Fields of papers citing papers by Charité Ricker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 61 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2005140
2 2020130
3 2018122
4 2012115
5 200772
6 201662
7 200656
8 200841
9 201639
10 201936
11 201733
12 200532
13 200632
14 202124
15 202023
16 201820
17 201718
18 201117
19 202016
20 202214

About Charité Ricker

Charité Ricker is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Oncology and Molecular Biology, having authored 61 papers that have together received 1.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (39 papers), Genetic factors in colorectal cancer (18 papers), Cancer Genomics and Diagnostics (13 papers), Genomics and Rare Diseases (9 papers), Family Support in Illness (4 papers), DNA Repair Mechanisms (3 papers), Colorectal Cancer Screening and Detection (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (770 citations), Cancer Research (169 citations), Pathology and Forensic Medicine (166 citations), Oncology (182 citations) and Public Health, Environmental and Occupational Health (153 citations). Charité Ricker has collaborated with scholars based in United States, Puerto Rico and Switzerland. Frequent co-authors include Jeffrey N. Weitzel, Kathleen R. Blazer, Veronica I. Lagos, Josef Herzog, Susan L. Neuhausen, Nancy Feldman, Katrina Lowstuter, Rebecca A. Nelson, Colleen McGuire and Deborah J. MacDonald. Their work appears in journals such as Journal of Clinical Oncology, Cancer Epidemiology Biomarkers & Prevention, Breast Cancer Research and Treatment, Gynecologic Oncology and Translational Behavioral Medicine.

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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