Deborah Ritter
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 23
- Genomics and Rare Diseases 19
- Genomic variations and chromosomal abnormalities 6
- BRCA gene mutations in cancer 6
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- Cancer Genomics and Diagnostics 12
- Co-authors
- Erin Rooney Riggs (5 shared papers)Daniel Pineda‐Alvarez (3 shared papers)Sarah T. South (3 shared papers)Erica Andersen (3 shared papers)Gordana Raca (4 shared papers)Erik C. Thorland (3 shared papers)Swaroop Aradhya (3 shared papers)Athena M. Cherry (2 shared papers)
- Journals
- Genetics in Medicine (10 papers)The American Journal of Human Genetics (4 papers)Human Mutation (4 papers)Genome Medicine (3 papers)Nature Genetics (2 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Deborah Ritter
43 papers receiving 3.3k citations
Deborah Ritter's Hit Papers
Peers
Comparison fields: 5 of 105
- Genetics 1.3k
- Cancer Research 636
- Pediatrics, Perinatology and Child Health 356
- Hematology 207
- Pathology and Forensic Medicine 302
Countries citing papers authored by Deborah Ritter
This map shows the geographic impact of Deborah Ritter'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 Deborah Ritter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deborah Ritter more than expected).
Fields of papers citing papers by Deborah Ritter
This network shows the impact of papers produced by Deborah Ritter. 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 Deborah Ritter. The network helps show where Deborah Ritter may publish in the future.
Co-authors
The 25 scholars most cited alongside Deborah Ritter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) Hit paper breakdown → | 2019 | 1139 |
| 2 | Pathogenic Germline Variants in 10,389 Adult Cancers Hit paper breakdown → | 2018 | 606 |
| 3 | 2013 | 255 | |
| 4 | Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC) Hit paper breakdown → | 2022 | 169 |
| 5 | 2016 | 135 | |
| 6 | 2018 | 117 | |
| 7 | 2015 | 116 | |
| 8 | 2020 | 115 | |
| 9 | 2016 | 77 | |
| 10 | 2020 | 59 | |
| 11 | 2018 | 56 | |
| 12 | 2016 | 55 | |
| 13 | 2009 | 54 | |
| 14 | 2022 | 50 | |
| 15 | 2018 | 44 | |
| 16 | 2010 | 40 | |
| 17 | 2012 | 36 | |
| 18 | 2024 | 27 | |
| 19 | 2023 | 23 | |
| 20 | 2022 | 22 |
About Deborah Ritter
Deborah Ritter is a scholar working on Genetics, Cancer Research, Pathology and Forensic Medicine, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 46 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (19 papers), Cancer Genomics and Diagnostics (12 papers), Genetic factors in colorectal cancer (7 papers), Genomic variations and chromosomal abnormalities (6 papers), BRCA gene mutations in cancer (6 papers), Genomics and Chromatin Dynamics (4 papers), DNA Repair Mechanisms (3 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Genetics (1.3k citations), Cancer Research (636 citations), Pediatrics, Perinatology and Child Health (356 citations), Hematology (207 citations) and Pathology and Forensic Medicine (302 citations). Deborah Ritter has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Erin Rooney Riggs, Daniel Pineda‐Alvarez, Sarah T. South, Erica Andersen, Gordana Raca, Erik C. Thorland, Swaroop Aradhya, Athena M. Cherry, Hutton M. Kearney and Sibel Kantarci. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Human Mutation, Genome Medicine and Nature 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.