Deborah Ritter
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 30
- Genomics and Rare Diseases 23
- Genomic variations and chromosomal abnormalities 3
- Race, Genetics, and Society 2
- BRCA gene mutations in cancer 2
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- Genomics and Chromatin Dynamics 4
- Genetics, Bioinformatics, and Biomedical Research 2
- Co-authors
- Erin Rooney Riggs (5 shared papers)Erica Andersen (3 shared papers)Hutton M. Kearney (3 shared papers)Swaroop Aradhya (3 shared papers)Erik C. Thorland (3 shared papers)Sibel Kantarci (3 shared papers)Athena M. Cherry (2 shared papers)Gordana Raca (4 shared papers)
- Journals
- Genetics in Medicine (11 papers)Human Mutation (4 papers)The American Journal of Human Genetics (4 papers)Genome Medicine (3 papers)Nature Genetics (2 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Deborah Ritter
42 papers receiving 3.4k citations
Deborah Ritter's Hit Papers
Peers
Comparison fields: 5 of 63
- Genetics 1.1k
- Pediatrics, Perinatology and Child Health 245
- Cancer Research 199
- Oncology 171
- Public Health, Environmental and Occupational Health 188
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 | 1164 |
| 2 | Pathogenic Germline Variants in 10,389 Adult Cancers Hit paper breakdown → | 2018 | 617 |
| 3 | 2013 | 261 | |
| 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 | 173 |
| 5 | 2016 | 136 | |
| 6 | 2018 | 120 | |
| 7 | 2020 | 120 | |
| 8 | 2015 | 115 | |
| 9 | 2016 | 77 | |
| 10 | 2020 | 61 | |
| 11 | 2018 | 56 | |
| 12 | 2009 | 55 | |
| 13 | 2016 | 54 | |
| 14 | 2022 | 54 | |
| 15 | 2018 | 45 | |
| 16 | 2010 | 40 | |
| 17 | 2012 | 38 | |
| 18 | 2024 | 30 | |
| 19 | 2023 | 24 | |
| 20 | 2022 | 23 |
About Deborah Ritter
Deborah Ritter is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pharmacology and Oncology, having authored 46 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Genomics and Chromatin Dynamics (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Race, Genetics, and Society (2 papers), BRCA gene mutations in cancer (2 papers), Genetics, Bioinformatics, and Biomedical Research (2 papers), Genetic factors in colorectal cancer (2 papers) and Acute Lymphoblastic Leukemia research (1 paper). The work is most often cited by research in Genetics (1.1k citations), Pediatrics, Perinatology and Child Health (245 citations), Cancer Research (199 citations), Oncology (171 citations) and Public Health, Environmental and Occupational Health (188 citations). Deborah Ritter has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Erin Rooney Riggs, Erica Andersen, Hutton M. Kearney, Swaroop Aradhya, Erik C. Thorland, Sibel Kantarci, Athena M. Cherry, Gordana Raca, Daniel Pineda‐Alvarez and Sarah T. South. Their work appears in journals such as Genetics in Medicine, Human Mutation, The American Journal of Human Genetics, 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.