Marilyn M. Li
Impact in
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
- Genetics top 1%
- Glioma Diagnosis and Treatment
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Cancer Genomics and Diagnostics 24
- Genetics 19
- Genomic variations and chromosomal abnormalities 15
- Genomics and Rare Diseases 15
- Glioma Diagnosis and Treatment 12
- Co-authors
- Daynna J. Wolff (4 shared papers)Cindy L. Vnencak‐Jones (2 shared papers)Somak Roy (2 shared papers)Eric Duncavage (1 shared paper)Michael Datto (1 shared paper)Anas Younes (1 shared paper)Apostolia Maria Tsimberidou (1 shared paper)Marina N. Nikiforova (1 shared paper)
- Journals
- Journal of Molecular Diagnostics (8 papers)Genetics in Medicine (5 papers)Haematologica (5 papers)Neuro-Oncology (3 papers)Pediatric Blood & Cancer (3 papers)
- Partner nations
- United StatesCanadaItaly
In The Last Decade
Marilyn M. Li
124 papers receiving 4.7k citations
Marilyn M. Li's Hit Papers
Peers
Comparison fields: 5 of 140
- Cancer Research 1.1k
- Genetics 798
- Hematology 379
- Oncology 728
- Pathology and Forensic Medicine 462
Countries citing papers authored by Marilyn M. Li
This map shows the geographic impact of Marilyn M. Li'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 Marilyn M. Li with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marilyn M. Li more than expected).
Fields of papers citing papers by Marilyn M. Li
This network shows the impact of papers produced by Marilyn M. Li. 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 Marilyn M. Li. The network helps show where Marilyn M. Li may publish in the future.
Co-authors
The 25 scholars most cited alongside Marilyn M. Li, 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 129 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer Hit paper breakdown → | 2016 | 1511 |
| 2 | Integrated Molecular and Clinical Analysis of 1,000 Pediatric Low-Grade Gliomas Hit paper breakdown → | 2020 | 337 |
| 3 | 2020 | 233 | |
| 4 | 2020 | 150 | |
| 5 | 2019 | 124 | |
| 6 | 1997 | 121 | |
| 7 | 2019 | 97 | |
| 8 | 2013 | 89 | |
| 9 | 2017 | 78 | |
| 10 | 2020 | 76 | |
| 11 | 2004 | 70 | |
| 12 | 2021 | 66 | |
| 13 | 2022 | 66 | |
| 14 | 2010 | 63 | |
| 15 | 2018 | 55 | |
| 16 | 2004 | 54 | |
| 17 | 2007 | 51 | |
| 18 | 2013 | 50 | |
| 19 | 2019 | 45 | |
| 20 | 2022 | 43 |
About Marilyn M. Li
Marilyn M. Li is a scholar working on Cancer Research, Genetics, Genetics, Pathology and Forensic Medicine and Neurology, having authored 129 papers that have together received 4.8k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (15 papers), Genomics and Rare Diseases (15 papers), Glioma Diagnosis and Treatment (12 papers), Neuroblastoma Research and Treatments (11 papers), Prenatal Screening and Diagnostics (8 papers), Acute Myeloid Leukemia Research (8 papers) and Acute Lymphoblastic Leukemia research (7 papers). The work is most often cited by research in Cancer Research (1.1k citations), Genetics (798 citations), Hematology (379 citations), Oncology (728 citations) and Pathology and Forensic Medicine (462 citations). Marilyn M. Li has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include Daynna J. Wolff, Cindy L. Vnencak‐Jones, Somak Roy, Eric Duncavage, Michael Datto, Anas Younes, Apostolia Maria Tsimberidou, Marina N. Nikiforova, Shashikant Kulkarni and Neal Ian Lindeman. Their work appears in journals such as Journal of Molecular Diagnostics, Genetics in Medicine, Haematologica, Neuro-Oncology and Pediatric Blood & Cancer.
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.