A FEINBERG
Impact in
- Molecular Biology top 0.01%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics
- Renal and related cancers
- Genetics top 0.01%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 110
- Genetic Syndromes and Imprinting 88
- Genetics and Neurodevelopmental Disorders 17
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- Epigenetics and DNA Methylation 146
- Genomics and Chromatin Dynamics 35
- RNA modifications and cancer 23
- Renal and related cancers 23
- Cancer-related gene regulation 22
- Co-authors
- B. Vogelstein (11 shared papers)Rafael A. Irizarry (20 shared papers)Benjamin Tycko (1 shared paper)Christine Ladd‐Acosta (17 shared papers)Martin J. Aryee (14 shared papers)Rolf I. OHLSSON (9 shared papers)Hengmi Cui (17 shared papers)Kasper D. Hansen (14 shared papers)
- Journals
- Nature Genetics (15 papers)Proceedings of the National Academy of Sciences (14 papers)Science (11 papers)The American Journal of Human Genetics (9 papers)Nature (8 papers)
- Partner nations
- United StatesSwedenJapan
In The Last Decade
A FEINBERG
231 papers receiving 62.2k citations
A FEINBERG's Hit Papers
Peers
Comparison fields: 5 of 202
- Molecular Biology 43.7k
- Genetics 15.0k
- Cancer Research 6.3k
- Pediatrics, Perinatology and Child Health 5.1k
- Oncology 5.6k
Countries citing papers authored by A FEINBERG
This map shows the geographic impact of A FEINBERG'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 A FEINBERG with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A FEINBERG more than expected).
Fields of papers citing papers by A FEINBERG
This network shows the impact of papers produced by A FEINBERG. 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 A FEINBERG. The network helps show where A FEINBERG may publish in the future.
Co-authors
The 25 scholars most cited alongside A FEINBERG, 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 239 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity Hit paper breakdown → | 1983 | 24030 |
| 2 | Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays Hit paper breakdown → | 2014 | 2715 |
| 3 | Hypomethylation distinguishes genes of some human cancers from their normal counterparts Hit paper breakdown → | 1983 | 1930 |
| 4 | The history of cancer epigenetics Hit paper breakdown → | 2004 | 1776 |
| 5 | The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores Hit paper breakdown → | 2009 | 1691 |
| 6 | The epigenetic progenitor origin of human cancer Hit paper breakdown → | 2005 | 1438 |
| 7 | Phenotypic plasticity and the epigenetics of human disease Hit paper breakdown → | 2007 | 1283 |
| 8 | DNMT1 and DNMT3b cooperate to silence genes in human cancer cells Hit paper breakdown → | 2002 | 1009 |
| 9 | Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts Hit paper breakdown → | 2009 | 923 |
| 10 | Increased methylation variation in epigenetic domains across cancer types Hit paper breakdown → | 2011 | 799 |
| 11 | Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19 Hit paper breakdown → | 2003 | 746 |
| 12 | Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis Hit paper breakdown → | 2013 | 725 |
| 13 | Hypomethylation of DNA from Benign and Malignant Human Colon Neoplasms Hit paper breakdown → | 1985 | 700 |
| 14 | Relaxation of imprinted genes in human cancer Hit paper breakdown → | 1993 | 691 |
| 15 | Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA Hit paper breakdown → | 2008 | 681 |
| 16 | Epigenetic modulators, modifiers and mediators in cancer aetiology and progression Hit paper breakdown → | 2016 | 655 |
| 17 | 2003 | 591 | |
| 18 | Comprehensive methylome map of lineage commitment from haematopoietic progenitors Hit paper breakdown → | 2010 | 496 |
| 19 | Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies Hit paper breakdown → | 2012 | 491 |
| 20 | 2011 | 489 |
About A FEINBERG
A FEINBERG is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cancer Research and Pathology and Forensic Medicine, having authored 239 papers that have together received 64.6k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (146 papers), Genetic Syndromes and Imprinting (88 papers), Prenatal Screening and Diagnostics (39 papers), Genomics and Chromatin Dynamics (35 papers), RNA modifications and cancer (23 papers), Renal and related cancers (23 papers), Cancer-related gene regulation (22 papers) and Genetics and Neurodevelopmental Disorders (17 papers). The work is most often cited by research in Molecular Biology (43.7k citations), Genetics (15.0k citations), Cancer Research (6.3k citations), Pediatrics, Perinatology and Child Health (5.1k citations) and Oncology (5.6k citations). A FEINBERG has collaborated with scholars based in United States, Sweden and Japan. Frequent co-authors include B. Vogelstein, Rafael A. Irizarry, Benjamin Tycko, Christine Ladd‐Acosta, Martin J. Aryee, Rolf I. OHLSSON, Hengmi Cui, Kasper D. Hansen, Andrew E. Jaffe and Steven Henikoff. Their work appears in journals such as Nature Genetics, Proceedings of the National Academy of Sciences, Science, The American Journal of Human Genetics and Nature.
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.