Ruth Shemer
Impact in
- Genetics top 1%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 30
- Cancer-related gene regulation 6
- RNA modifications and cancer 5
- Genetics 29
- Genetic Syndromes and Imprinting 18
- Genetics and Neurodevelopmental Disorders 6
- Co-authors
- Aharon Razin (25 shared papers)Howard Cedar (3 shared papers)Tal Kafri (2 shared papers)Yehudit Birger (3 shared papers)M. Silber Ariel (1 shared paper)John R. McCarrey (1 shared paper)Michael Brandeis (1 shared paper)Yuval Dor (26 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (7 papers)Human Molecular Genetics (4 papers)Nature Communications (3 papers)Gene (2 papers)Diabetes (2 papers)
- Partner nations
- IsraelUnited StatesCanada
In The Last Decade
Ruth Shemer
57 papers receiving 2.9k citations
Ruth Shemer's Hit Papers
Peers
Comparison fields: 5 of 103
- Genetics 1.4k
- Pediatrics, Perinatology and Child Health 580
- Molecular Biology 2.1k
- Cancer Research 350
- Developmental Neuroscience 35
Countries citing papers authored by Ruth Shemer
This map shows the geographic impact of Ruth Shemer'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 Ruth Shemer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruth Shemer more than expected).
Fields of papers citing papers by Ruth Shemer
This network shows the impact of papers produced by Ruth Shemer. 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 Ruth Shemer. The network helps show where Ruth Shemer may publish in the future.
Co-authors
The 25 scholars most cited alongside Ruth Shemer, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line. Hit paper breakdown → | 1992 | 591 |
| 2 | 1995 | 221 | |
| 3 | 1997 | 171 | |
| 4 | 1984 | 136 | |
| 5 | 2018 | 136 | |
| 6 | 2014 | 126 | |
| 7 | 2007 | 121 | |
| 8 | 1999 | 106 | |
| 9 | 2005 | 100 | |
| 10 | 2018 | 97 | |
| 11 | 2000 | 90 | |
| 12 | 2010 | 80 | |
| 13 | 2020 | 79 | |
| 14 | 2022 | 75 | |
| 15 | 1996 | 72 | |
| 16 | 1991 | 57 | |
| 17 | 1990 | 46 | |
| 18 | 1991 | 41 | |
| 19 | 2004 | 39 | |
| 20 | 2017 | 36 |
About Ruth Shemer
Ruth Shemer is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cancer Research and Surgery, having authored 60 papers that have together received 2.9k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (30 papers), Genetic Syndromes and Imprinting (18 papers), Cancer Genomics and Diagnostics (10 papers), Prenatal Screening and Diagnostics (9 papers), Genetics and Neurodevelopmental Disorders (6 papers), Cancer-related gene regulation (6 papers), Pancreatic function and diabetes (6 papers) and RNA modifications and cancer (5 papers). The work is most often cited by research in Genetics (1.4k citations), Pediatrics, Perinatology and Child Health (580 citations), Molecular Biology (2.1k citations), Cancer Research (350 citations) and Developmental Neuroscience (35 citations). Ruth Shemer has collaborated with scholars based in Israel, United States and Canada. Frequent co-authors include Aharon Razin, Howard Cedar, Tal Kafri, Yehudit Birger, M. Silber Ariel, John R. McCarrey, Michael Brandeis, Yuval Dor, Yotam Kaufman and Kirill Makedonski. Their work appears in journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics, Nature Communications, Gene and Diabetes.
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.