Ruth Shemer

7.0k citations
60 papers · 2.9k · 1 hit paper · h-index 26

Impact in

Papers in

    • Epigenetics and DNA Methylation 30
    • Cancer-related gene regulation 6
    • RNA modifications and cancer 5
    • Genetic Syndromes and Imprinting 18
    • Genetics and Neurodevelopmental Disorders 6

Ruth Shemer

57 papers receiving 2.9k citations

Ruth Shemer's Hit Papers

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line. 1992 · 591 citations
5910+11+22Years since publication100200300400500

Peers

Ruth Shemer
Comparison fields: 5 of 103
  • Genetics 1.4k
  • Pediatrics, Perinatology and Child Health 580
  • Molecular Biology 2.1k
  • Cancer Research 350
  • Developmental Neuroscience 35
Replace Joan Overhauser with:
Joan Overhauser United States
Howard R. Slater Australia
Ana Cristina Victorino Krepischi Brazil
Melissa A. Parisi United States
Sarah Howlett United Kingdom
Tibor A. Rauch United States
Diana Zélénika France
Antonio Novelli Italy
Takashi Tada Japan
Cédric Le Caignec France
Ruth Shemer relative to Joan Overhauser United States Joan Overhauser's profile →
Citations per field
00.5×10×17×
Joan Overhauser · 1×
Citations per year

Countries citing papers authored by Ruth Shemer

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Ruth Shemer Line = papers co-authored together Ruth Shemer links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

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 →
1992591
2 1995221
3 1997171
4 1984136
5 2018136
6 2014126
7 2007121
8 1999106
9 2005100
10 201897
11 200090
12 201080
13 202079
14 202275
15 199672
16 199157
17 199046
18 199141
19 200439
20 201736

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.

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