Steve Rozen
Impact in
- Genetics top 0.05%
- Genetic diversity and population structure
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities
- Cancer Research top 0.1%
- Cancer Genomics and Diagnostics
Papers in
-
- Cancer Genomics and Diagnostics 44
- Genetics 46
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 21
- Genomic variations and chromosomal abnormalities 12
- Co-authors
- Helen Skaletsky (17 shared papers)Ioana Cutcutache (9 shared papers)Triinu Kõressaar (1 shared paper)Andreas Untergasser (1 shared paper)Maido Remm (1 shared paper)Jian Ye (1 shared paper)Brant C. Faircloth (1 shared paper)Thomas Madden (1 shared paper)
- Journals
- Nature Genetics (17 papers)Nature (15 papers)Nature Communications (15 papers)Scientific Reports (7 papers)Gut (5 papers)
- Partner nations
- SingaporeUnited StatesUnited Kingdom
In The Last Decade
Steve Rozen
194 papers receiving 57k citations
Steve Rozen's Hit Papers
Peers
Comparison fields: 5 of 197
- Genetics 14.7k
- Cancer Research 6.2k
- Reproductive Medicine 3.8k
- Molecular Biology 14.6k
- Plant Science 6.1k
Countries citing papers authored by Steve Rozen
This map shows the geographic impact of Steve Rozen'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 Steve Rozen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steve Rozen more than expected).
Fields of papers citing papers by Steve Rozen
This network shows the impact of papers produced by Steve Rozen. 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 Steve Rozen. The network helps show where Steve Rozen may publish in the future.
Co-authors
The 25 scholars most cited alongside Steve Rozen, 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 197 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Primer3 on the WWW for General Users and for Biologist Programmers Hit paper breakdown → | 2003 | 13182 |
| 2 | Primer3—new capabilities and interfaces Hit paper breakdown → | 2012 | 7449 |
| 3 | Primer-BLAST: A tool to design target-specific primers for polymerase chain reaction Hit paper breakdown → | 2012 | 4798 |
| 4 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2401 |
| 5 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2169 |
| 6 | Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human Genome Hit paper breakdown → | 1998 | 1644 |
| 7 | The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes Hit paper breakdown → | 2003 | 1637 |
| 8 | Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene Hit paper breakdown → | 1995 | 1027 |
| 9 | A Gene Map of the Human Genome Hit paper breakdown → | 1996 | 811 |
| 10 | Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma Hit paper breakdown → | 2017 | 744 |
| 11 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 730 |
| 12 | 1995 | 634 | |
| 13 | The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men Hit paper breakdown → | 2001 | 575 |
| 14 | A comprehensive survey of genomic alterations in gastric cancer reveals systematic patterns of molecular exclusivity and co-occurrence among distinct therapeutic targets Hit paper breakdown → | 2012 | 574 |
| 15 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 564 |
| 16 | 1998 | 549 | |
| 17 | Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes Hit paper breakdown → | 2012 | 542 |
| 18 | Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators Hit paper breakdown → | 2014 | 500 |
| 19 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 489 |
| 20 | 2003 | 440 |
About Steve Rozen
Steve Rozen is a scholar working on Cancer Research, Genetics, Reproductive Medicine, Molecular Biology and Information Systems and Management, having authored 197 papers that have together received 58.3k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (44 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Sperm and Testicular Function (12 papers), Genomic variations and chromosomal abnormalities (12 papers), Advanced Database Systems and Queries (10 papers), Scientific Computing and Data Management (9 papers), Genomics and Phylogenetic Studies (8 papers) and Gastric Cancer Management and Outcomes (8 papers). The work is most often cited by research in Genetics (14.7k citations), Cancer Research (6.2k citations), Reproductive Medicine (3.8k citations), Molecular Biology (14.6k citations) and Plant Science (6.1k citations). Steve Rozen has collaborated with scholars based in Singapore, United States and United Kingdom. Frequent co-authors include Helen Skaletsky, Ioana Cutcutache, Triinu Kõressaar, Andreas Untergasser, Maido Remm, Jian Ye, Brant C. Faircloth, Thomas Madden, Jian Ye and David C. Page. Their work appears in journals such as Nature Genetics, Nature, Nature Communications, Scientific Reports and Gut.
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.