Karol Rubin
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
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- Hippo pathway signaling and YAP/TAZ
Papers in
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- Congenital heart defects research 1
- Retinal Development and Disorders 1
- Genetics 1
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Susan A. Berry (2 shared papers)Betsy Hirsch (1 shared paper)Michelle Dolan (1 shared paper)Leslie E. W. LaConte (1 shared paper)Stephanie DeLuca (1 shared paper)Konark Mukherjee (1 shared paper)Vrushali Chavan (1 shared paper)C. Gail Summers (1 shared paper)
- Journals
- American Journal of Medical Genetics Part A (2 papers)Journal of Genetic Counseling (1 paper)
- Partner nations
- United States
In The Last Decade
Karol Rubin
3 papers receiving 25 citations
Peers
Comparison fields: 5 of 13
- Genetics 24
- Cell Biology 11
- Pediatrics, Perinatology and Child Health 11
- Immunology and Allergy 2
- Molecular Biology 21
Countries citing papers authored by Karol Rubin
This map shows the geographic impact of Karol Rubin'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 Karol Rubin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karol Rubin more than expected).
Fields of papers citing papers by Karol Rubin
This network shows the impact of papers produced by Karol Rubin. 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 Karol Rubin. The network helps show where Karol Rubin may publish in the future.
Co-authors
The 10 scholars most cited alongside Karol Rubin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 18 | |
| 2 | 2011 | 16 | |
| 3 | 2018 | 2 |
About Karol Rubin
Karol Rubin is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Clinical Psychology and Sociology and Political Science, having authored 3 papers that have together received 36 indexed citations. Recurring topics across this work include Congenital heart defects research (1 paper), Prenatal Screening and Diagnostics (1 paper), Hippo pathway signaling and YAP/TAZ (1 paper), Family and Disability Support Research (1 paper), Cellular transport and secretion (1 paper), Family Support in Illness (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Retinal Development and Disorders (1 paper). The work is most often cited by research in Genetics (24 citations), Cell Biology (11 citations), Pediatrics, Perinatology and Child Health (11 citations), Immunology and Allergy (2 citations) and Molecular Biology (21 citations). Karol Rubin has collaborated with scholars based in United States. Frequent co-authors include Susan A. Berry, Betsy Hirsch, Michelle Dolan, Leslie E. W. LaConte, Stephanie DeLuca, Konark Mukherjee, Vrushali Chavan, C. Gail Summers, Bonnie S. LeRoy and Patricia McCarthy Veach. Their work appears in journals such as American Journal of Medical Genetics Part A and Journal of Genetic Counseling.
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.