Zoha Kibar
Impact in
- Cell Biology top 2%
- Hippo pathway signaling and YAP/TAZ
- Molecular Biology top 5%
- Wnt/β-catenin signaling in development and cancer
- Connexins and lens biology
- Developmental Biology and Gene Regulation
- Cancer-related gene regulation
Papers in
-
- Wnt/β-catenin signaling in development and cancer 16
- Kruppel-like factors research 7
- Connexins and lens biology 6
- Cancer-related gene regulation 4
- Genetics 17
- Connective tissue disorders research 6
- Co-authors
- Valeria Capra (23 shared papers)Patrizia De Marco (22 shared papers)Elisa Merello (21 shared papers)Philippe Gros (10 shared papers)Monica J. Justice (6 shared papers)D. Alan Underhill (3 shared papers)Alexander G. Bassuk (4 shared papers)Kyle Vogan (2 shared papers)
- Journals
- Birth Defects Research Part A Clinical and Molecular Teratology (6 papers)Human Mutation (5 papers)Genomics (5 papers)Human Molecular Genetics (4 papers)PLoS ONE (3 papers)
- Partner nations
- CanadaItalyUnited States
In The Last Decade
Zoha Kibar
54 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 93
- Cell Biology 491
- Molecular Biology 1.9k
- Genetics 636
- Sensory Systems 95
- Pediatrics, Perinatology and Child Health 317
Countries citing papers authored by Zoha Kibar
This map shows the geographic impact of Zoha Kibar'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 Zoha Kibar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zoha Kibar more than expected).
Fields of papers citing papers by Zoha Kibar
This network shows the impact of papers produced by Zoha Kibar. 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 Zoha Kibar. The network helps show where Zoha Kibar may publish in the future.
Co-authors
The 25 scholars most cited alongside Zoha Kibar, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 408 | |
| 2 | 2007 | 231 | |
| 3 | 1999 | 223 | |
| 4 | 2000 | 184 | |
| 5 | 2010 | 100 | |
| 6 | 2009 | 88 | |
| 7 | 2007 | 87 | |
| 8 | 2009 | 84 | |
| 9 | 2011 | 79 | |
| 10 | 2012 | 78 | |
| 11 | 2012 | 77 | |
| 12 | 2011 | 66 | |
| 13 | 2011 | 65 | |
| 14 | 2019 | 57 | |
| 15 | 2015 | 55 | |
| 16 | 1996 | 47 | |
| 17 | 2012 | 43 | |
| 18 | 2001 | 43 | |
| 19 | 2010 | 41 | |
| 20 | 2011 | 40 |
About Zoha Kibar
Zoha Kibar is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cell Biology and Surgery, having authored 54 papers that have together received 2.7k indexed citations. Recurring topics across this work include Wnt/β-catenin signaling in development and cancer (16 papers), Kruppel-like factors research (7 papers), Prenatal Screening and Diagnostics (7 papers), Spinal Dysraphism and Malformations (6 papers), Connective tissue disorders research (6 papers), Connexins and lens biology (6 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Cancer-related gene regulation (4 papers). The work is most often cited by research in Cell Biology (491 citations), Molecular Biology (1.9k citations), Genetics (636 citations), Sensory Systems (95 citations) and Pediatrics, Perinatology and Child Health (317 citations). Zoha Kibar has collaborated with scholars based in Canada, Italy and United States. Frequent co-authors include Valeria Capra, Patrizia De Marco, Elisa Merello, Philippe Gros, Monica J. Justice, D. Alan Underhill, Alexander G. Bassuk, Kyle Vogan, Normand Groulx and Guy A. Rouleau. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, Human Mutation, Genomics, Human Molecular Genetics and PLoS ONE.
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.