Fatima Abidi
Impact in
- Physiology top 1%
- Adenosine and Purinergic Signaling
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
-
- Ubiquitin and proteasome pathways 5
- Chromatin Remodeling and Cancer 5
- Fungal and yeast genetics research 3
- RNA and protein synthesis mechanisms 3
- Genetics 19
- Genetics and Neurodevelopmental Disorders 19
- Genomic variations and chromosomal abnormalities 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- Charles E. Schwartz (18 shared papers)Roger E. Stevenson (10 shared papers)Mark Griffiths (1 shared paper)David James Young (1 shared paper)Albert S. Baldwin (1 shared paper)Herbert A. Lubs (5 shared papers)David Schlessinger (3 shared papers)Elizabeth J. Keath (2 shared papers)
- Journals
- Genomics (5 papers)Clinical Genetics (3 papers)Journal of Medical Genetics (2 papers)European Journal of Human Genetics (2 papers)Human Mutation (2 papers)
- Partner nations
- United StatesFranceCanada
In The Last Decade
Fatima Abidi
40 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 84
- Physiology 280
- Genetics 659
- Transplantation 42
- Molecular Biology 1.0k
- Sensory Systems 45
Countries citing papers authored by Fatima Abidi
This map shows the geographic impact of Fatima Abidi'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 Fatima Abidi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fatima Abidi more than expected).
Fields of papers citing papers by Fatima Abidi
This network shows the impact of papers produced by Fatima Abidi. 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 Fatima Abidi. The network helps show where Fatima Abidi may publish in the future.
Co-authors
The 25 scholars most cited alongside Fatima Abidi, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 244 | |
| 2 | 2005 | 155 | |
| 3 | 2001 | 117 | |
| 4 | 2014 | 105 | |
| 5 | Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes. | 1990 | 83 |
| 6 | 2008 | 80 | |
| 7 | 2001 | 75 | |
| 8 | 2005 | 73 | |
| 9 | 2013 | 71 | |
| 10 | 1999 | 65 | |
| 11 | 1990 | 62 | |
| 12 | 1991 | 59 | |
| 13 | 1999 | 57 | |
| 14 | 2005 | 47 | |
| 15 | 2004 | 46 | |
| 16 | 1994 | 41 | |
| 17 | 2007 | 38 | |
| 18 | 2004 | 36 | |
| 19 | 1990 | 33 | |
| 20 | 2007 | 25 |
About Fatima Abidi
Fatima Abidi is a scholar working on Molecular Biology, Genetics, Plant Science, Cell Biology and Epidemiology, having authored 40 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (19 papers), Ubiquitin and proteasome pathways (5 papers), Chromosomal and Genetic Variations (5 papers), Chromatin Remodeling and Cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Fungal and yeast genetics research (3 papers), RNA and protein synthesis mechanisms (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). The work is most often cited by research in Physiology (280 citations), Genetics (659 citations), Transplantation (42 citations), Molecular Biology (1.0k citations) and Sensory Systems (45 citations). Fatima Abidi has collaborated with scholars based in United States, France and Canada. Frequent co-authors include Charles E. Schwartz, Roger E. Stevenson, Mark Griffiths, David James Young, Albert S. Baldwin, Herbert A. Lubs, David Schlessinger, Elizabeth J. Keath, Randall D. Little and Morimasa Wada. Their work appears in journals such as Genomics, Clinical Genetics, Journal of Medical Genetics, European Journal of Human Genetics and Human Mutation.
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.