Mala Isrie
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Fibroblast Growth Factor Research
- Epigenetics and DNA Methylation
- Ubiquitin and proteasome pathways
Papers in
- Genetics 5
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Genomics and Chromatin Dynamics 1
- Co-authors
- Hilde Van Esch (6 shared papers)Koenraad Devriendt (4 shared papers)Gunnar Buyse (1 shared paper)Aleksandra Siekierska (1 shared paper)Lieven Lagae (1 shared paper)Joris Vermeesch (2 shared papers)Yue Liu (1 shared paper)Peter de Witte (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)PLoS Genetics (1 paper)Neurology (1 paper)American Journal of Medical Genetics Part A (1 paper)Netherlands Heart Journal (1 paper)
- Partner nations
- BelgiumUnited StatesGermany
In The Last Decade
Mala Isrie
6 papers receiving 138 citations
Peers
Comparison fields: 5 of 39
- Genetics 79
- Molecular Biology 88
- Cell Biology 19
- Pediatrics, Perinatology and Child Health 10
- Aging 1
Countries citing papers authored by Mala Isrie
This map shows the geographic impact of Mala Isrie'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 Mala Isrie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mala Isrie more than expected).
Fields of papers citing papers by Mala Isrie
This network shows the impact of papers produced by Mala Isrie. 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 Mala Isrie. The network helps show where Mala Isrie may publish in the future.
Co-authors
The 25 scholars most cited alongside Mala Isrie, 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 | 2016 | 56 | |
| 2 | 2012 | 34 | |
| 3 | 2014 | 21 | |
| 4 | 2014 | 17 | |
| 5 | 2015 | 12 | |
| 6 | 2013 | 11 | |
| 7 | 2018 | 0 |
About Mala Isrie
Mala Isrie is a scholar working on Genetics, Molecular Biology, Plant Science, Cellular and Molecular Neuroscience and Neurology, having authored 7 papers that have together received 151 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper), Genomics and Chromatin Dynamics (1 paper) and Genetic Neurodegenerative Diseases (1 paper). The work is most often cited by research in Genetics (79 citations), Molecular Biology (88 citations), Cell Biology (19 citations), Pediatrics, Perinatology and Child Health (10 citations) and Aging (1 citation). Mala Isrie has collaborated with scholars based in Belgium, United States and Germany. Frequent co-authors include Hilde Van Esch, Koenraad Devriendt, Gunnar Buyse, Aleksandra Siekierska, Lieven Lagae, Joris Vermeesch, Yue Liu, Peter de Witte, Mitchell Goldfarb and Thomy de Ravel. Their work appears in journals such as European Journal of Medical Genetics, PLoS Genetics, Neurology, American Journal of Medical Genetics Part A and Netherlands Heart Journal.
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.