Mariam AlMulla
Impact in
-
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Neurogenetic and Muscular Disorders Research
Papers in
- Genetics 3
- Genomics and Rare Diseases 3
- Neurogenetic and Muscular Disorders Research 2
- Genomic variations and chromosomal abnormalities 2
- Hemoglobinopathies and Related Disorders 1
- Co-authors
- Noora Shahbeck (6 shared papers)Rehab Ali (6 shared papers)Mariam Al‐Mureikhi (5 shared papers)Laila Mahmoud (4 shared papers)Nader Al‐Dewik (4 shared papers)Angus Clarke (1 shared paper)Fowzan S. Alkuraya (2 shared papers)Abdulbari Bener (1 shared paper)
- Journals
- Human Genetics (1 paper)Gene Therapy (1 paper)American Journal of Medical Genetics Part A (3 papers)Molecular Genetics & Genomic Medicine (1 paper)International Journal of Applied and Basic Medical Research (1 paper)
- Partner nations
- QatarSaudi ArabiaUnited Kingdom
In The Last Decade
Mariam AlMulla
7 papers receiving 278 citations
Peers
Comparison fields: 5 of 58
- Genetics 125
- Genetics 44
- Clinical Biochemistry 17
- Cell Biology 30
- Pediatrics, Perinatology and Child Health 31
Countries citing papers authored by Mariam AlMulla
This map shows the geographic impact of Mariam AlMulla'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 Mariam AlMulla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mariam AlMulla more than expected).
Fields of papers citing papers by Mariam AlMulla
This network shows the impact of papers produced by Mariam AlMulla. 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 Mariam AlMulla. The network helps show where Mariam AlMulla may publish in the future.
Co-authors
The 24 scholars most cited alongside Mariam AlMulla, 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 | 2015 | 140 | |
| 2 | 2019 | 40 | |
| 3 | 2019 | 32 | |
| 4 | 2021 | 32 | |
| 5 | 2018 | 20 | |
| 6 | 2020 | 8 | |
| 7 | 2021 | 8 |
About Mariam AlMulla
Mariam AlMulla is a scholar working on Genetics, Genetics, Molecular Biology, Surgery and Cellular and Molecular Neuroscience, having authored 7 papers that have together received 280 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Metabolism and Genetic Disorders (1 paper), Cancer Genomics and Diagnostics (1 paper), Neurological diseases and metabolism (1 paper), Hemoglobinopathies and Related Disorders (1 paper) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (125 citations), Genetics (44 citations), Clinical Biochemistry (17 citations), Cell Biology (30 citations) and Pediatrics, Perinatology and Child Health (31 citations). Mariam AlMulla has collaborated with scholars based in Qatar, Saudi Arabia and United Kingdom. Frequent co-authors include Noora Shahbeck, Rehab Ali, Mariam Al‐Mureikhi, Laila Mahmoud, Nader Al‐Dewik, Angus Clarke, Fowzan S. Alkuraya, Abdulbari Bener, Shenela Lakhani and Patrik Vitazka. Their work appears in journals such as Human Genetics, Gene Therapy, American Journal of Medical Genetics Part A, Molecular Genetics & Genomic Medicine and International Journal of Applied and Basic Medical Research.
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.