Farid Ullah
Impact in
-
- Metabolism and Genetic Disorders
Papers in
-
- Hereditary Neurological Disorders 1
- Genetic Neurodegenerative Diseases 1
- Genetics 2
- Connective tissue disorders research 1
- Co-authors
- Shahid Mahmood Baig (4 shared papers)Uzma Abdullah (3 shared papers)Zafar Ali (3 shared papers)Johan Wikström (1 shared paper)Joakim Klar (1 shared paper)Niklas Dahl (1 shared paper)Muhammad Tariq (1 shared paper)Andrew Sinclair (1 shared paper)
In The Last Decade
Farid Ullah
4 papers receiving 42 citations
Peers
Comparison fields: 5 of 22
- Clinical Biochemistry 8
- Aging 2
- Developmental Biology 2
- Cellular and Molecular Neuroscience 12
- Molecular Biology 35
Countries citing papers authored by Farid Ullah
This map shows the geographic impact of Farid Ullah'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 Farid Ullah with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Farid Ullah more than expected).
Fields of papers citing papers by Farid Ullah
This network shows the impact of papers produced by Farid Ullah. 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 Farid Ullah. The network helps show where Farid Ullah may publish in the future.
Co-authors
The 22 scholars most cited alongside Farid Ullah, 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 | 2017 | 19 | |
| 2 | 2021 | 18 | |
| 3 | 2021 | 4 | |
| 4 | 2019 | 1 |
About Farid Ullah
Farid Ullah is a scholar working on Cellular and Molecular Neuroscience, Genetics, Molecular Biology, Oncology and Clinical Biochemistry, having authored 4 papers that have together received 42 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (1 paper), Hereditary Neurological Disorders (1 paper), Connective tissue disorders research (1 paper), Bone health and treatments (1 paper), Lysosomal Storage Disorders Research (1 paper), Genetic Neurodegenerative Diseases (1 paper), Mitochondrial Function and Pathology (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Clinical Biochemistry (8 citations), Aging (2 citations), Developmental Biology (2 citations), Cellular and Molecular Neuroscience (12 citations) and Molecular Biology (35 citations). Farid Ullah has collaborated with scholars based in Pakistan, Denmark and Australia. Frequent co-authors include Shahid Mahmood Baig, Uzma Abdullah, Zafar Ali, Johan Wikström, Joakim Klar, Niklas Dahl, Muhammad Tariq, Andrew Sinclair, Elena J. Tucker and Erica E. Davis. Their work appears in journals such as European Journal of Medical Genetics, Human Genetics, BMC Medical Genetics and International Journal of Neuroscience.
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.