Asmat Ullah
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
Papers in
-
- Hedgehog Signaling Pathway Studies 10
- RNA modifications and cancer 4
- Genetics 33
- Genomic variations and chromosomal abnormalities 10
- Connective tissue disorders research 8
- Genetic and Kidney Cyst Diseases 6
- Genetic Syndromes and Imprinting 5
- Co-authors
- Wasim Ahmad (47 shared papers)Muhammad Umair (16 shared papers)Farooq Ahmad (8 shared papers)Ali Ahmadian (1 shared paper)Mohd Yazid Bajuri (1 shared paper)Bruno Antonio Pansera (1 shared paper)Saif Ur Rehman (1 shared paper)Sulman Basit (13 shared papers)
- Journals
- Clinical Genetics (4 papers)European Journal of Medical Genetics (3 papers)Annals of Human Genetics (2 papers)Molecular Biology Reports (2 papers)Clinical and Experimental Dermatology (2 papers)
- Partner nations
- PakistanDenmarkSaudi Arabia
In The Last Decade
Asmat Ullah
72 papers receiving 658 citations
Peers
Comparison fields: 5 of 101
- Developmental Biology 130
- Genetics 259
- Molecular Biology 313
- Sensory Systems 21
- Pediatrics, Perinatology and Child Health 76
Countries citing papers authored by Asmat Ullah
This map shows the geographic impact of Asmat 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 Asmat Ullah with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Asmat Ullah more than expected).
Fields of papers citing papers by Asmat Ullah
This network shows the impact of papers produced by Asmat 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 Asmat Ullah. The network helps show where Asmat Ullah may publish in the future.
Co-authors
The 25 scholars most cited alongside Asmat 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
Showing the 20 most-cited of 86 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 78 | |
| 2 | 2017 | 39 | |
| 3 | 2017 | 26 | |
| 4 | 2018 | 25 | |
| 5 | Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families. | 2017 | 25 |
| 6 | 2017 | 22 | |
| 7 | 2021 | 21 | |
| 8 | 2014 | 21 | |
| 9 | 2017 | 20 | |
| 10 | 2016 | 20 | |
| 11 | 2016 | 20 | |
| 12 | 2018 | 20 | |
| 13 | 2019 | 16 | |
| 14 | 2018 | 16 | |
| 15 | 2022 | 16 | |
| 16 | 2014 | 15 | |
| 17 | Venous thromboembolism: application and effectiveness of the American College of Chest Physicians 2001 guidelines for prophylaxis. | 2006 | 15 |
| 18 | 2023 | 13 | |
| 19 | 2017 | 12 | |
| 20 | 2018 | 12 |
About Asmat Ullah
Asmat Ullah is a scholar working on Molecular Biology, Genetics, Developmental Biology, Surgery and Pediatrics, Perinatology and Child Health, having authored 86 papers that have together received 667 indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (10 papers), Congenital limb and hand anomalies (10 papers), Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (8 papers), Genetic and Kidney Cyst Diseases (6 papers), Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (5 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Developmental Biology (130 citations), Genetics (259 citations), Molecular Biology (313 citations), Sensory Systems (21 citations) and Pediatrics, Perinatology and Child Health (76 citations). Asmat Ullah has collaborated with scholars based in Pakistan, Denmark and Saudi Arabia. Frequent co-authors include Wasim Ahmad, Muhammad Umair, Farooq Ahmad, Ali Ahmadian, Mohd Yazid Bajuri, Bruno Antonio Pansera, Saif Ur Rehman, Sulman Basit, Muhammad Imran Asjad and Bader Alhaddad. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Annals of Human Genetics, Molecular Biology Reports and Clinical and Experimental Dermatology.
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.