Asmat Ullah
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
Papers in
-
- Hedgehog Signaling Pathway Studies 10
- Genetics 33
- Genomic variations and chromosomal abnormalities 10
- Connective tissue disorders research 8
- Genetic and Kidney Cyst Diseases 7
- Genetic Syndromes and Imprinting 5
- Co-authors
- Wasim Ahmad (47 shared papers)Muhammad Umair (16 shared papers)Farooq Ahmad (8 shared papers)Bruno Antonio Pansera (1 shared paper)Ali Ahmadian (1 shared paper)Saif Ur Rehman (1 shared paper)Sulman Basit (13 shared papers)Mohd Yazid Bajuri (1 shared paper)
- Journals
- Clinical Genetics (3 papers)Frontiers in Genetics (3 papers)European Journal of Medical Genetics (3 papers)Annals of Human Genetics (2 papers)Genes (2 papers)
- Partner nations
- PakistanDenmarkSaudi Arabia
In The Last Decade
Asmat Ullah
74 papers receiving 697 citations
Peers
Comparison fields: 5 of 102
- Developmental Biology 119
- Genetics 236
- Sensory Systems 22
- Internal Medicine 14
- Pediatrics, Perinatology and Child Health 68
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 | 83 | |
| 2 | 2017 | 41 | |
| 3 | 2017 | 27 | |
| 4 | Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families. | 2017 | 26 |
| 5 | 2018 | 25 | |
| 6 | 2021 | 23 | |
| 7 | 2017 | 22 | |
| 8 | 2014 | 21 | |
| 9 | 2017 | 21 | |
| 10 | 2016 | 21 | |
| 11 | 2018 | 21 | |
| 12 | 2016 | 20 | |
| 13 | 2018 | 18 | |
| 14 | 2023 | 17 | |
| 15 | 2014 | 16 | |
| 16 | 2022 | 16 | |
| 17 | 2019 | 16 | |
| 18 | Venous thromboembolism: application and effectiveness of the American College of Chest Physicians 2001 guidelines for prophylaxis. | 2006 | 15 |
| 19 | 2018 | 12 | |
| 20 | 2016 | 12 |
About Asmat Ullah
Asmat Ullah is a scholar working on Molecular Biology, Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 86 papers that have together received 707 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Congenital limb and hand anomalies (10 papers), Hedgehog Signaling Pathway Studies (10 papers), Connective tissue disorders research (8 papers), Genetic and Kidney Cyst Diseases (7 papers), Lysosomal Storage Disorders Research (5 papers), Genetic Syndromes and Imprinting (5 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Developmental Biology (119 citations), Genetics (236 citations), Sensory Systems (22 citations), Internal Medicine (14 citations) and Pediatrics, Perinatology and Child Health (68 citations). Asmat Ullah has collaborated with scholars based in Pakistan, Denmark and Saudi Arabia. Frequent co-authors include Wasim Ahmad, Muhammad Umair, Farooq Ahmad, Bruno Antonio Pansera, Ali Ahmadian, Saif Ur Rehman, Sulman Basit, Mohd Yazid Bajuri, Muhammad Imran Asjad and Thomas Meitinger. Their work appears in journals such as Clinical Genetics, Frontiers in Genetics, European Journal of Medical Genetics, Annals of Human Genetics and Genes.
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.