Sulman Basit
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Reproductive Medicine top 5%
- Ovarian function and disorders
Papers in
-
- RNA regulation and disease 10
- Wnt/β-catenin signaling in development and cancer 9
- Genetics 51
- Connective tissue disorders research 12
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 9
- Co-authors
- Wasim Ahmad (51 shared papers)Muhammad Jaseem Khan (3 shared papers)Anwar Ullah (1 shared paper)Khalid I. Khoshhal (7 shared papers)Muhammad Ansar (17 shared papers)Khushnooda Ramzan (27 shared papers)Muhammad Latif (7 shared papers)Saadullah Khan (13 shared papers)
- Journals
- Clinical Genetics (7 papers)European Journal of Medical Genetics (7 papers)Clinical and Experimental Dermatology (5 papers)Human Genetics (5 papers)Scientific Reports (4 papers)
- Partner nations
- Saudi ArabiaPakistanUnited States
In The Last Decade
Sulman Basit
124 papers receiving 1.8k citations
Sulman Basit's Hit Papers
Peers
Comparison fields: 5 of 113
- Developmental Biology 113
- Reproductive Medicine 233
- Sensory Systems 98
- Genetics 520
- Urology 116
Countries citing papers authored by Sulman Basit
This map shows the geographic impact of Sulman Basit'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 Sulman Basit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sulman Basit more than expected).
Fields of papers citing papers by Sulman Basit
This network shows the impact of papers produced by Sulman Basit. 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 Sulman Basit. The network helps show where Sulman Basit may publish in the future.
Co-authors
The 25 scholars most cited alongside Sulman Basit, 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 134 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | <p>Genetic Basis of Polycystic Ovary Syndrome (PCOS): Current Perspectives</p> Hit paper breakdown → | 2019 | 215 |
| 2 | 2014 | 149 | |
| 3 | 2013 | 119 | |
| 4 | 2017 | 82 | |
| 5 | 2013 | 79 | |
| 6 | 2009 | 53 | |
| 7 | 2010 | 50 | |
| 8 | 2017 | 46 | |
| 9 | 2016 | 39 | |
| 10 | 2014 | 39 | |
| 11 | 2011 | 35 | |
| 12 | 2017 | 30 | |
| 13 | 2008 | 29 | |
| 14 | 2015 | 29 | |
| 15 | 2010 | 27 | |
| 16 | 2011 | 25 | |
| 17 | 2011 | 25 | |
| 18 | 2018 | 23 | |
| 19 | 2017 | 22 | |
| 20 | 2016 | 21 |
About Sulman Basit
Sulman Basit is a scholar working on Molecular Biology, Genetics, Cell Biology, Genetics and Surgery, having authored 134 papers that have together received 1.9k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (14 papers), Connective tissue disorders research (12 papers), Genetics and Neurodevelopmental Disorders (12 papers), RNA regulation and disease (10 papers), Hair Growth and Disorders (10 papers), Genomics and Rare Diseases (9 papers), Wnt/β-catenin signaling in development and cancer (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). The work is most often cited by research in Developmental Biology (113 citations), Reproductive Medicine (233 citations), Sensory Systems (98 citations), Genetics (520 citations) and Urology (116 citations). Sulman Basit has collaborated with scholars based in Saudi Arabia, Pakistan and United States. Frequent co-authors include Wasim Ahmad, Muhammad Jaseem Khan, Anwar Ullah, Khalid I. Khoshhal, Muhammad Ansar, Khushnooda Ramzan, Muhammad Latif, Saadullah Khan, Sibtain Afzal and Kwangho Lee. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Clinical and Experimental Dermatology, Human Genetics and Scientific Reports.
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.