Salman Kirmani
Impact in
-
- Bone health and osteoporosis research
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 19
- Genomics and Rare Diseases 8
- BRCA gene mutations in cancer 5
- Neurogenetic and Muscular Disorders Research 4
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 4
- Connective tissue disorders research 4
- Co-authors
- William F. Young (1 shared paper)Sundeep Khosla (5 shared papers)Louise K. McCready (3 shared papers)Noralane M. Lindor (4 shared papers)David R. Deyle (1 shared paper)Sharonne N. Hayes (1 shared paper)Stanislav Henkin (1 shared paper)Timothy M. Olson (1 shared paper)
- Journals
- Journal of Bone and Mineral Research (4 papers)Journal of American Association for Pediatric Ophthalmology and Strabismus (2 papers)European Journal of Human Genetics (2 papers)Pediatric Blood & Cancer (2 papers)Endocrine Practice (2 papers)
- Partner nations
- PakistanUnited StatesSweden
In The Last Decade
Salman Kirmani
50 papers receiving 798 citations
Peers
Comparison fields: 5 of 77
- Orthopedics and Sports Medicine 95
- Genetics 275
- Cardiology and Cardiovascular Medicine 127
- Surgery 151
- Pediatrics, Perinatology and Child Health 63
Countries citing papers authored by Salman Kirmani
This map shows the geographic impact of Salman Kirmani'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 Salman Kirmani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Salman Kirmani more than expected).
Fields of papers citing papers by Salman Kirmani
This network shows the impact of papers produced by Salman Kirmani. 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 Salman Kirmani. The network helps show where Salman Kirmani may publish in the future.
Co-authors
The 25 scholars most cited alongside Salman Kirmani, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 119 | |
| 2 | 2013 | 97 | |
| 3 | 2014 | 68 | |
| 4 | 2013 | 59 | |
| 5 | 2012 | 49 | |
| 6 | Hereditary Paraganglioma-Pheochromocytoma Syndromes | 2014 | 49 |
| 7 | 2013 | 36 | |
| 8 | 2010 | 35 | |
| 9 | 2013 | 35 | |
| 10 | 2015 | 29 | |
| 11 | 2014 | 20 | |
| 12 | 2014 | 19 | |
| 13 | 2013 | 17 | |
| 14 | 2020 | 17 | |
| 15 | 2012 | 16 | |
| 16 | 2014 | 16 | |
| 17 | 2017 | 14 | |
| 18 | 2020 | 13 | |
| 19 | 2022 | 10 | |
| 20 | 2014 | 9 |
About Salman Kirmani
Salman Kirmani is a scholar working on Genetics, Molecular Biology, Genetics, Epidemiology and Surgery, having authored 57 papers that have together received 825 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), BRCA gene mutations in cancer (5 papers), Bone fractures and treatments (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Connective tissue disorders research (4 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Orthopedics and Sports Medicine (95 citations), Genetics (275 citations), Cardiology and Cardiovascular Medicine (127 citations), Surgery (151 citations) and Pediatrics, Perinatology and Child Health (63 citations). Salman Kirmani has collaborated with scholars based in Pakistan, United States and Sweden. Frequent co-authors include William F. Young, Sundeep Khosla, Louise K. McCready, Noralane M. Lindor, David R. Deyle, Sharonne N. Hayes, Stanislav Henkin, Timothy M. Olson, Marysia S. Tweet and Rajiv Gulati. Their work appears in journals such as Journal of Bone and Mineral Research, Journal of American Association for Pediatric Ophthalmology and Strabismus, European Journal of Human Genetics, Pediatric Blood & Cancer and Endocrine Practice.
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.