S. M. Jalal
- Molecular Biology
- Genetics top 5%
- Plant Science top 10%
- Pediatrics, Perinatology and Child Health top 10%
- Hematology top 10%
- Co-authors
- John T. MartsolfT. C. HsüSen PathakLarry BurdMary K. KukolichJacob KerbeshianRafaël FonsecaScott A. Van Wier
- Topics
- Genomic variations and chromosomal abnormalities (17 papers)Prenatal Screening and Diagnostics (10 papers)Chromosomal and Genetic Variations (8 papers)
- Cited by
- GeneticsHematology
- Partner nations
- United StatesSingaporeIran
In The Last Decade
S. M. Jalal
43 papers receiving 776 citations
Peers
Comparison fields: 5 of 88
- Molecular Biology 352
- Genetics 345
- Plant Science 236
- Pediatrics, Perinatology and Child Health 128
- Hematology 127
Countries citing papers authored by S. M. Jalal
This map shows the geographic impact of S. M. Jalal'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 S. M. Jalal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. M. Jalal more than expected).
Fields of papers citing papers by S. M. Jalal
This network shows the impact of papers produced by S. M. Jalal. 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 S. M. Jalal. The network helps show where S. M. Jalal may publish in the future.
Co-authorship network of co-authors of S. M. Jalal
This figure shows the co-authorship network connecting the top 25 collaborators of S. M. Jalal. A scholar is included among the top collaborators of S. M. Jalal based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with S. M. Jalal. S. M. Jalal is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | 69 | |
| 3 | 23 | |
| 4 | 1 | |
| 5 | 19 | |
| 6 | 13 | |
| 7 | 14 | |
| 8 | 19 | |
| 9 | 38 | |
| 10 | 10 | |
| 11 | 6 | |
| 12 | 17 | |
| 13 | 25 | |
| 14 | 20 | |
| 15 | 5 | |
| 16 | 34 | |
| 17 | 14 | |
| 18 | 2 | |
| 19 | 27 | |
| 20 | 9 |
About S. M. Jalal
S. M. Jalal is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 43 papers that have together received 808 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (10 papers) and Chromosomal and Genetic Variations (8 papers). The work is most often cited by research in Genetics (345 citations), Genetics (121 citations) and Hematology (127 citations). S. M. Jalal has collaborated with scholars based in United States, Singapore and Iran. Frequent co-authors include John T. Martsolf, T. C. Hsü, Sen Pathak, Larry Burd, Mary K. Kukolich, Jacob Kerbeshian, Rafaël Fonseca, Scott A. Van Wier, Morie A. Gertz and Martha Q. Lacy. Their work appears in journals such as Molecular Psychiatry, Experimental Cell Research and British Journal of Haematology.
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.