Ashwin Dalal
Impact in
- Genetics top 5%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 66
- Genomic variations and chromosomal abnormalities 19
- Genomics and Rare Diseases 17
- Connective tissue disorders research 14
- Genetic Syndromes and Imprinting 12
- Genetics and Neurodevelopmental Disorders 11
- Co-authors
- Shubha R. Phadke (27 shared papers)Aneek Das Bhowmik (22 shared papers)Shagun Aggarwal (27 shared papers)Vijaya Kumar Pidugu (10 shared papers)Mandakini Pradhan (5 shared papers)Prajnya Ranganath (30 shared papers)Katta M. Girisha (16 shared papers)Neerja Gupta (16 shared papers)
- Journals
- European Journal of Medical Genetics (12 papers)Gene (8 papers)Clinical Genetics (4 papers)European Journal of Human Genetics (3 papers)Prenatal Diagnosis (3 papers)
- Partner nations
- IndiaUnited StatesGermany
In The Last Decade
Ashwin Dalal
139 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 107
- Genetics 493
- Genetics 92
- Pediatrics, Perinatology and Child Health 160
- Developmental Biology 20
- Molecular Biology 595
Countries citing papers authored by Ashwin Dalal
This map shows the geographic impact of Ashwin Dalal'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 Ashwin Dalal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ashwin Dalal more than expected).
Fields of papers citing papers by Ashwin Dalal
This network shows the impact of papers produced by Ashwin Dalal. 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 Ashwin Dalal. The network helps show where Ashwin Dalal may publish in the future.
Co-authors
The 25 scholars most cited alongside Ashwin Dalal, 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 152 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 107 | |
| 2 | 2006 | 77 | |
| 3 | 2010 | 76 | |
| 4 | 2012 | 48 | |
| 5 | 2014 | 37 | |
| 6 | 2010 | 35 | |
| 7 | 2013 | 33 | |
| 8 | 2012 | 32 | |
| 9 | 2021 | 32 | |
| 10 | 2014 | 31 | |
| 11 | 2016 | 30 | |
| 12 | 2018 | 28 | |
| 13 | 2006 | 27 | |
| 14 | 2017 | 25 | |
| 15 | 2018 | 24 | |
| 16 | 2019 | 23 | |
| 17 | 2015 | 23 | |
| 18 | 2018 | 20 | |
| 19 | 2006 | 19 | |
| 20 | 2007 | 19 |
About Ashwin Dalal
Ashwin Dalal is a scholar working on Molecular Biology, Genetics, Physiology, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 152 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Genomics and Rare Diseases (17 papers), Lysosomal Storage Disorders Research (14 papers), Connective tissue disorders research (14 papers), Genetic Syndromes and Imprinting (12 papers), Prenatal Screening and Diagnostics (12 papers), Chromosomal and Genetic Variations (11 papers) and Genetics and Neurodevelopmental Disorders (11 papers). The work is most often cited by research in Genetics (493 citations), Genetics (92 citations), Pediatrics, Perinatology and Child Health (160 citations), Developmental Biology (20 citations) and Molecular Biology (595 citations). Ashwin Dalal has collaborated with scholars based in India, United States and Germany. Frequent co-authors include Shubha R. Phadke, Aneek Das Bhowmik, Shagun Aggarwal, Vijaya Kumar Pidugu, Mandakini Pradhan, Prajnya Ranganath, Katta M. Girisha, Neerja Gupta, Suraksha Agrawal and Faisal Ali Anwarali Khan. Their work appears in journals such as European Journal of Medical Genetics, Gene, Clinical Genetics, European Journal of Human Genetics and Prenatal Diagnosis.
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.