Trilochan Sahoo
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 59
- Genomic variations and chromosomal abnormalities 37
- Genetic Syndromes and Imprinting 17
- Genetics and Neurodevelopmental Disorders 8
- Bacterial Genetics and Biotechnology 7
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- Prenatal Screening and Diagnostics 25
- Co-authors
- Arthur L. Beaudet (20 shared papers)Sau Wai Cheung (14 shared papers)Sarika U. Peters (11 shared papers)Carlos A. Bacino (13 shared papers)Daniela del Gaudio (5 shared papers)Jennifer Ruth German (3 shared papers)Ankita Patel (12 shared papers)Richard Person (2 shared papers)
- Journals
- Genetics in Medicine (8 papers)European Journal of Human Genetics (7 papers)Molecular Cytogenetics (5 papers)Journal of Medical Genetics (4 papers)Journal of Biological Chemistry (3 papers)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Trilochan Sahoo
80 papers receiving 5.9k citations
Peers
Comparison fields: 5 of 112
- Genetics 4.0k
- Pediatrics, Perinatology and Child Health 1.4k
- Molecular Biology 2.6k
- Developmental Neuroscience 127
- Cognitive Neuroscience 612
Countries citing papers authored by Trilochan Sahoo
This map shows the geographic impact of Trilochan Sahoo'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 Trilochan Sahoo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Trilochan Sahoo more than expected).
Fields of papers citing papers by Trilochan Sahoo
This network shows the impact of papers produced by Trilochan Sahoo. 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 Trilochan Sahoo. The network helps show where Trilochan Sahoo may publish in the future.
Co-authors
The 25 scholars most cited alongside Trilochan Sahoo, 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 81 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 510 | |
| 2 | 2008 | 503 | |
| 3 | 1999 | 320 | |
| 4 | 2010 | 272 | |
| 5 | 2009 | 213 | |
| 6 | 2007 | 188 | |
| 7 | 2009 | 188 | |
| 8 | 2009 | 160 | |
| 9 | 2007 | 159 | |
| 10 | 2007 | 158 | |
| 11 | 2006 | 147 | |
| 12 | 2016 | 144 | |
| 13 | 2010 | 130 | |
| 14 | 2008 | 129 | |
| 15 | 2004 | 127 | |
| 16 | 2010 | 127 | |
| 17 | 2009 | 126 | |
| 18 | 2005 | 125 | |
| 19 | 2009 | 118 | |
| 20 | 2010 | 108 |
About Trilochan Sahoo
Trilochan Sahoo is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Genetics, having authored 81 papers that have together received 6.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (37 papers), Prenatal Screening and Diagnostics (25 papers), Genetic Syndromes and Imprinting (17 papers), Chromosomal and Genetic Variations (10 papers), Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (8 papers), Bacterial Genetics and Biotechnology (7 papers) and Epigenetics and DNA Methylation (7 papers). The work is most often cited by research in Genetics (4.0k citations), Pediatrics, Perinatology and Child Health (1.4k citations), Molecular Biology (2.6k citations), Developmental Neuroscience (127 citations) and Cognitive Neuroscience (612 citations). Trilochan Sahoo has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Arthur L. Beaudet, Sau Wai Cheung, Sarika U. Peters, Carlos A. Bacino, Daniela del Gaudio, Jennifer Ruth German, Ankita Patel, Richard Person, Chad A. Shaw and Marwan S. Shinawi. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, Molecular Cytogenetics, Journal of Medical Genetics and Journal of Biological Chemistry.
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.