Samarth Bhatt
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
- Birth, Development, and Health
Papers in
- Genetics 22
- Genomic variations and chromosomal abnormalities 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
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- Chromosomal and Genetic Variations 15
- Co-authors
- Darlene A. Kertes (7 shared papers)Thomas Liehr (19 shared papers)Hayley S. Kamin (5 shared papers)David A. Hughes (3 shared papers)Nicole C Rodney (3 shared papers)Connie J. Mulligan (4 shared papers)Kristin Mrasek (10 shared papers)Anja Weise (11 shared papers)
- Journals
- Molecular Cytogenetics (5 papers)Cytogenetic and Genome Research (3 papers)Psychoneuroendocrinology (2 papers)Human Reproduction (2 papers)Clinical Epigenetics (1 paper)
- Partner nations
- GermanyUnited StatesFrance
In The Last Decade
Samarth Bhatt
34 papers receiving 1000 citations
Peers
Comparison fields: 5 of 85
- Genetics 597
- Pediatrics, Perinatology and Child Health 301
- Behavioral Neuroscience 47
- Molecular Biology 448
- Pharmacy 30
Countries citing papers authored by Samarth Bhatt
This map shows the geographic impact of Samarth Bhatt'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 Samarth Bhatt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Samarth Bhatt more than expected).
Fields of papers citing papers by Samarth Bhatt
This network shows the impact of papers produced by Samarth Bhatt. 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 Samarth Bhatt. The network helps show where Samarth Bhatt may publish in the future.
Co-authors
The 25 scholars most cited alongside Samarth Bhatt, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 156 | |
| 2 | 2009 | 141 | |
| 3 | 2009 | 114 | |
| 4 | 2012 | 101 | |
| 5 | 2016 | 71 | |
| 6 | 2017 | 62 | |
| 7 | 2008 | 62 | |
| 8 | 2009 | 32 | |
| 9 | 2010 | 30 | |
| 10 | 2009 | 27 | |
| 11 | 2006 | 26 | |
| 12 | 2008 | 20 | |
| 13 | 2006 | 19 | |
| 14 | 2013 | 17 | |
| 15 | 2013 | 16 | |
| 16 | 2007 | 15 | |
| 17 | 2011 | 14 | |
| 18 | 2008 | 14 | |
| 19 | 2012 | 12 | |
| 20 | 2015 | 11 |
About Samarth Bhatt
Samarth Bhatt is a scholar working on Genetics, Plant Science, Pediatrics, Perinatology and Child Health, Molecular Biology and Social Psychology, having authored 34 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (15 papers), Prenatal Screening and Diagnostics (11 papers), Neuroendocrine regulation and behavior (5 papers), Genomics and Chromatin Dynamics (4 papers), Acute Myeloid Leukemia Research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (597 citations), Pediatrics, Perinatology and Child Health (301 citations), Behavioral Neuroscience (47 citations), Molecular Biology (448 citations) and Pharmacy (30 citations). Samarth Bhatt has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Darlene A. Kertes, Thomas Liehr, Hayley S. Kamin, David A. Hughes, Nicole C Rodney, Connie J. Mulligan, Kristin Mrasek, Anja Weise, Sau Wai Cheung and Franck Pellestor. Their work appears in journals such as Molecular Cytogenetics, Cytogenetic and Genome Research, Psychoneuroendocrinology, Human Reproduction and Clinical Epigenetics.
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.