Rani Sachdev
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
- Genetics 29
- Genomics and Rare Diseases 15
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 7
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- RNA modifications and cancer 7
- RNA Research and Splicing 6
- RNA and protein synthesis mechanisms 4
- Co-authors
- Rebecca Macintosh (12 shared papers)Elizabeth E. Palmer (12 shared papers)Alison Colley (2 shared papers)John Christodoulou (2 shared papers)Marcia L. Budarf (2 shared papers)Meredith J.C. Wilson (2 shared papers)Leon R. McQuade (2 shared papers)Beverly S. Emanuel (1 shared paper)
- Journals
- Genetics in Medicine (6 papers)The American Journal of Human Genetics (5 papers)European Journal of Paediatric Neurology (3 papers)European Journal of Human Genetics (3 papers)Genes (2 papers)
- Partner nations
- AustraliaUnited StatesFrance
In The Last Decade
Rani Sachdev
62 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 88
- Genetics 863
- Clinical Biochemistry 85
- Molecular Biology 642
- Psychiatry and Mental health 115
- Cancer Research 93
Countries citing papers authored by Rani Sachdev
This map shows the geographic impact of Rani Sachdev'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 Rani Sachdev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rani Sachdev more than expected).
Fields of papers citing papers by Rani Sachdev
This network shows the impact of papers produced by Rani Sachdev. 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 Rani Sachdev. The network helps show where Rani Sachdev may publish in the future.
Co-authors
The 25 scholars most cited alongside Rani Sachdev, 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 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 191 | |
| 2 | 2018 | 146 | |
| 3 | 2016 | 106 | |
| 4 | 2018 | 98 | |
| 5 | 2018 | 92 | |
| 6 | 2022 | 86 | |
| 7 | 2021 | 74 | |
| 8 | 2024 | 68 | |
| 9 | 2021 | 66 | |
| 10 | 1999 | 59 | |
| 11 | 2019 | 50 | |
| 12 | 2015 | 47 | |
| 13 | 2021 | 44 | |
| 14 | 2017 | 41 | |
| 15 | 2013 | 40 | |
| 16 | 2017 | 37 | |
| 17 | 2023 | 35 | |
| 18 | 2022 | 32 | |
| 19 | 2016 | 25 | |
| 20 | 2019 | 23 |
About Rani Sachdev
Rani Sachdev is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 65 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (15 papers), Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (7 papers), RNA modifications and cancer (7 papers), Epilepsy research and treatment (6 papers), RNA Research and Splicing (6 papers), RNA and protein synthesis mechanisms (4 papers) and Ethics and Legal Issues in Pediatric Healthcare (4 papers). The work is most often cited by research in Genetics (863 citations), Clinical Biochemistry (85 citations), Molecular Biology (642 citations), Psychiatry and Mental health (115 citations) and Cancer Research (93 citations). Rani Sachdev has collaborated with scholars based in Australia, United States and France. Frequent co-authors include Rebecca Macintosh, Elizabeth E. Palmer, Alison Colley, John Christodoulou, Marcia L. Budarf, Meredith J.C. Wilson, Leon R. McQuade, Beverly S. Emanuel, Michael A Cardamone and Paula W. Morris. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, European Journal of Paediatric Neurology, European Journal of Human Genetics and Genes.
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.