Rajan, Vani
Illumina (United States)
2 papers on CoChat
Most cited papers
- Verified
Detection of long repeat expansions from PCR-free whole-genome sequence data
Dolzhenko, E., van Vugt, J. J. F. A., Shaw, R. J., Bekritsky, M. A., van Blitterswijk, M., Narzisi, G., Ajay, S. S., Rajan, V., Lajoie, B. R., Johnson, N. H., et al. (2017) · Genome Research
Genomics and Rare DiseasesGenomics and Phylogenetic Studies
Cited by 388
- Verified
Whole exome sequencing in patients with white matter abnormalities
Vanderver, A., Simons, C., Helman, G., Crawford, J., Wolf, N. I., Bernard, G., Pizzino, A., Schmidt, J. L., Takanohashi, A., Miller, D., et al. (2016) · Annals of Neurology
Genomics and Rare DiseasesHereditary Neurological Disorders
Cited by 145
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