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Smoking + BMI in heart disease
WGS for cardiovascular outcomes
RNA-Seq in pancreatic cancer
Exome Sequencing of Chordoma Cases
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Overview
Selected Publications (4)
Variables (13)
Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma
M. Kelley, Jianxin Shi, Bari J. Ballew, et al. (2014). Human Genetics. Cited 57 times.
https://doi.org/10.1007/s00439-014-1463-z
Clinical findings in families with chordoma with and without T gene duplications and in patients with sporadic chordoma reported to the Surveillance, Epidemiology, and End Results program.
D. Parry, M. McMaster, N. Liebsch, et al. (2020). Journal of neurosurgery. Cited 10 times.
https://doi.org/10.3171/2020.4.JNS193505
Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma
B. Xia, K. Biswas, T. Foo, et al. (2022). Human Mutation. Cited 8 times.
https://doi.org/10.1002/humu.24427
Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility
Sally Yepes, Nirav N Shah, J. Bai, et al. (2021). Cancers. Cited 8 times.
https://doi.org/10.3390/cancers13112704