Brown, Garth R
National Institutes of Health · National Center for Biotechnology Information
5 papers on CoChat
Most cited papers
- Verified
ClinVar: improving access to variant interpretations and supporting evidence
Landrum, M. J., Lee, J. M., Benson, M., Brown, G. R., Chao, C., Chitipiralla, S., Gu, B., Hart, J., Hoffman, D., Jang, W., et al. (2018) · Nucleic Acids Research
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 4,196
- Verified
ClinVar: public archive of interpretations of clinically relevant variants
Landrum, M. J., Lee, J. M., Benson, M., Brown, G., Chao, C., Chitipiralla, S., Gu, B., Hart, J., Hoffman, D., Hoover, J., et al. (2016) · Nucleic Acids Research
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 2,758
- Verified
NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy
Pruitt, K. D., Tatusova, T., Brown, G. R., & Maglott, D. R. (2012) · Nucleic Acids Research
Genomics and Phylogenetic StudiesBiomedical Text Mining and Ontologies
Cited by 1,149
- Verified
ClinVar: improvements to accessing data
Landrum, M. J., Chitipiralla, S., Brown, G. R., Chen, C., Gu, B., Hart, J., Hoffman, D., Jang, W., Kaur, K., Liu, C., et al. (2020) · Nucleic Acids Research
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 994
- Verified
ClinVar: updates to support classifications of both germline and somatic variants
Landrum, M. J., Chitipiralla, S., Kaur, K., Brown, G., Chen, C., Hart, J., Hoffman, D., Jang, W., Liu, C., Maddipatla, Z., et al. (2025) · Nucleic Acids Research
Genomics and Rare DiseasesCancer Genomics and Diagnostics
Cited by 182
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