Guturu, Harendra

AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature

Birgmeier, J., Haeussler, M., Deisseroth, C. A., Steinberg, E. H., Jagadeesh, K. A., Ratner, A. J., Guturu, H., Wenger, A. M., Diekhans, M. E., Stenson, P. D., et al. (2020) · Science Translational Medicine

Genomics and Rare DiseasesBiomedical Text Mining and Ontologies

Cited by 118

Computational methods to detect conserved non-genic elements in phylogenetically isolated genomes: application to zebrafish

Hiller, M., Agarwal, S., Notwell, J. H., Parikh, R., Guturu, H., Wenger, A. M., & Bejerano, G. (2013) · Nucleic Acids Research

Genomics and Phylogenetic StudiesGenomics and Chromatin Dynamics

Cited by 72

Nanoparticle enrichment mass-spectrometry proteomics identifies protein-altering variants for precise pQTL mapping

Suhre, K., Venkataraman, G. R., Guturu, H., Halama, A., Stephan, N., Thareja, G., Sarwath, H., Motamedchaboki, K., Donovan, M. K. R., Siddiqui, A., et al. (2024) · Nature Communications

Advanced Proteomics Techniques and ApplicationsMass Spectrometry Techniques and Applications

Cited by 57

Phrank measures phenotype sets similarity to greatly improve Mendelian diagnostic disease prioritization

Jagadeesh, K. A., Birgmeier, J., Guturu, H., Deisseroth, C. A., Wenger, A. M., Bernstein, J. A., & Bejerano, G. (2019) · Genetics in Medicine

Genomics and Rare DiseasesBiomedical Text Mining and Ontologies

Cited by 56

A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform

Suhre, K., Chen, Q., Halama, A., Mendez, K., Dahlin, A., Stephan, N., Thareja, G., Sarwath, H., Guturu, H., Dwaraka, V. B., et al. (2025) · Nature Genetics

Genetic Associations and EpidemiologyAdvanced Proteomics Techniques and Applications

Cited by 14