• Source: Scopus
  • Calculated based on no. of publications stored in Pure and citations from Scopus
1984 …2022

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Dive into the research topics where Ravindranath Duggirala is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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  • Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

    Fernández-Rhodes, L., Graff, M., Buchanan, V. L., Justice, A. E., Highland, H. M., Guo, X., Zhu, W., Chen, H. H., Young, K. L., Adhikari, K., Palmer, N. D., Below, J. E., Bradfield, J., Pereira, A. C., Glover, L. S., Kim, D., Lilly, A. G., Shrestha, P., Thomas, A. G., Zhang, X. & 96 others, Chen, M., Chiang, C. W. K., Pulit, S., Horimoto, A., Krieger, J. E., Guindo-Martínez, M., Preuss, M., Schumann, C., Smit, R. A. J., Torres-Mejía, G., Acuña-Alonzo, V., Bedoya, G., Bortolini, M. C., Canizales-Quinteros, S., Gallo, C., González-José, R., Poletti, G., Rothhammer, F., Hakonarson, H., Igo, R., Adler, S. G., Iyengar, S. K., Nicholas, S. B., Gogarten, S. M., Isasi, C. R., Papnicolaou, G., Stilp, A. M., Qi, Q., Kho, M., Smith, J. A., Langefeld, C. D., Wagenknecht, L., Mckean-Cowdin, R., Gao, X. R., Nousome, D., Conti, D. V., Feng, Y., Allison, M. A., Arzumanyan, Z., Buchanan, T. A., Ida Chen, Y. D., Genter, P. M., Goodarzi, M. O., Hai, Y., Hsueh, W., Ipp, E., Kandeel, F. R., Lam, K., Li, X., Nadler, J. L., Raffel, L. J., Roll, K., Sandow, K., Tan, J., Taylor, K. D., Xiang, A. H., Yao, J., Audirac-Chalifour, A., de Jesus Peralta Romero, J., Hartwig, F., Horta, B., Blangero, J., Curran, J. E., Duggirala, R., Lehman, D. E., Puppala, S., Fejerman, L., John, E. M., Aguilar-Salinas, C., Burtt, N. P., Florez, J. C., García-Ortíz, H., González-Villalpando, C., Mercader, J., Orozco, L., Tusié-Luna, T., Blanco, E., Gahagan, S., Cox, N. J., Hanis, C., Butte, N. F., Cole, S. A., Comuzzie, A. G., Voruganti, V. S., Rohde, R., Wang, Y., Sofer, T., Ziv, E., Grant, S. F. A., Ruiz-Linares, A., Rotter, J. I., Haiman, C. A., Parra, E. J., Cruz, M., Loos, R. J. F. & North, K. E., Apr 14 2022, In: Human Genetics and Genomics Advances. 3, 2, 100099.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

    AMP-T2D-GENES, Myocardial Infarction Genetics Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & NHLBI TOPMed Lipids Working Group, Jan 6 2022, In: American Journal of Human Genetics. 109, 1, p. 81-96 16 p.

    Research output: Contribution to journalArticlepeer-review

  • Rare coding variants in RCN3 are associated with blood pressure

    Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Feb 19 2022, In: BMC genomics. 23, 1, p. 148 1 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

    NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Oct 2021, In: Nature Genetics. 53, 10, p. 1504-1516 13 p.

    Research output: Contribution to journalArticlepeer-review

  • APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups

    Goyal, S., Tanigawa, Y., Zhang, W., Chai, J. F., Almeida, M., Sim, X., Lerner, M., Chainakul, J., Ramiu, J. G., Seraphin, C., Apple, B., Vaughan, A., Muniu, J., Peralta, J., Lehman, D. M., Ralhan, S., Wander, G. S., Singh, J. R., Mehra, N. K., Sidorov, E. & 14 others, Peyton, M. D., Blackett, P. R., Curran, J. E., Tai, E. S., van Dam, R., Cheng, C. Y., Duggirala, R., Blangero, J. C., Chambers, J. C., Sabanayagam, C., Kooner, J. S., Rivas, M. A., Aston, C. E. & Sanghera, D. K., Dec 2021, In: Lipids in Health and Disease. 20, 1, 113.

    Research output: Contribution to journalArticlepeer-review

    Open Access