Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 18 Similar Profiles
von Willebrand Factor Medicine & Life Sciences
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Proteins Medicine & Life Sciences
Plasminogen Activator Inhibitor 1 Medicine & Life Sciences
Factor V Medicine & Life Sciences
Hemorrhage Medicine & Life Sciences
Thrombosis Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Grants 1987 2024

Research Output 1975 2017

1 Citations

A Critical Analysis of the Role of SNARE Protein SEC22B in Antigen Cross-Presentation

Wu, S. J., Niknafs, Y. S., Kim, S. H., Oravecz-Wilson, K., Zajac, C., Toubai, T., Sun, Y., Prasad, J., Peltier, D., Fujiwara, H., Hedig, I., Mathewson, N. D., Khoriaty, R., Ginsburg, D. & Reddy, P. Jun 27 2017 In : Cell Reports. 19, 13, p. 2645-2656 12 p.

Research output: Research - peer-reviewArticle

Cross-Priming
SNARE Proteins
Antigen Presentation
Dendritic Cells
Antigens

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

van Rooij, F. J. A. , Qayyum, R. , Smith, A. V. , Zhou, Y. , Trompet, S. , Tanaka, T. , Keller, M. F. , Chang, L. C. , Schmidt, H. , Yang, M. L. , Chen, M. H. , Hayes, J. , Johnson, A. D. , Yanek, L. R. , Mueller, C. , Lange, L. , Floyd, J. S. , Ghanbari, M. , Zonderman, A. B. , Jukema, J. W. & 80 others Hofman, A., van Duijn, C. M., Desch, K. C., Saba, Y., Ozel, A. B., Snively, B. M., Wu, J. Y., Schmidt, R., Fornage, M., Klein, R. J., Fox, C. S., Matsuda, K., Kamatani, N., Wild, P. S., Stott, D. J., Ford, I., Slagboom, P. E., Yang, J., Chu, A. Y., Lambert, A. J., Uitterlinden, A. G., Franco, O. H., Hofer, E., Ginsburg, D., Hu, B., Keating, B., Schick, U. M., Brody, J. A., Li, J. Z., Chen, Z., Zeller, T., Guralnik, J. M., Chasman, D. I., Peters, L. L., Kubo, M., Becker, D. M., Li, J., Eiriksdottir, G., Rotter, J. I., Levy, D., Grossmann, V., Patel, K. V., Chen, C. H., Ridker, P. M., Tang, H., Launer, L. J., Rice, K. M., Li-Gao, R., Ferrucci, L., Evans, M. K., Choudhuri, A., Trompouki, E., Abraham, B. J., Yang, S., Takahashi, A., Kamatani, Y., Kooperberg, C., Harris, T. B., Jee, S. H., Coresh, J., Tsai, F. J., Longo, D. L., Chen, Y. T., Felix, J. F., Yang, Q., Psaty, B. M., Boerwinkle, E., Becker, L. C., Mook-Kanamori, D. O., Wilson, J. G., Gudnason, V., O'Donnell, C. J., Dehghan, A., Cupples, L. A., Nalls, M. A., Morris, A. P., Okada, Y., Reiner, A. P., Zon, L. I. & Ganesh, S. K. Jan 5 2017 In : American Journal of Human Genetics. 100, 1, p. 51-63 13 p.

Research output: Research - peer-reviewArticle

Genetic Loci
Erythropoiesis
Genome-Wide Association Study
Meta-Analysis
Erythrocytes

Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci

Westrick, R. J., Tomberg, K., Siebert, A. E., Zhu, G., Winn, M. E., Dobies, S. L., Manning, S. L., Brake, M. A., Cleuren, A. C., Hobbs, L. M., Mishack, L. M., Johnston, A. J., Kotnik, E., Siemieniak, D. R., Xu, J., Li, J. Z., Saunders, T. L. & Ginsburg, D. Sep 5 2017 In : Proceedings of the National Academy of Sciences of the United States of America. 114, 36, p. 9659-9664 6 p.

Research output: Research - peer-reviewArticle

Ethylnitrosourea
Mutagenesis
Thrombosis
factor V Leiden
Haploinsufficiency
1 Citations

Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance

Ozel, A. B., McGee, B., Siemieniak, D., Jacobi, P. M., Haberichter, S. L., Brody, L. C., Mills, J. L., Molloy, A. M., Ginsburg, D., Li, J. Z. & Desch, K. C. Sep 1 2016 In : Journal of Thrombosis and Haemostasis. 14, 9, p. 1888-1898 11 p.

Research output: Research - peer-reviewArticle

von Willebrand Factor
Genome
Chromosomes, Human, Pair 2
Genome-Wide Association Study
Single Nucleotide Polymorphism
1 Citations

Pancreatic SEC23B deficiency is sufficient to explain the perinatal lethality of germline SEC23B deficiency in mice

Khoriaty, R., Everett, L., Chase, J., Zhu, G., Hoenerhoff, M., McKnight, B., Vasievich, M. P., Zhang, B., Tomberg, K., Williams, J., Maillard, I. & Ginsburg, D. Jun 14 2016 In : Scientific Reports. 6, 27802

Research output: Research - peer-reviewArticle

Congenital Dyserythropoietic Anemia
Transgenes
Mutation
Genes
Acinar Cells