Lisa Yanek

2023

Author Correction: Clonal haematopoiesis and risk of chronic liver disease (Nature, (2023), 616, 7958, (747-754), 10.1038/s41586-023-05857-4)

NHLBI TOPMed Hematology Working Group, Jul 20 2023, In: Nature. 619, 7970, p. E47

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2022

Correction: Association of low-frequency and rare coding variants with information processing speed (Translational Psychiatry, (2021), 11, 1, (613), 10.1038/s41398-021-01736-6)

Bressler, J., Davies, G., Smith, A. V., Saba, Y., Bis, J. C., Jian, X., Hayward, C., Yanek, L., Smith, J. A., Mirza, S. S., Wang, R., Adams, H. H. H., Becker, D., Boerwinkle, E., Campbell, A., Cox, S. R., Eiriksdottir, G., Fawns-Ritchie, C., Gottesman, R. F., Grove, M. L., & 35 othersGuo, X., Hofer, E., Kardia, S. L. R., Knol, M. J., Koini, M., Lopez, O. L., Marioni, R. E., Nyquist, P., Pattie, A., Polasek, O., Porteous, D. J., Rudan, I., Satizabal, C. L., Schmidt, H., Schmidt, R., Sidney, S., Simino, J., Smith, B. H., Turner, S. T., van der Lee, S. J., Ware, E. B., Whitmer, R. A., Yaffe, K., Yang, Q., Zhao, W., Gudnason, V., Launer, L. J., Fitzpatrick, A. L., Psaty, B. M., Fornage, M., Arfan Ikram, M., van Duijn, C. M., Seshadri, S., Mosley, T. H. & Deary, I. J., Dec 2022, In: Translational psychiatry. 12, 1, 88.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus (Nature Communications, (2022), 13, 1, (1222), 10.1038/s41467-022-28729-3)

CHARGE Hemostasis Working Group, Dec 2022, In: Nature communications. 13, 1, 1962.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2021

Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (Nature, (2020), 586, 7831, (763-768), 10.1038/s41586-020-2819-2)

NHLBI Trans-Omics for Precision Medicine Consortium, Mar 25 2021, In: Nature. 591, 7851, p. E27

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (Nature Genetics, (2021), 53, 10, (1504-1516), 10.1038/s41588-021-00935-7)

NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2021, In: Nature genetics. 53, 12, p. 1722 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

Erratum: Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program (The American Journal of Human Genetics (2021) 108(5) (874–893), (S0002929721001348), (10.1016/j.ajhg.2021.04.003))

the NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Jun 3 2021, In: American journal of human genetics. 108, 6, p. 1165 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2020

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (Nature Communications, (2018), 9, 1, (2606), 10.1038/s41467-018-04668-w)

NHLBI TOPMed Lipids Working Group, Dec 1 2020, In: Nature communications. 11, 1, 1715.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2018

Erratum: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations (PLoS Genet(2017)13: 5(e1006728)Doi: 10.1371/journal.pgen.1006728)

Liang, J., Le, T. H., Velez Edwards, D. R., Tayo, B. O., Gaulton, K. J., Smith, J. A., Lu, Y., Jensen, R. A., Chen, G., Yanek, L. R., Schwander, K., Tajuddin, S. M., Sofer, T., Kim, W., Kayima, J., McKenzie, C. A., Fox, E., Nalls, M. A., Hunter Young, J., Sun, Y. V., & 59 othersLane, J. M., Cechova, S., Zhou, J., Tang, H., Fornage, M., Musani, S. K., Wang, H., Lee, J., Adeyemo, A., Dreisbach, A. W., Forrester, T., Chu, P. L., Cappola, A., Evans, M. K., Morrison, A. C., Martin, L. W., Wiggins, K. L., Hui, Q., Zhao, W., Jackson, R. D., Ware, E. B., Faul, J. D., Reiner, A. P., Bray, M., Denny, J. C., Mosley, T. H., Palmas, W., Guo, X., Papanicolaou, G. J., Penman, A. D., Polak, J. F., Rice, K., Taylor, K. D., Boerwinkle, E., Bottinger, E. P., Liu, K., Risch, N., Hunt, S. C., Kooperberg, C., Zonderman, A. B., Laurie, C. C., Becker, D. M., Cai, J., Loos, R. J. F., Psaty, B. M., Weir, D. R., Kardia, S. L. R., Arnett, D. K., Won, S., Edwards, T. L., Redline, S., Cooper, R. S., Rao, D. C., Rotter, J. I., Rotimi, C., Levy, D., Chakravarti, A., Zhu, X. & Franceschini, N., May 11 2018, In: PLoS genetics. 14, 5, e1007345.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

1 Scopus citations

Erratum to: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (Nature Communications, (2018), 9, 1, (2606), 10.1038/s41467-018-04668-w)

NHLBI TOPMed Lipids Working Group, Dec 1 2018, In: Nature communications. 9, 1, 3493.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2016

Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016))

Polfus, L. M., Khajuria, R. K., Schick, U. M., Pankratz, N., Pazoki, R., Brody, J. A., Chen, M. H., Auer, P. L., Floyd, J. S., Huang, J., Lange, L., van Rooij, F. J. A., Gibbs, R. A., Metcalf, G., Muzny, D., Veeraraghavan, N., Walter, K., Chen, L., Yanek, L., Becker, L., & 36 othersPeloso, G. M., Wakabayashi, A., Kals, M., Metspalu, A., Esko, T., Fox, K., Wallace, R., Franceschini, N., Matijevic, N., Rice, K. M., Bartz, T. M., Lyytikäinen, L. P., Kähönen, M., Lehtimäki, T., Raitakari, O. T., Li-Gao, R., Mook-Kanamori, D. O., Lettre, G., van Duijn, C. M., Franco, O. H., Rich, S. S., Rivadeneira, F., Hofman, A., Uitterlinden, A. G., Wilson, J. G., Psaty, B. M., Soranzo, N., Dehghan, A., Boerwinkle, E., Zhang, X., Johnson, A. D., O'Donnell, C. J., Johnsen, J. M., Reiner, A. P., Ganesh, S. K. & Sankaran, V. G., Sep 1 2016, In: American journal of human genetics. 99, 3, p. 785 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

6 Scopus citations

Lisa Yanek

Research output

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