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2026 Journal Article Within-family heritability estimates for behavioural and disease phenotypes from 500,000 sibling pairs of diverse ancestriesYengo, Loic, Liang, Yanyu, 23andMe Research Team, Wang, Xin, Granka, Julie M., Evans, David M., Sidorenko, Julia and Visscher, Peter M. (2026). Within-family heritability estimates for behavioural and disease phenotypes from 500,000 sibling pairs of diverse ancestries. Nature Human Behaviour. doi: 10.1038/s41562-026-02599-x |
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2026 Journal Article Multiancestry conditional and joint analysis applied to GWAS summary statisticsWang, Xiaotong, Wang, Yong, Yang, Jian, Visscher, Peter M., Wray, Naomi R. and Yengo, Loic (2026). Multiancestry conditional and joint analysis applied to GWAS summary statistics. Nature Genetics. doi: 10.1038/s41588-026-02799-1 |
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2026 Journal Article Within-family effect of ancestry on complex traits in a Mexican populationWang, Siqi, Berumen, Jaime, Vergara-Lope, Alejandra, Baca, Paulina, Barrera, Elizabeth, Rivas, Fernando, Aguilar-Ramirez, Diego, Collins, Rory, Emberson, Jonathan R., Hill, Michael, Goddard, Michael E., Yengo, Loic, Young, Alexander Strudwick, Alegre-Díaz, Jesus, Kuri-Morales, Pablo, Tapia-Conyer, Roberto, Torres, Jason M. and Visscher, Peter M. (2026). Within-family effect of ancestry on complex traits in a Mexican population. Nature, 1-8. doi: 10.1038/s41586-026-11039-9 |
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2026 Journal Article Why pharmacogenomic biomarkers for chemotherapy-induced peripheral neuropathy fail: a systematic review of genetic associations, replication, and clinical translationMaganti, Aditya, Rankothge, Ishara, Sakadales, Hunter, Kok, Ethan, Britton, James, Rao, Neil, Shatunova, Svetlana, Shimell, Katherine, Zambrano, Paula Manuela Rojas, Park, Susanna B., Schweitzer, Daniel, Laakso, E-Liisa, Yengo, Loic, Vetter, Irina and Starobova, Hana (2026). Why pharmacogenomic biomarkers for chemotherapy-induced peripheral neuropathy fail: a systematic review of genetic associations, replication, and clinical translation. Frontiers in Pharmacology, 17 1842379. doi: 10.3389/fphar.2026.1842379 |
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2026 Journal Article Genetics of skeletal proportions across two different populationsBartell, Eric, Lin, Kuang, Tsuo, Kristin, Gan, Wei, Vedantam, Sailaja, Cole, Joanne B., Baronas, John M., Yengo, Loic, Marouli, Eirini, Amariuta, Tiffany, Chen, Zhengming, Li, Liming, Renthal, Nora E., Jacobsen, Christina M., Salem, Rany M., Walters, Robin G. and Hirschhorn, Joel N. (2026). Genetics of skeletal proportions across two different populations. The American Journal of Human Genetics, 113 (6), 1364-1364. doi: 10.1016/j.ajhg.2026.05.004 |
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2026 Journal Article Empirical evaluation of analytic validity of polygenic scoresLin, Tian, Zeng, Jian, Gordon, Scott D., Wallace, Leanne, Ziser, Laura, Shah, Sonia, Pain, Oliver, Nolte, Ilja M., Snieder, Harold, Lifelines Cohort Study, Aguirre-Gamboa, Raul, Deelen, Patrick, Franke, Lude, Kuivenhoven, Jan A, Lopera Maya, Esteban A, Sanna, Serena, Swertz, Morris A, Vonk, Judith M, Wijmenga, Cisca, James, Paul A., Martin, Nicholas G., Visscher, Peter M., Lee, Eric, Yengo, Loic, Henders, Anjali K. and Wray, Naomi R. (2026). Empirical evaluation of analytic validity of polygenic scores. Genome Medicine, 18 (1) 81, 1-13. doi: 10.1186/s13073-026-01654-6 |
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2026 Journal Article Genetics of skeletal proportions across two different populationsBartell, Eric, Lin, Kuang, Tsuo, Kristin, Gan, Wei, Vedantam, Sailaja, Cole, Joanne B., Baronas, John M., Yengo, Loic, Marouli, Eirini, Amariuta, Tiffany, Chen, Zhengming, Li, Liming, Renthal, Nora E., Jacobsen, Christina M., Salem, Rany M., Walters, Robin G. and Hirschhorn, Joel N. (2026). Genetics of skeletal proportions across two different populations. American Journal of Human Genetics, 113 (4), 794-808. doi: 10.1016/j.ajhg.2026.02.015 |
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2026 Journal Article Genome-wide fine-mapping improves identification of causal variantsWu, Yang, Zheng, Zhili, Thibaut, Loic, Lin, Tian, Feng, Qian, Cheng, Hao, Yengo, Loic, Goddard, Michael E., Wray, Naomi R., Visscher, Peter M. and Zeng, Jian (2026). Genome-wide fine-mapping improves identification of causal variants. Nature Genetics, 58 (4), 940-951. doi: 10.1038/s41588-026-02549-3 |
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2026 Conference Publication Genome-wide fine-mapping improves identification of causal variantsWu, Yang, Zheng, Zuduo, Thibaut, Loïc, Lin, Tian, Feng, Qian, Cheng, Hao, Yengo, Loic, Goddard, Mike, Wray, Naomi, Visscher, Peter and Zeng, Jian (2026). Genome-wide fine-mapping improves identification of causal variants. Iowa State University Digital Press. doi: 10.31274/wcgalp.23842 |
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2026 Journal Article Distinct genetic profiles influence body mass index between infancy and adolescenceWang, Geng, McEwan, Samuel, Zeng, Jian, Haile-Mariam, Mekonnen, Yengo, Loic, Goddard, Michael E., Kemper, Kathryn E. and Warrington, Nicole M. (2026). Distinct genetic profiles influence body mass index between infancy and adolescence. Nature Communications, 17 (1) 1594, 1-13. doi: 10.1038/s41467-026-69310-6 |
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2026 Journal Article Author Correction: Genome-wide fine-mapping improves identification of causal variants (Nature Genetics, (2026), 58, 4, (940-951), 10.1038/s41588-026-02549-3)Wu, Yang, Zheng, Zhili, Thibaut, Loic, Lin, Tian, Feng, Qian, Cheng, Hao, Yengo, Loic, Goddard, Michael E., Wray, Naomi R., Visscher, Peter M. and Zeng, Jian (2026). Author Correction: Genome-wide fine-mapping improves identification of causal variants (Nature Genetics, (2026), 58, 4, (940-951), 10.1038/s41588-026-02549-3). Nature Genetics, 58 (6), 1446-1446. doi: 10.1038/s41588-026-02627-6 |
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2025 Journal Article Estimation and mapping of the missing heritability of human phenotypesWainschtein, Pierrick, Zhang, Yuanxiang, Schwartzentruber, Jeremy, Kassam, Irfahan, Sidorenko, Julia, Fiziev, Petko P., Wang, Huanwei, McRae, Jeremy, Border, Richard, Zaitlen, Noah, Sankararaman, Sriram, Goddard, Michael E., Zeng, Jian, Visscher, Peter M., Farh, Kyle Kai-How and Yengo, Loic (2025). Estimation and mapping of the missing heritability of human phenotypes. Nature, 649 (8099), 1219-1227. doi: 10.1038/s41586-025-09720-6 |
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2025 Conference Publication Multi-ancestry conditional and joint analysis (MANC-COJO) of GWAS summary statisticsWang, Xiaotong, Wang, Yong, Visscher, Peter, Wray, Naomi and Yengo, Loic (2025). Multi-ancestry conditional and joint analysis (MANC-COJO) of GWAS summary statistics. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.136 |
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2025 Conference Publication A mixture model approach for correcting systematic measurement errors in sitting height data from UK biobankGe, Jieyu, Zeng, Jian, Yengo, Loic and Visscher, Peter (2025). A mixture model approach for correcting systematic measurement errors in sitting height data from UK biobank. 2025 Annual Meeting of the International Genetic Epidemiology Society, Cologne, Germany, 1 - 2 September 2025. Hoboken, NJ, United States: John Wiley & Sons. doi: 10.1002/gepi.70017 |
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2025 Journal Article The contribution of gametic phase disequilibrium to the heritability of complex traitsZhang, Yuanxiang, Sakaue, Saori, Morris, Sam, Graff, Mariaelisa, Yamamoto, Kenichi, Chen, Zhengming, Li, Liming, Keller, Matthew C., Goddard, Michael E., Walters, Robin G., Okada, Yukinori, Visscher, Peter M. and Yengo, Loic (2025). The contribution of gametic phase disequilibrium to the heritability of complex traits. Nature Genetics, 57 (6) e1006495, 1418-1425. doi: 10.1038/s41588-025-02192-4 |
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2025 Journal Article Author Correction: Heritable polygenic editing: the next frontier in genomic medicine?Visscher, Peter M., Gyngell, Christopher, Yengo, Loic and Savulescu, Julian (2025). Author Correction: Heritable polygenic editing: the next frontier in genomic medicine?. Nature, 640 (8058), E5-E5. doi: 10.1038/s41586-025-08904-4 |
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2025 Journal Article Heritable polygenic editing: the next frontier in genomic medicine?Visscher, Peter M., Gyngell, Christopher, Yengo, Loic and Savulescu, Julian (2025). Heritable polygenic editing: the next frontier in genomic medicine?. Nature, 637 (8046) 86, 637-645. doi: 10.1038/s41586-024-08300-4 |
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2025 Journal Article Insights from the largest diverse ancestry sex-specific disease map for genetically predicted heightPapadopoulou, A., Litkowski, E. M., Graff, M., Wang, Z., Smit, R. A. J., Chittoor, G., Dinsmore, I., Josyula, N. S., Lin, M., Shortt, J., Zhu, W., Vedantam, S. L., Yengo, L., Wood, A. R., Berndt, S. I., Holm, I. A., Mentch, F. D., Hakonarson, H., Kiryluk, K., Weng, C., Jarvik, G. P., Crosslin, D., Carrell, D., Kullo, I. J., Dikilitas, O., Hayes, M. G., Wei, W. -Q., Edwards, D. R. V., Assimes, T. L. ... Marouli, E. (2025). Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height. npj Genomic Medicine, 10 (1) 14, 1-10. doi: 10.1038/s41525-025-00464-w |
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2024 Conference Publication Distinct genetic profiles influence body mass index between infancy and adolescenceWang, Geng, McEwan, Samuel, Zeng, Jian, Haile-Mariam, Mekonnen, Yengo, Loic, Goddard, Michael, Kemper, Kathryn and Warrington, Nicole (2024). Distinct genetic profiles influence body mass index between infancy and adolescence. 57th European Society of Human Genetics (ESHG) Conference, Berlin, Germany, 1-4 June 2024. London, United Kingdom: Nature Publishing Group. |
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2024 Journal Article Functional genomics of human skeletal development and the patterning of height heritabilityRichard, Daniel, Muthuirulan, Pushpanathan, Young, Mariel, Yengo, Loic, Vedantam, Sailaja, Marouli, Eirini, Bartell, Eric, Hirschhorn, Joel and Capellini, Terence D. (2024). Functional genomics of human skeletal development and the patterning of height heritability. Cell, 188 (1), 15-32. doi: 10.1016/j.cell.2024.10.040 |
