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2023

He Y, Zheng W, Guo Y, Yue T, Cui C, Ouzhuluobu, Zhang H, Liu K, et al. (2023), Deep phenotyping of 11,880 highlanders reveals novel adaptive traits in native Tibetans. iScience 26:107677.

Yang J (2023), Expanding the genetic landscape of obesity. Cell Genomics 3:100400.

Wang H, Makowski C, Zhang Y, Qi A, Kaufmann T, Smeland OB, Fiecas M, Yang J, et al. (2023), Chromosomal inversion polymorphisms shape human brain morphology. Cell Reports 42.

Ma Y, Deng C, Zhou Y, Zhang Y, Qiu F, Jiang D, Zheng G, Li J, et al. Polygenic regression uncovers trait-relevant cellular contexts through pathway activation transformation of single-cell RNA sequencing data. Cell Genomics 3:100383.

Zhang R, Fang J, Qi T, Zhu S, Yao L, Fang G, Li Y, Zang X, et al. (2023), Maternal aging increases offspring adult body size via transmission of donut-shaped mitochondria. Cell Research 33:821-834.

Song L, Sun X, Qi T, Yang J (2023), Mixed model-based deconvolution of cell-state abundances (MeDuSA) along a one-dimensional trajectory. Nature Computational Science 3:630-643.

Wu Y, Qi T, Wray NR, Visscher PM, Zeng J, Yang J (2023), Joint analysis of GWAS and multi-omics QTL summary statistics reveals a large fraction of GWAS signals shared with molecular phenotypes. Cell Genomics 3:100344.

Pairo-Castineira E, Rawlik K, Bretherick AD, Qi T, Wu Y, Nassiri I, McConkey GA, Zechner M, et al. (2023), GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19. Nature 617:764-768.

Su J, Yuan J, Xu L, Xing S, Sun M, Yao Y, Ma Y, Chen F, et al. (2023), Sequencing of 19,219 exomes identifies a low-frequency variant in FKBP5 promoter predisposing to high myopia in a Han Chinese population. Cell Reports 42:112510.

Gu Y, Zhang T, Wang J, Song Y, Meng G, Wu H, Zhang S, Wang X, et al. (2023), Genetic risk, muscle strength and risk of incident major depressive disorder: results from the UK Biobank. Age and Ageing 52:afad021.

Makowski C, Wang H, Srinivasan A, Qi A, Qiu Y, van der Meer D, Frei O, Zou J, et al. (2023), Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Proceedings of the National Academy of Sciences 120:e2214834120.

Xu F, Yu EY-W, Cai X, Yue L, Jing L-p, Liang X, Fu Y, Miao Z, et al. (2023), Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature Communications 14:896.

Pan H, Liu Z, Ma J, Li Y, Zhao Y, Zhou X, Xiang Y, Wang Y, et al. (2023), Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese population. npj Parkinson's Disease 9:22.

Gu Y, Song Z, Li Q, Wang J, Song Y, Meng G, Wu H, Zhang S, et al. (2023), Association of thyroid-stimulating hormone with all-cause mortality: A two-sample Mendelian randomization study. The Journal of Clinical Endocrinology & Metabolism 108:e396-e403.

Li A, Liu S, Bakshi A, Jiang L, Chen W, Zheng Z, Sullivan PF, Visscher PM, et al. (2023), mBAT-combo: A more powerful test to detect gene-trait associations from GWAS data. The American Journal of Human Genetics 110:30-43.