Jiang L - Search Results

1

Power of transmission/disequilibrium tests in admixed populations.

Li MX, Jiang L, Song YQ, Sham PC. Li MX, et al. Among authors: jiang l. Genet Epidemiol. 2008 Jul;32(5):434-44. doi: 10.1002/gepi.20316. Genet Epidemiol. 2008. PMID: 18278814

2

IGG3: a tool to rapidly integrate large genotype datasets for whole-genome imputation and individual-level meta-analysis.

Li MX, Jiang L, Kao PY, Sham PC, Song YQ. Li MX, et al. Among authors: jiang l. Bioinformatics. 2009 Jun 1;25(11):1449-50. doi: 10.1093/bioinformatics/btp183. Epub 2009 Apr 3. Bioinformatics. 2009. PMID: 19346322

3

A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia.

Li M, Jiang L, Mak TSH, Kwan JSH, Xue C, Chen P, Leung HC, Cui L, Li T, Sham PC. Li M, et al. Among authors: jiang l. Bioinformatics. 2019 Feb 15;35(4):628-635. doi: 10.1093/bioinformatics/bty682. Bioinformatics. 2019. PMID: 30101339

4

WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation counts.

Jiang L, Zheng J, Kwan JSH, Dai S, Li C, Li MJ, Yu B, To KF, Sham PC, Zhu Y, Li M. Jiang L, et al. Nucleic Acids Res. 2019 Sep 19;47(16):e96. doi: 10.1093/nar/gkz566. Nucleic Acids Res. 2019. PMID: 31287869 Free PMC article.

5

DESE: estimating driver tissues by selective expression of genes associated with complex diseases or traits.

Jiang L, Xue C, Dai S, Chen S, Chen P, Sham PC, Wang H, Li M. Jiang L, et al. Genome Biol. 2019 Nov 6;20(1):233. doi: 10.1186/s13059-019-1801-5. Genome Biol. 2019. PMID: 31694669 Free PMC article.

6

Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases.

Jiang L, Jiang H, Dai S, Chen Y, Song Y, Tang CS, Pang SY, Ho SL, Wang B, Garcia-Barcelo MM, Tam PK, Cherny SS, Li MJ, Sham PC, Li M. Jiang L, et al. Among authors: jiang h. Nucleic Acids Res. 2022 Apr 8;50(6):e34. doi: 10.1093/nar/gkab1234. Nucleic Acids Res. 2022. PMID: 34931221 Free PMC article.

7

A conditional gene-based association framework integrating isoform-level eQTL data reveals new susceptibility genes for schizophrenia.

Li X, Jiang L, Xue C, Li MJ, Li M. Li X, et al. Among authors: jiang l. Elife. 2022 Apr 12;11:e70779. doi: 10.7554/eLife.70779. Elife. 2022. PMID: 35412455 Free PMC article.

8

Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization.

Jiang L, Miao L, Yi G, Li X, Xue C, Li MJ, Huang H, Li M. Jiang L, et al. Am J Hum Genet. 2022 May 5;109(5):838-856. doi: 10.1016/j.ajhg.2022.04.004. Epub 2022 Apr 22. Am J Hum Genet. 2022. PMID: 35460606 Free PMC article.

9

Dissecting the high-resolution genetic architecture of complex phenotypes by accurately estimating gene-based conditional heritability.

Miao L, Jiang L, Tang B, Sham PC, Li M. Miao L, et al. Among authors: jiang l. Am J Hum Genet. 2023 Sep 7;110(9):1534-1548. doi: 10.1016/j.ajhg.2023.08.006. Epub 2023 Aug 25. Am J Hum Genet. 2023. PMID: 37633278 Free PMC article.

10

PCGA: a comprehensive web server for phenotype-cell-gene association analysis.

Xue C, Jiang L, Zhou M, Long Q, Chen Y, Li X, Peng W, Yang Q, Li M. Xue C, et al. Among authors: jiang l. Nucleic Acids Res. 2022 Jul 5;50(W1):W568-W576. doi: 10.1093/nar/gkac425. Nucleic Acids Res. 2022. PMID: 35639771 Free PMC article.

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