Li J - Search Results

1

Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes.

Li K, Ling Z, Luo T, Zhao G, Zhou Q, Wang X, Xia K, Li J, Li B. Li K, et al. Among authors: li j, li b. Life (Basel). 2021 Mar 12;11(3):233. doi: 10.3390/life11030233. Life (Basel). 2021. PMID: 33809095 Free PMC article.

2

mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.

Li J, Jiang Y, Wang T, Chen H, Xie Q, Shao Q, Ran X, Xia K, Sun ZS, Wu J. Li J, et al. J Med Genet. 2015 Apr;52(4):275-81. doi: 10.1136/jmedgenet-2014-102656. Epub 2015 Jan 16. J Med Genet. 2015. PMID: 25596308

3

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.

Li J, Cai T, Jiang Y, Chen H, He X, Chen C, Li X, Shao Q, Ran X, Li Z, Xia K, Liu C, Sun ZS, Wu J. Li J, et al. Among authors: li z, li x. Mol Psychiatry. 2016 Feb;21(2):290-7. doi: 10.1038/mp.2015.40. Epub 2015 Apr 7. Mol Psychiatry. 2016. PMID: 25849321 Free PMC article.

4

Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.

Li J, Wang L, Yu P, Shi L, Zhang K, Sun ZS, Xia K. Li J, et al. Am J Med Genet B Neuropsychiatr Genet. 2017 Jul;174(5):568-577. doi: 10.1002/ajmg.b.32543. Epub 2017 Apr 13. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28407358

5

Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.

Li J, Wang L, Guo H, Shi L, Zhang K, Tang M, Hu S, Dong S, Liu Y, Wang T, Yu P, He X, Hu Z, Zhao J, Liu C, Sun ZS, Xia K. Li J, et al. Mol Psychiatry. 2017 Sep;22(9):1282-1290. doi: 10.1038/mp.2017.140. Epub 2017 Jul 25. Mol Psychiatry. 2017. PMID: 28831199

6

A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.

Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, Wu J, Xia K, Noonan JP, Sun ZS, He X. Liu Y, et al. Among authors: li z, li j. Am J Hum Genet. 2018 Jun 7;102(6):1031-1047. doi: 10.1016/j.ajhg.2018.03.023. Epub 2018 May 10. Am J Hum Genet. 2018. PMID: 29754769 Free PMC article.

7

A comparative study of the genetic components of three subcategories of autism spectrum disorder.

Li J, Hu S, Zhang K, Shi L, Zhang Y, Zhao T, Wang L, He X, Xia K, Liu C, Sun Z. Li J, et al. Mol Psychiatry. 2019 Nov;24(11):1720-1731. doi: 10.1038/s41380-018-0081-x. Epub 2018 Jun 6. Mol Psychiatry. 2019. PMID: 29875476

8

PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior.

Wang Y, Zeng C, Li J, Zhou Z, Ju X, Xia S, Li Y, Liu A, Teng H, Zhang K, Shi L, Bi C, Xie W, He X, Jia Z, Jiang Y, Cai T, Wu J, Xia K, Sun ZS. Wang Y, et al. Among authors: li y, li j. Cell Rep. 2018 Aug 21;24(8):2029-2041. doi: 10.1016/j.celrep.2018.07.061. Cell Rep. 2018. PMID: 30134165 Free article.

9

Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy.

Zeng S, Zhang MY, Wang XJ, Hu ZM, Li JC, Li N, Wang JL, Liang F, Yang Q, Liu Q, Fang L, Hao JW, Shi FD, Ding XB, Teng JF, Yin XM, Jiang H, Liao WP, Liu JY, Wang K, Xia K, Tang BS. Zeng S, et al. J Med Genet. 2019 Apr;56(4):265-270. doi: 10.1136/jmedgenet-2018-105484. Epub 2018 Sep 7. J Med Genet. 2019. PMID: 30194086

10

Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.

Wu J, Yu P, Jin X, Xu X, Li J, Li Z, Wang M, Wang T, Wu X, Jiang Y, Cai W, Mei J, Min Q, Xu Q, Zhou B, Guo H, Wang P, Zhou W, Hu Z, Li Y, Cai T, Wang Y, Xia K, Jiang YH, Sun ZS. Wu J, et al. Among authors: li y, li j, li z. J Genet Genomics. 2018 Oct 20;45(10):527-538. doi: 10.1016/j.jgg.2018.09.002. Epub 2018 Oct 21. J Genet Genomics. 2018. PMID: 30392784

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