Liu X - Search Results

1

Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates.

Liu X, Mei M, Chen X, Lu Y, Dong X, Hu L, Hu X, Cheng G, Cao Y, Yang L, Zhou W. Liu X, et al. Respir Res. 2019 Aug 5;20(1):174. doi: 10.1186/s12931-019-1148-1. Respir Res. 2019. PMID: 31382961 Free PMC article.

2

Clinical features and underlying genetic causes in neonatal encephalopathy: A large cohort study.

Yang L, Chen X, Liu X, Dong X, Ye C, Deng D, Lu Y, Lin Y, Zhou W. Yang L, et al. Among authors: liu x. Clin Genet. 2020 Oct;98(4):365-373. doi: 10.1111/cge.13818. Epub 2020 Sep 4. Clin Genet. 2020. PMID: 32712949

3

Genetic aetiology of early infant deaths in a neonatal intensive care unit.

Yang L, Liu X, Li Z, Zhang P, Wu B, Wang H, Hu L, Cheng G, Wang L, Zhou W. Yang L, et al. Among authors: liu x. J Med Genet. 2020 Mar;57(3):169-177. doi: 10.1136/jmedgenet-2019-106221. Epub 2019 Sep 9. J Med Genet. 2020. PMID: 31501239

4

A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development.

Yu X, Hu L, Liu X, Zhan G, Mei M, Wang H, Zhang X, Qiu Z, Zhou W, Yang L. Yu X, et al. Among authors: liu x. Neurosci Bull. 2018 Oct;34(5):854-858. doi: 10.1007/s12264-018-0236-4. Epub 2018 May 21. Neurosci Bull. 2018. PMID: 29786759 Free PMC article. No abstract available.

5

Clinical exome sequencing revealed that FLNC variants contribute to the early diagnosis of cardiomyopathies in infant patients.

Xiao F, Wei Q, Wu B, Liu X, Mading A, Yang L, Li Y, Liu F, Pan X, Wang H. Xiao F, et al. Among authors: liu x, liu f. Transl Pediatr. 2020 Feb;9(1):21-33. doi: 10.21037/tp.2019.12.02. Transl Pediatr. 2020. PMID: 32154132 Free PMC article.

6

Risk prediction for sporadic Alzheimer's disease using genetic risk score in the Han Chinese population.

Xiao Q, Liu ZJ, Tao S, Sun YM, Jiang D, Li HL, Chen H, Liu X, Lapin B, Wang CH, Zheng SL, Xu J, Wu ZY. Xiao Q, et al. Among authors: liu zj, liu x. Oncotarget. 2015 Nov 10;6(35):36955-64. doi: 10.18632/oncotarget.6271. Oncotarget. 2015. PMID: 26543236 Free PMC article. Clinical Trial.

7

Effect of genetic and coexisting polymorphisms on platelet response to clopidogrel in Chinese Han patients with acute coronary syndrome.

Liu X, Luo Y, Lai Y, Yao Y, Li J, Wang Y, Zheng SL, Xu J, Liu X. Liu X, et al. J Genet. 2016 Jun;95(2):231-7. doi: 10.1007/s12041-016-0618-1. J Genet. 2016. PMID: 27350664

8

Preimplantation genetic haplotyping for six Chinese pedigrees with thalassemia using a single nucleotide polymorphism microarray.

Liu X, Xu Y, Sun J, Zhang Z, Wang J, Ding C, Zheng SL, Xu J, Zhou C. Liu X, et al. Prenat Diagn. 2017 May;37(5):460-468. doi: 10.1002/pd.5033. Epub 2017 Mar 27. Prenat Diagn. 2017. PMID: 28258706

9

Adding genetic risk score to family history identifies twice as many high-risk men for prostate cancer: Results from the prostate cancer prevention trial.

Chen H, Liu X, Brendler CB, Ankerst DP, Leach RJ, Goodman PJ, Lucia MS, Tangen CM, Wang L, Hsu FC, Sun J, Kader AK, Isaacs WB, Helfand BT, Zheng SL, Thompson IM, Platz EA, Xu J. Chen H, et al. Among authors: liu x. Prostate. 2016 Sep;76(12):1120-9. doi: 10.1002/pros.23200. Epub 2016 May 16. Prostate. 2016. PMID: 27197965 Free PMC article. Clinical Trial.

10

Correlations between CYP3A4 polymorphism and susceptibility to breast cancer in Chinese Han population.

Liu X, Huang X, Zhang S, Niu F, Ouyang Y, Shou Z, Liu J. Liu X, et al. Among authors: liu j. Int J Clin Oncol. 2019 Feb;24(2):179-188. doi: 10.1007/s10147-018-1346-8. Epub 2018 Sep 14. Int J Clin Oncol. 2019. PMID: 30218411

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