These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 29129660)

  • 1. Microduplication of 10q26.3 in a Chinese hypertriglyceridemia patient.
    Li JJ; Chen YQ; Fan LL; Jin JY; Guo S; Xiang R
    Mol Cell Probes; 2018 Feb; 37():28-31. PubMed ID: 29129660
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study.
    Yang TL; Guo Y; Shen H; Li J; Glessner JT; Qiu C; Deng FY; Tian Q; Yu P; Liu YZ; Liu YJ; Hakonarson H; Grant SF; Deng HW
    J Clin Endocrinol Metab; 2013 Jan; 98(1):E191-5. PubMed ID: 23175694
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genome-wide copy number scan in Chinese patients with premature ovarian failure].
    Zhen XM; Sun YM; Qiao J; Li R; Wang LN; Liu P
    Beijing Da Xue Xue Bao Yi Xue Ban; 2013 Dec; 45(6):841-7. PubMed ID: 24343059
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population.
    Sha BY; Yang TL; Zhao LJ; Chen XD; Guo Y; Chen Y; Pan F; Zhang ZX; Dong SS; Xu XH; Deng HW
    J Hum Genet; 2009 Apr; 54(4):199-202. PubMed ID: 19229253
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial
    Dron JS; Wang J; McIntyre AD; Cao H; Robinson JF; Duell PB; Manjoo P; Feng J; Movsesyan I; Malloy MJ; Pullinger CR; Kane JP; Hegele RA
    J Lipid Res; 2019 Nov; 60(11):1953-1958. PubMed ID: 31519763
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Identification of a pathogenic microduplication in a Chinese split-hand/split-foot malformation family].
    Liu Y; Huang Y; Yang W; Zhang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):276-9. PubMed ID: 24928001
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic screening of the lipoprotein lipase gene for mutations in Chinese subjects with or without hypertriglyceridemia.
    Yang Y; Mu Y; Zhao Y; Liu X; Zhao L; Wang J; Xie Y
    J Genet Genomics; 2007 May; 34(5):381-91. PubMed ID: 17560523
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations.
    Yang TL; Guo Y; Li SM; Li SK; Tian Q; Liu YJ; Deng HW
    Int J Obes (Lond); 2013 Feb; 37(2):188-90. PubMed ID: 22391884
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interaction between obesity and genetic polymorphisms in the apolipoprotein CIII gene and lipoprotein lipase gene on the risk of hypertriglyceridemia in Chinese.
    Ko YL; Ko YS; Wu SM; Teng MS; Chen FR; Hsu TS; Chiang CW; Lee YS
    Hum Genet; 1997 Sep; 100(3-4):327-33. PubMed ID: 9272150
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ohnologs are overrepresented in pathogenic copy number mutations.
    McLysaght A; Makino T; Grayton HM; Tropeano M; Mitchell KJ; Vassos E; Collier DA
    Proc Natl Acad Sci U S A; 2014 Jan; 111(1):361-6. PubMed ID: 24368850
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic polymorphisms in CYP2E1: association with schizophrenia susceptibility and risperidone response in the Chinese Han population.
    Huo R; Tang K; Wei Z; Shen L; Xiong Y; Wu X; Niu J; Han X; Tian Z; Yang L; Feng G; He L; Qin S
    PLoS One; 2012; 7(5):e34809. PubMed ID: 22606226
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation.
    Dai L; Deng Y; Li N; Xie L; Mao M; Zhu J
    BMC Med Genet; 2013 Apr; 14():45. PubMed ID: 23596994
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical whole exome sequencing in severe hypertriglyceridemia.
    Tada H; Nomura A; Okada H; Nakahashi T; Nozue T; Hayashi K; Nohara A; Yagi K; Inazu A; Michishita I; Mabuchi H; Yamagishi M; Kawashiri MA
    Clin Chim Acta; 2019 Jan; 488():31-39. PubMed ID: 30389453
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene-gene interaction between CETP and APOE polymorphisms confers higher risk for hypertriglyceridemia in oldest-old Chinese women.
    Sun L; Hu C; Zheng C; Huang Z; Lv Z; Huang J; Liang S; Shi X; Zhu X; Yuan H; Yang Z
    Exp Gerontol; 2014 Jul; 55():129-33. PubMed ID: 24746514
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetic analysis of a pedigree affected with congenital split-hand/foot malformation].
    Li Q; Tong M; Chen C; Ji Y; Zhou K; Xu G; Hu S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):467-470. PubMed ID: 32219839
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe hypertriglyceridemia is primarily polygenic.
    Dron JS; Wang J; Cao H; McIntyre AD; Iacocca MA; Menard JR; Movsesyan I; Malloy MJ; Pullinger CR; Kane JP; Hegele RA
    J Clin Lipidol; 2019; 13(1):80-88. PubMed ID: 30466821
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration.
    Cantsilieris S; White SJ; Richardson AJ; Guymer RH; Baird PN
    PLoS One; 2012; 7(4):e35255. PubMed ID: 22558131
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Frequency of rare mutations and common genetic variations in severe hypertriglyceridemia in the general population of Spain.
    Lamiquiz-Moneo I; Blanco-Torrecilla C; Bea AM; Mateo-Gallego R; Pérez-Calahorra S; Baila-Rueda L; Cenarro A; Civeira F; de Castro-Orós I
    Lipids Health Dis; 2016 Apr; 15():82. PubMed ID: 27108409
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.
    Chen CH; Chen HI; Liao HM; Chen YJ; Fang JS; Lee KF; Gau SS
    Psychiatr Genet; 2017 Feb; 27(1):23-33. PubMed ID: 27846046
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gene copy number variation analysis reveals dosage-insensitive expression of CYP2E1.
    Tremmel R; Klein K; Winter S; Schaeffeler E; Zanger UM
    Pharmacogenomics J; 2016 Nov; 16(6):551-558. PubMed ID: 26503817
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.