BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 28789618)

  • 1. Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.
    Chung RH; Chiu YF; Hung YJ; Lee WJ; Wu KD; Chen HL; Lin MW; Chen YI; Quertermous T; Hsiung CA
    BMC Genomics; 2017 Aug; 18(1):591. PubMed ID: 28789618
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Quantitative candidate gene association studies of metabolic traits in Han Chinese type 2 diabetes patients.
    Wei FJ; Cai CY; Yu P; Lv J; Ling C; Shi WT; Jiao HX; Chang BC; Yang FH; Tian Y; Li MS; Wang YH; Zou L; Shi JM; Chen LM; Li WD
    Genet Mol Res; 2015 Dec; 14(4):15471-81. PubMed ID: 26634513
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide copy number variation-, validation- and screening study implicates a new copy number polymorphism associated with suicide attempts in major depressive disorder.
    Rao S; Shi M; Han X; Lam MHB; Chien WT; Zhou K; Liu G; Wing YK; So HC; Waye MMY
    Gene; 2020 Sep; 755():144901. PubMed ID: 32554045
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study.
    Yang HC; Liang YJ; Chen JW; Chiang KM; Chung CM; Ho HY; Ting CT; Lin TH; Sheu SH; Tsai WC; Chen JH; Leu HB; Yin WH; Chiu TY; Chern CL; Lin SJ; Tomlinson B; Guo Y; Sham PC; Cherny SS; Lam TH; Thomas GN; Pan WH
    PLoS One; 2012; 7(3):e32907. PubMed ID: 22479346
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heritability and genome-wide association analyses of fasting plasma glucose in Chinese adult twins.
    Wang W; Zhang C; Liu H; Xu C; Duan H; Tian X; Zhang D
    BMC Genomics; 2020 Jul; 21(1):491. PubMed ID: 32682390
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose.
    Chung RH; Chiu YF; Wang WC; Hwu CM; Hung YJ; Lee IT; Chuang LM; Quertermous T; Rotter JI; Chen YI; Chang IS; Hsiung CA
    Diabetologia; 2021 Jul; 64(7):1613-1625. PubMed ID: 33842983
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity.
    Shrine N; Tobin MD; Schurmann C; Soler Artigas M; Hui J; Lehtimäki T; Raitakari OT; Pennell CE; Ang QW; Strachan DP; Homuth G; Gläser S; Felix SB; Evans DM; Henderson J; Granell R; Palmer LJ; Huffman J; Hayward C; Scotland G; Malarstig A; Musk B; James AL; ; Wain LV
    BMC Genet; 2016 Aug; 17(1):116. PubMed ID: 27514831
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
    Liu J; Zhou Y; Liu S; Song X; Yang XZ; Fan Y; Chen W; Akdemir ZC; Yan Z; Zuo Y; Du R; Liu Z; Yuan B; Zhao S; Liu G; Chen Y; Zhao Y; Lin M; Zhu Q; Niu Y; Liu P; Ikegawa S; Song YQ; Posey JE; Qiu G; ; Zhang F; Wu Z; Lupski JR; Wu N
    Hum Genet; 2018 Jul; 137(6-7):553-567. PubMed ID: 30019117
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy number variations in the genome of the Qatari population.
    Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
    BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus.
    Zhou Y; Utsunomiya YT; Xu L; Hay el HA; Bickhart DM; Alexandre PA; Rosen BD; Schroeder SG; Carvalheiro R; de Rezende Neves HH; Sonstegard TS; Van Tassell CP; Ferraz JB; Fukumasu H; Garcia JF; Liu GE
    BMC Genomics; 2016 Jun; 17():419. PubMed ID: 27245577
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Divergent patterns of genic copy number variation in KCNIP1 gene reveal risk locus of type 2 diabetes in Chinese population.
    Xu Y; Shi W; Song R; Long W; Guo H; Yuan S; Zhang T
    Endocr J; 2018 May; 65(5):537-545. PubMed ID: 29491224
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PPARD rs2016520 polymorphism is associated with metabolic traits in a large population of Chinese adults.
    Tang L; Lü Q; Cao H; Yang Q; Tong N
    Gene; 2016 Jul; 585(2):191-5. PubMed ID: 26915488
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease.
    Frenkel S; Bernstein CN; Sargent M; Kuang Q; Jiang W; Wei J; Thiruvahindrapuram B; Spriggs E; Scherer SW; Hu P
    PLoS One; 2019; 14(6):e0217846. PubMed ID: 31185018
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Associations of MYH3 gene copy number variations with transcriptional expression and growth traits in Chinese cattle.
    Xu Y; Shi T; Cai H; Zhou Y; Lan X; Zhang C; Lei C; Qi X; Chen H
    Gene; 2014 Feb; 535(2):106-11. PubMed ID: 24316128
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease.
    Glessner JT; Li J; Desai A; Palmer M; Kim D; Lucas AM; Chang X; Connolly JJ; Almoguera B; Harley JB; Jarvik GP; Ritchie MD; Sleiman PMA; Roden DM; Crosslin D; Hakonarson H
    Int J Cardiol; 2020 Jan; 298():107-113. PubMed ID: 31447229
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people.
    Lin L; Quan H; Fang T; Lin L; Ou Q; Zhang H; Chen K; Zhou Z
    Endokrynol Pol; 2022; 73(5):856-862. PubMed ID: 35971929
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide Association Study (GWAS) of Germline Copy Number Variations (CNVs) Reveal Genetic Risks of Prostate Cancer in Chinese population.
    Wu Y; Chen H; Jiang G; Mo Z; Ye D; Wang M; Qi J; Lin X; Zheng SL; Zhang N; Na R; Ding Q; Xu J; Sun Y
    J Cancer; 2018; 9(5):923-928. PubMed ID: 29581771
    [No Abstract]   [Full Text] [Related]  

  • 19. Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population.
    Hebbar P; Abu-Farha M; Alkayal F; Nizam R; Elkum N; Melhem M; John SE; Channanath A; Abubaker J; Bennakhi A; Al-Ozairi E; Tuomilehto J; Pitkaniemi J; Alsmadi O; Al-Mulla F; Thanaraj TA
    Sci Rep; 2020 Jan; 10(1):152. PubMed ID: 31932636
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.