BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 21041550)

  • 1. The identification of a novel locus for mandibular prognathism in the Han Chinese population.
    Li Q; Li X; Zhang F; Chen F
    J Dent Res; 2011 Jan; 90(1):53-7. PubMed ID: 21041550
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome scan for locus involved in mandibular prognathism in pedigrees from China.
    Li Q; Zhang F; Li X; Chen F
    PLoS One; 2010 Sep; 5(9):. PubMed ID: 20844756
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K; Neumann A; Kleensang A; Lohnau T; Muhle H; Djarmati A; König IR; Pramstaller PP; Schwinger E; Kramer PL; Ziegler A; Stephani U; Klein C
    Neurology; 2008 Feb; 70(9):686-94. PubMed ID: 18032746
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
    Holliday EG; McLean DE; Nyholt DR; Mowry BJ
    Arch Gen Psychiatry; 2009 Oct; 66(10):1058-67. PubMed ID: 19805696
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microsatellite genome-wide association study for mandibular prognathism.
    Ikuno K; Kajii TS; Oka A; Inoko H; Ishikawa H; Iida J
    Am J Orthod Dentofacial Orthop; 2014 Jun; 145(6):757-62. PubMed ID: 24880846
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R
    Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
    Zhang Q; Guo X; Xiao X; Yi J; Jia X; Hejtmancik JF
    Mol Vis; 2004 Nov; 10():890-900. PubMed ID: 15570218
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.
    Wilson SG; Adam G; Langdown M; Reneland R; Braun A; Andrew T; Surdulescu GL; Norberg M; Dudbridge F; Reed PW; Sambrook PN; Kleyn PW; Spector TD
    Eur J Hum Genet; 2006 Mar; 14(3):340-8. PubMed ID: 16391564
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genomewide scan and fine mapping of quantitative trait loci for intraocular pressure on 5q and 14q in West Africans.
    Rotimi CN; Chen G; Adeyemo AA; Jones LS; Agyenim-Boateng K; Eghan BA; Zhou J; Doumatey A; Lashley K; Huang H; Fasanmade O; Akinsola FB; Ezepue F; Amoah A; Akafo S; Chen Y; Oli J; Johnson T
    Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3262-7. PubMed ID: 16877390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR
    Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
    Ocaka L; Zhao C; Reed JA; Ebenezer ND; Brice G; Morley T; Mehta M; O'Dowd J; Weber JL; Hardcastle AJ; Child AH
    J Med Genet; 2008 Feb; 45(2):87-92. PubMed ID: 17932119
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage analysis in keratoconus: replication of locus 5q21.2 and identification of other suggestive Loci.
    Bisceglia L; De Bonis P; Pizzicoli C; Fischetti L; Laborante A; Di Perna M; Giuliani F; Delle Noci N; Buzzonetti L; Zelante L
    Invest Ophthalmol Vis Sci; 2009 Mar; 50(3):1081-6. PubMed ID: 18978346
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P; Blair MA; Andermann E; Andermann F; D'Agostino D; Taylor KA; Chahine L; Pandolfo M; Bradford Y; Haines JL; Abou-Khalil B
    Neurology; 2007 Jun; 68(24):2107-12. PubMed ID: 17377072
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A genomewide scan for the susceptibility gene loci to ankylosing spondylitis in Chinese Han population].
    Gu MM; Yuan WT; Yang JQ; Zhang J; Xiong XY; Yao FJ; Lu ZY; Wang ZG; Huang W; Fan LA
    Yi Chuan Xue Bao; 2004 Mar; 31(3):217-20. PubMed ID: 15195556
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.
    de Kovel CG; Hol FA; Heister JG; Willemen JJ; Sandkuijl LA; Franke B; Padberg GW
    J Med Genet; 2004 Sep; 41(9):652-7. PubMed ID: 15342694
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population].
    Cai G; Wu X; Li T; Collier DA; Liu X; Feng B; Deng H; Tong D; Li J; Ou J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Dec; 19(6):491-4. PubMed ID: 12476422
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.
    Ye X; Shi L; Yin W; Meng L; Wang QK; Bian Z
    J Clin Periodontol; 2009 Aug; 36(8):627-33. PubMed ID: 19552635
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymorphisms in the Matrilin-1 gene and risk of mandibular prognathism in Koreans.
    Jang JY; Park EK; Ryoo HM; Shin HI; Kim TH; Jang JS; Park HS; Choi JY; Kwon TG
    J Dent Res; 2010 Nov; 89(11):1203-7. PubMed ID: 20739701
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.