BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 12402251)

  • 1. A susceptibility gene for late-onset idiopathic Parkinson's disease.
    Hicks AA; Pétursson H; Jónsson T; Stefánsson H; Jóhannsdóttir HS; Sainz J; Frigge ML; Kong A; Gulcher JR; Stefánsson K; Sveinbjörnsdóttir S
    Ann Neurol; 2002 Nov; 52(5):549-55. PubMed ID: 12402251
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [The alpha-synuclein gene microsatellite polymorphism and late-onset sporadic Parkinson's disease susceptibility].
    Zhao XP; Zheng HM; Xie HJ; Ding SJ; Ren DM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):339-41. PubMed ID: 15300629
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New Alzheimer's disease locus on chromosome 8.
    Giedraitis V; Hedlund M; Skoglund L; Blom E; Ingvast S; Brundin R; Lannfelt L; Glaser A
    J Med Genet; 2006 Dec; 43(12):931-5. PubMed ID: 16825432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.
    Pankratz N; Nichols WC; Uniacke SK; Halter C; Murrell J; Rudolph A; Shults CW; Conneally PM; Foroud T;
    Hum Mol Genet; 2003 Oct; 12(20):2599-608. PubMed ID: 12925570
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage.
    Thompson SD; Moroldo MB; Guyer L; Ryan M; Tombragel EM; Shear ES; Prahalad S; Sudman M; Keddache MA; Brown WM; Giannini EH; Langefeld CD; Rich SS; Nichols WC; Glass DN
    Arthritis Rheum; 2004 Sep; 50(9):2920-30. PubMed ID: 15457461
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new locus for coeliac disease mapped to chromosome 15 in a population isolate.
    Woolley N; Holopainen P; Ollikainen V; Mustalahti K; Mäki M; Kere J; Partanen J
    Hum Genet; 2002 Jul; 111(1):40-5. PubMed ID: 12136234
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q.
    Curtis D; Kalsi G; Brynjolfsson J; McInnis M; O'Neill J; Smyth C; Moloney E; Murphy P; McQuillin A; Petursson H; Gurling H
    Psychiatr Genet; 2003 Jun; 13(2):77-84. PubMed ID: 12782963
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes.
    Chu K; Koller DL; Snyder R; Fishburn T; Lai D; Waguespack SG; Foroud T; Econs MJ
    Bone; 2005 Nov; 37(5):655-61. PubMed ID: 16120485
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of a susceptibility locus for SLE, SLEB5, on chromosome 4p14-13.
    Johansson CM; Kristjánsdottir H; Gröndal G; Steinsson K; Alarcón-Riquelme ME
    Scand J Immunol; 2006 Sep; 64(3):308-13. PubMed ID: 16918700
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Collection of a Chinese pedigree with Parkinson's disease and linkage analysis of nine susceptibility genes].
    Sun H; Zhang CJ; Shu Q; Tian YY; Shi L; Yu JK; Qian YP; Chu JY
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2006 Jun; 28(3):368-71. PubMed ID: 16900635
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Mapping of a familial essential tremor gene, FET1, to chromosome 3q13.
    Gulcher JR; Jónsson P; Kong A; Kristjánsson K; Frigge ML; Kárason A; Einarsdóttir IE; Stefánsson H; Einarsdóttir AS; Sigurthoardóttir S; Baldursson S; Björnsdóttir S; Hrafnkelsdóttir SM; Jakobsson F; Benedickz J; Stefánsson K
    Nat Genet; 1997 Sep; 17(1):84-7. PubMed ID: 9288103
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome scan on Swedish Alzheimer's disease families.
    Sillén A; Forsell C; Lilius L; Axelman K; Björk BF; Onkamo P; Kere J; Winblad B; Graff C
    Mol Psychiatry; 2006 Feb; 11(2):182-6. PubMed ID: 16288313
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations.
    Sharma M; Mueller JC; Zimprich A; Lichtner P; Hofer A; Leitner P; Maass S; Berg D; Dürr A; Bonifati V; De Michele G; Oostra B; Brice A; Wood NW; Muller-Myhsok B; Gasser T;
    J Med Genet; 2006 Jul; 43(7):557-62. PubMed ID: 16443856
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12.
    Shink E; Morissette J; Sherrington R; Barden N
    Mol Psychiatry; 2005 Jun; 10(6):545-52. PubMed ID: 15494705
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I; Camuzat A; Berger E; Hannequin D; Laquerrière A; Golfier V; Seilhean D; Viennet G; Couratier P; Verpillat P; Heath S; Camu W; Martinaud O; Lacomblez L; Vercelletto M; Salachas F; Sellal F; Didic M; Thomas-Anterion C; Puel M; Michel BF; Besse C; Duyckaerts C; Meininger V; Campion D; Dubois B; Brice A;
    Neurology; 2009 May; 72(19):1669-76. PubMed ID: 19433740
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease.
    Martinez M; Brice A; Vaughan JR; Zimprich A; Breteler MM; Meco G; Filla A; Farrer MJ; Bétard C; Hardy J; De Michele G; Bonifati V; Oostra B; Gasser T; Wood NW; Dürr A; ;
    J Med Genet; 2004 Dec; 41(12):900-7. PubMed ID: 15591275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes.
    Gasser T; Wszolek ZK; Trofatter J; Ozelius L; Uitti RJ; Lee CS; Gusella J; Pfeiffer RF; Calne DB; Breakefield XO
    Ann Neurol; 1994 Sep; 36(3):387-96. PubMed ID: 7915897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q.
    Dauvilliers Y; Blouin JL; Neidhart E; Carlander B; Eliaou JF; Antonarakis SE; Billiard M; Tafti M
    Ann Neurol; 2004 Sep; 56(3):382-8. PubMed ID: 15349865
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.