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 *

355 related articles for article (PubMed ID: 30704416)

  • 81. Genome-wide scan of African-American and white families for linkage to myopia.
    Ciner E; Ibay G; Wojciechowski R; Dana D; Holmes TN; Bailey-Wilson JE; Stambolian D
    Am J Ophthalmol; 2009 Mar; 147(3):512-517.e2. PubMed ID: 19026404
    [TBL] [Abstract][Full Text] [Related]  

  • 82. Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.
    Cicek MS; Cunningham JM; Fridley BL; Serie DJ; Bamlet WR; Diergaarde B; Haile RW; Le Marchand L; Krontiris TG; Younghusband HB; Gallinger S; Newcomb PA; Hopper JL; Jenkins MA; Casey G; Schumacher F; Chen Z; DeRycke MS; Templeton AS; Winship I; Green RC; Green JS; Macrae FA; Parry S; Young GP; Young JP; Buchanan D; Thomas DC; Bishop DT; Lindor NM; Thibodeau SN; Potter JD; Goode EL;
    PLoS One; 2012; 7(5):e38175. PubMed ID: 22675446
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Linkage analysis of circulating levels of adiponectin in Hispanic children.
    Tejero ME; Cai G; Göring HH; Diego V; Cole SA; Bacino CA; Butte NF; Comuzzie AG
    Int J Obes (Lond); 2007 Mar; 31(3):535-42. PubMed ID: 16894363
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13.
    Costantino F; Chaplais E; Leturcq T; Said-Nahal R; Leboime A; Zinovieva E; Zelenika D; Gut I; Charon C; Chiocchia G; Breban M; Garchon HJ
    Ann Rheum Dis; 2016 Jul; 75(7):1380-5. PubMed ID: 26275432
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.
    Li J; Gao B; Guan L; Xiao X; Zhang J; Li S; Jiang H; Jia X; Yang J; Guo X; Yin Y; Wang J; Zhang Q
    Invest Ophthalmol Vis Sci; 2015 Jun; 56(6):4150-5. PubMed ID: 26114493
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Genome-wide study of families with absolute pitch reveals linkage to 8q24.21 and locus heterogeneity.
    Theusch E; Basu A; Gitschier J
    Am J Hum Genet; 2009 Jul; 85(1):112-9. PubMed ID: 19576568
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12.
    Schäche M; Chen CY; Pertile KK; Richardson AJ; Dirani M; Mitchell P; Baird PN
    Mol Vis; 2009; 15():722-30. PubMed ID: 19365569
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Deciphering the genetics of hereditary non-syndromic colorectal cancer.
    Papaemmanuil E; Carvajal-Carmona L; Sellick GS; Kemp Z; Webb E; Spain S; Sullivan K; Barclay E; Lubbe S; Jaeger E; Vijayakrishnan J; Broderick P; Gorman M; Martin L; Lucassen A; Bishop DT; Evans DG; Maher ER; Steinke V; Rahner N; Schackert HK; Goecke TO; Holinski-Feder E; Propping P; Van Wezel T; Wijnen J; Cazier JB; Thomas H; Houlston RS; Tomlinson I;
    Eur J Hum Genet; 2008 Dec; 16(12):1477-86. PubMed ID: 18628789
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.
    Ratnamala U; Lyle R; Rawal R; Singh R; Vishnupriya S; Himabindu P; Rao V; Aggarwal S; Paluru P; Bartoloni L; Young TL; Paoloni-Giacobino A; Morris MA; Nath SK; Antonarakis SE; Radhakrishna U
    Invest Ophthalmol Vis Sci; 2011 Aug; 52(9):6814-9. PubMed ID: 21357393
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer.
    Toma C; Díaz-Gay M; Franch-Expósito S; Arnau-Collell C; Overs B; Muñoz J; Bonjoch L; Soares de Lima Y; Ocaña T; Cuatrecasas M; Castells A; Bujanda L; Balaguer F; Cubiella J; Caldés T; Fullerton JM; Castellví-Bel S
    Int J Cancer; 2020 Mar; 146(6):1568-1577. PubMed ID: 31525256
    [TBL] [Abstract][Full Text] [Related]  

  • 91. A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.
    Zhang Q; Guo X; Xiao X; Jia X; Li S; Hejtmancik JF
    Mol Vis; 2005 Jul; 11():554-60. PubMed ID: 16052171
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Chromosome 2p14 is linked to susceptibility to leprosy.
    Yang Q; Liu H; Low HQ; Wang H; Yu Y; Fu X; Yu G; Chen M; Yan X; Chen S; Huang W; Liu J; Zhang F
    PLoS One; 2012; 7(1):e29747. PubMed ID: 22238647
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismus.
    Shaaban S; Matsuo T; Fujiwara H; Itoshima E; Furuse T; Hasebe S; Zhang Q; Ott J; Ohtsuki H
    Invest Ophthalmol Vis Sci; 2009 Feb; 50(2):654-61. PubMed ID: 18824738
    [TBL] [Abstract][Full Text] [Related]  

  • 94. A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11.
    Kinirons P; Verlaan DJ; Dubé MP; Poirier J; Deacon C; Lortie A; Clément JF; Desbiens R; Carmant L; Cieuta-Walti C; Shevell M; Rouleau GA; Cossette P
    Am J Med Genet A; 2008 Mar; 146A(5):578-84. PubMed ID: 18241056
    [TBL] [Abstract][Full Text] [Related]  

  • 95. Familial high myopia linkage to chromosome 18p.
    Lam DS; Tam PO; Fan DS; Baum L; Leung YF; Pang CP
    Ophthalmologica; 2003; 217(2):115-8. PubMed ID: 12592049
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease.
    Schiff ER; Frampton M; Ben-Yosef N; Avila BE; Semplici F; Pontikos N; Bloom SL; McCartney SA; Vega R; Lovat LB; Wood E; Hart A; Israeli E; Crespi D; Furman MA; Mann S; Murray CD; Segal AW; Levine AP
    Hum Genet; 2018 Sep; 137(9):723-734. PubMed ID: 30167848
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.
    Simpson CL; Wojciechowski R; Oexle K; Murgia F; Portas L; Li X; Verhoeven VJ; Vitart V; Schache M; Hosseini SM; Hysi PG; Raffel LJ; Cotch MF; Chew E; Klein BE; Klein R; Wong TY; van Duijn CM; Mitchell P; Saw SM; Fossarello M; Wang JJ; ; Polašek O; Campbell H; Rudan I; Oostra BA; Uitterlinden AG; Hofman A; Rivadeneira F; Amin N; Karssen LC; Vingerling JR; Döring A; Bettecken T; Bencic G; Gieger C; Wichmann HE; Wilson JF; Venturini C; Fleck B; Cumberland PM; Rahi JS; Hammond CJ; Hayward C; Wright AF; Paterson AD; Baird PN; Klaver CC; Rotter JI; Pirastu M; Meitinger T; Bailey-Wilson JE; Stambolian D
    PLoS One; 2014; 9(9):e107110. PubMed ID: 25233373
    [TBL] [Abstract][Full Text] [Related]  

  • 98. An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome.
    Jaeger EE; Woodford-Richens KL; Lockett M; Rowan AJ; Sawyer EJ; Heinimann K; Rozen P; Murday VA; Whitelaw SC; Ginsberg A; Atkin WS; Lynch HT; Southey MC; Debinski H; Eng C; Bodmer WF; Talbot IC; Hodgson SV; Thomas HJ; Tomlinson IP
    Am J Hum Genet; 2003 May; 72(5):1261-7. PubMed ID: 12696020
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families.
    Bailey-Wilson JE; Childs EJ; Cropp CD; Schaid DJ; Xu J; Camp NJ; Cannon-Albright LA; Farnham JM; George A; Powell I; Carpten JD; Giles GG; Hopper JL; Severi G; English DR; Foulkes WD; Mæhle L; Møller P; Eeles R; Easton D; Guy M; Edwards S; Badzioch MD; Whittemore AS; Oakley-Girvan I; Hsieh CL; Dimitrov L; Stanford JL; Karyadi DM; Deutsch K; McIntosh L; Ostrander EA; Wiley KE; Isaacs SD; Walsh PC; Thibodeau SN; McDonnell SK; Hebbring S; Lange EM; Cooney KA; Tammela TL; Schleutker J; Maier C; Bochum S; Hoegel J; Grönberg H; Wiklund F; Emanuelsson M; Cancel-Tassin G; Valeri A; Cussenot O; Isaacs WB;
    BMC Med Genet; 2012 Jun; 13():46. PubMed ID: 22712434
    [TBL] [Abstract][Full Text] [Related]  

  • 100. American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12.
    Brant SR; Fu Y; Fields CT; Baltazar R; Ravenhill G; Pickles MR; Rohal PM; Mann J; Kirschner BS; Jabs EW; Bayless TM; Hanauer SB; Cho JH
    Gastroenterology; 1998 Nov; 115(5):1056-61. PubMed ID: 9797357
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.