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Journal Abstract Search

174 related items for PubMed ID: 18301393

  • 1. Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.
    Romanos M, Freitag C, Jacob C, Craig DW, Dempfle A, Nguyen TT, Halperin R, Walitza S, Renner TJ, Seitz C, Romanos J, Palmason H, Reif A, Heine M, Windemuth-Kieselbach C, Vogler C, Sigmund J, Warnke A, Schäfer H, Meyer J, Stephan DA, Lesch KP.
    Mol Psychiatry; 2008 May; 13(5):522-30. PubMed ID: 18301393
    [Abstract] [Full Text] [Related]

  • 2. Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
    Friedel S, Saar K, Sauer S, Dempfle A, Walitza S, Renner T, Romanos M, Freitag C, Seitz C, Palmason H, Scherag A, Windemuth-Kieselbach C, Schimmelmann BG, Wewetzer C, Meyer J, Warnke A, Lesch KP, Reinhardt R, Herpertz-Dahlmann B, Linder M, Hinney A, Remschmidt H, Schäfer H, Konrad K, Hübner N, Hebebrand J.
    Mol Psychiatry; 2007 Oct; 12(10):923-33. PubMed ID: 17579611
    [Abstract] [Full Text] [Related]

  • 3. A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.
    Hebebrand J, Dempfle A, Saar K, Thiele H, Herpertz-Dahlmann B, Linder M, Kiefl H, Remschmidt H, Hemminger U, Warnke A, Knölker U, Heiser P, Friedel S, Hinney A, Schäfer H, Nürnberg P, Konrad K.
    Mol Psychiatry; 2006 Feb; 11(2):196-205. PubMed ID: 16222334
    [Abstract] [Full Text] [Related]

  • 4. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
    Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
    [Abstract] [Full Text] [Related]

  • 5. Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan.
    Kemp Z, Carvajal-Carmona L, Spain S, Barclay E, Gorman M, Martin L, Jaeger E, Brooks N, Bishop DT, Thomas H, Tomlinson I, Papaemmanuil E, Webb E, Sellick GS, Wood W, Evans G, Lucassen A, Maher ER, Houlston RS, ColoRectal tumour Gene Identification (CoRGI) Study Consortium.
    Hum Mol Genet; 2006 Oct 01; 15(19):2903-10. PubMed ID: 16923799
    [Abstract] [Full Text] [Related]

  • 6. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.
    Loo SK, Fisher SE, Francks C, Ogdie MN, MacPhie IL, Yang M, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL.
    Mol Psychiatry; 2004 May 01; 9(5):485-93. PubMed ID: 14625563
    [Abstract] [Full Text] [Related]

  • 7. Distinct loci on chromosome 1q21 and 6q22 predispose to familial nonmedullary thyroid cancer: a SNP array-based linkage analysis of 38 families.
    Suh I, Filetti S, Vriens MR, Guerrero MA, Tumino S, Wong M, Shen WT, Kebebew E, Duh QY, Clark OH.
    Surgery; 2009 Dec 01; 146(6):1073-80. PubMed ID: 19958934
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 37(5):655-61. PubMed ID: 16120485
    [Abstract] [Full Text] [Related]

  • 9. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.
    Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M, Park N, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Knowles JA, Ott J, Gilliam TC, Baron M.
    Mol Psychiatry; 2003 Mar 01; 8(3):333-42. PubMed ID: 12660806
    [Abstract] [Full Text] [Related]

  • 10. Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.
    Gayán J, Willcutt EG, Fisher SE, Francks C, Cardon LR, Olson RK, Pennington BF, Smith SD, Monaco AP, DeFries JC.
    J Child Psychol Psychiatry; 2005 Oct 01; 46(10):1045-56. PubMed ID: 16178928
    [Abstract] [Full Text] [Related]

  • 11. Genome-wide linkage scan for bladder exstrophy-epispadias complex.
    Ludwig M, Rüschendorf F, Saar K, Hübner N, Siekmann L, Boyadjiev SA, Reutter H.
    Birth Defects Res A Clin Mol Teratol; 2009 Feb 01; 85(2):174-8. PubMed ID: 19086019
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 50(3):1081-6. PubMed ID: 18978346
    [Abstract] [Full Text] [Related]

  • 13. Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica.
    DeLisi LE, Mesen A, Rodriguez C, Bertheau A, LaPrade B, Llach M, Riondet S, Razi K, Relja M, Byerley W, Sherrington R.
    Am J Med Genet; 2002 Jul 08; 114(5):497-508. PubMed ID: 12116183
    [Abstract] [Full Text] [Related]

  • 14. Genome-wide linkage scan of schizophrenia: a cross-isolate study.
    Bulayeva KB, Glatt SJ, Bulayev OA, Pavlova TA, Tsuang MT.
    Genomics; 2007 Feb 08; 89(2):167-77. PubMed ID: 17140763
    [Abstract] [Full Text] [Related]

  • 15. A genome-wide scan maps a novel high myopia locus to 5p15.
    Lam CY, Tam PO, Fan DS, Fan BJ, Wang DY, Lee CW, Pang CP, Lam DS.
    Invest Ophthalmol Vis Sci; 2008 Sep 08; 49(9):3768-78. PubMed ID: 18421076
    [Abstract] [Full Text] [Related]

  • 16. Review: Genetics of attention deficit/hyperactivity disorder.
    Wallis D, Russell HF, Muenke M.
    J Pediatr Psychol; 2008 Sep 08; 33(10):1085-99. PubMed ID: 18522996
    [Abstract] [Full Text] [Related]

  • 17. Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.
    Walitza S, Renner TJ, Dempfle A, Konrad K, Wewetzer Ch, Halbach A, Herpertz-Dahlmann B, Remschmidt H, Smidt J, Linder M, Flierl L, Knölker U, Friedel S, Schäfer H, Gross C, Hebebrand J, Warnke A, Lesch KP.
    Mol Psychiatry; 2005 Dec 08; 10(12):1126-32. PubMed ID: 16116490
    [Abstract] [Full Text] [Related]

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  • 20. Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies.
    Dempfle A, Wudy SA, Saar K, Hagemann S, Friedel S, Scherag A, Berthold LD, Alzen G, Gortner L, Blum WF, Hinney A, Nürnberg P, Schäfer H, Hebebrand J.
    Hum Mol Genet; 2006 Sep 15; 15(18):2772-83. PubMed ID: 16905557
    [Abstract] [Full Text] [Related]

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