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Journal Abstract Search

337 related items for PubMed ID: 23190410

  • 1. Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.
    Field LL, Shumansky K, Ryan J, Truong D, Swiergala E, Kaplan BJ.
    Genes Brain Behav; 2013 Feb; 12(1):56-69. PubMed ID: 23190410
    [Abstract] [Full Text] [Related]

  • 2. Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.
    Arcos-Burgos M, Castellanos FX, Pineda D, Lopera F, Palacio JD, Palacio LG, Rapoport JL, Berg K, Bailey-Wilson JE, Muenke M.
    Am J Hum Genet; 2004 Dec; 75(6):998-1014. PubMed ID: 15497111
    [Abstract] [Full Text] [Related]

  • 3. Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.
    Nijmeijer JS, Arias-Vásquez A, Rommelse NN, Altink ME, Anney RJ, Asherson P, Banaschewski T, Buschgens CJ, Fliers EA, Gill M, Minderaa RB, Poustka L, Sergeant JA, Buitelaar JK, Franke B, Ebstein RP, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sonuga-Barke EJ, Steinhausen HC, Faraone SV, Hartman CA, Hoekstra PJ.
    J Am Acad Child Adolesc Psychiatry; 2010 Jul; 49(7):675-85. PubMed ID: 20610137
    [Abstract] [Full Text] [Related]

  • 4. The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.
    Strug LJ, Addis L, Chiang T, Baskurt Z, Li W, Clarke T, Hardison H, Kugler SL, Mandelbaum DE, Novotny EJ, Wolf SM, Pal DK.
    PLoS One; 2012 Jul; 7(7):e40696. PubMed ID: 22815793
    [Abstract] [Full Text] [Related]

  • 5. Toward localizing genes underlying cerebral asymmetry and mental health.
    Smalley SL, Loo SK, Yang MH, Cantor RM.
    Am J Med Genet B Neuropsychiatr Genet; 2005 May 05; 135B(1):79-84. PubMed ID: 15806584
    [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 05; 9(5):485-93. PubMed ID: 14625563
    [Abstract] [Full Text] [Related]

  • 7. 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 05; 13(5):522-30. PubMed ID: 18301393
    [Abstract] [Full Text] [Related]

  • 8. A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.
    Kaminen N, Hannula-Jouppi K, Kestilä M, Lahermo P, Muller K, Kaaranen M, Myllyluoma B, Voutilainen A, Lyytinen H, Nopola-Hemmi J, Kere J.
    J Med Genet; 2003 May 05; 40(5):340-5. PubMed ID: 12746395
    [Abstract] [Full Text] [Related]

  • 9. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.
    Schmidt S, Scott WK, Postel EA, Agarwal A, Hauser ER, De La Paz MA, Gilbert JR, Weeks DE, Gorin MB, Haines JL, Pericak-Vance MA.
    BMC Genet; 2004 Jul 06; 5():18. PubMed ID: 15238159
    [Abstract] [Full Text] [Related]

  • 10. Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.
    Zhou K, Asherson P, Sham P, Franke B, Anney RJ, Buitelaar J, Ebstein R, Gill M, Brookes K, Buschgens C, Campbell D, Chen W, Christiansen H, Fliers E, Gabriëls I, Johansson L, Marco R, Mulas F, Müller U, Mulligan A, Neale BM, Rijsdijk F, Rommelse N, Uebel H, Psychogiou L, Xu X, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Faraone SV.
    Biol Psychiatry; 2008 Oct 01; 64(7):571-6. PubMed ID: 18439570
    [Abstract] [Full Text] [Related]

  • 11. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
    Hoffmann K, Mattheisen M, Dahm S, Nürnberg P, Roe C, Johnson J, Cox NJ, Wichmann HE, Wienker TF, Schulze J, Schwarz PE, Lindner TH.
    Diabetologia; 2007 Jul 01; 50(7):1418-22. PubMed ID: 17464498
    [Abstract] [Full Text] [Related]

  • 12. Genome-wide linkage scan of bipolar disorder in a Colombian population isolate replicates Loci on chromosomes 7p21-22, 1p31, 16p12 and 21q21-22 and identifies a novel locus on chromosome 12q.
    Kremeyer B, García J, Müller H, Burley MW, Herzberg I, Parra MV, Duque C, Vega J, Montoya P, López MC, Bedoya G, Reus V, Palacio C, López C, Ospina-Duque J, Freimer NB, Ruiz-Linares A.
    Hum Hered; 2010 Jul 01; 70(4):255-68. PubMed ID: 21071953
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 12(4):376-84. PubMed ID: 17179998
    [Abstract] [Full Text] [Related]

  • 14. Linkage genome scan for loci predisposing to panic disorder or agoraphobia.
    Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.
    Am J Med Genet; 2001 Aug 08; 105(6):548-57. PubMed ID: 11496373
    [Abstract] [Full Text] [Related]

  • 15. 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 08; 11(2):196-205. PubMed ID: 16222334
    [Abstract] [Full Text] [Related]

  • 16. Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.
    Huc-Chabrolle M, Charon C, Guilmatre A, Vourc'h P, Tripi G, Barthez MA, Sizaret E, Thepault RA, Le Gallic S, Hager J, Toutain A, Raynaud M, Andres C, Campion D, Laumonnier F, Bonnet-Brilhault F.
    Behav Genet; 2013 Mar 08; 43(2):132-40. PubMed ID: 23307483
    [Abstract] [Full Text] [Related]

  • 17. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family.
    Carrion-Castillo A, Estruch SB, Maassen B, Franke B, Francks C, Fisher SE.
    Hum Genet; 2021 Aug 08; 140(8):1183-1200. PubMed ID: 34076780
    [Abstract] [Full Text] [Related]

  • 18. 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 08; 46(10):1045-56. PubMed ID: 16178928
    [Abstract] [Full Text] [Related]

  • 19. A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.
    Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Crawford LR, Palmer CG, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL.
    Am J Hum Genet; 2002 May 08; 70(5):1183-96. PubMed ID: 11923911
    [Abstract] [Full Text] [Related]

  • 20. 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 08; 41(9):652-7. PubMed ID: 15342694
    [Abstract] [Full Text] [Related]

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