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Journal Abstract Search

66 related items for PubMed ID: 8825900

  • 21. 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
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  • 25. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.
    Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582
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  • 28. 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 26; 70(9):686-94. PubMed ID: 18032746
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  • 29. Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype.
    Eisenberg J, Mei-Tal G, Steinberg A, Tartakovsky E, Zohar A, Gritsenko I, Nemanov L, Ebstein RP.
    Am J Med Genet; 1999 Oct 15; 88(5):497-502. PubMed ID: 10490706
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  • 31. Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region.
    Adams J, Crosbie J, Wigg K, Ickowicz A, Pathare T, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL, Barr CL.
    Mol Psychiatry; 2004 May 15; 9(5):494-9. PubMed ID: 14699423
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  • 32. Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD.
    Smoller JW, Biederman J, Arbeitman L, Doyle AE, Fagerness J, Perlis RH, Sklar P, Faraone SV.
    Biol Psychiatry; 2006 Mar 01; 59(5):460-7. PubMed ID: 16197923
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  • 33. Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred.
    Plasilova M, Russell AM, Wanner A, Wolf A, Dobbie Z, Müller HJ, Heinimann K.
    Eur J Hum Genet; 2004 May 01; 12(5):365-71. PubMed ID: 14735163
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  • 34. Refining the ADHD phenotype using affected sibling pair families.
    Smalley SL, McCracken J, McGough J.
    Am J Med Genet; 2001 Jan 08; 105(1):31-3. PubMed ID: 11424989
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  • 35. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 08; 56(3):105-52. PubMed ID: 19728970
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  • 36. Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees.
    Arcos-Burgos M, Castellanos FX, Lopera F, Pineda D, Palacio JD, Garcia M, Henao GC, Palacio LG, Berg K, Bailey-Wilson JE, Muenke M.
    Clin Genet; 2002 May 08; 61(5):335-43. PubMed ID: 12081716
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  • 37. Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder.
    Barr CL, Feng Y, Wigg K, Bloom S, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL.
    Mol Psychiatry; 2000 Jul 08; 5(4):405-9. PubMed ID: 10889551
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  • 38. Coloboma mouse mutant as an animal model of hyperkinesis and attention deficit hyperactivity disorder.
    Wilson MC.
    Neurosci Biobehav Rev; 2000 Jan 08; 24(1):51-7. PubMed ID: 10654661
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  • 40. [Analysis of hypotheses and simulation of selection for a suppressor affecting the manifestations of the fused gene in mice].
    Shindialov IN, Ruvinskiĭ AO, Agul'nik AI.
    Genetika; 1987 Mar 08; 23(3):568-70. PubMed ID: 3569900
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