BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 15133308)

  • 21. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.
    Shao Y; Raiford KL; Wolpert CM; Cope HA; Ravan SA; Ashley-Koch AA; Abramson RK; Wright HH; DeLong RG; Gilbert JR; Cuccaro ML; Pericak-Vance MA
    Am J Hum Genet; 2002 Apr; 70(4):1058-61. PubMed ID: 11875756
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism.
    Talebizadeh Z; Arking DE; Hu VW
    PLoS One; 2013; 8(6):e67569. PubMed ID: 23840741
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Full-genome scans with autistic disorder: a review.
    Gutknecht L
    Behav Genet; 2001 Jan; 31(1):113-23. PubMed ID: 11529268
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.
    SLI Consortium (SLIC)
    Am J Hum Genet; 2004 Jun; 74(6):1225-38. PubMed ID: 15133743
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.
    McCauley JL; Olson LM; Dowd M; Amin T; Steele A; Blakely RD; Folstein SE; Haines JL; Sutcliffe JS
    Am J Med Genet B Neuropsychiatr Genet; 2004 May; 127B(1):104-12. PubMed ID: 15108191
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits.
    Smith M; Woodroffe A; Smith R; Holguin S; Martinez J; Filipek PA; Modahl C; Moore B; Bocian ME; Mays L; Laulhere T; Flodman P; Spence MA
    Cytogenet Genome Res; 2002; 98(4):233-9. PubMed ID: 12826745
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genome-wide linkage in Utah autism pedigrees.
    Allen-Brady K; Robison R; Cannon D; Varvil T; Villalobos M; Pingree C; Leppert MF; Miller J; McMahon WM; Coon H
    Mol Psychiatry; 2010 Oct; 15(10):1006-15. PubMed ID: 19455147
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Examination of AVPR1a as an autism susceptibility gene.
    Wassink TH; Piven J; Vieland VJ; Pietila J; Goedken RJ; Folstein SE; Sheffield VC
    Mol Psychiatry; 2004 Oct; 9(10):968-72. PubMed ID: 15098001
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
    Hum Mol Genet; 1998 Mar; 7(3):571-8. PubMed ID: 9546821
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.
    Ramoz N; Reichert JG; Smith CJ; Silverman JM; Bespalova IN; Davis KL; Buxbaum JD
    Am J Psychiatry; 2004 Apr; 161(4):662-9. PubMed ID: 15056512
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.
    Auranen M; Nieminen T; Majuri S; Vanhala R; Peltonen L; Järvelä I
    Mol Psychiatry; 2000 May; 5(3):320-2. PubMed ID: 10889536
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The molecular genetics of autism.
    Wassink TH; Piven J
    Curr Psychiatry Rep; 2000 Apr; 2(2):170-5. PubMed ID: 11122951
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Localisation of a gene implicated in a severe speech and language disorder.
    Fisher SE; Vargha-Khadem F; Watkins KE; Monaco AP; Pembrey ME
    Nat Genet; 1998 Feb; 18(2):168-70. PubMed ID: 9462748
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.
    Molloy CA; Keddache M; Martin LJ
    Mol Psychiatry; 2005 Aug; 10(8):741-6. PubMed ID: 15940295
    [TBL] [Abstract][Full Text] [Related]  

  • 36. No association between the WNT2 gene and autistic disorder.
    McCoy PA; Shao Y; Wolpert CM; Donnelly SL; Ashley-Koch A; Abel HL; Ravan SA; Abramson RK; Wright HH; DeLong GR; Cuccaro ML; Gilbert JR; Pericak-Vance MA
    Am J Med Genet; 2002 Jan; 114(1):106-9. PubMed ID: 11840514
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
    Rabionet R; Jaworski JM; Ashley-Koch AE; Martin ER; Sutcliffe JS; Haines JL; Delong GR; Abramson RK; Wright HH; Cuccaro ML; Gilbert JR; Pericak-Vance MA
    Neurosci Lett; 2004 Dec; 372(3):209-14. PubMed ID: 15542242
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families.
    Simmons TR; Flax JF; Azaro MA; Hayter JE; Justice LM; Petrill SA; Bassett AS; Tallal P; Brzustowicz LM; Bartlett CW
    Hum Hered; 2010; 70(4):232-44. PubMed ID: 20948219
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.
    Lennon PA; Cooper ML; Peiffer DA; Gunderson KL; Patel A; Peters S; Cheung SW; Bacino CA
    Am J Med Genet A; 2007 Apr; 143A(8):791-8. PubMed ID: 17330859
    [TBL] [Abstract][Full Text] [Related]  

  • 40. No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.
    Nabi R; Zhong H; Serajee FJ; Huq AH
    Am J Med Genet B Neuropsychiatr Genet; 2003 May; 119B(1):98-101. PubMed ID: 12707945
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.