BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

99 related articles for article (PubMed ID: 19259978)

  • 1. Association of the alpha4 integrin subunit gene (ITGA4) with autism.
    Correia C; Coutinho AM; Almeida J; Lontro R; Lobo C; Miguel TS; Martins M; Gallagher L; Conroy J; Gill M; Oliveira G; Vicente AM
    Am J Med Genet B Neuropsychiatr Genet; 2009 Dec; 150B(8):1147-51. PubMed ID: 19259978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.
    Conroy J; Cochrane L; Anney RJ; Sutcliffe JS; Carthy P; Dunlop A; Mullarkey M; O'hici B; Green AJ; Ennis S; Gill M; Gallagher L
    Am J Med Genet B Neuropsychiatr Genet; 2009 Jun; 150B(4):535-44. PubMed ID: 18846500
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.
    Ramoz N; Cai G; Reichert JG; Silverman JM; Buxbaum JD
    Am J Med Genet B Neuropsychiatr Genet; 2008 Oct; 147B(7):1152-8. PubMed ID: 18348195
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample.
    Cochrane LE; Tansey KE; Gill M; Gallagher L; Anney RJ
    Autism Res; 2010 Dec; 3(6):342-4. PubMed ID: 21182210
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ITGA4 polymorphisms and susceptibility to multiple sclerosis.
    O'Doherty C; Roos IM; Antiguedad A; Aransay AM; Hillert J; Vandenbroeck K
    J Neuroimmunol; 2007 Sep; 189(1-2):151-7. PubMed ID: 17689671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.
    Philippi A; Tores F; Carayol J; Rousseau F; Letexier M; Roschmann E; Lindenbaum P; Benajjou A; Fontaine K; Vazart C; Gesnouin P; Brooks P; Hager J
    BMC Med Genet; 2007 Dec; 8():74. PubMed ID: 18053270
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.
    McCauley JL; Olson LM; Delahanty R; Amin T; Nurmi EL; Organ EL; Jacobs MM; Folstein SE; Haines JL; Sutcliffe JS
    Am J Med Genet B Neuropsychiatr Genet; 2004 Nov; 131B(1):51-9. PubMed ID: 15389768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families.
    Romano V; Calì F; Seidita G; Mirisola M; D'Anna RP; Gambino G; Schinocca P; Romano S; Ayala GF; Canziani F; De Leo G; Elia M
    Psychiatr Genet; 2005 Jun; 15(2):149-50. PubMed ID: 15900231
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A population-based association study of glutamate decarboxylase 1 as a candidate gene for autism.
    Buttenschøn HN; Lauritsen MB; El Daoud A; Hollegaard M; Jorgensen M; Tvedegaard K; Hougaard D; Børglum A; Thorsen P; Mors O
    J Neural Transm (Vienna); 2009 Mar; 116(3):381-8. PubMed ID: 19139806
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.
    Hutcheson HB; Olson LM; Bradford Y; Folstein SE; Santangelo SL; Sutcliffe JS; Haines JL
    BMC Med Genet; 2004 May; 5():12. PubMed ID: 15128462
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genetics of autism.
    Muhle R; Trentacoste SV; Rapin I
    Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Lack of association between autism and SLC25A12.
    Rabionet R; McCauley JL; Jaworski JM; Ashley-Koch AE; Martin ER; Sutcliffe JS; Haines JL; DeLong GR; Abramson RK; Wright HH; Cuccaro ML; Gilbert JR; Pericak-Vance MA
    Am J Psychiatry; 2006 May; 163(5):929-31. PubMed ID: 16648338
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.
    Wermter AK; Kamp-Becker I; Hesse P; Schulte-Körne G; Strauch K; Remschmidt H
    Am J Med Genet B Neuropsychiatr Genet; 2010 Mar; 153B(2):629-639. PubMed ID: 19777562
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
    Wassink TH; Piven J; Vieland VJ; Jenkins L; Frantz R; Bartlett CW; Goedken R; Childress D; Spence MA; Smith M; Sheffield VC
    Am J Med Genet B Neuropsychiatr Genet; 2005 Jul; 136B(1):36-44. PubMed ID: 15892143
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
    Nurmi EL; Amin T; Olson LM; Jacobs MM; McCauley JL; Lam AY; Organ EL; Folstein SE; Haines JL; Sutcliffe JS
    Mol Psychiatry; 2003 Jun; 8(6):624-34, 570. PubMed ID: 12851639
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.
    Philippi A; Roschmann E; Tores F; Lindenbaum P; Benajou A; Germain-Leclerc L; Marcaillou C; Fontaine K; Vanpeene M; Roy S; Maillard S; Decaulne V; Saraiva JP; Brooks P; Rousseau F; Hager J
    Mol Psychiatry; 2005 Oct; 10(10):950-60. PubMed ID: 16027742
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
    Maestrini E; Pagnamenta AT; Lamb JA; Bacchelli E; Sykes NH; Sousa I; Toma C; Barnby G; Butler H; Winchester L; Scerri TS; Minopoli F; Reichert J; Cai G; Buxbaum JD; Korvatska O; Schellenberg GD; Dawson G; de Bildt A; Minderaa RB; Mulder EJ; Morris AP; Bailey AJ; Monaco AP;
    Mol Psychiatry; 2010 Sep; 15(9):954-68. PubMed ID: 19401682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.