These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 16773125)

  • 21. Association analysis of the glutamic acid decarboxylase 2 and the glutamine synthetase genes (GAD2, GLUL) with schizophrenia.
    Arai S; Shibata H; Sakai M; Ninomiya H; Iwata N; Ozaki N; Fukumaki Y
    Psychiatr Genet; 2009 Feb; 19(1):6-13. PubMed ID: 19125103
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach.
    Gloyn AL; Mackay DJ; Weedon MN; McCarthy MI; Walker M; Hitman G; Knight BA; Owen KR; Hattersley AT; Frayling TM
    Diabetes; 2006 Aug; 55(8):2272-6. PubMed ID: 16873690
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.
    Addington AM; Gornick MC; Shaw P; Seal J; Gogtay N; Greenstein D; Clasen L; Coffey M; Gochman P; Long R; Rapoport JL
    Mol Psychiatry; 2007 Feb; 12(2):195-205. PubMed ID: 17033632
    [TBL] [Abstract][Full Text] [Related]  

  • 24. DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands.
    Kroes HY; van Zon PH; Fransen van de Putte D; Nelen MR; Nievelstein RJ; Wittebol-Post D; van Nieuwenhuizen O; Mancini GM; van der Knaap MS; Kwee ML; Maas SM; Cobben JM; De Nef JE; Lindhout D; Sinke RJ
    Eur J Med Genet; 2008; 51(1):24-34. PubMed ID: 18054307
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families.
    Liu CM; Liu YL; Fann CS; Chen WJ; Yang WC; Ouyang WC; Chen CY; Jou YS; Hsieh MH; Liu SK; Hwang TJ; Faraone SV; Tsuang MT; Hwu HG
    Genes Brain Behav; 2007 Aug; 6(6):497-502. PubMed ID: 17054719
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Linkage disequilibrium analyses within chromosome 19p in multiple sclerosis.
    Vyshkina T; Kalman B
    Mult Scler; 2008 May; 14(4):433-9. PubMed ID: 18208878
    [TBL] [Abstract][Full Text] [Related]  

  • 27. GABRB2 association with schizophrenia: commonalities and differences between ethnic groups and clinical subtypes.
    Lo WS; Harano M; Gawlik M; Yu Z; Chen J; Pun FW; Tong KL; Zhao C; Ng SK; Tsang SY; Uchimura N; Stober G; Xue H
    Biol Psychiatry; 2007 Mar; 61(5):653-60. PubMed ID: 16950232
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32.
    Adamovic S; Amundsen SS; Lie BA; Hellqvist A; Gudjónsdóttir AH; Ek J; Nilsson S; Wahlström J; Ascher H; Sollid LM; Naluai AT
    Tissue Antigens; 2008 Jan; 71(1):27-34. PubMed ID: 17971050
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Excitement and confusion on chromosome 6q: the challenges of neuropsychiatric genetics in microcosm.
    Kohn Y; Lerer B
    Mol Psychiatry; 2005 Dec; 10(12):1062-73. PubMed ID: 16172614
    [TBL] [Abstract][Full Text] [Related]  

  • 30. RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.
    Liu YL; Fann CS; Liu CM; Chen WJ; Wu JY; Hung SI; Chen CH; Jou YS; Liu SK; Hwang TJ; Hsieh MH; Chang CC; Yang WC; Lin JJ; Chou FH; Faraone SV; Tsuang MT; Hwu HG
    Biol Psychiatry; 2008 Nov; 64(9):789-96. PubMed ID: 18571626
    [TBL] [Abstract][Full Text] [Related]  

  • 31. No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).
    Thiselton DL; Webb BT; Neale BM; Ribble RC; O'Neill FA; Walsh D; Riley BP; Kendler KS
    Mol Psychiatry; 2004 Aug; 9(8):777-83; image 729. PubMed ID: 15197397
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.
    Alkelai A; Kohn Y; Olender T; Sarner-Kanyas K; Rigbi A; Hamdan A; Ben-Asher E; Lancet D; Lerer B
    Am J Med Genet B Neuropsychiatr Genet; 2009 Oct; 150B(7):914-25. PubMed ID: 19152384
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adults.
    Close J; Game L; Clark B; Bergounioux J; Gerovassili A; Thein SL
    BMC Genomics; 2004 May; 5(1):33. PubMed ID: 15169551
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.
    Ingason A; Giegling I; Cichon S; Hansen T; Rasmussen HB; Nielsen J; Jürgens G; Muglia P; Hartmann AM; Strengman E; Vasilescu C; Mühleisen TW; Djurovic S; Melle I; Lerer B; Möller HJ; Francks C; Pietiläinen OP; Lonnqvist J; Suvisaari J; Tuulio-Henriksson A; Walshe M; Vassos E; Di Forti M; Murray R; Bonetto C; Tosato S; ; Cantor RM; Rietschel M; Craddock N; Owen MJ; Peltonen L; Andreassen OA; Nöthen MM; St Clair D; Ophoff RA; O'Donovan MC; Collier DA; Werge T; Rujescu D
    Hum Mol Genet; 2010 Apr; 19(7):1379-86. PubMed ID: 20071346
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genomic profiling of interpopulation diversity guides prioritization of candidate-genes for autoimmunity.
    Grossman I; Avidan N; Singer C; Paperna T; Lancet D; Beckmann JS; Miller A
    Genes Immun; 2004 Sep; 5(6):493-504. PubMed ID: 15269719
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia.
    Duan J; Martinez M; Sanders AR; Hou C; Saitou N; Kitano T; Mowry BJ; Crowe RR; Silverman JM; Levinson DF; Gejman PV
    Am J Hum Genet; 2004 Oct; 75(4):624-38. PubMed ID: 15329799
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic association of NALP1 with generalized vitiligo in Jordanian Arabs.
    Alkhateeb A; Qarqaz F
    Arch Dermatol Res; 2010 Oct; 302(8):631-4. PubMed ID: 20574744
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association of common variants in the Joubert syndrome gene (AHI1) with autism.
    Alvarez Retuerto AI; Cantor RM; Gleeson JG; Ustaszewska A; Schackwitz WS; Pennacchio LA; Geschwind DH
    Hum Mol Genet; 2008 Dec; 17(24):3887-96. PubMed ID: 18782849
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
    Teltsh O; Kanyas K; Karni O; Levi A; Korner M; Ben-Asher E; Lancet D; Hamdan A; Lerer B; Kohn Y
    Am J Med Genet B Neuropsychiatr Genet; 2008 Mar; 147B(2):209-15. PubMed ID: 17823922
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Association between golli-MBP and schizophrenia in the Jewish Ashkenazi population: are regulatory regions involved?
    Baruch K; Silberberg G; Aviv A; Shamir E; Bening-Abu-Shach U; Baruch Y; Darvasi A; Navon R
    Int J Neuropsychopharmacol; 2009 Aug; 12(7):885-94. PubMed ID: 19154657
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.