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 *

216 related articles for article (PubMed ID: 22405623)

  • 1. Mutation analysis of the NRXN1 gene in a Chinese autism cohort.
    Liu Y; Hu Z; Xun G; Peng Y; Lu L; Xu X; Xiong Z; Xia L; Liu D; Li W; Zhao J; Xia K
    J Psychiatr Res; 2012 May; 46(5):630-4. PubMed ID: 22405623
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population.
    Yue W; Yang Y; Zhang Y; Lu T; Hu X; Wang L; Ruan Y; Lv L; Zhang D
    Behav Brain Funct; 2011 Apr; 7():7. PubMed ID: 21477380
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
    Liu Y; Du Y; Liu W; Yang C; Liu Y; Wang H; Gong X
    PLoS One; 2013; 8(2):e56639. PubMed ID: 23468870
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disruption of the neurexin 1 gene is associated with schizophrenia.
    Rujescu D; Ingason A; Cichon S; Pietiläinen OP; Barnes MR; Toulopoulou T; Picchioni M; Vassos E; Ettinger U; Bramon E; Murray R; Ruggeri M; Tosato S; Bonetto C; Steinberg S; Sigurdsson E; Sigmundsson T; Petursson H; Gylfason A; Olason PI; Hardarsson G; Jonsdottir GA; Gustafsson O; Fossdal R; Giegling I; Möller HJ; Hartmann AM; Hoffmann P; Crombie C; Fraser G; Walker N; Lonnqvist J; Suvisaari J; Tuulio-Henriksson A; Djurovic S; Melle I; Andreassen OA; Hansen T; Werge T; Kiemeney LA; Franke B; Veltman J; Buizer-Voskamp JE; ; Sabatti C; Ophoff RA; Rietschel M; Nöthen MM; Stefansson K; Peltonen L; St Clair D; Stefansson H; Collier DA
    Hum Mol Genet; 2009 Mar; 18(5):988-96. PubMed ID: 18945720
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
    Xu X; Xiong Z; Zhang L; Liu Y; Lu L; Peng Y; Guo H; Zhao J; Xia K; Hu Z
    Mol Biol Rep; 2014 Jun; 41(6):4133-40. PubMed ID: 24570023
    [TBL] [Abstract][Full Text] [Related]  

  • 6. RELN gene polymorphisms and susceptibility to autism in Chinese Han population.
    Tian P
    Neurol India; 2012; 60(6):581-4. PubMed ID: 23287318
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorder.
    Yangngam S; Plong-On O; Sripo T; Roongpraiwan R; Hansakunachai T; Wirojanan J; Sombuntham T; Ruangdaraganon N; Limprasert P
    Genet Test Mol Biomarkers; 2014 Jul; 18(7):510-5. PubMed ID: 24832020
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neurexin gene family variants as risk factors for autism spectrum disorder.
    Wang J; Gong J; Li L; Chen Y; Liu L; Gu H; Luo X; Hou F; Zhang J; Song R
    Autism Res; 2018 Jan; 11(1):37-43. PubMed ID: 29045040
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association between neurexin 1 (NRXN1) polymorphisms and the smoking behavior of elderly Japanese.
    Sato N; Kageyama S; Chen R; Suzuki M; Tanioka F; Kamo T; Shinmura K; Nozawa A; Sugimura H
    Psychiatr Genet; 2010 Jun; 20(3):135-6. PubMed ID: 20414139
    [No Abstract]   [Full Text] [Related]  

  • 10. High frequency of neurexin 1beta signal peptide structural variants in patients with autism.
    Feng J; Schroer R; Yan J; Song W; Yang C; Bockholt A; Cook EH; Skinner C; Schwartz CE; Sommer SS
    Neurosci Lett; 2006 Nov; 409(1):10-3. PubMed ID: 17034946
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population.
    Wang L; Li J; Shuang M; Lu T; Wang Z; Zhang T; Yue W; Jia M; Ruan Y; Liu J; Wu Z; Zhang D; Wang L
    Transl Psychiatry; 2018 Aug; 8(1):152. PubMed ID: 30108208
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population.
    Li J; Liu J; Zhao L; Ma Y; Jia M; Lu T; Ruan Y; Li Q; Yue W; Zhang D; Wang L
    Prog Neuropsychopharmacol Biol Psychiatry; 2013 Jul; 44():226-32. PubMed ID: 23333377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders.
    Voineskos AN; Lett TA; Lerch JP; Tiwari AK; Ameis SH; Rajji TK; Müller DJ; Mulsant BH; Kennedy JL
    PLoS One; 2011; 6(6):e20982. PubMed ID: 21687627
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.
    Nag A; Bochukova EG; Kremeyer B; Campbell DD; Muller H; Valencia-Duarte AV; Cardona J; Rivas IC; Mesa SC; Cuartas M; Garcia J; Bedoya G; Cornejo W; Herrera LD; Romero R; Fournier E; Reus VI; Lowe TL; Farooqi IS; ; Mathews CA; McGrath LM; Yu D; Cook E; Wang K; Scharf JM; Pauls DL; Freimer NB; Plagnol V; Ruiz-Linares A
    PLoS One; 2013; 8(3):e59061. PubMed ID: 23533600
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.
    Béna F; Bruno DL; Eriksson M; van Ravenswaaij-Arts C; Stark Z; Dijkhuizen T; Gerkes E; Gimelli S; Ganesamoorthy D; Thuresson AC; Labalme A; Till M; Bilan F; Pasquier L; Kitzis A; Dubourgm C; Rossi M; Bottani A; Gagnebin M; Sanlaville D; Gilbert-Dussardier B; Guipponi M; van Haeringen A; Kriek M; Ruivenkamp C; Antonarakis SE; Anderlid BM; Slater HR; Schoumans J
    Am J Med Genet B Neuropsychiatr Genet; 2013 Jun; 162B(4):388-403. PubMed ID: 23533028
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.
    Qin J; Jia M; Wang L; Lu T; Ruan Y; Liu J; Guo Y; Zhang J; Yang X; Yue W; Zhang D
    BMC Med Genet; 2009 Jun; 10():61. PubMed ID: 19566951
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.
    Schaaf CP; Boone PM; Sampath S; Williams C; Bader PI; Mueller JM; Shchelochkov OA; Brown CW; Crawford HP; Phalen JA; Tartaglia NR; Evans P; Campbell WM; Tsai AC; Parsley L; Grayson SW; Scheuerle A; Luzzi CD; Thomas SK; Eng PA; Kang SH; Patel A; Stankiewicz P; Cheung SW
    Eur J Hum Genet; 2012 Dec; 20(12):1240-7. PubMed ID: 22617343
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population.
    Yang P; Shu BC; Hallmayer JF; Lung FW
    Neuropsychobiology; 2010; 62(2):104-15. PubMed ID: 20523082
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.
    Sharma JR; Arieff Z; Gameeldien H; Davids M; Kaur M; van der Merwe L
    Genet Test Mol Biomarkers; 2013 Feb; 17(2):93-8. PubMed ID: 23216241
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare NRXN1 promoter variants in patients with schizophrenia.
    Shah AK; Tioleco NM; Nolan K; Locker J; Groh K; Villa C; Stopkova P; Pedrosa E; Lachman HM
    Neurosci Lett; 2010 May; 475(2):80-4. PubMed ID: 20347009
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.