BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 17171652)

  • 1. HOXA1 gene variants influence head growth rates in humans.
    Muscarella LA; Guarnieri V; Sacco R; Militerni R; Bravaccio C; Trillo S; Schneider C; Melmed R; Elia M; Mascia ML; Rucci E; Piemontese MR; D'Agruma L; Persico AM
    Am J Med Genet B Neuropsychiatr Genet; 2007 Apr; 144B(3):388-90. PubMed ID: 17171652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.
    Conciatori M; Stodgell CJ; Hyman SL; O'Bara M; Militerni R; Bravaccio C; Trillo S; Montecchi F; Schneider C; Melmed R; Elia M; Crawford L; Spence SJ; Muscarella L; Guarnieri V; D'Agruma L; Quattrone A; Zelante L; Rabinowitz D; Pascucci T; Puglisi-Allegra S; Reichelt KL; Rodier PM; Persico AM
    Biol Psychiatry; 2004 Feb; 55(4):413-9. PubMed ID: 14960295
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project.
    Collins JS; Schroer RJ; Bird J; Michaelis RC
    J Autism Dev Disord; 2003 Jun; 33(3):343-8. PubMed ID: 12908836
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HOXA1 A218G polymorphism is associated with smaller cerebellar volume in healthy humans.
    Canu E; Boccardi M; Ghidoni R; Benussi L; Duchesne S; Testa C; Binetti G; Frisoni GB
    J Neuroimaging; 2009 Oct; 19(4):353-8. PubMed ID: 19018953
    [TBL] [Abstract][Full Text] [Related]  

  • 5. No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD).
    Talebizadeh Z; Bittel DC; Miles JH; Takahashi N; Wang CH; Kibiryeva N; Butler MG
    J Med Genet; 2002 Nov; 39(11):e70. PubMed ID: 12414832
    [No Abstract]   [Full Text] [Related]  

  • 6. No association between allelic variants of HOXA1/HOXB1 and autism.
    Gallagher L; Hawi Z; Kearney G; Fitzgerald M; Gill M
    Am J Med Genet B Neuropsychiatr Genet; 2004 Jan; 124B(1):64-7. PubMed ID: 14681917
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An integrated meta-analysis of two variants in HOXA1/HOXB1 and their effect on the risk of autism spectrum disorders.
    Song RR; Zou L; Zhong R; Zheng XW; Zhu BB; Chen W; Liu L; Miao XP
    PLoS One; 2011; 6(9):e25603. PubMed ID: 21980499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
    Devlin B; Bennett P; Cook EH; Dawson G; Gonen D; Grigorenko EL; McMahon W; Pauls D; Smith M; Spence MA; Schellenberg GD;
    Am J Med Genet; 2002 Aug; 114(6):667-72. PubMed ID: 12210285
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.
    Li J; Tabor HK; Nguyen L; Gleason C; Lotspeich LJ; Spiker D; Risch N; Myers RM
    Am J Med Genet; 2002 Jan; 114(1):24-30. PubMed ID: 11840501
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders.
    Ingram JL; Stodgell CJ; Hyman SL; Figlewicz DA; Weitkamp LR; Rodier PM
    Teratology; 2000 Dec; 62(6):393-405. PubMed ID: 11091361
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lack of association of HOXA1 and HOXB1 variants with autism in the Indian population.
    Sen B; Sinha S; Ahmed S; Ghosh S; Gangopadhyay PK; Usha R
    Psychiatr Genet; 2007 Feb; 17(1):1. PubMed ID: 17167333
    [No Abstract]   [Full Text] [Related]  

  • 12. Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients.
    Romano V; Calì F; Mirisola M; Gambino G; D' Anna R; Di Rosa P; Seidita G; Chiavetta V; Aiello F; Canziani F; De Leo G; Ayala GF; Elia M
    Mol Psychiatry; 2003 Aug; 8(8):716-7. PubMed ID: 12888798
    [No Abstract]   [Full Text] [Related]  

  • 13. Allelic variation within the putative autism spectrum disorder risk gene homeobox A1 and cerebellar maturation in typically developing children and adolescents.
    Raznahan A; Lee Y; Vaituzis C; Tran L; Mackie S; Tiemeier H; Clasen L; Lalonde F; Greenstein D; Pierson R; Giedd JN
    Autism Res; 2012 Apr; 5(2):93-100. PubMed ID: 22359339
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.
    Baker EK; Arpone M; Aliaga SM; Bretherton L; Kraan CM; Bui M; Slater HR; Ling L; Francis D; Hunter MF; Elliott J; Rogers C; Field M; Cohen J; Cornish K; Santa Maria L; Faundes V; Curotto B; Morales P; Trigo C; Salas I; Alliende AM; Amor DJ; Godler DE
    Mol Autism; 2019; 10():21. PubMed ID: 31073396
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Candidate gene study of HOXB1 in autism spectrum disorder.
    Muscarella LA; Guarnieri V; Sacco R; Curatolo P; Manzi B; Alessandrelli R; Giana G; Militerni R; Bravaccio C; Lenti C; Saccani M; Schneider C; Melmed R; D'Agruma L; Persico AM
    Mol Autism; 2010 May; 1(1):9. PubMed ID: 20678259
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.
    Hatton DD; Sideris J; Skinner M; Mankowski J; Bailey DB; Roberts J; Mirrett P
    Am J Med Genet A; 2006 Sep; 140A(17):1804-13. PubMed ID: 16700053
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Accelerated head and body growth in infants later diagnosed with autism spectrum disorders: a comparative study of optimal outcome children.
    Mraz KD; Dixon J; Dumont-Mathieu T; Fein D
    J Child Neurol; 2009 Jul; 24(7):833-45. PubMed ID: 19617459
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The fragile X marker and autism in perspective.
    Payton JB; Steele MW; Wenger SL; Minshew NJ
    J Am Acad Child Adolesc Psychiatry; 1989 May; 28(3):417-21. PubMed ID: 2738009
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autism and the fragile X syndrome.
    Fisch GS; Cohen IL; Wolf EG; Brown WT; Jenkins EC; Gross A
    Am J Psychiatry; 1986 Jan; 143(1):71-3. PubMed ID: 3455802
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical characterization of the HOXA1 syndrome BSAS variant.
    Bosley TM; Salih MA; Alorainy IA; Oystreck DT; Nester M; Abu-Amero KK; Tischfield MA; Engle EC
    Neurology; 2007 Sep; 69(12):1245-53. PubMed ID: 17875913
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.