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 *

116 related articles for article (PubMed ID: 19548260)

  • 1. A longitudinal follow-up study of autistic symptoms in children and adults with duplications of 15q11-13.
    Simon EW; Haas-Givler B; Finucane B
    Am J Med Genet B Neuropsychiatr Genet; 2010 Mar; 153B(2):463-467. PubMed ID: 19548260
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autistic symptoms among children and young adults with isodicentric chromosome 15.
    Rineer S; Finucane B; Simon EW
    Am J Med Genet; 1998 Sep; 81(5):428-33. PubMed ID: 9754629
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders.
    Keller K; Williams C; Wharton P; Paulk M; Bent-Williams A; Gray B; Ward A; Stalker H; Wallace M; Carter R; Zori R
    Am J Med Genet A; 2003 Mar; 117A(2):105-11. PubMed ID: 12567405
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.
    Sutcliffe JS; Nurmi EL; Lombroso PJ
    J Am Acad Child Adolesc Psychiatry; 2003 Feb; 42(2):253-6. PubMed ID: 12544187
    [No Abstract]   [Full Text] [Related]  

  • 7. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.
    Cook EH; Courchesne RY; Cox NJ; Lord C; Gonen D; Guter SJ; Lincoln A; Nix K; Haas R; Leventhal BL; Courchesne E
    Am J Hum Genet; 1998 May; 62(5):1077-83. PubMed ID: 9545402
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.
    Simic M; Turk J
    Eur Child Adolesc Psychiatry; 2004 Dec; 13(6):389-93. PubMed ID: 15619052
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.
    Cook EH; Lindgren V; Leventhal BL; Courchesne R; Lincoln A; Shulman C; Lord C; Courchesne E
    Am J Hum Genet; 1997 Apr; 60(4):928-34. PubMed ID: 9106540
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.
    Kwasnicka-Crawford DA; Roberts W; Scherer SW
    J Autism Dev Disord; 2007 Apr; 37(4):694-702. PubMed ID: 17006779
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
    Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial dysfunction in autistic patients with 15q inverted duplication.
    Filipek PA; Juranek J; Smith M; Mays LZ; Ramos ER; Bocian M; Masser-Frye D; Laulhere TM; Modahl C; Spence MA; Gargus JJ
    Ann Neurol; 2003 Jun; 53(6):801-4. PubMed ID: 12783428
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism.
    Wegiel J; Schanen NC; Cook EH; Sigman M; Brown WT; Kuchna I; Nowicki K; Wegiel J; Imaki H; Ma SY; Marchi E; Wierzba-Bobrowicz T; Chauhan A; Chauhan V; Cohen IL; London E; Flory M; Lach B; Wisniewski T
    J Neuropathol Exp Neurol; 2012 May; 71(5):382-97. PubMed ID: 22487857
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B; Hallmayer J; Rogers T; Kalaydjieva L; Petersen PB; Nicholas P; Pingree C; McMahon W; Spiker D; Lotspeich L; Kraemer H; McCague P; Dimiceli S; Nouri N; Pitts T; Yang J; Hinds D; Myers RM; Risch N
    Am J Med Genet; 1999 Oct; 88(5):551-6. PubMed ID: 10490715
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.
    Bolton PF; Dennis NR; Browne CE; Thomas NS; Veltman MW; Thompson RJ; Jacobs P
    Am J Med Genet; 2001 Dec; 105(8):675-85. PubMed ID: 11803514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication.
    Orrico A; Zollino M; Galli L; Buoni S; Marangi G; Sorrentino V
    Am J Med Genet A; 2009 May; 149A(5):1033-5. PubMed ID: 19396834
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature.
    Charalsawadi C; Maisrikhaw W; Praphanphoj V; Wirojanan J; Hansakunachai T; Roongpraiwan R; Sombuntham T; Ruangdaraganon N; Limprasert P
    Cytogenet Genome Res; 2014; 144(1):1-8. PubMed ID: 25171325
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder.
    Silva AE; Vayego-Lourenco SA; Fett-Conte AC; Goloni-Bertollo EM; Varella-Garcia M
    Arq Neuropsiquiatr; 2002 Jun; 60(2-A):290-4. PubMed ID: 12068363
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A modified screening tool for autism (Checklist for Autism in Toddlers [CHAT-23]) for Chinese children.
    Wong V; Hui LH; Lee WC; Leung LS; Ho PK; Lau WL; Fung CW; Chung B
    Pediatrics; 2004 Aug; 114(2):e166-76. PubMed ID: 15286253
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation screening of the UBE3A/E6-AP gene in autistic disorder.
    Veenstra-VanderWeele J; Gonen D; Leventhal BL; Cook EH
    Mol Psychiatry; 1999 Jan; 4(1):64-7. PubMed ID: 10089011
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.