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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

314 related items for PubMed ID: 11543639

  • 1. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
    Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, Folstein SE, Haines JL, Sutcliffe JS.
    Genomics; 2001 Sep; 77(1-2):105-13. PubMed ID: 11543639
    [Abstract] [Full Text] [Related]

  • 2. 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 15; 131B(1):51-9. PubMed ID: 15389768
    [Abstract] [Full Text] [Related]

  • 3. An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.
    Curran S, Roberts S, Thomas S, Veltman M, Browne J, Medda E, Pickles A, Sham P, Bolton PF.
    Am J Med Genet B Neuropsychiatr Genet; 2005 Aug 05; 137B(1):25-8. PubMed ID: 15952184
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 88(5):551-6. PubMed ID: 10490715
    [Abstract] [Full Text] [Related]

  • 5. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
    Samaco RC, Hogart A, LaSalle JM.
    Hum Mol Genet; 2005 Feb 15; 14(4):483-92. PubMed ID: 15615769
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.
    Menold MM, Shao Y, Wolpert CM, Donnelly SL, Raiford KL, Martin ER, Ravan SA, Abramson RK, Wright HH, Delong GR, Cuccaro ML, Pericak-Vance MA, Gilbert JR.
    J Neurogenet; 2001 Feb 15; 15(3-4):245-59. PubMed ID: 12092907
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 8(6):624-34, 570. PubMed ID: 12851639
    [Abstract] [Full Text] [Related]

  • 9. The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression.
    Herzing LB, Kim SJ, Cook EH, Ledbetter DH.
    Am J Hum Genet; 2001 Jun 15; 68(6):1501-5. PubMed ID: 11353404
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. [Autism, chromosome 15 and the GAbaergic dysfunction hypothesis].
    Solís-Añez E, Delgado-Luengo W, Hernández ML.
    Invest Clin; 2007 Dec 15; 48(4):529-41. PubMed ID: 18271397
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
    Kim SJ, Brune CW, Kistner EO, Christian SL, Courchesne EH, Cox NJ, Cook EH.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Oct 05; 147B(7):1116-25. PubMed ID: 18361419
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. 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 15; 66(4):349-59. PubMed ID: 19278672
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.