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 *

290 related articles for article (PubMed ID: 9545402)

  • 1. 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]  

  • 2. Association between a GABRB3 polymorphism and autism.
    Buxbaum JD; Silverman JM; Smith CJ; Greenberg DA; Kilifarski M; Reichert J; Cook EH; Fang Y; Song CY; Vitale R
    Mol Psychiatry; 2002; 7(3):311-6. PubMed ID: 11920158
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.
    Martin ER; Menold MM; Wolpert CM; Bass MP; Donnelly SL; Ravan SA; Zimmerman A; Gilbert JR; Vance JM; Maddox LO; Wright HH; Abramson RK; DeLong GR; Cuccaro ML; Pericak-Vance MA
    Am J Med Genet; 2000 Feb; 96(1):43-8. PubMed ID: 10686550
    [TBL] [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; 88(5):551-6. PubMed ID: 10490715
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 137B(1):25-8. PubMed ID: 15952184
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 131B(1):51-9. PubMed ID: 15389768
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic studies in autistic disorder and chromosome 15.
    Bass MP; Menold MM; Wolpert CM; Donnelly SL; Ravan SA; Hauser ER; Maddox LO; Vance JM; Abramson RK; Wright HH; Gilbert JR; Cuccaro ML; DeLong GR; Pericak-Vance MA
    Neurogenetics; 2000 Mar; 2(4):219-26. PubMed ID: 10983717
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
    Maddox LO; Menold MM; Bass MP; Rogala AR; Pericak-Vance MA; Vance JM; Gilbert JR
    Genomics; 1999 Dec; 62(3):325-31. PubMed ID: 10644429
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 8(6):624-34, 570. PubMed ID: 12851639
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 15(3-4):245-59. PubMed ID: 12092907
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios.
    Kim SA; Kim JH; Park M; Cho IH; Yoo HJ
    Neuropsychobiology; 2006; 54(3):160-5. PubMed ID: 17230033
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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; 147B(7):1116-25. PubMed ID: 18361419
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
    Shao Y; Cuccaro ML; Hauser ER; Raiford KL; Menold MM; Wolpert CM; Ravan SA; Elston L; Decena K; Donnelly SL; Abramson RK; Wright HH; DeLong GR; Gilbert JR; Pericak-Vance MA
    Am J Hum Genet; 2003 Mar; 72(3):539-48. PubMed ID: 12567325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.
    Maestrini E; Lai C; Marlow A; Matthews N; Wallace S; Bailey A; Cook EH; Weeks DE; Monaco AP
    Am J Med Genet; 1999 Oct; 88(5):492-6. PubMed ID: 10490705
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Association study of the commonly recognized breakpoints in chromosome 15q11-q13 in Japanese autistic patients.
    Kato C; Tochigi M; Koishi S; Kawakubo Y; Yamamoto K; Matsumoto H; Hashimoto O; Kim SY; Watanabe K; Kano Y; Nanba E; Kato N; Sasaki T
    Psychiatr Genet; 2008 Jun; 18(3):133-6. PubMed ID: 18496211
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.