BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 37958807)

  • 1. Structural Variation Evolution at the 15q11-q13 Disease-Associated Locus.
    Paparella A; L'Abbate A; Palmisano D; Chirico G; Porubsky D; Catacchio CR; Ventura M; Eichler EE; Maggiolini FAM; Antonacci F
    Int J Mol Sci; 2023 Oct; 24(21):. PubMed ID: 37958807
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
    Kalsner L; Chamberlain SJ
    Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
    Isles AR; Ingason A; Lowther C; Walters J; Gawlick M; Stöber G; Rees E; Martin J; Little RB; Potter H; Georgieva L; Pizzo L; Ozaki N; Aleksic B; Kushima I; Ikeda M; Iwata N; Levinson DF; Gejman PV; Shi J; Sanders AR; Duan J; Willis J; Sisodiya S; Costain G; Werge TM; Degenhardt F; Giegling I; Rujescu D; Hreidarsson SJ; Saemundsen E; Ahn JW; Ogilvie C; Girirajan SD; Stefansson H; Stefansson K; O'Donovan MC; Owen MJ; Bassett A; Kirov G
    PLoS Genet; 2016 May; 12(5):e1005993. PubMed ID: 27153221
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus.
    Maggiolini FAM; Cantsilieris S; D'Addabbo P; Manganelli M; Coe BP; Dumont BL; Sanders AD; Pang AWC; Vollger MR; Palumbo O; Palumbo P; Accadia M; Carella M; Eichler EE; Antonacci F
    PLoS Genet; 2019 Mar; 15(3):e1008075. PubMed ID: 30917130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.
    Ingason A; Kirov G; Giegling I; Hansen T; Isles AR; Jakobsen KD; Kristinsson KT; le Roux L; Gustafsson O; Craddock N; Möller HJ; McQuillin A; Muglia P; Cichon S; Rietschel M; Ophoff RA; Djurovic S; Andreassen OA; Pietiläinen OP; Peltonen L; Dempster E; Collier DA; St Clair D; Rasmussen HB; Glenthøj BY; Kiemeney LA; Franke B; Tosato S; Bonetto C; Saemundsen E; Hreidarsson SJ; ; Nöthen MM; Gurling H; O'Donovan MC; Owen MJ; Sigurdsson E; Petursson H; Stefansson H; Rujescu D; Stefansson K; Werge T
    Am J Psychiatry; 2011 Apr; 168(4):408-17. PubMed ID: 21324950
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
    Christian SL; Fantes JA; Mewborn SK; Huang B; Ledbetter DH
    Hum Mol Genet; 1999 Jun; 8(6):1025-37. PubMed ID: 10332034
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
    Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
    Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletions and duplications of the 15q11-q13 region in spermatozoa from Prader-Willi syndrome fathers.
    Molina O; Blanco J; Vidal F
    Mol Hum Reprod; 2010 May; 16(5):320-8. PubMed ID: 20083560
    [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. [Variation analysis of the number of copies and methylene patterns in region 15q11-q13].
    Laurito S; Roqué M
    Medicina (B Aires); 2018; 78(1):1-5. PubMed ID: 29360068
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes.
    Makoff AJ; Flomen RH
    Genome Biol; 2007; 8(6):R114. PubMed ID: 17573966
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.
    Hogart A; Wu D; LaSalle JM; Schanen NC
    Neurobiol Dis; 2010 May; 38(2):181-91. PubMed ID: 18840528
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
    Aypar U; Brodersen PR; Lundquist PA; Dawson DB; Thorland EC; Hoppman N
    Am J Med Genet A; 2014 Oct; 164A(10):2514-20. PubMed ID: 24975781
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
    Thomas NS; Durkie M; Potts G; Sandford R; Van Zyl B; Youings S; Dennis NR; Jacobs PA
    Eur J Hum Genet; 2006 Jul; 14(7):831-7. PubMed ID: 16617304
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder.
    Delorme R; Moreno-De-Luca D; Gennetier A; Maier W; Chaste P; Mössner R; Grabe HJ; Ruhrmann S; Falkai P; Mouren MC; Leboyer M; Wagner M; Betancur C
    BMC Med Genet; 2010 Jun; 11():100. PubMed ID: 20565924
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.
    Wang NJ; Parokonny AS; Thatcher KN; Driscoll J; Malone BM; Dorrani N; Sigman M; LaSalle JM; Schanen NC
    BMC Genet; 2008 Jan; 9():2. PubMed ID: 18177502
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An evolutionary driver of interspersed segmental duplications in primates.
    Cantsilieris S; Sunkin SM; Johnson ME; Anaclerio F; Huddleston J; Baker C; Dougherty ML; Underwood JG; Sulovari A; Hsieh P; Mao Y; Catacchio CR; Malig M; Welch AE; Sorensen M; Munson KM; Jiang W; Girirajan S; Ventura M; Lamb BT; Conlon RA; Eichler EE
    Genome Biol; 2020 Aug; 21(1):202. PubMed ID: 32778141
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.