BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 38616334)

  • 1. Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region.
    Mim RA; Soorajkumar A; Kosaji N; Rahman MM; Sarker S; Karuvantevida N; Eshaque TB; Rahaman MA; Islam A; Chowdhury MSJ; Shams N; Uddin KMF; Akter H; Uddin M
    Brain Behav; 2024 Apr; 14(4):e3437. PubMed ID: 38616334
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC; Driscoll DJ; Yang TP; Nicholls RD
    Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.
    Jiang YH; Wauki K; Liu Q; Bressler J; Pan Y; Kashork CD; Shaffer LG; Beaudet AL
    BMC Genomics; 2008 Jan; 9():50. PubMed ID: 18226259
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. IPSC Models of Chromosome 15Q Imprinting Disorders: From Disease Modeling to Therapeutic Strategies.
    Germain ND; Levine ES; Chamberlain SJ
    Adv Neurobiol; 2020; 25():55-77. PubMed ID: 32578144
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The mechanisms involved in formation of deletions and duplications of 15q11-q13.
    Robinson WP; Dutly F; Nicholls RD; Bernasconi F; Peñaherrera M; Michaelis RC; Abeliovich D; Schinzel AA
    J Med Genet; 1998 Feb; 35(2):130-6. PubMed ID: 9580159
    [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. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
    Lee S; Wevrick R
    Am J Hum Genet; 2000 Mar; 66(3):848-58. PubMed ID: 10712201
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
    Hassan M; Butler MG
    Eur J Med Genet; 2016 Nov; 59(11):584-589. PubMed ID: 27659713
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Prader-Willi syndrome: reflections on seminal studies and future therapies.
    Chung MS; Langouët M; Chamberlain SJ; Carmichael GG
    Open Biol; 2020 Sep; 10(9):200195. PubMed ID: 32961075
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
    Procter M; Chou LS; Tang W; Jama M; Mao R
    Clin Chem; 2006 Jul; 52(7):1276-83. PubMed ID: 16690734
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mechanisms of imprinting of the Prader-Willi/Angelman region.
    Horsthemke B; Wagstaff J
    Am J Med Genet A; 2008 Aug; 146A(16):2041-52. PubMed ID: 18627066
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.
    Kitsiou-Tzeli S; Tzetis M; Sofocleous C; Vrettou C; Xaidara A; Giannikou K; Pampanos A; Mavrou A; Kanavakis E
    Am J Med Genet A; 2010 Aug; 152A(8):1925-32. PubMed ID: 20575009
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.
    Glenn CC; Nicholls RD; Robinson WP; Saitoh S; Niikawa N; Schinzel A; Horsthemke B; Driscoll DJ
    Hum Mol Genet; 1993 Sep; 2(9):1377-82. PubMed ID: 8242060
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The imprinting box of the Prader-Willi/Angelman syndrome domain.
    Shemer R; Hershko AY; Perk J; Mostoslavsky R; Tsuberi B; Cedar H; Buiting K; Razin A
    Nat Genet; 2000 Dec; 26(4):440-3. PubMed ID: 11101841
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.