BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 26064710)

  • 1. PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication.
    Dawson AJ; Cox J; Hovanes K; Spriggs E
    Case Rep Genet; 2015; 2015():474097. PubMed ID: 26064710
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Prader-Willi and Angelman syndromes: case series diagnosed by MS-MLPA assay].
    Rios-Flores IM; Bobadilla-Morales L; Peña Padilla C; Corona-Rivera A; Acosta-Fernández E; Santana-Hernández J; Brukman-Jiménez SA; Corona Rivera JR
    Rev Med Inst Mex Seguro Soc; 2021 Jun; 59(2):170-178. PubMed ID: 34232598
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
    Henkhaus RS; Kim SJ; Kimonis VE; Gold JA; Dykens EM; Driscoll DJ; Butler MG
    Genet Test Mol Biomarkers; 2012 Mar; 16(3):178-86. PubMed ID: 21977908
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.
    Cai G; Edelmann L; Goldsmith JE; Cohen N; Nakamine A; Reichert JG; Hoffman EJ; Zurawiecki DM; Silverman JM; Hollander E; Soorya L; Anagnostou E; Betancur C; Buxbaum JD
    BMC Med Genomics; 2008 Oct; 1():50. PubMed ID: 18925931
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome.
    Kim B; Park Y; Cho SI; Kim MJ; Chae JH; Kim JY; Seong MW; Park SS
    Ann Lab Med; 2022 Jan; 42(1):79-88. PubMed ID: 34374352
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome].
    Li MR; Wang XZ; Liu XY; Yang YL; Bao XH; Zhang YH; Xiong H; Zhong N; Qin J; Wu XR; Pan H
    Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3257-61. PubMed ID: 19159549
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS features.
    Aypar U; Hoppman NL; Thorland EC; Dawson DB
    Mol Cytogenet; 2016; 9():26. PubMed ID: 27006693
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
    Driscoll DJ; Waters MF; Williams CA; Zori RT; Glenn CC; Avidano KM; Nicholls RD
    Genomics; 1992 Aug; 13(4):917-24. PubMed ID: 1505981
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.
    Zilina O; Kahre T; Talvik I; Oiglane-Shlik E; Tillmann V; Ounap K
    Eur J Med Genet; 2014; 57(6):279-83. PubMed ID: 24704109
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 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. Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.
    Wu J; Lei M; Wang X; Liu N; Xu X; Gu C; Yu Y; Liu W
    Ital J Pediatr; 2022 Dec; 48(1):204. PubMed ID: 36582000
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities.
    Bittel DC; Kibiryeva N; Butler MG
    Genet Test; 2007; 11(4):467-75. PubMed ID: 18294067
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.