229 related articles for article (PubMed ID: 23111162)
1. Uniparental disomy analysis in trios using genome-wide SNP array and whole-genome sequencing data imply segmental uniparental isodisomy in general populations.
Sasaki K; Mishima H; Miura K; Yoshiura K
Gene; 2013 Jan; 512(2):267-74. PubMed ID: 23111162
[TBL] [Abstract][Full Text] [Related]
2. A rapid microarray based whole genome analysis for detection of uniparental disomy.
Altug-Teber O; Dufke A; Poths S; Mau-Holzmann UA; Bastepe M; Colleaux L; Cormier-Daire V; Eggermann T; Gillessen-Kaesbach G; Bonin M; Riess O
Hum Mutat; 2005 Aug; 26(2):153-9. PubMed ID: 15968682
[TBL] [Abstract][Full Text] [Related]
3. Complex and segmental uniparental disomy updated.
Kotzot D
J Med Genet; 2008 Sep; 45(9):545-56. PubMed ID: 18524837
[TBL] [Abstract][Full Text] [Related]
4. Uniparental disomy in a population of 32,067 clinical exome trios.
Scuffins J; Keller-Ramey J; Dyer L; Douglas G; Torene R; Gainullin V; Juusola J; Meck J; Retterer K
Genet Med; 2021 Jun; 23(6):1101-1107. PubMed ID: 33495530
[TBL] [Abstract][Full Text] [Related]
5. Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11.
Flotho C; Steinemann D; Mullighan CG; Neale G; Mayer K; Kratz CP; Schlegelberger B; Downing JR; Niemeyer CM
Oncogene; 2007 Aug; 26(39):5816-21. PubMed ID: 17353900
[TBL] [Abstract][Full Text] [Related]
6. Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array.
Tamura M; Isojima T; Kawashima M; Yoshida H; Yamamoto K; Kitaoka T; Namba N; Oka A; Ozono K; Tokunaga K; Kitanaka S
PLoS One; 2015; 10(7):e0131157. PubMed ID: 26153892
[TBL] [Abstract][Full Text] [Related]
7. Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.
Cooper WN; Curley R; Macdonald F; Maher ER
Genomics; 2007 May; 89(5):613-7. PubMed ID: 17337339
[TBL] [Abstract][Full Text] [Related]
8. Global analysis of uniparental disomy using high density genotyping arrays.
Bruce S; Leinonen R; Lindgren CM; Kivinen K; Dahlman-Wright K; Lipsanen-Nyman M; Hannula-Jouppi K; Kere J
J Med Genet; 2005 Nov; 42(11):847-51. PubMed ID: 15879501
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide UPD screening in patients with intellectual disability.
Schroeder C; Ekici AB; Moog U; Grasshoff U; Mau-Holzmann U; Sturm M; Vosseler V; Poths S; Rappold G; Riess A; Riess O; Dufke A; Bonin M
Eur J Hum Genet; 2014 Oct; 22(10):1233-5. PubMed ID: 24801762
[TBL] [Abstract][Full Text] [Related]
10. Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency.
Cho SY; Goh DL; Lau KC; Ong HT; Lam CW
Clin Chim Acta; 2013 Nov; 426():13-7. PubMed ID: 23994568
[TBL] [Abstract][Full Text] [Related]
11. Accurate detection of clinically relevant uniparental disomy from exome sequencing data.
Yauy K; de Leeuw N; Yntema HG; Pfundt R; Gilissen C
Genet Med; 2020 Apr; 22(4):803-808. PubMed ID: 31767986
[TBL] [Abstract][Full Text] [Related]
12. Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis.
Faas BH; van der Burgt I; Kooper AJ; Pfundt R; Hehir-Kwa JY; Smits AP; de Leeuw N
J Med Genet; 2010 Sep; 47(9):586-94. PubMed ID: 20577003
[TBL] [Abstract][Full Text] [Related]
13. SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory.
Ngo C; Baluyot M; Bennetts B; Carmichael J; Clark A; Darmanian A; Gayagay T; Jones L; Nash B; Clark M; Jose N; Robinson S; St Heaps L; Wright D
Pathology; 2023 Oct; 55(6):818-826. PubMed ID: 37414616
[TBL] [Abstract][Full Text] [Related]
14. A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.
Talseth-Palmer BA; Bowden NA; Meldrum C; Nicholl J; Thompson E; Friend K; Liebelt J; Bratkovic D; Haan E; Yu S; Scott RJ
Cytogenet Genome Res; 2009; 124(1):94-101. PubMed ID: 19372674
[TBL] [Abstract][Full Text] [Related]
15. High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
Boultwood J; Perry J; Zaman R; Fernandez-Santamaria C; Littlewood T; Kusec R; Pellagatti A; Wang L; Clark RE; Wainscoat JS
Leukemia; 2010 Jun; 24(6):1139-45. PubMed ID: 20410925
[TBL] [Abstract][Full Text] [Related]
16. SNP-based arrays complement classic cytogenetics in the detection of chromosomal aberrations in Wilms' tumor.
Zin R; Pham K; Ashleigh M; Ravine D; Waring P; Charles A
Cancer Genet; 2012 Mar; 205(3):80-93. PubMed ID: 22469507
[TBL] [Abstract][Full Text] [Related]
17. Multiple methods used for type detection of uniparental disomy in paternity testing.
Su H; Sun T; Chen M; Liu J; Wang X; Chen Y; Ren W; Zhang G; Yan J; Yun K
Int J Legal Med; 2020 May; 134(3):885-893. PubMed ID: 31807870
[TBL] [Abstract][Full Text] [Related]
18. Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technology.
Cottrell CE; Mendell J; Hart-Kothari M; Ell D; Thrush DL; Astbury C; Pastore M; Gastier-Foster JM; Pyatt RE
Clin Genet; 2012 Jun; 81(6):578-83. PubMed ID: 21480868
[TBL] [Abstract][Full Text] [Related]
19. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.
Yin D; Ogawa S; Kawamata N; Tunici P; Finocchiaro G; Eoli M; Ruckert C; Huynh T; Liu G; Kato M; Sanada M; Jauch A; Dugas M; Black KL; Koeffler HP
Mol Cancer Res; 2009 May; 7(5):665-77. PubMed ID: 19435819
[TBL] [Abstract][Full Text] [Related]
20. Uniparental disomy in the human blastocyst is exceedingly rare.
Gueye NA; Devkota B; Taylor D; Pfundt R; Scott RT; Treff NR
Fertil Steril; 2014 Jan; 101(1):232-6. PubMed ID: 24083874
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
