170 related articles for article (PubMed ID: 35065533)
1. Whole-chromosome arm acquired uniparental disomy in cancer development is a consequence of isochromosome formation.
Tuna M; Amos CI; Mills GB
Neoplasia; 2022 Mar; 25():9-17. PubMed ID: 35065533
[TBL] [Abstract][Full Text] [Related]
2. Common and distinct patterns of acquired uniparental disomy and homozygous deletions between lung squamous cell carcinomas and lung adenocarcinoma.
Tuna M; Mills GB; Amos CI
Neoplasia; 2023 Nov; 45():100932. PubMed ID: 37801862
[TBL] [Abstract][Full Text] [Related]
3. Genome-Wide Analysis of Head and Neck Squamous Cell Carcinomas Reveals HPV, TP53, Smoking and Alcohol-Related Allele-Based Acquired Uniparental Disomy Genomic Alterations.
Tuna M; Amos CI; Mills GB
Neoplasia; 2019 Feb; 21(2):197-205. PubMed ID: 30616092
[TBL] [Abstract][Full Text] [Related]
4. Quantitative analysis of somatically acquired and constitutive uniparental disomy in gastrointestinal cancers.
Torabi K; Erola P; Alvarez-Mora MI; Díaz-Gay M; Ferrer Q; Castells A; Castellví-Bel S; Milà M; Lozano JJ; Miró R; Ried T; Ponsa I; Camps J
Int J Cancer; 2019 Feb; 144(3):513-524. PubMed ID: 30350313
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements.
Kotzot D
J Med Genet; 2001 Aug; 38(8):497-507. PubMed ID: 11483637
[TBL] [Abstract][Full Text] [Related]
7. Prader-Willi syndrome and Tay-Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq.
Zeesman S; McCready E; Sadikovic B; Nowaczyk MJ
Am J Med Genet A; 2015 Jan; 167A(1):180-4. PubMed ID: 25287655
[TBL] [Abstract][Full Text] [Related]
8. Prognostic relevance of acquired uniparental disomy in serous ovarian cancer.
Tuna M; Ju Z; Smid M; Amos CI; Mills GB
Mol Cancer; 2015 Feb; 14(1):29. PubMed ID: 25644622
[TBL] [Abstract][Full Text] [Related]
9. Genome-Wide Profiling of Acquired Uniparental Disomy Reveals Prognostic Factors in Head and Neck Squamous Cell Carcinoma.
Tuna M; Liu W; Amos CI; Mills GB
Neoplasia; 2019 Nov; 21(11):1102-1109. PubMed ID: 31734631
[TBL] [Abstract][Full Text] [Related]
10. Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.
Berend SA; Feldman GL; McCaskill C; Czarnecki P; Van Dyke DL; Shaffer LG
Am J Med Genet; 1999 Jan; 82(3):275-81. PubMed ID: 10215554
[TBL] [Abstract][Full Text] [Related]
11. Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15.
Poyatos D; Guitart M; Gabau E; Brun C; Mila M; Vaquerizo J; Coll MD
J Med Genet; 2002 Feb; 39(2):E4. PubMed ID: 11836373
[No Abstract] [Full Text] [Related]
12. Association between acquired uniparental disomy and homozygous mutations and HER2/ER/PR status in breast cancer.
Tuna M; Smid M; Zhu D; Martens JW; Amos CI
PLoS One; 2010 Nov; 5(11):e15094. PubMed ID: 21152100
[TBL] [Abstract][Full Text] [Related]
13. Tetrasomy 5p mosaicism due to an additional isochromosome 5p in a man with normal phenotype.
Venci A; Bettio D
Am J Med Genet A; 2009 Dec; 149A(12):2889-91. PubMed ID: 19938082
[No Abstract] [Full Text] [Related]
14. Robertsonian translocations: mechanisms of formation, aneuploidy, and uniparental disomy and diagnostic considerations.
Kim SR; Shaffer LG
Genet Test; 2002; 6(3):163-8. PubMed ID: 12490055
[TBL] [Abstract][Full Text] [Related]
15. Acquired uniparental disomy of chromosome 9p in hematologic malignancies.
Wang L; Wheeler DA; Prchal JT
Exp Hematol; 2016 Aug; 44(8):644-52. PubMed ID: 26646991
[TBL] [Abstract][Full Text] [Related]
16. Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.
Wang JC; Vaccarello-Cruz M; Ross L; Owen R; Pratt VM; Lightman K; Liu Y; Hafezi K; Cherif D; Sahoo T
Am J Med Genet A; 2013 Jul; 161A(7):1695-701. PubMed ID: 23686718
[TBL] [Abstract][Full Text] [Related]
17. Soft tissue sarcoma subtypes exhibit distinct patterns of acquired uniparental disomy.
Tuna M; Ju Z; Amos CI; Mills GB
BMC Med Genomics; 2012 Dec; 5():60. PubMed ID: 23217126
[TBL] [Abstract][Full Text] [Related]
18. Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocations.
Berend SA; Bejjani BA; McCaskill C; Shaffer LG
Am J Med Genet; 2002 Sep; 111(4):362-5. PubMed ID: 12210293
[TBL] [Abstract][Full Text] [Related]
19. The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements.
McGowan KD; Weiser JJ; Horwitz J; Berend SA; McCaskill C; Sutton VR; Shaffer LG
Prenat Diagn; 2002 Feb; 22(2):141-3. PubMed ID: 11857621
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report.
Chen CL; Lee CN; Lin MW; Hsu WW; Tai YY; Lin SY
J Formos Med Assoc; 2019 Mar; 118(3):739-742. PubMed ID: 30616993
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
