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Page 1
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas.
Díaz de Ståhl T, Hansson CM, de Bustos C, Mantripragada KK, Piotrowski A, Benetkiewicz M, Jarbo C, Wiklund L, Mathiesen T, Nyberg G, Collins VP, Evans DG, Ichimura K, Dumanski JP. Díaz de Ståhl T, et al. Among authors: mantripragada kk. Hum Genet. 2005 Oct;118(1):35-44. doi: 10.1007/s00439-005-0002-3. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16078050
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
Jarbo C, Buckley PG, Piotrowski A, Mantripragada KK, Benetkiewicz M, Diaz de Ståhl T, Langford CF, Gregory SG, Dralle H, Gimm O, Bäckdahl M, Geli J, Larsson C, Westin G, Akerström G, Dumanski JP. Jarbo C, et al. Among authors: mantripragada kk. Int J Cancer. 2006 Mar 1;118(5):1159-64. doi: 10.1002/ijc.21385. Int J Cancer. 2006. PMID: 16161042
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.
Buckley PG, Mantripragada KK, Díaz de Ståhl T, Piotrowski A, Hansson CM, Kiss H, Vetrie D, Ernberg IT, Nordenskjöld M, Bolund L, Sainio M, Rouleau GA, Niimura M, Wallace AJ, Evans DG, Grigelionis G, Menzel U, Dumanski JP. Buckley PG, et al. Among authors: mantripragada kk. Hum Mutat. 2005 Dec;26(6):540-9. doi: 10.1002/humu.20255. Hum Mutat. 2005. PMID: 16287142
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.
de Bustos C, Díaz de Ståhl T, Piotrowski A, Mantripragada KK, Buckley PG, Darai E, Hansson CM, Grigelionis G, Menzel U, Dumanski JP. de Bustos C, et al. Among authors: mantripragada kk. Genomics. 2006 Aug;88(2):152-62. doi: 10.1016/j.ygeno.2006.03.016. Epub 2006 May 18. Genomics. 2006. PMID: 16713171 Free article.
Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer.
Piotrowski A, Benetkiewicz M, Menzel U, Díaz de Ståhl T, Mantripragada K, Grigelionis G, Buckley PG, Jankowski M, Hoffman J, Bała D, Srutek E, Laskowski R, Zegarski W, Dumanski JP. Piotrowski A, et al. Among authors: mantripragada k. Genes Chromosomes Cancer. 2006 Jul;45(7):656-67. doi: 10.1002/gcc.20331. Genes Chromosomes Cancer. 2006. PMID: 16575877
Array-CGH and multipoint FISH to decode complex chromosomal rearrangements.
Darai-Ramqvist E, Diaz de Ståhl T, Sandlund A, Mantripragada K, Klein G, Dumanski J, Imreh S, Kost-Alimova M. Darai-Ramqvist E, et al. Among authors: mantripragada k. BMC Genomics. 2006 Dec 29;7:330. doi: 10.1186/1471-2164-7-330. BMC Genomics. 2006. PMID: 17196103 Free PMC article.
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH.
Mantripragada KK, Thuresson AC, Piotrowski A, Díaz de Ståhl T, Menzel U, Grigelionis G, Ferner RE, Griffiths S, Bolund L, Mautner V, Nordling M, Legius E, Vetrie D, Dahl N, Messiaen L, Upadhyaya M, Bruder CE, Dumanski JP. Mantripragada KK, et al. J Med Genet. 2006 Jan;43(1):28-38. doi: 10.1136/jmg.2005.033795. Epub 2005 Jun 8. J Med Genet. 2006. PMID: 15944227 Free PMC article.
75 results