Dumanski JP - Search Results

1

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. Among authors: dumanski jp. 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.

2

Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3.

Nesslinger NJ, Gorski JL, Kurczynski TW, Shapira SK, Siegel-Bartelt J, Dumanski JP, Cullen RF Jr, French BN, McDermid HE. Nesslinger NJ, et al. Among authors: dumanski jp. Am J Hum Genet. 1994 Mar;54(3):464-72. Am J Hum Genet. 1994. PMID: 7906921 Free PMC article.

3

Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12.

Xie YG, Han FY, Peyrard M, Ruttledge MH, Fransson I, DeJong P, Collins J, Dunham I, Nordenskjöld M, Dumanski JP. Xie YG, et al. Among authors: dumanski jp. Hum Mol Genet. 1993 Sep;2(9):1361-8. doi: 10.1093/hmg/2.9.1361. Hum Mol Genet. 1993. PMID: 8242058

4

1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization.

Carlson KM, Bruder C, Nordenskjöld M, Dumanski JP. Carlson KM, et al. Among authors: dumanski jp. Genes Chromosomes Cancer. 1997 Dec;20(4):419-24. Genes Chromosomes Cancer. 1997. PMID: 9408760

5

Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity.

Sulman EP, Dumanski JP, White PS, Zhao H, Maris JM, Mathiesen T, Bruder C, Cnaan A, Brodeur GM. Sulman EP, et al. Among authors: dumanski jp. Cancer Res. 1998 Aug 1;58(15):3226-30. Cancer Res. 1998. PMID: 9699646

6

The mouse ortholog of the human SMARCB1 gene encodes two splice forms.

Bruder CE, Dumanski JP, Kedra D. Bruder CE, et al. Among authors: dumanski jp. Biochem Biophys Res Commun. 1999 Apr 21;257(3):886-90. doi: 10.1006/bbrc.1999.0563. Biochem Biophys Res Commun. 1999. PMID: 10208879

7

Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?

Bruder CE, Ichimura K, Blennow E, Ikeuchi T, Yamaguchi T, Yuasa Y, Collins VP, Dumanski JP. Bruder CE, et al. Among authors: dumanski jp. Genes Chromosomes Cancer. 1999 Jun;25(2):184-90. Genes Chromosomes Cancer. 1999. PMID: 10338003

8

A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene.

Bruder CE, Ichimura K, Tingby O, Hirakawa K, Komatsuzaki A, Tamura A, Yuasa Y, Collins VP, Dumanski JP. Bruder CE, et al. Among authors: dumanski jp. Hum Genet. 1999 May;104(5):418-24. doi: 10.1007/s004390050978. Hum Genet. 1999. PMID: 10394935

9

A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3.

Kiss H, Kedra D, Yang Y, Kost-Alimova M, Kiss C, O'Brien KP, Fransson I, Klein G, Imreh S, Dumanski JP. Kiss H, et al. Among authors: dumanski jp. Hum Genet. 1999 Dec;105(6):552-9. doi: 10.1007/s004399900188. Hum Genet. 1999. PMID: 10647888

10

Fine mapping of the constitutional translocation t(11;22)(q23;q11).

Tapia-Páez I, O'Brien KP, Kost-Alimova M, Sahlén S, Kedra D, Bruder CE, Andersson B, Roe BA, Hu P, Imreh S, Blennow E, Dumanski JP. Tapia-Páez I, et al. Among authors: dumanski jp. Hum Genet. 2000 May;106(5):506-16. doi: 10.1007/s004390000287. Hum Genet. 2000. PMID: 10914680

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