Bruder C - Search Results

1

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: bruder c. Cancer Res. 1998 Aug 1;58(15):3226-30. Cancer Res. 1998. PMID: 9699646

2

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: bruder c. Genes Chromosomes Cancer. 1997 Dec;20(4):419-24. Genes Chromosomes Cancer. 1997. PMID: 9408760

3

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. Genes Chromosomes Cancer. 1999 Jun;25(2):184-90. Genes Chromosomes Cancer. 1999. PMID: 10338003

4

High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH.

Mantripragada KK, Buckley PG, Benetkiewicz M, De Bustos C, Hirvelä C, Jarbo C, Bruder CE, Wensman H, Mathiesen T, Nyberg G, Papi L, Collins VP, Ichimura K, Evans G, Dumanski JP. Mantripragada KK, et al. Among authors: bruder ce. Int J Oncol. 2003 Mar;22(3):615-22. Int J Oncol. 2003. PMID: 12579316

5

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

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

6

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. Hum Genet. 1999 May;104(5):418-24. doi: 10.1007/s004390050978. Hum Genet. 1999. PMID: 10394935

7

A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.

Erickson RP, Díaz de Ståhl T, Bruder CE, Dumanski JP. Erickson RP, et al. Am J Med Genet A. 2007 Dec 15;143A(24):3302-8. doi: 10.1002/ajmg.a.32025. Am J Med Genet A. 2007. PMID: 18000907

8

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH.

Bruder CE, Hirvelä C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Evans DG, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, Poptodorov G, Jordanova A, Rask-Andersen H, Kluwe L, Mautner V, Sainio M, Hung G, Mathiesen T, Möller C, Pulst SM, Harder H, Heiberg A, Honda M, Niimura M, Sahlén S, Blennow E, Albertson DG, Pinkel D, Dumanski JP. Bruder CE, et al. Hum Mol Genet. 2001 Feb 1;10(3):271-82. doi: 10.1093/hmg/10.3.271. Hum Mol Genet. 2001. PMID: 11159946 Free article.

9

Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis.

Sandgren J, Diaz de Ståhl T, Andersson R, Menzel U, Piotrowski A, Nord H, Bäckdahl M, Kiss NB, Brauckhoff M, Komorowski J, Dralle H, Hessman O, Larsson C, Akerström G, Bruder C, Dumanski JP, Westin G. Sandgren J, et al. Among authors: bruder c. Endocr Relat Cancer. 2010 Jun 3;17(3):561-79. doi: 10.1677/ERC-09-0310. Print 2010 Sep. Endocr Relat Cancer. 2010. PMID: 20410162

10

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: bruder ce. 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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

95 results

Search Page

Filters