Schwab M - Search Results

1

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.

Neuhausen SL, Godwin AK, Gershoni-Baruch R, Schubert E, Garber J, Stoppa-Lyonnet D, Olah E, Csokay B, Serova O, Lalloo F, Osorio A, Stratton M, Offit K, Boyd J, Caligo MA, Scott RJ, Schofield A, Teugels E, Schwab M, Cannon-Albright L, Bishop T, Easton D, Benitez J, King MC, Ponder BA, Weber B, Devilee P, Borg A, Narod SA, Goldgar D. Neuhausen SL, et al. Among authors: schwab m. Am J Hum Genet. 1998 Jun;62(6):1381-8. doi: 10.1086/301885. Am J Hum Genet. 1998. PMID: 9585613 Free PMC article.

2

An interstitial tandem duplication of 9p23-24 coexists with a mutation in the BRCA2 gene in the germ line of three brothers with breast cancer.

Savelyeva L, Claas A, Gier S, Schlag P, Finke L, Mangion J, Stratton MR, Schwab M. Savelyeva L, et al. Among authors: schwab m. Cancer Res. 1998 Mar 1;58(5):863-6. Cancer Res. 1998. PMID: 9500439

3

Constitutional genomic instability with inversions, duplications, and amplifications in 9p23-24 in BRCA2 mutation carriers.

Savelyeva L, Claas A, Matzner I, Schlag P, Hofmann W, Scherneck S, Weber B, Schwab M. Savelyeva L, et al. Among authors: schwab m. Cancer Res. 2001 Jul 1;61(13):5179-85. Cancer Res. 2001. PMID: 11431357

4

BRCA2: a genetic risk factor for breast cancer.

Schwab M, Claas A, Savelyeva L. Schwab M, et al. Cancer Lett. 2002 Jan 10;175(1):1-8. doi: 10.1016/s0304-3835(01)00752-2. Cancer Lett. 2002. PMID: 11734330 Review.

5

Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells.

Savelyeva L, Corvi R, Schwab M. Savelyeva L, et al. Among authors: schwab m. Am J Hum Genet. 1994 Aug;55(2):334-40. Am J Hum Genet. 1994. PMID: 8037210 Free PMC article.

6

The neurobeachin gene spans the common fragile site FRA13A.

Savelyeva L, Sagulenko E, Schmitt JG, Schwab M. Savelyeva L, et al. Among authors: schwab m. Hum Genet. 2006 Jan;118(5):551-8. doi: 10.1007/s00439-005-0083-z. Epub 2005 Oct 22. Hum Genet. 2006. PMID: 16244873

7

The FRA2C common fragile site maps to the borders of MYCN amplicons in neuroblastoma and is associated with gross chromosomal rearrangements in different cancers.

Blumrich A, Zapatka M, Brueckner LM, Zheglo D, Schwab M, Savelyeva L. Blumrich A, et al. Among authors: schwab m. Hum Mol Genet. 2011 Apr 15;20(8):1488-501. doi: 10.1093/hmg/ddr027. Epub 2011 Jan 21. Hum Mol Genet. 2011. PMID: 21258086

8

Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats.

Brueckner LM, Sagulenko E, Hess EM, Zheglo D, Blumrich A, Schwab M, Savelyeva L. Brueckner LM, et al. Among authors: schwab m. Hum Genet. 2012 Aug;131(8):1345-59. doi: 10.1007/s00439-012-1165-3. Epub 2012 Apr 5. Hum Genet. 2012. PMID: 22476624

9

Increased rates of spontaneous sister chromatid exchange in lymphocytes of BRCA2+/- carriers of familial breast cancer clusters.

Kim MK, Zitzmann S, Westermann F, Arnold K, Brouwers S, Schwab M, Savelyeva L. Kim MK, et al. Among authors: schwab m. Cancer Lett. 2004 Jul 8;210(1):85-94. doi: 10.1016/j.canlet.2004.01.014. Cancer Lett. 2004. PMID: 15172125

10

Retention of imprinting of the human apoptosis-related gene TSSC3 in human brain tumors.

Müller S, van den Boom D, Zirkel D, Köster H, Berthold F, Schwab M, Westphal M, Zumkeller W. Müller S, et al. Among authors: schwab m. Hum Mol Genet. 2000 Mar 22;9(5):757-63. doi: 10.1093/hmg/9.5.757. Hum Mol Genet. 2000. PMID: 10749982

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