Kiechle M - Search Results

1

Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer.

Kast K, Rhiem K, Wappenschmidt B, Hahnen E, Hauke J, Bluemcke B, Zarghooni V, Herold N, Ditsch N, Kiechle M, Braun M, Fischer C, Dikow N, Schott S, Rahner N, Niederacher D, Fehm T, Gehrig A, Mueller-Reible C, Arnold N, Maass N, Borck G, de Gregorio N, Scholz C, Auber B, Varon-Manteeva R, Speiser D, Horvath J, Lichey N, Wimberger P, Stark S, Faust U, Weber BH, Emons G, Zachariae S, Meindl A, Schmutzler RK, Engel C; German Consortium for Hereditary Breast and Ovarian Cancer (GC-HBOC). Kast K, et al. Among authors: kiechle m. J Med Genet. 2016 Jul;53(7):465-71. doi: 10.1136/jmedgenet-2015-103672. Epub 2016 Feb 29. J Med Genet. 2016. PMID: 26928436

2

[Clinical counseling and care of women with genetic predisposition to breast and ovarian carcinoma].

Schmutzler RK, Kempe A, Kiechle M, Beckmann MW. Schmutzler RK, et al. Among authors: kiechle m. Dtsch Med Wochenschr. 1999 May 7;124(18):563-6. doi: 10.1055/s-2007-1024360. Dtsch Med Wochenschr. 1999. PMID: 10356583 Review. German. No abstract available.

3

A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC.

Gross E, Arnold N, Goette J, Schwarz-Boeger U, Kiechle M. Gross E, et al. Among authors: kiechle m. Hum Genet. 1999 Jul-Aug;105(1-2):72-8. doi: 10.1007/s004399900092. Hum Genet. 1999. PMID: 10480358

4

A highly sensitive, fast, and economical technique for mutation analysis in hereditary breast and ovarian cancers.

Arnold N, Gross E, Schwarz-Boeger U, Pfisterer J, Jonat W, Kiechle M. Arnold N, et al. Among authors: kiechle m. Hum Mutat. 1999;14(4):333-9. doi: 10.1002/(SICI)1098-1004(199910)14:4<333::AID-HUMU9>3.0.CO;2-C. Hum Mutat. 1999. PMID: 10502781

5

FISH-microdissection (FISH-MD) analysis of complex chromosome rearrangements.

Weimer J, Kiechle M, Arnold N. Weimer J, et al. Among authors: kiechle m. Cytogenet Cell Genet. 2000;88(1-2):114-8. doi: 10.1159/000015502. Cytogenet Cell Genet. 2000. PMID: 10773683

6

Delineation of a complex karyotypic rearrangement by microdissection and CGH in a family affected with split foot.

Weimer J, Kiechle M, Wiedemann U, Tönnies H, Neitzel H, Ruhenstroth E, Ovens-Raeder A, Arnold N. Weimer J, et al. Among authors: kiechle m. J Med Genet. 2000 Jun;37(6):442-5. doi: 10.1136/jmg.37.6.442. J Med Genet. 2000. PMID: 10851255 Free PMC article.

7

Identification of specific BRCA1 and BRCA2 variants by DHPLC.

Gross E, Arnold N, Pfeifer K, Bandick K, Kiechle M. Gross E, et al. Among authors: kiechle m. Hum Mutat. 2000 Oct;16(4):345-53. doi: 10.1002/1098-1004(200010)16:4<345::AID-HUMU7>3.0.CO;2-#. Hum Mutat. 2000. PMID: 11013445

8

Ten novel BRCA1 and BRCA2 mutations in breast and/or ovarian cancer families from northern Germany.

Kiechle M, Gross E, Schwarz-Boeger U, Pfisterer J, Jonat W, Gerber WD, Albacht B, Fischer B, Schlegelberger B, Arnold N. Kiechle M, et al. Hum Mutat. 2000 Dec;16(6):529-30. doi: 10.1002/1098-1004(200012)16:6<529::AID-HUMU14>3.0.CO;2-K. Hum Mutat. 2000. PMID: 11102986

9

Comparison of comparative genomic hybridization and interphase fluorescence in situ hybridization in ovarian carcinomas: possibilities and limitations of both techniques.

Jacobsen A, Arnold N, Weimer J, Kiechle M. Jacobsen A, et al. Among authors: kiechle m. Cancer Genet Cytogenet. 2000 Oct 1;122(1):7-12. doi: 10.1016/s0165-4608(00)00263-6. Cancer Genet Cytogenet. 2000. PMID: 11104025

10

Mutation analysis of p53 in ovarian tumors by DHPLC.

Gross E, Kiechle M, Arnold N. Gross E, et al. Among authors: kiechle m. J Biochem Biophys Methods. 2001 Jan 30;47(1-2):73-81. doi: 10.1016/s0165-022x(00)00153-6. J Biochem Biophys Methods. 2001. PMID: 11179763

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