Kiechle M - Search Results

1

Breast cancer risk in BRCA1/2 mutation carriers and noncarriers under prospective intensified surveillance.

Engel C, Fischer C, Zachariae S, Bucksch K, Rhiem K, Giesecke J, Herold N, Wappenschmidt B, Hübbel V, Maringa M, Reichstein-Gnielinski S, Hahnen E, Bartram CR, Dikow N, Schott S, Speiser D, Horn D, Fallenberg EM, Kiechle M, Quante AS, Vesper AS, Fehm T, Mundhenke C, Arnold N, Leinert E, Just W, Siebers-Renelt U, Weigel S, Gehrig A, Wöckel A, Schlegelberger B, Pertschy S, Kast K, Wimberger P, Briest S, Loeffler M, Bick U, Schmutzler RK; German Consortium for Hereditary Breast and Ovarian Cancer (GC-HBOC). Engel C, et al. Among authors: kiechle m. Int J Cancer. 2020 Feb 15;146(4):999-1009. doi: 10.1002/ijc.32396. Epub 2019 May 22. Int J Cancer. 2020. PMID: 31081934

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

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

7

Breastfeeding and breast cancer risk by age 50 among women in Germany.

Chang-Claude J, Eby N, Kiechle M, Bastert G, Becher H. Chang-Claude J, et al. Among authors: kiechle m. Cancer Causes Control. 2000 Sep;11(8):687-95. doi: 10.1023/a:1008907901087. Cancer Causes Control. 2000. PMID: 11065005

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

Comparative genomic hybridization detects genetic imbalances in primary ovarian carcinomas as correlated with grade of differentiation.

Kiechle M, Jacobsen A, Schwarz-Boeger U, Hedderich J, Pfisterer J, Arnold N. Kiechle M, et al. Cancer. 2001 Feb 1;91(3):534-40. Cancer. 2001. PMID: 11169935

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