Kearney L - Search Results

1

New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization.

Saracoglu K, Brown J, Kearney L, Uhrig S, Azofeifa J, Fauth C, Speicher MR, Eils R. Saracoglu K, et al. Among authors: kearney l. Cytometry. 2001 May 1;44(1):7-15. doi: 10.1002/1097-0320(20010501)44:1<7::aid-cyto1076>3.0.co;2-g. Cytometry. 2001. PMID: 11309803 Free article.

2

A new strategy for the detection of subtelomeric rearrangements.

Fauth C, Zhang H, Harabacz S, Brown J, Saracoglu K, Lederer G, Rittinger O, Rost I, Eils R, Kearney L, Speicher MR. Fauth C, et al. Among authors: kearney l. Hum Genet. 2001 Dec;109(6):576-83. doi: 10.1007/s00439-001-0629-7. Epub 2001 Nov 9. Hum Genet. 2001. PMID: 11810269

3

A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay.

Brown J, Jawad M, Twigg SR, Saracoglu K, Sauerbrey A, Thomas AE, Eils R, Harbott J, Kearney L. Brown J, et al. Among authors: kearney l. Blood. 2002 Apr 1;99(7):2526-31. doi: 10.1182/blood.v99.7.2526. Blood. 2002. PMID: 11895789 Free article.

4

Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.

Brown J, Horsley SW, Jung C, Saracoglu K, Janssen B, Brough M, Daschner M, Beedgen B, Kerkhoffs G, Eils R, Harris PC, Jauch A, Kearney L. Brown J, et al. Among authors: kearney l. Eur J Hum Genet. 2000 Dec;8(12):903-10. doi: 10.1038/sj.ejhg.5200545. Eur J Hum Genet. 2000. PMID: 11175277

5

Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.

Popp S, Schulze B, Granzow M, Keller M, Holtgreve-Grez H, Schoell B, Brough M, Hager HD, Tariverdian G, Brown J, Kearney L, Jauch A. Popp S, et al. Among authors: kearney l. Hum Genet. 2002 Jul;111(1):31-9. doi: 10.1007/s00439-002-0739-x. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136233

6

Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL).

Brown J, Saracoglu K, Uhrig S, Speicher MR, Eils R, Kearney L. Brown J, et al. Among authors: kearney l. Nat Med. 2001 Apr;7(4):497-501. doi: 10.1038/86581. Nat Med. 2001. PMID: 11283680 No abstract available.

7

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG).

Jaju RJ, Haas OA, Neat M, Harbott J, Saha V, Boultwood J, Brown JM, Pirc-Danoewinata H, Krings BW, Müller U, Morris SW, Wainscoat JS, Kearney L. Jaju RJ, et al. Among authors: kearney l. Blood. 1999 Jul 15;94(2):773-80. Blood. 1999. PMID: 10397745 Free article.

8

Fluorescence in situ hybridization for cancer-related studies.

Kearney L, Shipley J. Kearney L, et al. Methods Mol Biol. 2012;878:149-74. doi: 10.1007/978-1-61779-854-2_10. Methods Mol Biol. 2012. PMID: 22674132

9

Molecular cytogenetics.

Kearney L. Kearney L. Best Pract Res Clin Haematol. 2001 Sep;14(3):645-69. doi: 10.1053/beha.2001.0159. Best Pract Res Clin Haematol. 2001. PMID: 11640874 Review.

10

Specialized fluorescence in situ hybridization (FISH) techniques for leukaemia research.

Kearney L, Colman S. Kearney L, et al. Methods Mol Biol. 2009;538:57-70. doi: 10.1007/978-1-59745-418-6_4. Methods Mol Biol. 2009. PMID: 19277577

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