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1

Molecular cytogenetic analysis of telomere rearrangements.

Lese CM, Ledbetter DH. Lese CM, et al. Curr Protoc Hum Genet. 2001 May;Chapter 8:Unit 8.11. doi: 10.1002/0471142905.hg0811s24. Curr Protoc Hum Genet. 2001. PMID: 18428312 Review.

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2

Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature.

Tepperberg J, Pettenati MJ, Rao PN, Lese CM, Rita D, Wyandt H, Gersen S, White B, Schoonmaker MM. Tepperberg J, et al. Among authors: Lese CM. Prenat Diagn. 2001 Apr;21(4):293-301. doi: 10.1002/pd.57. Prenat Diagn. 2001. PMID: 11288120 Review.

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3

Visualization of INT2 and HST1 amplification in oral squamous cell carcinomas.

Lese CM, Rossie KM, Appel BN, Reddy JK, Johnson JT, Myers EN, Gollin SM. Lese CM, et al. Genes Chromosomes Cancer. 1995 Apr;12(4):288-95. doi: 10.1002/gcc.2870120409. Genes Chromosomes Cancer. 1995. PMID: 7539284

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4

An optimized set of human telomere clones for studying telomere integrity and architecture.

Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S, Regan R, Brenan M, Nicod A, Lawrie NM, Cardy DL, Nguyen H, Hudson TJ, Riethman HC, Ledbetter DH, Flint J. Knight SJ, et al. Among authors: Lese CM. Am J Hum Genet. 2000 Aug;67(2):320-32. doi: 10.1086/302998. Epub 2000 Jun 22. Am J Hum Genet. 2000. PMID: 10869233 Free PMC article.

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5

Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q.

Fantes JA, Mewborn SK, Lese CM, Hedrick J, Brown RL, Dyomin V, Chaganti RS, Christian SL, Ledbetter DH. Fantes JA, et al. Among authors: Lese CM. J Med Genet. 2002 Mar;39(3):170-7. doi: 10.1136/jmg.39.3.170. J Med Genet. 2002. PMID: 11897815 Free PMC article.

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6

Characterization of physical gap sizes at human telomeres.

Lese CM, Fantes JA, Riethman HC, Ledbetter DH. Lese CM, et al. Genome Res. 1999 Sep;9(9):888-94. doi: 10.1101/gr.9.9.888. Genome Res. 1999. PMID: 10508848 Free PMC article.

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7

A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage-fusion-bridge cycle model for 11q13 amplification.

Shuster MI, Han L, Le Beau MM, Davis E, Sawicki M, Lese CM, Park NH, Colicelli J, Gollin SM. Shuster MI, et al. Among authors: Lese CM. Genes Chromosomes Cancer. 2000 Jun;28(2):153-63. Genes Chromosomes Cancer. 2000. PMID: 10825000

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8

Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities.

Das S, Lese CM, Song M, Jensen JL, Wells LA, Barnoski BL, Roseberry JA, Camacho JM, Ledbetter DH, Schnur RE. Das S, et al. Among authors: Lese CM. Am J Hum Genet. 2000 Dec;67(6):1586-91. doi: 10.1086/316897. Epub 2000 Oct 18. Am J Hum Genet. 2000. PMID: 11038325 Free PMC article.

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9

Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements.

Kaiser-Rogers KA, Rao KW, Michaelis RC, Lese CM, Powell CM. Kaiser-Rogers KA, et al. Among authors: Lese CM. Am J Med Genet. 2000 Nov 6;95(1):28-35. doi: 10.1002/1096-8628(20001106)95:1<28::aid-ajmg7>3.0.co;2-c. Am J Med Genet. 2000. PMID: 11074491

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10

Two 22q telomere deletions serendipitously detected by FISH.

Precht KS, Lese CM, Spiro RP, Huttenlocher PR, Johnston KM, Baker JC, Christian SL, Kittikamron K, Ledbetter DH. Precht KS, et al. Among authors: Lese CM. J Med Genet. 1998 Nov;35(11):939-42. doi: 10.1136/jmg.35.11.939. J Med Genet. 1998. PMID: 9832042 Free PMC article.

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