Hirschhorn K - Search Results

1

Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai.

Scott SA, Owusu Obeng A, Botton MR, Yang Y, Scott ER, Ellis SB, Wallsten R, Kaszemacher T, Zhou X, Chen R, Nicoletti P, Naik H, Kenny EE, Vega A, Waite E, Diaz GA, Dudley J, Halperin JL, Edelmann L, Kasarskis A, Hulot JS, Peter I, Bottinger EP, Hirschhorn K, Sklar P, Cho JH, Desnick RJ, Schadt EE. Scott SA, et al. Among authors: hirschhorn k. Pharmacogenomics. 2017 Oct;18(15):1381-1386. doi: 10.2217/pgs-2017-0137. Epub 2017 Oct 6. Pharmacogenomics. 2017. PMID: 28982267 Free PMC article. Review.

2

Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.

Edelmann L, Hirschhorn K. Edelmann L, et al. Among authors: hirschhorn k. Ann N Y Acad Sci. 2009 Jan;1151:157-66. doi: 10.1111/j.1749-6632.2008.03610.x. Ann N Y Acad Sci. 2009. PMID: 19154522 Review.

3

Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization.

Levy B, Gershin IF, Desnick RJ, Babu A, Gelb BD, Hirschhorn K, Cotter PD. Levy B, et al. Among authors: hirschhorn k. Cytogenet Cell Genet. 1997;76(1-2):68-71. doi: 10.1159/000134518. Cytogenet Cell Genet. 1997. PMID: 9154131

4

Multiple hemangiomas in a patient with a t(3q;4p) translocation: an infrequent association with Wolf-Hirschhorn syndrome.

Pardo S, Blitman N, Han B, Cohen N, Edelmann L, Hirschhorn K. Pardo S, et al. Among authors: hirschhorn k. Am J Med Genet A. 2008 Jan 15;146A(2):219-24. doi: 10.1002/ajmg.a.32033. Am J Med Genet A. 2008. PMID: 18076104

5

Paternal uniparental disomy for chromosome 14: a case report and review.

Cotter PD, Kaffe S, McCurdy LD, Jhaveri M, Willner JP, Hirschhorn K. Cotter PD, et al. Among authors: hirschhorn k. Am J Med Genet. 1997 May 2;70(1):74-9. doi: 10.1002/(sici)1096-8628(19970502)70:1<74::aid-ajmg14>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9129745 Review.

6

Jumping translocations in spontaneous abortions.

Levy B, Dunn TM, Hirschhorn K, Kardon N. Levy B, et al. Among authors: hirschhorn k. Cytogenet Cell Genet. 2000;88(1-2):25-9. doi: 10.1159/000015478. Cytogenet Cell Genet. 2000. PMID: 10773659

7

Clinical applications of comparative genomic hybridization.

Levy B, Dunn TM, Kaffe S, Kardon N, Hirschhorn K. Levy B, et al. Among authors: hirschhorn k. Genet Med. 1998 Nov-Dec;1(1):4-12. doi: 10.1097/00125817-199811000-00004. Genet Med. 1998. PMID: 11261428 Free article.

8

Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4.

Cotter PD, Kaffe S, Li L, Gershin IF, Hirschhorn K. Cotter PD, et al. Among authors: hirschhorn k. Am J Med Genet. 2001 Jul 22;102(1):76-80. doi: 10.1002/1096-8628(20010722)102:1<76::aid-ajmg1389>3.0.co;2-4. Am J Med Genet. 2001. PMID: 11471177

9

Molecular cytogenetic analysis of uterine leiomyoma and leiomyosarcoma by comparative genomic hybridization.

Levy B, Mukherjee T, Hirschhorn K. Levy B, et al. Among authors: hirschhorn k. Cancer Genet Cytogenet. 2000 Aug;121(1):1-8. doi: 10.1016/s0165-4608(00)00225-9. Cancer Genet Cytogenet. 2000. PMID: 10958933

10

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.

Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P. Levy B, et al. Among authors: hirschhorn k. Cytogenet Cell Genet. 2000;91(1-4):165-70. doi: 10.1159/000056839. Cytogenet Cell Genet. 2000. PMID: 11173851

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