Finegold DN - Search Results

1

Truncating mutations in FOXC2 cause multiple lymphedema syndromes.

Finegold DN, Kimak MA, Lawrence EC, Levinson KL, Cherniske EM, Pober BR, Dunlap JW, Ferrell RE. Finegold DN, et al. Hum Mol Genet. 2001 May 15;10(11):1185-9. doi: 10.1093/hmg/10.11.1185. Hum Mol Genet. 2001. PMID: 11371511

2

Research perspectives in inherited lymphatic disease: an update.

Ferrell RE, Finegold DN. Ferrell RE, et al. Among authors: finegold dn. Ann N Y Acad Sci. 2008;1131:134-9. doi: 10.1196/annals.1413.012. Ann N Y Acad Sci. 2008. PMID: 18519966 Review.

3

HGF and MET mutations in primary and secondary lymphedema.

Finegold DN, Schacht V, Kimak MA, Lawrence EC, Foeldi E, Karlsson JM, Baty CJ, Ferrell RE. Finegold DN, et al. Lymphat Res Biol. 2008;6(2):65-8. doi: 10.1089/lrb.2008.1524. Lymphat Res Biol. 2008. PMID: 18564920 Free PMC article.

4

Candidate gene analysis in primary lymphedema.

Ferrell RE, Kimak MA, Lawrence EC, Finegold DN. Ferrell RE, et al. Among authors: finegold dn. Lymphat Res Biol. 2008;6(2):69-76. doi: 10.1089/lrb.2007.1022. Lymphat Res Biol. 2008. PMID: 18564921

5

GJC2 missense mutations cause human lymphedema.

Ferrell RE, Baty CJ, Kimak MA, Karlsson JM, Lawrence EC, Franke-Snyder M, Meriney SD, Feingold E, Finegold DN. Ferrell RE, et al. Among authors: finegold dn. Am J Hum Genet. 2010 Jun 11;86(6):943-8. doi: 10.1016/j.ajhg.2010.04.010. Epub 2010 May 27. Am J Hum Genet. 2010. PMID: 20537300 Free PMC article.

6

Age of onset in hereditary lymphedema.

Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN. Levinson KL, et al. Among authors: finegold dn. J Pediatr. 2003 Jun;142(6):704-8. doi: 10.1067/mpd.2003.235. J Pediatr. 2003. PMID: 12838201

7

Hereditary lymphedema: evidence for linkage and genetic heterogeneity.

Ferrell RE, Levinson KL, Esman JH, Kimak MA, Lawrence EC, Barmada MM, Finegold DN. Ferrell RE, et al. Among authors: finegold dn. Hum Mol Genet. 1998 Dec;7(13):2073-8. doi: 10.1093/hmg/7.13.2073. Hum Mol Genet. 1998. PMID: 9817924

8

Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment.

Finegold DN, Baty CJ, Knickelbein KZ, Perschke S, Noon SE, Campbell D, Karlsson JM, Huang D, Kimak MA, Lawrence EC, Feingold E, Meriney SD, Brufsky AM, Ferrell RE. Finegold DN, et al. Clin Cancer Res. 2012 Apr 15;18(8):2382-90. doi: 10.1158/1078-0432.CCR-11-2303. Epub 2012 Feb 20. Clin Cancer Res. 2012. PMID: 22351697 Free PMC article.

9

Lymphedema-distichiasis syndrome and FOXC2 gene mutation.

Traboulsi EI, Al-Khayer K, Matsumoto M, Kimak MA, Crowe S, Wilson SE, Finegold DN, Ferrell RE, Meisler DM. Traboulsi EI, et al. Among authors: finegold dn. Am J Ophthalmol. 2002 Oct;134(4):592-6. doi: 10.1016/s0002-9394(02)01642-2. Am J Ophthalmol. 2002. PMID: 12383817

10

African American hypertensive nephropathy maps to a new locus on chromosome 9q31-q32.

Chung KW, Ferrell RE, Ellis D, Barmada M, Moritz M, Finegold DN, Jaffe R, Vats A. Chung KW, et al. Among authors: finegold dn. Am J Hum Genet. 2003 Aug;73(2):420-9. doi: 10.1086/377184. Epub 2003 Jul 1. Am J Hum Genet. 2003. PMID: 12840782 Free PMC article.

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