Publications

The following are recent publications from the members of this lab. Click on the title of a publication to read its abstract, or follow the Pubmed ID link to view the Pubmed entry.

Mutations in the RNA granule component TDRD7 cause cataract and glaucoma.

Lachke SA, Alkuraya FS, Kneeland SC, Ohn T, Aboukhalil A, Howell GR, Saadi I, Cavallesco R, Yue Y, Tsai AC, Nair KS, Cosma MI, Smith RS, Hodges E, Alfadhli SM, Al-Hajeri A, Shamseldin HE, Behbehani A, Hannon GJ, Bulyk ML, Drack AV, Anderson PJ, John SW,

Science Mar 25 2011
Pubmed ID: 21436445
Genotype-phenotype analysis of the branchio-oculo-facial syndrome.

Milunsky JM, Maher TM, Zhao G, Wang Z, Mulliken JB, Chitayat D, Clemens M, Stalker HJ, Bauer M, Burch M, Chénier S, Cunningham ML, Drack AV, Janssens S, Karlea A, Klatt R, Kini U, Klein O, Lachmeijer AM, Megarbane A, Mendelsohn NJ, Meschino WS, Mortier G

American journal of medical genetics. Part A. Dec 22 2010
Pubmed ID: 21204207
From the laboratory to the clinic: molecular genetic testing in pediatric ophthalmology.

Drack AV, Lambert SR, Stone EM.

American Journal of Ophthalmology Jan 1 2010
Pubmed ID: 20103038
Which Leber congenital amaurosis patients are eligible for gene therapy trials?

Drack AV, Johnston R, Stone EM.

Journal of AAPOS Oct 17 2009
Pubmed ID: 19840725
Pediatric golf-related ophthalmic injuries.

Hink EM, Oliver SC, Drack AV, Hawes MJ, Wojno TH, On AV, Durairaj VD.

Archives of ophthalmology Sep 8 2008
Pubmed ID: 18779486
Giant orbital cysts after strabismus surgery.

Curtis TH, Stout AU, Drack AV, Durairaj VD.

American Journal of Ophthalmology Sep 30 2006
Pubmed ID: 17011875
Retinopathy of prematurity.

Drack A

Advances in Pediatrics Sep 23 2006
Pubmed ID: 17089868
Longitudinal changes in the refractive errors of children with tears in Descemet's membrane following forceps injuries.

Lambert SR, Drack AV, Hutchinson AK.

Journal of AAPOS Aug 5 2004
Pubmed ID: 15314599
Refractive surgery for unilateral high myopia in children.

Nucci P, Drack AV.

Journal of AAPOS May 25 2002
Pubmed ID: 11753253
Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1).

Kerrison JB, Giorda R, Lenart TD, Drack AV, Maumenee IH.

Ophthalmic Genetics Dec 1 2001
Pubmed ID: 11803490

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