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Results: 10

1.

A crystallin gene network in the mouse retina.

Templeton JP, Wang X, Freeman NE, Ma Z, Lu A, Hejtmancik F, Geisert EE.

Exp Eye Res. 2013 Nov;116:129-40. doi: 10.1016/j.exer.2013.08.001. Epub 2013 Aug 24.

2.

Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry.

Liu Y, Hauser MA, Akafo SK, Qin X, Miura S, Gibson JR, Wheeler J, Gaasterland DE, Challa P, Herndon LW; International Consortium of African Ancestry REsearch in Glaucoma, Ritch R, Moroi SE, Pasquale LR, Girkin CA, Budenz DL, Wiggs JL, Richards JE, Ashley-Koch AE, Allingham RR.

Invest Ophthalmol Vis Sci. 2013 Sep 17;54(9):6248-54. doi: 10.1167/iovs.13-12779.

3.

Association of complement factor H tyrosine 402 histidine genotype with posterior involvement in sarcoid-related uveitis.

Thompson IA, Liu B, Sen HN, Jiao X, Katamay R, Li Z, Hu M, Hejtmancik F, Nussenblatt RB.

Am J Ophthalmol. 2013 Jun;155(6):1068-1074.e1. doi: 10.1016/j.ajo.2013.01.019. Epub 2013 Mar 14.

PMID:
23497844
4.

High-throughput retina-array for screening 93 genes involved in inherited retinal dystrophy.

Song J, Smaoui N, Ayyagari R, Stiles D, Benhamed S, MacDonald IM, Daiger SP, Tumminia SJ, Hejtmancik F, Wang X.

Invest Ophthalmol Vis Sci. 2011 Nov 25;52(12):9053-60. doi: 10.1167/iovs.11-7978.

5.

A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma.

Nemesure B, Jiao X, He Q, Leske MC, Wu SY, Hennis A, Mendell N, Redman J, Garchon HJ, Agarwala R, Schäffer AA, Hejtmancik F; Barbados Family Study Group.

Hum Genet. 2003 May;112(5-6):600-9. Epub 2003 Mar 4.

PMID:
12616399
6.

Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14.

Caldwell GM, Eddy RL, Day CD, Haley LH, Cooper PR, Sait SS, Hejtmancik F, Smith RJ, Morton CC, Higgins MJ, Shows TB.

Cytogenet Cell Genet. 2001;92(1-2):103-7.

PMID:
11306805
7.

Recurrent missense (R197C) and nonsense (Y89X) mutations in the XLRS1 gene in families with X-linked retinoschisis.

Shastry BS, Hejtmancik FJ, Trese MT.

Biochem Biophys Res Commun. 1999 Mar 16;256(2):317-9.

PMID:
10079181
8.

Contig maps and genomic sequencing identify candidate genes in the usher 1C locus.

Higgins MJ, Day CD, Smilinich NJ, Ni L, Cooper PR, Nowak NJ, Davies C, de Jong PJ, Hejtmancik F, Evans GA, Smith RJ, Shows TB.

Genome Res. 1998 Jan;8(1):57-68.

9.

Linkage mapping of new X-linked juvenile retinoschisis kindreds using microsatellite markers.

Shastry BS, Hejtmancik FJ, Margherio RT, Trese MT.

Biochem Biophys Res Commun. 1996 Mar 27;220(3):824-7.

PMID:
8607849
10.

DMD carrier detection and prenatal diagnosis via recombinant DNA methods.

Caskey CT, Ward P, Hejtmancik F.

Adv Neurol. 1988;48:83-91. No abstract available.

PMID:
2891260
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