Ayyagari R - Search Results

1

IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis.

Chekuri A, Guru AA, Biswas P, Branham K, Borooah S, Soto-Hermida A, Hicks M, Khan NW, Matsui H, Alapati A, Raghavendra PB, Roosing S, Sarangapani S, Mathavan S, Telenti A, Heckenlively JR, Riazuddin SA, Frazer KA, Sieving PA, Ayyagari R. Chekuri A, et al. Among authors: ayyagari r. Hum Genet. 2018 Jul;137(6-7):447-458. doi: 10.1007/s00439-018-1897-9. Epub 2018 Jul 5. Hum Genet. 2018. PMID: 29978320 Free PMC article.

2

Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.

Padma T, Ayyagari R, Murty JS, Basti S, Fletcher T, Rao GN, Kaiser-Kupfer M, Hejtmancik JF. Padma T, et al. Among authors: ayyagari r. Am J Hum Genet. 1995 Oct;57(4):840-5. Am J Hum Genet. 1995. PMID: 7573044 Free PMC article.

3

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.

Ayyagari R, Kakuk LE, Coats CL, Bingham EL, Toda Y, Felius J, Sieving PA. Ayyagari R, et al. Mol Vis. 1999 Jul 28;5:13. Mol Vis. 1999. PMID: 10427103 Free article.

4

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.

Hiriyanna KT, Bingham EL, Yashar BM, Ayyagari R, Fishman G, Small KW, Weinberg DV, Weleber RG, Lewis RA, Andreasson S, Richards JE, Sieving PA. Hiriyanna KT, et al. Among authors: ayyagari r. Hum Mutat. 1999;14(5):423-7. doi: 10.1002/(SICI)1098-1004(199911)14:5<423::AID-HUMU8>3.0.CO;2-D. Hum Mutat. 1999. PMID: 10533068 Free article.

5

Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.

Griesinger IB, Sieving PA, Ayyagari R. Griesinger IB, et al. Among authors: ayyagari r. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):248-55. Invest Ophthalmol Vis Sci. 2000. PMID: 10634627

6

Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene.

Ayyagari R, Griesinger IB, Bingham E, Lark KK, Moroi SE, Sieving PA. Ayyagari R, et al. Arch Ophthalmol. 2000 Jan;118(1):85-92. doi: 10.1001/archopht.118.1.85. Arch Ophthalmol. 2000. PMID: 10636420

7

Juvenile retinoschisis: a model for molecular diagnostic testing of X-linked ophthalmic disease.

Sieving PA, Yashar BM, Ayyagari R. Sieving PA, et al. Among authors: ayyagari r. Trans Am Ophthalmol Soc. 1999;97:451-64; discussion 464-9. Trans Am Ophthalmol Soc. 1999. PMID: 10703138 Free PMC article.

8

A 5-base insertion in the gammaC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract.

Ren Z, Li A, Shastry BS, Padma T, Ayyagari R, Scott MH, Parks MM, Kaiser-Kupfer MI, Hejtmancik JF. Ren Z, et al. Among authors: ayyagari r. Hum Genet. 2000 May;106(5):531-7. doi: 10.1007/s004390000289. Hum Genet. 2000. PMID: 10914683 Free article.

9

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene.

Eksandh LC, Ponjavic V, Ayyagari R, Bingham EL, Hiriyanna KT, Andréasson S, Ehinger B, Sieving PA. Eksandh LC, et al. Among authors: ayyagari r. Arch Ophthalmol. 2000 Aug;118(8):1098-104. doi: 10.1001/archopht.118.8.1098. Arch Ophthalmol. 2000. PMID: 10922205

10

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy.

Ayyagari R, Kakuk LE, Bingham EL, Szczesny JJ, Kemp J, Toda Y, Felius J, Sieving PA. Ayyagari R, et al. Hum Genet. 2000 Jul;107(1):75-82. doi: 10.1007/s004390000338. Hum Genet. 2000. PMID: 10982039 Free article.

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