Shankar SP - Search Results

1

Prioritizing regions of candidate genes for efficient mutation screening.

Braun TA, Shankar SP, Davis S, O'Leary B, Scheetz TE, Clark AF, Sheffield VC, Casavant TL, Stone EM. Braun TA, et al. Among authors: shankar sp. Hum Mutat. 2006 Feb;27(2):195-200. doi: 10.1002/humu.20247. Hum Mutat. 2006. PMID: 16395665

2

Familial cavitary optic disk anomalies: identification of a novel genetic locus.

Fingert JH, Honkanen RA, Shankar SP, Affatigato LM, Ehlinger MA, Moore MD, Jampol LM, Sheffield VC, Stone EM, Alward WL. Fingert JH, et al. Among authors: shankar sp. Am J Ophthalmol. 2007 May;143(5):795-800. doi: 10.1016/j.ajo.2007.01.042. Epub 2007 Mar 19. Am J Ophthalmol. 2007. PMID: 17368552 Free PMC article.

3

Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy.

Shankar SP, Fingert JH, Carelli V, Valentino ML, King TM, Daiger SP, Salomao SR, Berezovsky A, Belfort R Jr, Braun TA, Sheffield VC, Sadun AA, Stone EM. Shankar SP, et al. Ophthalmic Genet. 2008 Mar;29(1):17-24. doi: 10.1080/13816810701867607. Ophthalmic Genet. 2008. PMID: 18363168

4

Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies.

Shankar SP, Birch DG, Ruiz RS, Hughbanks-Wheaton DK, Sullivan LS, Bowne SJ, Stone EM, Daiger SP. Shankar SP, et al. JAMA Ophthalmol. 2015 May;133(5):511-7. doi: 10.1001/jamaophthalmol.2014.6115. JAMA Ophthalmol. 2015. PMID: 25675413 Free PMC article.

5

Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers.

Shankar SP, Hughbanks-Wheaton DK, Birch DG, Sullivan LS, Conneely KN, Bowne SJ, Stone EM, Daiger SP. Shankar SP, et al. Invest Ophthalmol Vis Sci. 2016 Feb;57(2):349-59. doi: 10.1167/iovs.15-16965. Invest Ophthalmol Vis Sci. 2016. PMID: 26842753 Free PMC article.

6

No association between variations in the WDR36 gene and primary open-angle glaucoma.

Fingert JH, Alward WL, Kwon YH, Shankar SP, Andorf JL, Mackey DA, Sheffield VC, Stone EM. Fingert JH, et al. Among authors: shankar sp. Arch Ophthalmol. 2007 Mar;125(3):434-6. doi: 10.1001/archopht.125.3.434-b. Arch Ophthalmol. 2007. PMID: 17353431 No abstract available.

7

Genetic factors modifying clinical expression of autosomal dominant RP.

Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, Daw EW, Stone EM, Heckenlively JR. Daiger SP, et al. Among authors: shankar sp. Adv Exp Med Biol. 2006;572:3-8. doi: 10.1007/0-387-32442-9_1. Adv Exp Med Biol. 2006. PMID: 17249547 Free PMC article. Review. No abstract available.

8

Retinal vascular abnormalities and dragged maculae in a carrier with a new NDP mutation (c.268delC) that caused severe Norrie disease in the proband.

Lin P, Shankar SP, Duncan J, Slavotinek A, Stone EM, Rutar T. Lin P, et al. Among authors: shankar sp. J AAPOS. 2010 Feb;14(1):93-6. doi: 10.1016/j.jaapos.2009.11.012. J AAPOS. 2010. PMID: 20227630

9

Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.

Sullivan LS, Bowne SJ, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Lewis RA, Garcia CA, Ruiz RS, Blanton SH, Northrup H, Gire AI, Seaman R, Duzkale H, Spellicy CJ, Zhu J, Shankar SP, Daiger SP. Sullivan LS, et al. Among authors: shankar sp. Invest Ophthalmol Vis Sci. 2006 Jul;47(7):3052-64. doi: 10.1167/iovs.05-1443. Invest Ophthalmol Vis Sci. 2006. PMID: 16799052 Free PMC article.

10

Alignment efficiency and three-dimensional assessment of root resorption after alignment with conventional and copper-nickel-titanium archwires: A randomized controlled trial.

Bhatia NK, Chugh VK, Shankar SP, Vinay A P R, Singh S, Moungkhom P, Sardana R. Bhatia NK, et al. Among authors: shankar sp. Dental Press J Orthod. 2024 Jan 8;28(6):e2323177. doi: 10.1590/2177-6709.28.6.e2323177.oar. eCollection 2024. Dental Press J Orthod. 2024. PMID: 38198391 Free PMC article. Clinical Trial.

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