Alessandro Iannaccone
Alessandro Iannaccone
Professor of Ophthalmology, Duke University Eye Center
Verified email at duke.edu
Title
Cited by
Cited by
Year
Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years
SG Jacobson, AV Cideciyan, R Ratnakaram, E Heon, SB Schwartz, ...
Archives of ophthalmology 130 (1), 9-24, 2012
5742012
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
K Mykytyn, T Braun, R Carmi, NB Haider, CC Searby, M Shastri, G Beck, ...
Nature genetics 28 (2), 188-191, 2001
2842001
Positional cloning of a novel gene on chromosome 16q causing Bardet–Biedl syndrome (BBS2)
DY Nishimura, CC Searby, R Carmi, K Elbedour, L Van Maldergem, ...
Human Molecular Genetics 10 (8), 865-874, 2001
2732001
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa
DK Breuer, BM Yashar, E Filippova, S Hiriyanna, RH Lyons, AJ Mears, ...
The American Journal of Human Genetics 70 (6), 1545-1554, 2002
2242002
Pigment epithelium-derived factor supports normal development of photoreceptor neurons and opsin expression after retinal pigment epithelium removal
MM Jablonski, J Tombran-Tink, DA Mrazek, A Iannaccone
Journal of Neuroscience 20 (19), 7149-7157, 2000
2072000
Human CHN1 mutations hyperactivate α2-chimaerin and cause Duane's retraction syndrome
N Miyake, J Chilton, M Psatha, L Cheng, C Andrews, WM Chan, K Law, ...
Science 321 (5890), 839-843, 2008
1352008
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa
SG Jacobson, AV Cideciyan, A Iannaccone, RG Weleber, GA Fishman, ...
Investigative ophthalmology & visual science 41 (7), 1898-1908, 2000
1302000
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)
K Mykytyn, DY Nishimura, CC Searby, G Beck, K Bugge, HL Haines, ...
The American Journal of Human Genetics 72 (2), 429-437, 2003
1252003
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing
X Wang, H Wang, V Sun, HF Tuan, V Keser, K Wang, H Ren, I Lopez, ...
Journal of medical genetics 50 (10), 674-688, 2013
1172013
Macular pigment optical density is related to cognitive function in older people
R Vishwanathan, A Iannaccone, TM Scott, SB Kritchevsky, BJ Jennings, ...
Age and ageing 43 (2), 271-275, 2014
1142014
Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation
A Iannaccone, DK Breuer, XF Wang, SF Kuo, EM Normando, E Filippova, ...
Journal of medical genetics 40 (11), e118-e118, 2003
1132003
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease
K Branham, M Othman, M Brumm, AJ Karoukis, P Atmaca-Sonmez, ...
Investigative ophthalmology & visual science 53 (13), 8232-8237, 2012
972012
Pigment epithelium‐derived factor supports normal Müller cell development and glutamine synthetase expression after removal of the retinal pigment epithelium
MM Jablonski, J Tombran‐Tink, DA Mrazek, A Iannaccone
Glia 35 (1), 14-25, 2001
902001
Correlates of serum lutein+ zeaxanthin: findings from the Third National Health and Nutrition Examination Survey
M Gruber, R Chappell, A Millen, T LaRowe, SM Moeller, A Iannaccone, ...
The Journal of nutrition 134 (9), 2387-2394, 2004
802004
Diagnostic sensitivity and specificity of dark adaptometry for detection of age-related macular degeneration
GR Jackson, IU Scott, IK Kim, DA Quillen, A Iannaccone, JG Edwards
Investigative ophthalmology & visual science 55 (3), 1427-1431, 2014
742014
Kinetics of visual field loss in Usher syndrome Type II
A Iannaccone, SB Kritchevsky, ML Ciccarelli, SA Tedesco, C Macaluso, ...
Investigative ophthalmology & visual science 45 (3), 784-792, 2004
702004
Macular pigment optical density in the elderly: findings in a large biracial Midsouth population sample
A Iannaccone, M Mura, KT Gallaher, EJ Johnson, WA Todd, E Kenyon, ...
Investigative ophthalmology & visual science 48 (4), 1458-1465, 2007
682007
Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications
A Iannaccone, NC Kerr, TR Kinnick, JI Calzada, EM Stone
Archives of ophthalmology 129 (2), 211-217, 2011
672011
Clinical evidence of decreased olfaction in Bardet–Biedl syndrome caused by a deletion in the BBS4 Gene
A Iannaccone, K Mykytyn, AM Persico, CC Searby, A Baldi, MM Jablonski, ...
American Journal of Medical Genetics Part A 132 (4), 343-346, 2005
662005
Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium
DA Thompson, RR Ali, E Banin, KE Branham, JG Flannery, DM Gamm, ...
Investigative ophthalmology & visual science 56 (2), 918-931, 2015
652015
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