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Hendrik Scholl
Hendrik Scholl
其他姓名Hendrik Peter Scholl, Hendrik Peter Nicolas Scholl
在 unibas.ch 的电子邮件经过验证
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引用次数
引用次数
年份
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
14562016
Progression of geographic atrophy and impact of fundus autofluorescence patterns in age-related macular degeneration
FG Holz, A Bindewald-Wittich, M Fleckenstein, J Dreyhaupt, HPN Scholl, ...
American journal of ophthalmology 143 (3), 463-472. e2, 2007
6612007
Complement factor H binds malondialdehyde epitopes and protects from oxidative stress
D Weismann, K Hartvigsen, N Lauer, KL Bennett, HPN Scholl, PC Issa, ...
Nature 478 (7367), 76-81, 2011
5982011
Systemic complement activation in age-related macular degeneration
HPN Scholl, PC Issa, M Walier, S Janzer, B Pollok-Kopp, F Börncke, ...
PloS one 3 (7), e2593, 2008
4702008
Cell types of the human retina and its organoids at single-cell resolution
CS Cowan, M Renner, M De Gennaro, B Gross-Scherf, D Goldblum, ...
Cell 182 (6), 1623-1640. e34, 2020
4282020
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration
A Rivera, K White, H Stöhr, K Steiner, N Hemmrich, T Grimm, B Jurklies, ...
The American Journal of Human Genetics 67 (4), 800-813, 2000
3952000
Macular telangiectasia type 2
PC Issa, MC Gillies, EY Chew, AC Bird, TFC Heeren, T Peto, FG Holz, ...
Progress in retinal and eye research 34, 49-77, 2013
3922013
High-resolution spectral domain-OCT imaging in geographic atrophy associated with age-related macular degeneration
M Fleckenstein, PC Issa, HM Helb, S Schmitz-Valckenberg, RP Finger, ...
Investigative ophthalmology & visual science 49 (9), 4137-4144, 2008
3222008
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
I Ebermann, HPN Scholl, P Charbel Issa, E Becirovic, J Lamprecht, ...
Human genetics 121, 203-211, 2007
2532007
Pseudoxanthoma elasticum: genetics, clinical manifestations and therapeutic approaches
RP Finger, PC Issa, MS Ladewig, C Götting, C Szliska, HPN Scholl, ...
Survey of ophthalmology 54 (2), 272-285, 2009
2502009
Fundus autofluorescence and progression of age-related macular degeneration
S Schmitz-Valckenberg, M Fleckenstein, HPN Scholl, FG Holz
Survey of ophthalmology 54 (1), 96-117, 2009
2472009
Emerging therapies for inherited retinal degeneration
HPN Scholl, RW Strauss, MS Singh, D Dalkara, B Roska, S Picaud, ...
Science translational medicine 8 (368), 368rv6-368rv6, 2016
2322016
Correlation between the area of increased autofluorescence surrounding geographic atrophy and disease progression in patients with AMD
S Schmitz-Valckenberg, A Bindewald-Wittich, J Dolar-Szczasny, ...
Investigative ophthalmology & visual science 47 (6), 2648-2654, 2006
2152006
An update on the genetics of age-related macular degeneration
HPN Scholl, M Fleckenstein, PC Issa, C Keilhauer, FG Holz, BHF Weber
Molecular vision 13, 196, 2007
2082007
Photopic and scotopic fine matrix mapping of retinal areas of increased fundus autofluorescence in patients with age-related maculopathy
HPN Scholl, C Bellmann, SS Dandekar, AC Bird, FW Fitzke
Investigative ophthalmology & visual science 45 (2), 574-583, 2004
1762004
Genetic control of the alternative pathway of complement in humans and age-related macular degeneration
LA Hecker, AO Edwards, E Ryu, N Tosakulwong, KH Baratz, WL Brown, ...
Human molecular genetics 19 (1), 209-215, 2010
1742010
Targeting neuronal and glial cell types with synthetic promoter AAVs in mice, non-human primates and humans
J Jüttner, A Szabo, B Gross-Scherf, RK Morikawa, SB Rompani, P Hantz, ...
Nature Neuroscience 22 (8), 1345-1356, 2019
1732019
L/M cone ratios in human trichromats assessed by psychophysics, electroretinography, and retinal densitometry
J Kremers, HPN Scholl, H Knau, TTJM Berendschot, T Usui, LT Sharpe
JOSA A 17 (3), 517-526, 2000
1622000
The natural history of the progression of atrophy secondary to Stargardt disease (ProgStar) studies: design and baseline characteristics: ProgStar Report No. 1
RW Strauss, A Ho, B Muñoz, AV Cideciyan, JA Sahel, JS Sunness, ...
Ophthalmology 123 (4), 817-828, 2016
1572016
Incidence of blindness and severe visual impairment in Germany: projections for 2030
RP Finger, R Fimmers, FG Holz, HPN Scholl
Investigative ophthalmology & visual science 52 (7), 4381-4389, 2011
1522011
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