☰

Hendrik Peter Nicolas Scholl - Publications

Affiliations: 
1997-2001 Eberhard Karls Universität Tübingen, Tübingen, Baden-Württemberg, Germany 
 2001-2003 Moorfields Eye Hospital 
 2003-2010 University of Bonn, Bonn, Nordrhein-Westfalen, Germany 
 2010-2016 Wilmer Eye Institute Johns Hopkins University, Baltimore, MD 
 2016- Department of ophthalmology University of Basel, Basel, Basel-Stadt, Switzerland 
 2018- Institute of Molecular and Clinical Ophthalmology Basel 
Tree Info Grants Similar researchers Related pubs Distance to... Nearest Nobel PubMed Report error

50 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Bocquet B, Borday C, Erkilic N, Mamaeva D, Donval A, Masson-Garcia C, Parain K, Kaminska K, Quinodoz M, Perea-Romero I, Garcia-Garcia G, Jimenez-Medina C, Boukhaddaoui H, Coget A, Leboucq N, ... ... Scholl HP, et al. TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa. Jci Insight. PMID 37768732 DOI: 10.1172/jci.insight.169426  0.333
2016 Scholl HP, Strauss RW, Singh MS, Dalkara D, Roska B, Picaud S, Sahel JA. Emerging therapies for inherited retinal degeneration. Science Translational Medicine. 8: 368rv6. PMID 27928030 DOI: 10.1126/Scitranslmed.Aaf2838  0.314
2016 Strauss RW, Ho A, Muñoz B, Cideciyan AV, Sahel JA, Sunness JS, Birch DG, Bernstein PS, Michaelides M, Traboulsi EI, Zrenner E, Sadda S, Ervin AM, West S, Scholl HP, et al. The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1. Ophthalmology. 123: 817-28. PMID 26786511 DOI: 10.1016/J.Ophtha.2015.12.009  0.394
2016 Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/Ng.3448  0.531
2015 Scholl HP, Moore AT, Koenekoop RK, Wen Y, Fishman GA, van den Born LI, Bittner A, Bowles K, Fletcher EC, Collison FT, Dagnelie G, Degli Eposti S, Michaelides M, Saperstein DA, Schuchard RA, et al. Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT). Plos One. 10: e0143846. PMID 26656277 DOI: 10.1371/Journal.Pone.0143846  0.516
2015 Heeren TF, Clemons T, Scholl HP, Bird AC, Holz FG, Charbel Issa P. Progression of Vision Loss in Macular Telangiectasia Type 2. Investigative Ophthalmology & Visual Science. 56: 3905-12. PMID 26070062 DOI: 10.1167/Iovs.15-16915  0.699
2014 Charbel Issa P, Scholl HP, Holz FG. Short-term effects of intravitreal bevacizumab in type ii idiopathic macular telangiectasia. Retinal Cases & Brief Reports. 1: 189-91. PMID 25390973 DOI: 10.1097/icb.0b013e31809ed9b6  0.53
2014 Chen C, Khurana RN, Scholl H, Goldberg M. Macular caldera in North Carolina macular dystrophy: only an illusion of posterior pole staphyloma. Jama Ophthalmology. 132: 786-7. PMID 24921177 DOI: 10.1001/jamaophthalmol.2014.1705  0.306
2014 Ratnapriya R, Zhan X, Fariss RN, Branham KE, Zipprer D, Chakarova CF, Sergeev YV, Campos MM, Othman M, Friedman JS, Maminishkis A, Waseem NH, Brooks M, Rajasimha HK, Edwards AO, ... ... Scholl HP, et al. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Human Molecular Genetics. 23: 5827-37. PMID 24899048 DOI: 10.1093/Hmg/Ddu276  0.303
2013 Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, ... ... Scholl HP, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578  0.673
2013 Charbel Issa P, Gillies MC, Chew EY, Bird AC, Heeren TF, Peto T, Holz FG, Scholl HP. Macular telangiectasia type 2. Progress in Retinal and Eye Research. 34: 49-77. PMID 23219692 DOI: 10.1016/J.Preteyeres.2012.11.002  0.721
2012 Fritsche LG, Fleckenstein M, Fiebig BS, Schmitz-Valckenberg S, Bindewald-Wittich A, Keilhauer CN, Renner AB, Mackensen F, Mößner A, Pauleikhoff D, Adrion C, Mansmann U, Scholl HP, Holz FG, Weber BH. A subgroup of age-related macular degeneration is associated with mono-allelic sequence variants in the ABCA4 gene. Investigative Ophthalmology & Visual Science. 53: 2112-8. PMID 22427542 DOI: 10.1167/Iovs.11-8785  0.529
2011 Finger RP, Fenwick E, Marella M, Charbel Issa P, Scholl HP, Holz FG, Lamoureux EL. The relative impact of vision impairment and cardiovascular disease on quality of life: the example of pseudoxanthoma elasticum. Health and Quality of Life Outcomes. 9: 113. PMID 22152229 DOI: 10.1186/1477-7525-9-113  0.483
2011 Lauer N, Mihlan M, Hartmann A, Schlötzer-Schrehardt U, Keilhauer C, Scholl HP, Charbel Issa P, Holz F, Weber BH, Skerka C, Zipfel PF. Complement regulation at necrotic cell lesions is impaired by the age-related macular degeneration-associated factor-H His402 risk variant. Journal of Immunology (Baltimore, Md. : 1950). 187: 4374-83. PMID 21930971 DOI: 10.4049/Jimmunol.1002488  0.508
2011 Finger RP, Charbel Issa P, Hendig D, Scholl HP, Holz FG. Monthly ranibizumab for choroidal neovascularizations secondary to angioid streaks in pseudoxanthoma elasticum: a one-year prospective study. American Journal of Ophthalmology. 152: 695-703. PMID 21704964 DOI: 10.1016/J.Ajo.2011.03.022  0.504
2011 Finger RP, Fimmers R, Holz FG, Scholl HP. Incidence of blindness and severe visual impairment in Germany: projections for 2030. Investigative Ophthalmology & Visual Science. 52: 4381-9. PMID 21447690 DOI: 10.1167/Iovs.10-6987  0.494
2011 Finger RP, Fimmers R, Holz FG, Scholl HP. Prevalence and causes of registered blindness in the largest federal state of Germany. The British Journal of Ophthalmology. 95: 1061-7. PMID 21378005 DOI: 10.1136/Bjo.2010.194712  0.499
2011 Charbel Issa P, Finger RP, Kruse K, Baumüller S, Scholl HP, Holz FG. Monthly ranibizumab for nonproliferative macular telangiectasia type 2: a 12-month prospective study. American Journal of Ophthalmology. 151: 876-886.e1. PMID 21334595 DOI: 10.1016/J.Ajo.2010.11.019  0.538
2010 Finger RP, Krohne TU, Charbel Issa P, Scholl HP, Holz FG. No evidence to support the use of plasmapheresis for age-related macular degeneration. Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society For Apheresis, the Japanese Society For Apheresis, the Japanese Society For Dialysis Therapy. 14: 607-8; author reply . PMID 21118372 DOI: 10.1111/J.1744-9987.2010.00879.X  0.528
2010 Charbel Issa P, Troeger E, Finger R, Holz FG, Wilke R, Scholl HP. Structure-function correlation of the human central retina. Plos One. 5: e12864. PMID 20877651 DOI: 10.1371/Journal.Pone.0012864  0.533
2010 Baumüller S, Charbel Issa P, Scholl HP, Schmitz-Valckenberg S, Holz FG. Outer retinal hyperreflective spots on spectral-domain optical coherence tomography in macular telangiectasia type 2. Ophthalmology. 117: 2162-8. PMID 20557944 DOI: 10.1016/J.Ophtha.2010.02.014  0.57
2010 Szental JA, Baird PN, Richardson AJ, Islam FM, Scholl HP, Charbel Issa P, Holz FG, Gillies M, Guymer RH. Analysis of glutathione S-transferase Pi isoform (GSTP1) single-nucleotide polymorphisms and macular telangiectasia type 2. International Ophthalmology. 30: 645-50. PMID 20499266 DOI: 10.1007/S10792-010-9374-Z  0.496
2010 Charbel Issa P, Finger RP, Götting C, Hendig D, Holz FG, Scholl HP. Centrifugal fundus abnormalities in pseudoxanthoma elasticum. Ophthalmology. 117: 1406-14. PMID 20189652 DOI: 10.1016/J.Ophtha.2009.11.008  0.585
2009 Finger RP, Charbel Issa P, Ladewig M, Götting C, Holz FG, Scholl HP. Fundus autofluorescence in Pseudoxanthoma elasticum. Retina (Philadelphia, Pa.). 29: 1496-505. PMID 19823106 DOI: 10.1097/Iae.0B013E3181Aade47  0.593
2009 Gillies MC, Zhu M, Chew E, Barthelmes D, Hughes E, Ali H, Holz FG, Scholl HP, Charbel Issa P. Familial asymptomatic macular telangiectasia type 2. Ophthalmology. 116: 2422-9. PMID 19815294 DOI: 10.1016/J.Ophtha.2009.05.010  0.553
2009 Charbel Issa P, Holz FG, Scholl HP. Metamorphopsia in patients with macular telangiectasia type 2. Documenta Ophthalmologica. Advances in Ophthalmology. 119: 133-40. PMID 19711108 DOI: 10.1007/S10633-009-9190-9  0.588
2009 Charbel Issa P, Finger RP, Holz FG, Scholl HP. Multimodal imaging including spectral domain OCT and confocal near infrared reflectance for characterization of outer retinal pathology in pseudoxanthoma elasticum. Investigative Ophthalmology & Visual Science. 50: 5913-8. PMID 19553619 DOI: 10.1167/Iovs.09-3541  0.548
2009 Charbel Issa P, Holz FG, Scholl HP. The article by Kovach and Rosenfeld. Retina (Philadelphia, Pa.). 29: 717; author reply 71. PMID 19430284 DOI: 10.1097/Iae.0B013E31819Ed6D1  0.427
2009 Finger RP, Charbel Issa P, Ladewig MS, Götting C, Szliska C, Scholl HP, Holz FG. Pseudoxanthoma elasticum: genetics, clinical manifestations and therapeutic approaches. Survey of Ophthalmology. 54: 272-85. PMID 19298904 DOI: 10.1016/J.Survophthal.2008.12.006  0.609
2009 Charbel Issa P, van der Veen RL, Stijfs A, Holz FG, Scholl HP, Berendschot TT. Quantification of reduced macular pigment optical density in the central retina in macular telangiectasia type 2. Experimental Eye Research. 89: 25-31. PMID 19233170 DOI: 10.1016/J.Exer.2009.02.006  0.638
2009 Finger RP, Charbel Issa P, Fimmers R, Holz FG, Rubin GS, Scholl HP. Reading performance is reduced by parafoveal scotomas in patients with macular telangiectasia type 2. Investigative Ophthalmology & Visual Science. 50: 1366-70. PMID 18997085 DOI: 10.1167/Iovs.08-2032  0.557
2008 Helb HM, Charbel Issa P, VAN DER Veen RL, Berendschot TT, Scholl HP, Holz FG. Abnormal macular pigment distribution in type 2 idiopathic macular telangiectasia. Retina (Philadelphia, Pa.). 28: 808-16. PMID 18536596 DOI: 10.1097/Iae.0B013E31816D81Aa  0.6
2008 Meyer CH, Scholl HP, Eter N, Helb HM, Holz FG. Combined treatment of acute subretinal haemorrhages with intravitreal recombined tissue plasminogen activator, expansile gas and bevacizumab: a retrospective pilot study. Acta Ophthalmologica. 86: 490-4. PMID 18221499 DOI: 10.1111/J.1600-0420.2007.01125.X  0.592
2008 Ladewig MS, Karl SE, Hamelmann V, Helb HM, Scholl HP, Holz FG, Eter N. Combined intravitreal bevacizumab and photodynamic therapy for neovascular age-related macular degeneration. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fã¼R Klinische Und Experimentelle Ophthalmologie. 246: 17-25. PMID 17701197 DOI: 10.1007/S00417-007-0654-X  0.653
2007 Reinhard J, Messias A, Dietz K, Mackeben M, Lakmann R, Scholl HP, Apfelstedt-Sylla E, Weber BH, Seeliger MW, Zrenner E, Trauzettel-Klosinski S. Quantifying fixation in patients with Stargardt disease. Vision Research. 47: 2076-85. PMID 17562343 DOI: 10.1016/J.Visres.2007.04.012  0.465
2007 Ebermann I, Scholl HP, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, Millán JM, Aller E, Mitter D, Bolz H. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss. Human Genetics. 121: 203-11. PMID 17171570 DOI: 10.1007/S00439-006-0304-0  0.327
2006 Ladewig MS, Götting C, Szliska C, Issa PC, Helb HM, Bedenicki I, Scholl HP, Holz FG. [Pseudoxanthoma elasticum]. Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft. 103: 537-51; quiz 552-3. PMID 16763870 DOI: 10.1007/S00347-006-1353-4  0.732
2006 Schmitz-Valckenberg S, Bindewald-Wittich A, Dolar-Szczasny J, Dreyhaupt J, Wolf S, Scholl HP, Holz FG. Correlation between the area of increased autofluorescence surrounding geographic atrophy and disease progression in patients with AMD. Investigative Ophthalmology & Visual Science. 47: 2648-54. PMID 16723482 DOI: 10.1167/Iovs.05-0892  0.607
2006 Scholl HP, Wheeler-Schilling TH, Zrenner E, Holz FG. [Establishing ophthalmology in the research framework programs of the European Union]. Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft. 103: 91-9. PMID 16437232 DOI: 10.1007/S00347-005-1308-1  0.415
2006 Zrenner E, Cunha-Vaz J, Sahel JA, Sillito A, Scholl HP, Wheeler-Schilling TH. [The European Vision Institute. Opening up new frontiers?]. Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft. 103: 100-3. PMID 16432731 DOI: 10.1007/S00347-005-1307-2  0.492
2006 Scholl HP, Kremers J, Besch D, Zrenner E, Jägle H. Progressive cone dystrophy with deutan genotype and phenotype. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fã¼R Klinische Und Experimentelle Ophthalmologie. 244: 183-91. PMID 16082559 DOI: 10.1007/S00417-005-0022-7  0.507
2005 Dandekar SS, Jenkins SA, Peto T, Scholl HP, Sehmi KS, Fitzke FW, Bird AC, Webster AR. Autofluorescence imaging of choroidal neovascularization due to age-related macular degeneration. Archives of Ophthalmology (Chicago, Ill. : 1960). 123: 1507-13. PMID 16286612 DOI: 10.1001/Archopht.123.11.1507  0.636
2004 Scholl HP, Chong NH, Robson AG, Holder GE, Moore AT, Bird AC. Fundus autofluorescence in patients with leber congenital amaurosis. Investigative Ophthalmology & Visual Science. 45: 2747-52. PMID 15277500 DOI: 10.1167/Iovs.03-1208  0.636
2004 Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE. Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness. Investigative Ophthalmology & Visual Science. 45: 2355-60. PMID 15223817 DOI: 10.1167/Iovs.03-1090  0.617
2004 Scholl HP, Bellmann C, Dandekar SS, Bird AC, Fitzke FW. Photopic and scotopic fine matrix mapping of retinal areas of increased fundus autofluorescence in patients with age-related maculopathy. Investigative Ophthalmology & Visual Science. 45: 574-83. PMID 14744901 DOI: 10.1167/Iovs.03-0495  0.657
2003 Besch D, Jägle H, Scholl HP, Seeliger MW, Zrenner E. Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects. Vision Research. 43: 3095-108. PMID 14611947 DOI: 10.1016/J.Visres.2003.09.020  0.48
2002 Scholl HP, Schuster AM, Vonthein R, Zrenner E. Mapping of retinal function in Best macular dystrophy using multifocal electroretinography. Vision Research. 42: 1053-61. PMID 11934455 DOI: 10.1016/S0042-6989(02)00034-2  0.504
2001 Scholl HP, Langrová H, Weber BH, Zrenner E, Apfelstedt-Sylla E. Clinical electrophysiology of two rod pathways: normative values and clinical application. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fã¼R Klinische Und Experimentelle Ophthalmologie. 239: 71-80. PMID 11372548 DOI: 10.1007/S004170000232  0.532
2000 Scholl HP, Kremers J, Apfelstedt-Sylla E, Zrenner E. L- and M-cone driven ERGs are differently altered in Best's macular dystrophy. Vision Research. 40: 3159-68. PMID 10996618 DOI: 10.1016/S0042-6989(00)00160-7  0.425
2000 Scholl HP, Zrenner E. Electrophysiology in the investigation of acquired retinal disorders. Survey of Ophthalmology. 45: 29-47. PMID 10946080 DOI: 10.1016/S0039-6257(00)00125-9  0.52
Show low-probability matches.