Paul A. Sieving, MD, PhD

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Samuel G. JacobsonProfessor of Ophthalmology, University of PennsylvaniaDirección de correo verificada de mail.med.upenn.edu
Sten KjellstromLund University, NIH, NIDCD, NEIDirección de correo verificada de med.lu.se
Robert FarissChief, Biological Imaging Core, National Eye Institute-NIHDirección de correo verificada de nei.nih.gov
Jeff JamisonOphthy-DS Inc.Dirección de correo verificada de ophthy-ds.com
Konstantin PetrukhinProfessor of Ophthalmic Science, Department of Ophthalmology, Columbia UniversityDirección de correo verificada de cumc.columbia.edu
Brett JeffreyStaff Scientist, National Eye Institute, NIHDirección de correo verificada de nei.nih.gov
Ricardo Fujita, Ph.D.Centro de Genética y Biología Molecular, Facultad de Medicina, Universidad de San Martin de PorresDirección de correo verificada de usmp.pe
Dario MarangoniUniversity of Trieste, Department of Medicine, Surgery and Health SciencesDirección de correo verificada de units.it
Michael BoehnkeProfessor of Biostatistics, University of MichiganDirección de correo verificada de umich.edu
Wai T WongVP Retinal Discovery, Janssen R&DDirección de correo verificada de alum.mit.edu
David BirchChief Scientific and Executive Officer, Retina Foundation of the SouthwestDirección de correo verificada de retinafoundation.org
Kang ZhangMacau University of Science and TechnologyDirección de correo verificada de must.edu.mo
Zubair AhmedUniversity of MarylandDirección de correo verificada de som.umaryland.edu
Eberhart ZrennerProfessor of Ophthalmology, Univ. of Tuebingen - Germany, Instit. for Opht. Research, Retina ClinicDirección de correo verificada de uni-tuebingen.de
Laura FrishmanProfessor of Vision Science, University of HoustonDirección de correo verificada de uh.edu
Monica M. JablonskiUniversity of Tennessee Health Science CenterDirección de correo verificada de uthsc.edu
susan vitaleDirección de correo verificada de nei.nih.gov
Thomas B. FriedmanNIDCD?NIHDirección de correo verificada de nidcd.nih.gov
Joost Felius, PhDBaylor Scott & White Research Institute, Baylor University Medical Center, Dallas TXDirección de correo verificada de bswhealth.org
Lee M JampolFeinberg Professor, Northwestern UNiversityDirección de correo verificada de northwestern.edu

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Paul A. Sieving, MD, PhD

University of California Davis

Dirección de correo verificada de ucdavis.edu

medicine ophthalmology genetics neuroscience


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
Nrl is required for rod photoreceptor development AJ Mears, M Kondo, PK Swain, Y Takada, RA Bush, TL Saunders, ... Nature genetics 29 (4), 447-452, 2001	1009	2001
Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants PA Sieving, RC Caruso, W Tao, HR Coleman, DJS Thompson, ... Proceedings of the National Academy of Sciences 103 (10), 3896-3901, 2006	702	2006
Retinopathy induced in mice by targeted disruption of the rhodopsin gene MM Humphries, D Rancourt, GJ Farrar, P Kenna, M Hazel, RA Bush, ... Nature genetics 15 (2), 216-219, 1997	640	1997
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy K Zhang, M Kniazeva, M Han, W Li, Z Yu, Z Yang, Y Li, ML Metzker, ... Nature genetics 27 (1), 89-93, 2001	522	2001
Multiple evanescent white dot syndrome: I. Clinical findings LM Jampol, PA Sieving, D Pugh, GA Fishman, H Gilbert Archives of ophthalmology 102 (5), 671-674, 1984	514	1984
Push–pull model of the primate photopic electroretinogram: A role for hyperpolarizing neurons in shaping the b-wave PA Sieving, K Murayama, F Naarendorp Visual neuroscience 11 (3), 519-532, 1994	481	1994
Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to … S Kohl, B Baumann, M Broghammer, H Jägle, P Sieving, U Kellner, ... Human molecular genetics 9 (14), 2107-2116, 2000	358	2000
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23 ZM Ahmed, S Riazuddin, J Ahmad, SL Bernstein, Y Guo, MF Sabar, ... Human molecular genetics 12 (24), 3215-3223, 2003	328	2003
A proximal retinal component in the primate photopic ERG a-wave. RA Bush, PA Sieving Investigative ophthalmology & visual science 35 (2), 635-645, 1994	324	1994
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration DA Thompson, P Gyürüs, LL Fleischer, EL Bingham, CL McHenry, ... Investigative ophthalmology & visual science 41 (13), 4293-4299, 2000	303	2000
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration PK Swain, S Chen, QL Wang, LM Affatigato, CL Coats, KD Brady, ... Neuron 19 (6), 1329-1336, 1997	301	1997
Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration RA Radu, NL Mata, S Nusinowitz, X Liu, PA Sieving, GH Travis Proceedings of the National Academy of Sciences 100 (8), 4742-4747, 2003	292	2003
Biology and therapy of inherited retinal degenerative disease: insights from mouse models S Veleri, CH Lazar, B Chang, PA Sieving, E Banin, A Swaroop Disease models & mechanisms 8 (2), 109-129, 2015	289	2015
P23H rhodopsin transgenic rat: correlation of retinal function with histopathology S Machida, M Kondo, JA Jamison, NW Khan, LT Kononen, T Sugawara, ... Investigative ophthalmology & visual science 41 (10), 3200-3209, 2000	282	2000
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	279	2002
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia S Kohl, B Varsanyi, GA Antunes, B Baumann, CB Hoyng, H Jägle, ... European Journal of Human Genetics 13 (3), 302-308, 2005	267	2005
CNTF and retina R Wen, W Tao, Y Li, PA Sieving Progress in retinal and eye research 31 (2), 136-151, 2012	250	2012
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease GR Abecasis, BM Yashar, Y Zhao, NM Ghiasvand, S Zareparsi, ... The American Journal of Human Genetics 74 (3), 482-494, 2004	235	2004
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the … A Swaroop, QL Wang, W Wu, J Cook, C Coats, S Xu, S Chen, DJ Zack, ... Human molecular genetics 8 (2), 299-305, 1999	231	1999
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy DA Thompson, Y Li, CL McHenry, TJ Carlson, X Ding, PA Sieving, ... Nature genetics 28 (2), 123-124, 2001	228	2001

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