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P. Nishina · SciRah

Researcher profile · Semantic Scholar

P. Nishina

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P. Nishina — researcher profile on SciRah

h-index: 59
Works: 212
Citations: 9,846

Most-cited papers

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
N. Peachey, Thomas A. Ray, R. Florijn, Lucy B. Rowe +23 more
2012American Journal of Human Genetics167 citations Open access
Semantic Scholar
Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice
K. Boldt, D. A. Mans, Jungyeon Won, J. van Reeuwijk +15 more
2011Cilia110 citations Open access
Semantic Scholar
Mutations in Lama1 Disrupt Retinal Vascular Development and Inner Limiting Membrane Formation*
M. Edwards, E. Mammadova-Bach, F. Alpy, A. Klein +10 more
2010Journal of Biological Chemistry97 citations Open access
Semantic Scholar
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
G. B. Collin, Navdeep Gogna, B. Chang, Nattaya Damkham +6 more
2020Cells92 citations Open access
Semantic Scholar
Survey of common eye diseases in laboratory mouse strains.
B. Chang, R. Hurd, Jie-ping Wang, P. Nishina
2013Investigative Ophthalmology and Visual Science92 citations Open access
Semantic Scholar
Nr2e3-Directed Transcriptional Regulation of Genes Involved in Photoreceptor Development and Cell-Type Specific Phototransduction
N. Haider, N. Mollema, Meghan Gaule, Yang Yuan +4 more
2009Experimental Eye Research89 citations Open access
Semantic Scholar
A novel dwarfism with gonadal dysfunction due to loss-of-function allele of the collagen receptor gene, Ddr2, in the mouse.
K. Kano, C. D. de Evsikova, James Young, Christopher Wnek +3 more
2008Molecular Endocrinology86 citations Open access
Semantic Scholar
Mouse Model Resources for Vision Research
Jungyeon Won, L. Shi, W. Hicks, Jie-ping Wang +4 more
2010Journal of Ophthalmology83 citations Open access
Semantic Scholar
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development.
Jungyeon Won, Caralina Marín de Evsikova, Richard S. Smith, W. Hicks +5 more
2011Human Molecular Genetics78 citations Open access
Semantic Scholar
Elevation of 20-carbon long chain bases due to a mutation in serine palmitoyltransferase small subunit b results in neurodegeneration
Lihong Zhao, Stefka D. Spassieva, K. Gable, Sita D. Gupta +9 more
2015Proceedings of the National Academy of Sciences of the United States of America73 citations Open access
Semantic Scholar
RPGRIP1 is essential for normal rod photoreceptor outer segment elaboration and morphogenesis.
Jungyeon Won, Elaine J. Gifford, Richard S. Smith, Hai-Qing Yi +5 more
2009Human Molecular Genetics69 citations Open access
Semantic Scholar
Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosa.
K. Wert, Richard J. Davis, J. Sancho-Pellúz, P. Nishina +1 more
2013Human Molecular Genetics63 citations Open access
Semantic Scholar
Correction of the Crb1rd8 allele and retinal phenotype in C57BL/6N mice via TALEN-mediated homology-directed repair.
B. Low, Mark P. Krebs, J. K. Joung, Shengdar Q. Tsai +2 more
2014Investigative Ophthalmology and Visual Science62 citations Open access
Semantic Scholar
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity
N. Saksens, M. Krebs, Frederieke E. Schoenmaker-Koller, W. Hicks +21 more
2015Nature Genetics60 citations Open access
Semantic Scholar
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation.
G. B. Collin, Dirk Hubmacher, J. Charette, W. Hicks +7 more
2015Human Molecular Genetics59 citations Open access
Semantic Scholar
Prefoldin 5 Is Required for Normal Sensory and Neuronal Development in a Murine Model*
Yongsuk Lee, Richard S. Smith, W. Jordan, B. King +4 more
2010Journal of Biological Chemistry53 citations Open access
Semantic Scholar
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
N. Peachey, J. Pearring, Pasano Bojang, Matthew E. Hirschtritt +10 more
2012Journal of Neurophysiology52 citations Open access
Semantic Scholar
Mouse models of human ocular disease for translational research
M. Krebs, G. B. Collin, W. Hicks, Min-Zhong Yu +6 more
2017PLoS ONE48 citations Open access
Semantic Scholar
Degradation of IRS1 leads to impaired glucose uptake in adipose tissue of the type 2 diabetes mouse model TALLYHO/Jng
Yun Wang, P. Nishina, J. Naggert
2009Journal of Endocrinology47 citations Open access
Semantic Scholar
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease.
Scott H. Greenwald, J. Charette, M. Staniszewska, L. Shi +9 more
2016American Journal of Pathology44 citations Open access
Semantic Scholar
Full-field electroretinography and marked variability in clinical phenotype of Alström syndrome.
Eva Malm, V. Ponjavic, P. Nishina, J. Naggert +4 more
2008A M A Archives of Ophthalmology41 citations Open access
Semantic Scholar
Identification of genes required for eye development by high-throughput screening of mouse knockouts
B. Moore, B. Leonard, L. Sebbag, Sydney G. Edwards +65 more
2018Communications Biology40 citations Open access
Semantic Scholar
Mutations of the Opsin Gene (Y102H and I307N) Lead to Light-induced Degeneration of Photoreceptors and Constitutive Activation of Phototransduction in Mice*
E. Budzynski, Alecia K. Gross, Suzanne D. McAlear, N. Peachey +8 more
2010Journal of Biological Chemistry40 citations Open access
Semantic Scholar
Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis.
G. B. Collin, Jungyeon Won, W. Hicks, S. Cook +2 more
2012Investigative Ophthalmology and Visual Science35 citations Open access
Semantic Scholar
Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2.
M. Edwards, C. D. de Evsikova, G. B. Collin, Elaine J. Gifford +9 more
2010Investigative Ophthalmology and Visual Science34 citations Open access
Semantic Scholar
Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments
Jungyeon Won, Richard S. Smith, N. Peachey, Jiang Wu +3 more
2008Visual Neuroscience31 citations Open access
Semantic Scholar
Gene Profiling of Postnatal Mfrprd6 Mutant Eyes Reveals Differential Accumulation of Prss56, Visual Cycle and Phototransduction mRNAs
R. Soundararajan, Jungyeon Won, Timothy M. Stearns, J. Charette +5 more
2014PLoS ONE26 citations Open access
Semantic Scholar
Human genome meeting 2016
A. K. Srivastava, Y. Wang, R. Huang, C. Skinner +496 more
2016Human Genomics23 citations Open access
Semantic Scholar
A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia.
D. Maddox, G. B. Collin, Akihiro Ikeda, C. H. Pratt +8 more
2015Investigative Ophthalmology and Visual Science23 citations Open access
Semantic Scholar
An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant Mice.
D. Maddox, Sakae Ikeda, Akihiro Ikeda, Weidong Zhang +3 more
2012Investigative Ophthalmology and Visual Science22 citations Open access
Semantic Scholar
Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness.
Ji-Yun Song, Puya Aravand, S. Nikonov, L. Leo +24 more
2018Molecular Therapy20 citations Open access
Semantic Scholar
A murine RP1 missense mutation causes protein mislocalization and slowly progressive photoreceptor degeneration.
Delu Song, S. Grieco, Ya-Feng Li, A. Hunter +10 more
2014American Journal of Pathology20 citations Open access
Semantic Scholar
Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele
B. Chang, B. Fitzmaurice, Jie-ping Wang, B. Low +2 more
2018Investigative Ophthalmology and Visual Science18 citations Open access
Semantic Scholar
A new mouse model of metabolic syndrome and associated complications
Yun Wang, Yue Zheng, P. Nishina, J. Naggert
2009Journal of Endocrinology18 citations Open access
Semantic Scholar
Transcriptome analysis reveals an unexpected role of a collagen tyrosine kinase receptor gene, Ddr2, as a regulator of ovarian function.
Hirokazu Matsumura, K. Kano, C. D. de Evsikova, J. Young +3 more
2009Physiological Genomics17 citations Open access
Semantic Scholar
Disruption in murine Eml1 perturbs retinal lamination during early development
G. B. Collin, Jungyeon Won, Mark P. Krebs, W. Hicks +3 more
2020Scientific Reports16 citations Open access
Semantic Scholar
Bright-Field Imaging and Optical Coherence Tomography of the Mouse Posterior Eye.
M. Krebs, Xiao Mei, Keith S. Sheppard, W. Hicks +1 more
2016Methods in molecular biology16 citations
Semantic Scholar
An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration.
D. Maddox, W. Hicks, D. Vollrath, M. Lavail +2 more
2011Investigative Ophthalmology and Visual Science16 citations Open access
Semantic Scholar
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Ye-Ming Yang, Xiao Li, Jie-ping Wang, Junkai Tan +8 more
2021Cell Death and Disease15 citations Open access
Semantic Scholar
Translational vision research models program.
Jungyeon Won, L. Shi, W. Hicks, Jie-ping Wang +2 more
2012Advances in Experimental Medicine and Biology15 citations
Semantic Scholar
Lysosomal Trafficking Regulator (LYST).
Xiaojie Ji, B. Chang, J. Naggert, P. Nishina
2016Advances in Experimental Medicine and Biology14 citations
Semantic Scholar
A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects
J. Charette, Ivy S. Samuels, Min-Zhong Yu, Lisa Stone +6 more
2016Advances in Experimental Medicine and Biology14 citations Open access
Semantic Scholar
The Impact of Adherens and Tight Junctions on Physiological Function and Pathological Changes in the Retina.
Y. Kong, J. Naggert, P. Nishina
2018Advances in Experimental Medicine and Biology12 citations
Semantic Scholar
Myosin 6 is required for iris development and normal function of the outer retina.
Ivy S. Samuels, B. Bell, Gwen M. Sturgill-Short, Lindsey A. Ebke +4 more
2013Investigative Ophthalmology and Visual Science12 citations Open access
Semantic Scholar
Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium
Ravi S. Pandey, M. Krebs, M. Bolisetty, J. Charette +4 more
2022International Journal of Molecular Sciences11 citations Open access
Semantic Scholar
An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency
Y. Kong, Lihong Zhao, J. Charette, W. Hicks +3 more
2018Human Molecular Genetics11 citations Open access
Semantic Scholar
Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model
Sonia M. Weatherly, G. B. Collin, J. Charette, Lisa Stone +8 more
2021bioRxiv10 citations Open access
Semantic Scholar
A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density
J. Charette, Sarah E. Earp, B. Bell, C. Ackert-Bicknell +5 more
2017Molecular Vision10 citations
Semantic Scholar
Genetic modifier loci of mouse Mfrprd6 identified by quantitative trait locus analysis
Jungyeon Won, J. Charette, V. Philip, Timothy M. Stearns +4 more
2013Experimental Eye Research10 citations Open access
Semantic Scholar
Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ
Xiaojie Ji, Ye Liu, R. Hurd, Jie-ping Wang +3 more
2016Investigative Ophthalmology and Visual Science9 citations Open access
Semantic Scholar

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