Anand Swaroop

Q: What Schools Are Affiliated With Anand Swaroop

Anand Swaroop is affiliated with the following schools: University of California, Berkeley, University of Michigan, Massachusetts Institute of Technology, Stanford University, Kyoto University, Harvard University, University of Nebraska Medical Center

Anand Swaroop's AcademicInfluence.com Rankings

Anand Swaroop

Computer Science

#5084

World Rank

#5370

Historical Rank

Computational Linguistics

#623

World Rank

#635

Historical Rank

Machine Learning

#1211

World Rank

#1231

Historical Rank

Artificial Intelligence

#1444

World Rank

#1473

Historical Rank

computer-science Degrees

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Computer Science

Anand Swaroop's Degrees

PhD Computer Science Stanford University
Masters Computer Science University of California, Berkeley
Bachelors Computer Science University of California, Berkeley

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Anand Swaroop's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Next-generation genotype imputation service and methods (2016) (2190)
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants (2015) (1024)
Nrl is required for rod photoreceptor development (2001) (869)
Retinal repair by transplantation of photoreceptor precursors (2006) (853)
Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region (1991) (850)
Seven New Loci Associated with Age-Related Macular Degeneration (2013) (741)
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4 (2006) (560)
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration (2010) (508)
Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina (2010) (493)
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration (2007) (453)
Age-related macular degeneration: genetics and biology coming together. (2014) (398)
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa. (1998) (381)
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin (2005) (379)
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse. (2006) (375)
Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration. (2005) (365)
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration (2006) (360)
Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors. (2006) (317)
A conserved retina-specific gene encodes a basic motif/leucine zipper domain. (1992) (314)
Unraveling a multifactorial late-onset disease: from genetic susceptibility to disease mechanisms for age-related macular degeneration. (2009) (294)
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies (2009) (275)
Mutations in the Cone-Rod Homeobox Gene Are Associated with the Cone-Rod Dystrophy Photoreceptor Degeneration (1997) (261)
CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease. (2008) (254)
E2-2 protein and Fuchs's corneal dystrophy. (2010) (247)
High-resolution imaging with adaptive optics in patients with inherited retinal degeneration. (2007) (246)
Meta-analysis of genome scans of age-related macular degeneration. (2005) (245)
Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa (2012) (240)
Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors. (2004) (237)
Transcriptome analysis and molecular signature of human retinal pigment epithelium (2010) (236)
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa. (2002) (229)
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa (1999) (226)
Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse. (2005) (219)
Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice (2017) (214)
The Leucine Zipper of NRL Interacts with the CRX Homeodomain (2000) (211)
Biology and therapy of inherited retinal degenerative disease: insights from mouse models (2015) (209)
The basic motif-leucine zipper transcription factor Nrl can positively regulate rhodopsin gene expression. (1996) (207)
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 development of photoreceptor function. (1999) (194)
Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration. (2005) (185)
Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting complex disease traits. (2007) (181)
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration. (2003) (179)
Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl. (2004) (173)
Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration (2013) (171)
Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL (2007) (162)
RPGR-ORF15, Which Is Mutated in Retinitis Pigmentosa, Associates with SMC1, SMC3, and Microtubule Transport Proteins* (2005) (162)
Molecular Anatomy of the Developing Human Retina. (2017) (160)
Biomarkers of cardiovascular disease as risk factors for age-related macular degeneration. (2005) (154)
Association of apolipoprotein E alleles with susceptibility to age-related macular degeneration in a large cohort from a single center. (2004) (150)
Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration (2019) (147)
Molecular analysis of the cDNA for human SPARC/osteonectin/BM-40: sequence, expression, and localization of the gene to chromosome 5q31-q33. (1988) (145)
Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons (2007) (145)
Free radical scavenging, antioxidant and cancer chemoprevention by grape seed proanthocyanidin: an overview. (2014) (145)
The bZIP Transcription Factor Nrl Stimulates Rhodopsin Promoter Activity in Primary Retinal Cell Cultures* (1996) (142)
Centrosomal‐ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis (2007) (141)
Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins (2012) (137)
Photoreceptors of Nrl −/− Mice Coexpress Functional S- and M-cone Opsins Having Distinct Inactivation Mechanisms (2005) (136)
Transcriptome Dynamics of Developing Photoreceptors in Three‐Dimensional Retina Cultures Recapitulates Temporal Sequence of Human Cone and Rod Differentiation Revealing Cell Surface Markers and Gene Networks (2015) (134)
Multiple Phosphorylated Isoforms of NRL Are Expressed in Rod Photoreceptors* (2001) (132)
Evidence of association of APOE with age‐related macular degeneration ‐ a pooled analysis of 15 studies (2011) (130)
A comprehensive analysis of the expression of crystallins in mouse retina. (2003) (129)
Ancestry estimation and control of population stratification for sequence-based association studies (2014) (128)
Barrier to Autointegration Factor Interacts with the Cone-Rod Homeobox and Represses Its Transactivation Function* (2002) (124)
Retinoid-related orphan nuclear receptor RORβ is an early-acting factor in rod photoreceptor development (2009) (123)
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration. (2006) (122)
Accelerated and Improved Differentiation of Retinal Organoids from Pluripotent Stem Cells in Rotating-Wall Vessel Bioreactors (2017) (121)
In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development. (2006) (120)
Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors (2008) (120)
Age-Related Macular Degeneration: A High-Resolution Genome Scan for Susceptibility Loci in a Population Enriched for Late-Stage Disease (2004) (120)
Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation (2003) (119)
GRK1-Dependent Phosphorylation of S and M Opsins and Their Binding to Cone Arrestin during Cone Phototransduction in the Mouse Retina (2003) (119)
Transcriptional Regulation of Rod Photoreceptor Homeostasis Revealed by In Vivo NRL Targetome Analysis (2012) (118)
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy. (2011) (114)
A small plant with big benefits: Fenugreek (Trigonella foenum‐graecum Linn.) for disease prevention and health promotion (2017) (114)
Microarray analysis of gene expression in the aging human retina. (2002) (113)
Long-term survival and differentiation of retinal neurons derived from human embryonic stem cell lines in un-immunosuppressed mouse retina (2012) (111)
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome (2004) (111)
RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin. (2005) (109)
Next-generation sequencing facilitates quantitative analysis of wild-type and Nrl−/− retinal transcriptomes (2011) (109)
Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome. (2009) (108)
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations. (2007) (107)
Human SEC13Rp functions in yeast and is located on transport vesicles budding from the endoplasmic reticulum (1995) (106)
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. (2012) (101)
Progression of Geographic Atrophy in Age-related Macular Degeneration: AREDS2 Report Number 16. (2018) (100)
Developing Rods Transplanted into the Degenerating Retina of Crx‐Knockout Mice Exhibit Neural Activity Similar to Native Photoreceptors (2013) (100)
Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration (2010) (99)
Genome-wide association study and meta-analysis of intraocular pressure (2013) (99)
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration. (2004) (99)
CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies. (2015) (98)
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa. (1997) (97)
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function. (2004) (96)
Complement factor D in age-related macular degeneration. (2011) (96)
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations. (2017) (96)
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. (2011) (93)
Recruitment of Rod Photoreceptors from Short-Wavelength-Sensitive Cones during the Evolution of Nocturnal Vision in Mammals. (2016) (93)
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa. (2009) (93)
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene. (1997) (93)
MicroRNA profile of the developing mouse retina. (2010) (91)
Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). (2011) (90)
Quantification of Oxygen Consumption in Retina Ex Vivo Demonstrates Limited Reserve Capacity of Photoreceptor Mitochondria. (2015) (90)
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease. (2004) (88)
NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors. (2016) (86)
Chondroitinase ABC Treatment Enhances Synaptogenesis between Transplant and Host Neurons in Model of Retinal Degeneration (2007) (86)
Recruitment of the Rod Pathway by Cones in the Absence of Rods (2004) (86)
QRX, a novel homeobox gene, modulates photoreceptor gene expression. (2004) (85)
Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina. (2004) (85)
No clinically significant association between CFH and ARMS2 genotypes and response to nutritional supplements: AREDS report number 38. (2014) (84)
Biochemical Characterization and Subcellular Localization of the Mouse Retinitis Pigmentosa GTPase Regulator (mRpgr)* (1998) (84)
Evaluation and optimization of procedures for target labeling and hybridization of cDNA microarrays. (2002) (83)
Heat exposure and hypothyroid conditions decrease hydrogen peroxide generation in liver mitochondria. (1985) (83)
Genetic studies of age-related macular degeneration: lessons, challenges, and opportunities for disease management. (2012) (83)
Toll-like receptor polymorphisms and age-related macular degeneration. (2008) (82)
Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy. (2007) (81)
The mRNA of a human class I gene HLA G/HLA 6.0 exhibits a restricted pattern of expression. (1990) (81)
Two Transcription Factors Can Direct Three Photoreceptor Outcomes from Rod Precursor Cells in Mouse Retinal Development (2011) (80)
Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis. (2012) (79)
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. (2012) (79)
Localization of the gene for pigment epithelium-derived factor (PEDF) to chromosome 17p13.1 and expression in cultured human retinoblastoma cells. (1994) (76)
Conditional knockdown of DNA methyltransferase 1 reveals a key role of retinal pigment epithelium integrity in photoreceptor outer segment morphogenesis (2013) (76)
Loss of RPGR glutamylation underlies the pathogenic mechanism of retinal dystrophy caused by TTLL5 mutations (2016) (76)
Epigenetic control of gene regulation during development and disease: A view from the retina (2018) (76)
Differential expression of novel Gsα signal transduction protein cDNA species (1991) (75)
Gene expression changes in aging retinal microglia: relationship to microglial support functions and regulation of activation (2013) (75)
Three-dimensional retinal organoids from mouse pluripotent stem cells mimic in vivo development with enhanced stratification and rod photoreceptor differentiation (2016) (74)
The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development. (2010) (70)
Subunit Dissociation and Diffusion Determine the Subcellular Localization of Rod and Cone Transducins (2007) (69)
Activation of signaling pathways and stress-response genes in an experimental model of retinal detachment. (2006) (69)
Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development. (2010) (69)
A simple and efficient cDNA library subtraction procedure: isolation of human retina-specific cDNA clones. (1991) (68)
Expression of the bZIP transcription factor gene Nrl in the developing nervous system. (1996) (68)
Radioprotective and antioxidant activity of fractionated extracts of berries of Hippophae rhamnoides. (2007) (67)
Rd9 Is a Naturally Occurring Mouse Model of a Common Form of Retinitis Pigmentosa Caused by Mutations in RPGR-ORF15 (2012) (66)
Efficacy of a Novel Fenugreek Seed Extract (Trigonella foenum-graecum, FurocystTM) in Polycystic Ovary Syndrome (PCOS) (2015) (66)
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness. (2014) (65)
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families. (1997) (65)
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies (2015) (65)
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa. (1999) (64)
Retinoic Acid Regulates the Expression of Photoreceptor Transcription Factor NRL* (2006) (64)
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15. (2000) (63)
A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27. (1998) (63)
A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degeneration. (2015) (63)
Expressed sequence tags and chromosomal localization of cDNA clones from a subtracted retinal pigment epithelium library. (1992) (63)
Increased retinal mtDNA damage in the CFH variant associated with age-related macular degeneration. (2016) (62)
Altered Expression of Genes of the Bmp/Smad and Wnt/Calcium Signaling Pathways in the Cone-only Nrl-/- Mouse Retina, Revealed by Gene Profiling Using Custom cDNA Microarrays* (2004) (62)
Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesis (2014) (62)
Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3 (2009) (62)
Deletion of aryl hydrocarbon receptor AHR in mice leads to subretinal accumulation of microglia and RPE atrophy. (2014) (62)
Autosomal recessive retinitis pigmentosa with early macular affectation caused by premature truncation in PROM1. (2010) (62)
Improved Retinal Organoid Differentiation by Modulating Signaling Pathways Revealed by Comparative Transcriptome Analyses with Development In Vivo (2019) (62)
Functional analysis of the rod photoreceptor cGMP phosphodiesterase alpha-subunit gene promoter: Nrl and Crx are required for full transcriptional activity. (2004) (61)
Centrosomal protein CP110 controls maturation of the mother centriole during cilia biogenesis (2016) (61)
RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa. (2010) (61)
Evaluation of the ELOVL4 gene in patients with age-related macular degeneration (2001) (60)
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene. (1997) (59)
Next generation sequencing technology and genomewide data analysis: Perspectives for retinal research (2016) (59)
High Throughput Screening of Co-Expressed Gene Pairs with Controlled False Discovery Rate (FDR) and Minimum Acceptable Strength (MAS) (2005) (59)
Mechanisms of aging in senescence-accelerated mice (2005) (59)
RPGR-associated retinal degeneration in human X-linked RP and a murine model. (2012) (59)
The cellular and compartmental profile of mouse retinal glycolysis, tricarboxylic acid cycle, oxidative phosphorylation, and ~P transferring kinases (2016) (58)
Sequence analysis of the complete cDNA and encoded polypeptide for the Glued gene of Drosophila melanogaster. (1987) (58)
Clinical and Genetic Factors Associated with Progression of Geographic Atrophy Lesions in Age-Related Macular Degeneration (2015) (58)
Pluripotent stem cell‐derived retinal organoids for disease modeling and development of therapies (2020) (58)
Genome-wide analysis of disease progression in age-related macular degeneration (2018) (58)
Deep-learning-based Prediction of Late Age-Related Macular Degeneration Progression (2019) (58)
Preservation of Cone Photoreceptors after a Rapid yet Transient Degeneration and Remodeling in Cone-Only Nrl−/− Mouse Retina (2012) (57)
Differential DNA methylation identified in the blood and retina of AMD patients (2015) (56)
Vision from next generation sequencing: Multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease (2015) (56)
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. (2014) (55)
Minireview: the role of nuclear receptors in photoreceptor differentiation and disease. (2012) (55)
Ablation of the X-linked retinitis pigmentosa 2 (Rp2) gene in mice results in opsin mislocalization and photoreceptor degeneration. (2013) (55)
Age-related macular degeneration-associated variants at chromosome 10q26 do not significantly alter ARMS2 and HTRA1 transcript levels in the human retina (2010) (55)
Pharmacologic fibroblast reprogramming into photoreceptors restores vision (2020) (55)
Generation of H2O2 in Brain Mitochondria (1986) (55)
Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent (2010) (53)
Ciliary Neurotrophic Factor Induces Genes Associated with Inflammation and Gliosis in the Retina: A Gene Profiling Study of Flow-Sorted, Müller Cells (2011) (53)
Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits (2017) (53)
Cloning and functional expression of human retinal kir2.4, a pH-sensitive inwardly rectifying K(+) channel. (2000) (53)
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 mice (2010) (52)
A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration (2011) (52)
Simultaneous Determination of Quercetin, Rutin and Coumaric Acid in Flowers of Rhododendron arboreum by HPTLC1 (2005) (52)
Inflammation in the pathogenesis of age-related macular degeneration (2008) (52)
An isoform of retinoid-related orphan receptor β directs differentiation of retinal amacrine and horizontal interneurons (2013) (51)
TOPORS, implicated in retinal degeneration, is a cilia-centrosomal protein. (2011) (51)
A multicenter clinical study to determine the efficacy of a novel fenugreek seed (Trigonella foenum-graecum) extract (Fenfuro™) in patients with type 2 diabetes (2016) (51)
Annotation and analysis of 10,000 expressed sequence tags from developing mouse eye and adult retina (2003) (50)
Lens-Specific Gene Recruitment of ζ-Crystallin through Pax6, Nrl-Maf, and Brain Suppressor Sites (1998) (50)
Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene. (2008) (50)
XIAP therapy increases survival of transplanted rod precursors in a degenerating host retina. (2011) (50)
Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: Insights into X-linked Retinitis Pigmentosa and associated ciliopathies (2008) (50)
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL (2010) (49)
Transcriptome analysis using next generation sequencing reveals molecular signatures of diabetic retinopathy and efficacy of candidate drugs (2012) (49)
Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects (2012) (49)
Null and hypomorph Prickle1 alleles in mice phenocopy human Robinow syndrome and disrupt signaling downstream of Wnt5a (2014) (48)
Dietary nutrient intake and progression to late age-related macular degeneration in the Age-Related Eye Disease Studies 1 and 2. (2020) (47)
Transcriptome-based molecular staging of human stem cell-derived retinal organoids uncovers accelerated photoreceptor differentiation by 9-cis retinal (2019) (47)
Rdh12 Activity and Effects on Retinoid Processing in the Murine Retina* (2009) (47)
Rapid, Dynamic Activation of Müller Glial Stem Cell Responses in Zebrafish (2016) (47)
Distinct nuclear localization patterns of DNA methyltransferases in developing and mature mammalian retina (2011) (47)
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity (2007) (47)
Sumoylation of bZIP Transcription Factor NRL Modulates Target Gene Expression during Photoreceptor Differentiation* (2010) (47)
Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk Scores (2017) (46)
Regulation of retinal progenitor expansion by Frizzled receptors: implications for microphthalmia and retinal coloboma. (2012) (46)
Prickle1 is expressed in distinct cell populations of the central nervous system and contributes to neuronal morphogenesis. (2013) (46)
Molecular genetics of a transposon-induced dominant mutation in the Drosophila locus Glued. (1985) (46)
Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors. (2011) (46)
Mouse eye gene microarrays for investigating ocular development and disease (2002) (45)
Strong Association of the Y 402 H Variant in Complement Factor H at 1 q 32 with Susceptibility to Age-Related Macular Degeneration (2005) (44)
Transcriptome analysis of the retina (2002) (43)
Interaction of retinal bZIP transcription factor NRL with Flt3-interacting zinc-finger protein Fiz1: possible role of Fiz1 as a transcriptional repressor. (2003) (43)
What can we learn about age-related macular degeneration from other retinal diseases? (1999) (42)
The Transcription Factor Neural Retina Leucine Zipper (NRL) Controls Photoreceptor-specific Expression of Myocyte Enhancer Factor Mef2c from an Alternative Promoter* (2011) (42)
The Minimal Transactivation Domain of the Basic Motif-Leucine Zipper Transcription Factor NRL Interacts with TATA-binding Protein* (2004) (42)
Gene expression profile of native human retinal pigment epithelium. (2002) (42)
Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15. (2002) (42)
Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments. (2008) (41)
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. (2016) (41)
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosa. (2003) (40)
Afferent Control of Horizontal Cell Morphology Revealed by Genetic Respecification of Rods and Cones (2007) (40)
Declarative Querying for Biological Sequences (2006) (40)
A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma. (2016) (40)
Treatment Paradigms for Retinal and Macular Diseases Using 3-D Retina Cultures Derived From Human Reporter Pluripotent Stem Cell Lines (2016) (40)
Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degeneration. (2013) (39)
Combinatorial Regulation of Photoreceptor Differentiation Factor, Neural Retina Leucine Zipper Gene Nrl, Revealed by in Vivo Promoter Analysis* (2011) (39)
Long-term rescue of cone photoreceptor degeneration in retinitis pigmentosa 2 (RP2)-knockout mice by gene replacement therapy. (2015) (39)
Primary cilia biogenesis and associated retinal ciliopathies (2020) (38)
Multicriteria Gene Screening for Analysis of Differential Expression with DNA Microarrays (2004) (37)
Genetic association study of age‐related macular degeneration in the Spanish population (2011) (37)
Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma. (2017) (36)
Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing (2013) (35)
Sequence analysis, expression and chromosomal localization of a gene, isolated from a subtracted human retina cDNA library, that encodes an insulin-like growth factor binding protein (IGFBP2). (1991) (35)
Development and Plasticity of Outer Retinal Circuitry Following Genetic Removal of Horizontal Cells (2013) (35)
Madeline 2.0 PDE: a new program for local and web-based pedigree drawing (2007) (35)
Distinct Signature of Altered Homeostasis in Aging Rod Photoreceptors: Implications for Retinal Diseases (2010) (35)
Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6. (1994) (34)
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration. (1997) (33)
Spatial and temporal expression of AP-1 responsive rod photoreceptor genes and bZIP transcription factors during development of the rat retina. (1998) (32)
A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3 (2009) (32)
Safety, efficacy and toxicological evaluation of a novel, patented anti-diabetic extract of Trigonella Foenum-Graecum seed extract (Fenfuro) (2014) (32)
RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction (2009) (32)
Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutations. (2013) (32)
Transgenic mice expressing Cre-recombinase specifically in M- or S-cone photoreceptors. (2004) (32)
Efficacy of FurosapTM, a novel Trigonella foenum-graecum seed extract, in Enhancing Testosterone Level and Improving Sperm Profile in Male Volunteers (2017) (31)
EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression (2017) (31)
The transcription-splicing protein NonO/p54nrb and three NonO-interacting proteins bind to distal enhancer region and augment rhodopsin expression. (2014) (31)
Generation of hydrogen peroxide on oxidation of NADH by hepatic plasma membranes (1981) (30)
Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in Israel. (2014) (30)
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration. (2016) (30)
Connexin 36 in photoreceptor cells: studies on transgenic rod-less and cone-less mouse retinas. (2004) (29)
Molecular characterization of the murine neural retina leucine zipper gene, Nrl. (1993) (29)
Gene Expression Changes In Retinal Microglia And Macrophages In Response To Ciliary Neurotrophic Factor (2011) (29)
Increasing evidence for syndromic phenotypes associated with RPGR mutations. (2004) (28)
Long-term follow-up of a family with dominant X-linked retinitis pigmentosa (2010) (28)
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration (2020) (28)
Pareto analysis for gene filtering in microarray experiments (2002) (27)
A CEP290 C-Terminal Domain Complements the Mutant CEP290 of Rd16 Mice In Trans and Rescues Retinal Degeneration. (2018) (27)
Synergistically acting agonists and antagonists of G protein–coupled receptors prevent photoreceptor cell degeneration (2016) (27)
Gene therapy of dominant CRX-Leber congenital amaurosis using patient stem cell-derived retinal organoids. (2021) (27)
A simple and efficient method for generating human retinal organoids (2020) (27)
A micromethod for the determination of urinary inorganic sulfates. (1973) (27)
Expression Profile and Chromosomal Location of cDNA Clones, Identified from an Enriched Adult Human Retina Library (2000) (27)
Regulation of a novel isoform of Receptor Expression Enhancing Protein REEP6 in rod photoreceptors by bZIP transcription factor NRL. (2014) (27)
Mitochondrial Respiration in Outer Retina Contributes to Light-Evoked Increase in Hydration In Vivo (2018) (26)
Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes (2003) (26)
NRL S50T mutation and the importance of ‘founder effects’ in inherited retinal dystrophies (2000) (25)
A Deep Phenotype Association Study Reveals Specific Phenotype Associations with Genetic Variants in Age-related Macular Degeneration: Age-Related Eye Disease Study 2 (AREDS2) Report No. 14. (2018) (25)
Adherence to the Mediterranean diet and progression to late age-related macular degeneration in the Age-Related Eye Disease Studies 1 and 2. (2020) (25)
RNA Biology in Retinal Development and Disease. (2018) (25)
Mini and customized low-cost bioreactors for optimized high-throughput generation of tissue organoids. (2018) (25)
Molecular organization and expression of the genetic locus glued in Drosophila melanogaster. (1986) (25)
X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60. (1998) (25)
Differential expression of novel Gs alpha signal transduction protein cDNA species. (1991) (25)
Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1 (2020) (24)
Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to CEP290 Mutation: Determining the Timing and Expectation of Therapy (2014) (24)
Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP). (2010) (24)
Retinal transcriptome profiling by directional next-generation sequencing using 100 ng of total RNA. (2012) (24)
Charon BS(+) and (-), versatile lambda phage vectors for constructing directional cDNA libraries and their efficient transfer to plasmids. (1988) (23)
Regulation of Noncoding Transcriptome in Developing Photoreceptors by Rod Differentiation Factor NRL (2017) (23)
Adherence to a Mediterranean diet and cognitive function in the Age‐Related Eye Disease Studies 1 & 2 (2020) (23)
Patient iPSC‐derived neural stem cells exhibit phenotypes in concordance with the clinical severity of mucopolysaccharidosis I (2018) (23)
Feedback Induction of a Photoreceptor-specific Isoform of Retinoid-related Orphan Nuclear Receptor β by the Rod Transcription Factor NRL* (2014) (23)
FGF19 exhibits neuroprotective effects on adult mammalian photoreceptors in vitro. (2008) (22)
cDNA libraries from human tissues and cell lines. (1993) (22)
An efficient chemoselective strategy for the preparation of (E)-cinnamic esters from cinnamaldehydes using heterogeneous catalyst and DDQ (2007) (22)
REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival (2017) (22)
Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration. (2019) (22)
Retinal disease in ciliopathies: Recent advances with a focus on stem cell-based therapies (2019) (22)
Origin of mutations in two families with X-linked chronic granulomatous disease. (1990) (21)
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene. (2010) (21)
Expression profile and chromosomal location of cDNA clones, identified from an enriched adult retina library. (2000) (20)
Genetic components in diabetic retinopathy (2016) (20)
Inhibition of H2O2 generation in rat liver mitochondria by radical quenchers and phenolic compounds. (1981) (20)
The combination of whole‐exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies (2019) (19)
Association of age-related macular degeneration with complement activation products, smoking, and single nucleotide polymorphisms in South Carolinians of European and African descent (2019) (19)
Toll-like receptor 4 variant D 299 G is associated with susceptibility to age-related macular degeneration (2005) (19)
Characterization and sequence analysis of the human homeobox-containing gene GBX2. (1996) (19)
Preventing polyglutamine-induced activation of c-Jun delays neuronal dysfunction in a mouse model of SCA7 retinopathy (2007) (18)
An optimized protocol for retina single-cell RNA sequencing (2020) (18)
Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing (2016) (18)
Nutraceuticals and Functional Foods in Human Health and Disease Prevention (2015) (18)
Centrosomal protein CP110 controls maturation of the mother centriole during cilia biogenesis (2016) (17)
Nonsyndromic Early‐Onset Cone‐Rod Dystrophy and Limb‐Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF (2015) (17)
Geographic atrophy in age-related macular degeneration and TLR3. (2009) (17)
A mega-analysis of expression quantitative trait loci in retinal tissue (2020) (17)
A role for prenylated rab acceptor 1 in vertebrate photoreceptor development (2012) (16)
The golden era of ocular disease gene discovery: Race to the finish (2013) (16)
Family-based exome sequencing identifies rare coding variants in age-related macular degeneration (2020) (16)
Examining the Relationship Between Nonalcoholic Fatty Liver Disease and the Metabolic Syndrome in Nondiabetic Subjects (2018) (16)
Phenotype of an X-linked retinitis pigmentosa family with a novel splice defect in the RPGR gene. (1998) (15)
Seeing the unseen: Microarray-based gene expression profiling in vision. (2004) (15)
Increasing evidence for syndromic phenotypes associated with RPGR mutations [3] (multiple letters) (2004) (15)
RPGR: part one of the X-linked retinitis pigmentosa story. (1996) (15)
Expression and chromosomal localization of cDNA clones from an enriched human retinal pigment epithelial (RPE) cell line library: identification of two RPE-specific genes. (1995) (15)
Senile panretinal cone dysfunction in age-related macular degeneration (AMD): a report of 52 amd patients compared to age-matched controls. (2006) (15)
Clustering gene expression signals from retinal microarray data (2002) (15)
X-Linked Retinitis Pigmentosa: Current Status (2001) (15)
Gene‐Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions (2016) (14)
Letter to the Editor: A Carboxy-terminal Truncation of 99 Amino Acids Resulting from a Novel Mutation (Arg555→stop) in theCHMGene leads to Choroideremia (1997) (14)
A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa. (1998) (14)
Protective Gene Expression Changes Elicited by an Inherited Defect in Photoreceptor Structure (2012) (14)
Global expression profiling of peripheral Qa-1-restricted CD8αα+TCRαβ+ regulatory T cells reveals innate-like features: implications for immune-regulatory repertoire. (2012) (14)
Aging of the Retina: Molecular and Metabolic Turbulences and Potential Interventions. (2021) (14)
Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual (2016) (13)
Tbx2a modulates switching of RH2 and LWS opsin gene expression. (2020) (13)
Cone‐rod homeobox CRX controls presynaptic active zone formation in photoreceptors of mammalian retina (2018) (13)
Noradrenaline treatment of rats stimulates H2O2 generation in liver mitochondria. (1983) (13)
Proneural genes define ground-state rules to regulate neurogenic patterning and cortical folding (2020) (13)
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration. (2018) (12)
Neural retina-specific leucine zipper gene NRL (D14S46E) maps to human chromosome 14q11.1-q11.2. (1992) (12)
A Review on Antioxidant, Anti-Inflammatory and Gastroprotective Abilities of Mango (Magnifera indica) Leaf Extract and Mangiferin (2018) (12)
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene. (2003) (12)
No CFH or ARMS2 Interaction with Omega-3 Fatty Acids, Low versus High Zinc, or β-Carotene versus Lutein and Zeaxanthin on Progression of Age-Related Macular Degeneration in the Age-Related Eye Disease Study 2: Age-Related Eye Disease Study 2 Report No. 18. (2019) (12)
Genome-wide Profiling Identifies DNA Methylation Signatures of Aging in Rod Photoreceptors Associated with Alterations in Energy Metabolism. (2020) (12)
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3. (1996) (12)
General Lack of Correlations between Age and Signs of the Metabolic Syndrome in Subjects with Non-diabetic Fasting Glucose Values (2017) (12)
Gene discovery using Pareto depth sampling distributions (2004) (11)
Furostanolic saponins from Trigonella foenum-graecum alleviate diet-induced glucose intolerance and hepatic fat accumulation. (2015) (11)
Isolation and characterization of 1,3-dicapryloyl-2-linoleoylglycerol: a novel triglyceride from berries of Hippophae rhamnoides. (2005) (11)
Five novel RPGR mutations in families with X‐linked retinitis pigmentosa (2001) (11)
Competing peroxidase and oxidase reactions in scopoletin-dependent H2O2-initiated oxidation of NADH by horseradish peroxidase. (1994) (11)
RP 2 Phenotype and Pathogenetic Correlations in X-Linked Retinitis Pigmentosa (2010) (10)
Exome sequencing: capture and sequencing of all human coding regions for disease gene discovery. (2012) (10)
Green Coffee Bean Extract in Human Health (2016) (10)
A unique PRDM13-associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique CFH variant (2020) (10)
Nucleotide sequence of a cDNA for the beta 2 subunit isoform of Na+,K(+)-ATPase from human retina. (1994) (10)
A carboxy-terminal truncation of 99 amino acids resulting from a novel mutation (Arg555-->stop) in the CHM gene leads to choroideremia. (1997) (10)
Characterization of new transcripts enriched in the mouse retina and identification of candidate retinal disease genes. (2004) (10)
The Transcription Factor GTF2IRD1 Regulates the Topology and Function of Photoreceptors by Modulating Photoreceptor Gene Expression across the Retina (2014) (9)
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. (2016) (9)
Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes (2020) (9)
Expression of deubiquitinating enzyme genes in the developing mammal retina (2019) (8)
Author Correction: Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration (2019) (8)
Longitudinal Examination of Links Between Risk Factors for the Metabolic Syndrome and Both Age and Fasting Glucose Levels in Nondiabetic Subjects (2018) (8)
Antioxidant Additives in Food Preservation and Human Health (2016) (8)
Mango (Mangifera indica Linn) and Anti-Inflammatory Benefits: Versatile Roles in Mitochondrial Bio-Energetics and Exercise Physiology (2018) (8)
Association of Rare Predicted Loss-of-Function Variants in Cellular Pathways with Sub-Phenotypes in Age-Related Macular Degeneration. (2017) (8)
Clinical assessment of functional outcome in lateral epicondylitis managed by local infiltration of autologous blood (2010) (8)
Blood Pressure Regulation: Reviewing Evidence for Interplay Between Common Dietary Sugars and Table Salt (2017) (7)
Genomics, Proteomics and Metabolomics in Nutraceuticals and Functional Foods: Bagchi/Genomics, Proteomics and Metabolomics in Nutraceuticals and Functional Foods (2015) (7)
Accelerated Development of Rod Photoreceptors in Retinal Organoids Derived from Human Pluripotent Stem Cells by Supplementation with 9-cis Retinal (2020) (7)
Accelerated and Improved Differentiation of Retinal Organoids from Pluripotent Stem Cells in Rotating-Wall Vessel Bioreactors (2021) (7)
Genome-Wide Association Studies-Based Machine Learning for Prediction of Age-Related Macular Degeneration Risk (2021) (7)
Pias3 is necessary for dorso-ventral patterning and visual response of retinal cones but is not required for rod photoreceptor differentiation (2017) (7)
Plasmodium falciparum: drug-resistant malaria complicating leukemias and lymphomas in children. (1999) (7)
Mutations associated with retinopathies alter mitogen-activated protein kinase-induced phosphorylation of neural retina leucine-zipper (2007) (6)
From disease genes to cellular pathways: a progress report. (2004) (6)
Transcriptome profiling of NIH3T3 cell lines expressing opsin and the P23H opsin mutant identifies candidate drugs for the treatment of retinitis pigmentosa (2017) (6)
Soy protein nanofiber scaffolds for uniform maturation of hiPSC-derived retinal pigment epithelium. (2020) (6)
Targeted deletion of an NRL‐ and CRX‐regulated alternative promoter specifically silences FERM and PDZ domain containing 1 (Frmpd1) in rod photoreceptors (2018) (6)
Dose–Response: An Overview and Signicance in Food Toxicology (2016) (6)
Chromosomal localization and cDNA sequence of humanralB, a GTP binding protein (1990) (6)
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype. (1998) (6)
Naturally Occurring Toxicants as Etiologic Agents of Foodborne Disease (2016) (6)
Changes in mitochondrial oxidative metabolism under conditions of heat stress. (1982) (6)
High-resolution genome topology of human retina uncovers super enhancer-promoter interactions at tissue-specific and multifactorial disease loci (2022) (5)
Hypomethylation of the IL 17 RC Promoter in Peripheral Blood Leukocytes Is Not A Hallmark of Age-Related Macular Degeneration (2014) (5)
A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration (2021) (5)
Photoreceptor Development: Early Steps/Fate (2010) (5)
Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degeneration (2020) (5)
Chronic epidural intracranial actinomycosis: A rare case (2009) (5)
Alu-vector PCR with biotinylated primers to isolate YAC ends ready for sequencing. (1995) (5)
Pareto depth sampling distributions for gene ranking (2004) (5)
Methylation of two-component response regulator MtrA in mycobacteria negatively modulates its DNA binding and transcriptional activation. (2020) (5)
Reticular Pseudodrusen Status, ARMS2/HTRA1 Genotype, and Geographic Atrophy Enlargement: Age-Related Eye Disease Study 2 Report 32. (2022) (5)
Nutraceuticals and Their Role in Human Health: A Review (2015) (4)
Functional Analysis of the Rod Photoreceptor cGMP Phosphodiesterase α-Subunit Gene Promoter (2004) (4)
Divergent Effects of HSP70 Overexpression in Photoreceptors During Inherited Retinal Degeneration (2020) (4)
Remapping of the RP 15 Locus for X-Linked Cone-Rod Degeneration to Xp 11 . 4p 21 . 1 , and Identification of a De Novo Insertion in the RPGR Exon ORF 15 (4)
Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype–Phenotype Correlation in 228 Patients (2021) (4)
pSH4: a mammalian cDNA expression vector. (1990) (4)
Assessment Of Results Of Open Arthrolysis In Post Traumatic Stiff Elbows (2008) (4)
Functional Rods Are Required For Photopic ERG Amplitude Increase During Light Adaptation: Study Of Nrl–/– And Rho–/– Mice. (2004) (3)
A Study on Incidence of Adverse Drug Reaction of Anti-Tubercular Drugs in New Cases of Pulmonary Tuberculosis in a Tertiary Care Teaching Hospital (2016) (3)
Deep-learning-based prediction of late age-related macular degeneration progression (2020) (3)
stem cells and neuronal repair (2009) (3)
Multi-omics analyses reveal early metabolic imbalance and mitochondrial stress in neonatal photoreceptors leading to cell death in Pde6brd1/rd1 mouse model of retinal degeneration. (2022) (3)
Safety and Free Testosterone Boosting Efficacy of a Novel Curculigo orchioides Extract (Blamus™) in Male Rats (2017) (3)
Dispersion Relations in Gold (1971) (3)
Modeling ciliogenesis in Leber congenital amaurosis using fibroblasts from patients with CEP290 mutations (2016) (3)
Construction of Directional cDNA Libraries from Human Retinal Tissue/Cells and Their Enrichment for Specific Genes Using an Efficient Subtraction Procedure (1993) (3)
Declarative Querying for Biological Sequence Databases (2005) (3)
Genetics and therapy for pediatric eye diseases (2021) (3)
HiCRes: a computational method to estimate and predict the resolution of HiC libraries (2020) (3)
What's in a name? RPGR mutations redefine the genetic and phenotypic landscape in retinal degenerative diseases. (2013) (3)
Genome Wide Association Study (GWAS) of Age-Related Macular Degeneration (AMD) (2009) (3)
Salient Features for Designing a Functional Beverage Formulation to Boost Energy (2017) (3)
transcriptional activator in rod photoreceptors (2004) (3)
Safety and Efficacy of a Novel Green Coffee Bean Extract (GCB‐70) in Overweight Subjects (2017) (3)
Safety and efficacy of a novel Prunus domestica extract (Sitoprin, CR002) on testosterone-induced benign prostatic hyperplasia (BPH) in male Wistar rats (2015) (3)
Safety and Efficacy of a Novel Curculigo orchioides Extract in Boosting Testosterone Levels in Male Rats (2018) (3)
Food Security and Foodborne Mycotoxicoses, Risk Assessment, Preventive Measures, and Underestimated Hazard of Masked Mycotoxins or Joint Mycotoxin Interaction (2016) (3)
Choline-Dependent H2o2 Generation In Mitochondria Responds To Altered Status Of Thyroxine And Thermogenesis (1981) (3)
Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene. (2008) (3)
A novel protodioscin-enriched fenugreek seed extract (Trigonella foenum-graecum, family Fabaceae) improves free testosterone level and sperm profile in healthy volunteers (2017) (3)
Towards Declarative Querying for Biological Sequences (2005) (3)
Molecular dissection of cone photoreceptor‐enriched genes encoding transmembrane and secretory proteins (2018) (3)
Retinal pigment epithelium transcriptome analysis in chronic smoking reveals a suppressed innate immune response and activation of differentiation pathways. (2020) (3)
Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration (2019) (3)
An overview of gluten-free foods and related disorders (2019) (2)
Expression and subcellular localization of USH1C/harmonin in the human retina provides insights into pathophysiology and therapy of Usher syndrome (2021) (2)
Soy Protein Nanoﬁber Scaffolds for Uniform Maturation of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium (2020) (2)
Explorer A Secreted WNT-Ligand Binding Domain of FZD 5 Generated by a Frameshift Mutation Causes Autosomal Dominant Coloboma (2016) (2)
COMBINATORIAL REGULATION OF PHOTORECEPTOR DIFFERENTIATION FACTOR GENE NRL , REVEALED BY IN VIVO PROMOTER ANALYSIS (2011) (2)
Targeting Cancer Stem Cells by Functional Foods and Their Constituents (2016) (2)
X-Linked Recessive Mutations in Simplex Males With Retinitis Pigmentosa (2010) (2)
Microarray Analysis of Mouse Models of Diabetic Retinopathy Reveals Dramatic Modulation of Crystallin Genes in the Retina (2003) (2)
Determination of posttranslational modifications of photoreceptor differentiation factor NRL: focus on SUMOylation. (2012) (2)
Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration (2018) (2)
Customized rotating wall vessel bioreactors produce improved retinal organoids with reduced operational costs and less frequent experimental failure (2019) (2)
Glycogen Synthase Kinase 3 regulates the genesis of the rare displaced ganglion cell retinal subtype (2021) (2)
Canine Rod Cone Dysplasia Type 2 (rcd2) Is the Canine Ortholog of Human and Murine RD3 (2008) (2)
Dinucleotide repeat polymorphism at the DXS977 locus. (1994) (2)
Glycogen Synthase Kinase 3 Regulates the Genesis of Displaced Retinal Ganglion Cells3 (2021) (2)
SSBP1 faux pas in mitonuclear tango causes optic neuropathy. (2019) (2)
Safety and Antidiabetic Efficacy of a Novel Trigonella foenum-graecum Seed Extract (2018) (2)
Distinct Expression of Heat Shock Proteins in Mouse Models of Retinal Degeneration (2016) (2)
Making Biological Sense of Genetic Studies of Age-Related Macular Degeneration. (2021) (2)
HIPRO: A High-Efficiency, Hypoxia-Induced Protocol for Generation of Photoreceptors in Retinal Organoids from Mouse Pluripotent Stem Cells (2020) (2)
Protective Ability of Vitamin E Against Acetylsalicylic Acid-Induced Glutathione Depletion, Acetylcholinesterase and (Na+,K+)-ATPase Activities, and Erythrocyte Osmotic Fragility (2018) (2)
Transgenic Mice Lines Expressing Cre-Recombinase Specifically in the Photoreceptors or Retinal Pigment Epithelium: Towards Somatic Mutagenesis in Retinal Cell Types (2003) (2)
GATD3A, a mitochondrial deglycase with evolutionary origins from gammaproteobacteria, restricts the formation of advanced glycation end products (2022) (2)
Developmental genome-wide occupancy analysis of bZIP transcription factor NRL uncovers the role of c-Jun in early differentiation of rod photoreceptors in the mammalian retina. (2022) (2)
A mutation in the bZIP transcription factor NRL is associated with autosomal dominant retinitis pigmentosa in a family linked to a novel locus on 14p (1999) (2)
Association of Apolipoprotein E Alleles with Age-Related Macular Degeneration in a Large Cohort of Patients (2003) (2)
AMP-activated-protein kinase (AMPK) is an essential sensor and metabolic regulator of retinal neurons and their integrated metabolism with RPE (2020) (2)
Lattice dynamics of calcium and strontium (1973) (2)
Nutrition and Nutraceutical Supplements for the Treatment of Hypertension (2015) (2)
Proteostasis in aging-associated ocular disease. (2022) (2)
Effects of Different Dietary Fibers on Sugar-Induced Blood Pressure Elevations in Hypertensive Rats: Focus on Viscosity (2015) (1)
Safety and efficacy of a novel KD120 MEC multi‐enzyme complex (N‐Sorb®) in human volunteers (2017) (1)
Antimicrobial Properties of Wild Oregano Extracts: A Compilation and Review of Current Research (2015) (1)
Stress, Parkinson’s, and Alzheimer’s Disease: Role of Dietary Supplements (2015) (1)
Safety and Efficacy of Furosap, a novel Trigonella foenum‐graecum seed extract, in Enhancing Testosterone Level and Improving Sperm Profile in Male Human Volunteers (2017) (1)
Occurrence in Plants andIn Vitro, Animal and Human Metabolism of Chlorogenic Acids (2016) (1)
Novel Energy Beverage Formulations: Efficacious, Healthy, and Safe (2018) (1)
Measurement of Toxicants and Toxicity (2016) (1)
Efficacy of a novel fenugreek seed extract (Furocyst) in polycystic ovary syndrome (PCOS) (2016) (1)
Functional Foods in the Treatment of Processed Food Addiction and the Metabolic Syndrome (2015) (1)
Herbal Treatment for Hair Loss and Alopecia: An Overview (2015) (1)
Green Coffee Bean Extract and Chlorogenic Acids: Chemistry and Novel Antioxidant Benefits (2016) (1)
A Review on Food-Associated Carcinogenesis (2016) (1)
Lumbar para-spinal haemangioma as a rare differential diagnosis of lumbar disc prolapse (2008) (1)
Absorption of Food Toxicants: An Overview on Polycyclic Aromatic Hydrocarbons (2016) (1)
Anti‐Diabetic Efficacy of a Novel Fenugreek Seed (Trigonella foenum‐graecum, Fenfuro) Extract in Patients with Type‐2 Diabetes (2016) (1)
Uric acid levels in neurological and psychiatric disorders. (1976) (1)
Huperzine A and Shankhapushpi in Brain Health (2017) (1)
Efficacy of a novel green coffee bean extract (GCB‐70) in weight management (1107.2) (2014) (1)
Kidney lipids of weanling rats fed lysine threonine deficient rice diets (1979) (1)
Global Nutraceutical Regulations for Functional Beverages (2016) (1)
CK Isoenzyme Variants in Electrophoresis (1989) (1)
A synergistic combination of Huperzine A, Convolvulus pluricaulis and Celastrus paniculatus promote cognitive function and health (2018) (1)
Prebiotics, Probiotics, and Synbiotics for the Management of Respiratory Disease (2015) (1)
A Simple and Cost-effective Technique for Vertebroplasty (2015) (1)
Functional Characterization of Prickle 2, a core Planar Cell Polarity protein, in mouse retina (2012) (1)
λSHK and λAASV : phage vectors for efficient cDNA cloning and expression in mammalian cells (1993) (1)
Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits (2017) (1)
Cloning and functional expression of human retinal Kir2.4, a pH-sensitive inwardly rectifying K 1 channel (2000) (1)
Role of Epigenetics (DNA Methylation) in RPE and Photoreceptor Development (2010) (1)
Towards an Expression Profile of Native Human Retinal Pigment Epithelium and Identification of RPE-Specific Genes (2002) (1)
What can we learn about AMD from other retinal diseases ? (1999) (1)
Loss of Lysophosphatidylcholine Acyltransferase 1 (LPCAT1) Leads to Photoreceptor Degeneration in rd11 Mice (2010) (1)
GWAS-based Machine Learning for Prediction of Age-Related Macular Degeneration Risk (2019) (1)
Genomewide search for genetic modifiers in patients with Leber congenital amaurosis using whole exome sequencing (2014) (1)
Transgenic Mice Expressing Cre-Recombinase Specifically in Mor SCone Photoreceptors (2003) (1)
NRL- and CRX-guided gene network modulates photoreceptor presynapse size and positioning during retinal development (2019) (1)
Transducin Translocation And The Role Of Frmpd1 And Gpsm2 In Rod To Rod Bipolar Cell Synaptic Transmission. (2020) (1)
A Sandwich-Hybridization Method for Specific and Efficient Selection of cDNA Clones from Genomic Regions (1994) (1)
Mapping of the Epitope Recognized by a Monoclonal Antibody Specific for RPE65 and the Retinal Pigment Epithelium (2003) (1)
Nicotinamide Promotes Formation of Retinal Organoids From Human Pluripotent Stem Cells via Enhanced Neural Cell Fate Commitment (2022) (1)
The Role of Dnmt1 in Retinal Differentiation (2011) (1)
Retinal Degeneration in the Rd16 Mouse Is Associated With a Deletion in a Novel Centrosomal Protein CEP290/NPHP6 That Interacts With Retinitis Pigmentosa GTPase Regulator (RPGR) (2006) (1)
RPGR Interacts With a Novel Ciliary IQ Domain Protein Nephrocystin 5, Mutated in Senior–Loken Syndrome (Nephronophthisis With Retinitis Pigmentosa) (2005) (1)
Early mitochondrial stress and metabolic imbalance lead to photoreceptor cell death in retinal degeneration (2021) (1)
Expression and subcellular localization of USH1C/harmonin in human retina provides insights into pathomechanisms and therapy (2022) (1)
Epigenetic Regulation of Rod Photoreceptor Development (2013) (1)
Gene Expression Changes in Aging Retinal Microglia: Relationship to Microglial Support Functions and Regulation of Microglial Activation (2013) (1)
Unsupervised posterior analysis of signaling pathways from gene microarray data (2005) (1)
Isolated population helps tease out a third locus underlying a multigenic form of canine RPGRIP1 cone-rod dystrophy (2018) (1)
Determination of Mitochondrial Oxygen Consumption in the Retina Ex Vivo: Applications for Retinal Disease. (2018) (1)
Next-generation sequencing facilitates quantitative analysis of wild-type and Nrl (2011) (1)
Expression of the Igf–1 Receptor in Developing Photoreceptors of the Mouse Retina and the Importance of Igf–1 Signaling During Photoreceptor Differentiation (2006) (1)
RDH12 Expression Relative to Other Short Chain Dehydrogenase/Reductase Isoforms Present in the Retina (2007) (1)
Associations of CFHR 1 – CFHR 3 deletion and a CFH snp to age-related macular degeneration (2010) (1)
Regulation of NRL Expression by Retinoic Acid and Trophic Factors (2003) (1)
266. In Vivo Rod Photoreceptor Reprogramming Using AAV-Delivered CRISPR/Cas9 Rescues Retinal Degeneration (2016) (1)
Identification of putative small open reading frame peptides in the retinal transcriptome (2018) (1)
GATD3A, a mitochondrial deglycase with evolutionary origins from gammaproteobacteria, restricts the formation of advanced glycation end products (2022) (1)
Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients (2016) (1)
Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13 (1995) (1)
Erratum: Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis (Journal of Clinical Investigation (2012) 122, 4, (1233-1245) DOI: 10.1172/JCI60981) (2012) (1)
Functional Properties of Photocurrents of Single Photoreceptors of the Nrl-/- Mouse (2003) (1)
In vitro modeling and rescue of ciliopathy associated with IQCB1/NPHP5 mutations using patient-derived cells (2022) (1)
Probiotics and Dental Health: An Overview (2015) (0)
Genetics Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG 2 as a Candidate Gene for Age-Related Macular Degeneration (2019) (0)
Differential miRNA Expression In Geographic Atrophy Retina And Retinal Pigment Epithelium (2011) (0)
Evaluation of Selected Human Embryonic Stem Cell Lines for Differentiation to Retinal Cells and for Cell-Based Therapy (2009) (0)
HLA Genotypes and Age Related Macular Degeneration: A Replication Study in a North American Cohort (2007) (0)
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Identification of Genes Altered in Aging Retina Using Gene Microarrays (2002) (0)
Gene Expression Changes Precede Cellular and Morphological Alterations in the rd1 Mouse Retina (2006) (0)
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Genome-wide association study and meta-analysis of intraocular pressure (2013) (0)
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Gene Expression Profiles of Crystallins During Development and Aging in Mouse Retina (2005) (0)
RNA-Seq Approach for the Refinement of a Modifier Locus in a Canine Model of Cone-Rod Dystrophy (2013) (0)
Disruption of ocular development and function in Prickle 1 (Pk1) mutant mouse (2013) (0)
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Nutrition, Functional Foods, and Exercise: A Review (2015) (0)
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A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1. (1995) (0)
Restoration of vision by chemically reprogrammed photoreceptors (2019) (0)
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Subretinal Transplantation of Purifed Cone Precursors in Mouse Cone Degeneration Mutants (2007) (0)
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Complement activation products, single nucleotide polymorphisms and age-related macular degeneration (AMD). (2018) (0)
Protein kinase CK2 modulates the activity of Maf-family bZIP transcription factor NRL in rod photoreceptors of mammalian retina. (2022) (0)
Neurotrophic activity and gene analysis of a pigment epithelium-derived factor (PEDF) (1992) (0)
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Blood DNA Methylation Analysis Reveals Differential Methylation in AMD (2014) (0)
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Nrl Knockout Mice Lacking Rpe65 Do Not Synthesize 11–cis Retinal (2006) (0)
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Transcriptome analysis of AMD retina reveals convergent molecular pathology (2017) (0)
Differential Gene Expression between Macular and Equatorial Human RPE Cells in Response to Oxidative Stress (2007) (0)
The adRP Gene KLHL7 And Its Potential Role In Ubiquitination And Photoreceptor Degeneration (2011) (0)
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Genetic studies of age-related macular degeneration - eScholarship (1999) (0)
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Systematic Reviews and Meta- and Pooled Analyses Variations in Apolipoprotein E FrequencyWith Age in a Pooled Analysis of a Large Group of Older People (2011) (0)
Development of a Synergistic Combination of Huperzia serrata, Convolvulus pluricaulis, and Celastrus paniculatus for Optimal Brain Health and Functions (2020) (0)
Identification and Characterisation of Novel Cone Photoreceptor-Enriched Factors Conserved in Zebrafish, Mouse and Human (2016) (0)
Transgenic Analysis of Nrl Promoter: Towards Identification of Rod Precursors (2002) (0)
Functional Characterization Of Prickle1 Gene In Mouse Retina (2012) (0)
Sexual Dysfunctions and Nutraceutical Therapy: An Examination of Human Research (2015) (0)
Functional Beverages in Weight Management (2016) (0)
X-Linked Recessive RPGR Mutation Causes Incomplete Congenital Stationary Night Blindness (2003) (0)
Search for Interactors of Retinal Degeneration 3 (RD3) (2009) (0)
Cell-based Therapy In A Mouse Model Of Leber Congenital Amaurosis (2012) (0)
Expression And Function Of Planar Cell Polarity Gene Prickle1 During Retinal Development (2011) (0)
Anti‐diabetic efficacy of Fenfuroœ, a novel, patented Trigonella foenum‐graecum seed extract (1019.14) (2014) (0)
EVALUATION OF PERMEABILITY AND BIOAVAILABILITY OF A LEAD ANTILEISHMANIAL COMPOUND BUPARVAQUONE IN ANIMAL MODELS (2009) (0)
Determination of Mitochondrial Respiration and Glycolysis in Ex Vivo Retinal Tissue Samples. (2021) (0)
Co-expression of UV- and M- Cone Opsins in Photoreceptors of Nrl-/- Mouse (2003) (0)
Olfactory Dysfunction in LCA Patients With CEP290/NPHP6 Defects: A Comparison With Other RP and LCA Genotypes (2007) (0)
Integrity and Ciliary Localization of the RPGR-SMC Protein Complex Are Critical for Normal Photoreceptor Function (2009) (0)
Myocyte Enhancer Factor 2C and bHLH Proteins Regulate the Expression of Nrl, the bZIP Transcription Factor Essential for Rod Differentiation (2003) (0)
Contrast-enhanced MRI of Brain Abnormalities and Cerebrospinal Fluid (CSF) Buildup in CEP290 Knockout (ko) Mice: Effect of Ciliogenesis on Volumetry of CSF, Cerebrum and Cerebellum (2013) (0)
Cc2d2a is required for cilia axoneme development (2013) (0)
Developmental Expression of DNA Methyltransferases in the Mammalian Retina (2010) (0)
Rare Variant Pathway Analysis in the Age-Related Eye Disease Study 2 (2017) (0)
The minimal transactivation domain of the basic motif–leucine zipper protein NRL interacts with TATA–binding protein (2004) (0)
Integrated transcriptome and epigenome analysis of developing mouse rod photoreceptors reveals dynamic epigenetic control of lineage priming and developmental plasticity (2015) (0)
Müller Cell/Microglia Interactions in CNTF-Mediated Photoreceptor Neuroprotection (2009) (0)
Author response: Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes (2020) (0)
Gene Expression Changes Associated with Retinal Aging Identified by Gene Microarrays (2003) (0)
Author Correction: Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration (2019) (0)
Gene Patterning and Genomic Location Analysis of Late-Born Retinal Cells in the Developing Mouse Retina (2008) (0)
Molecular organization and expression of the genetic locus glued in Drosophila melanogaster (1986) (0)
Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1 (2020) (0)
Interaction of Genotypic Risks and the AREDS Supplements for Progression to Late Age-Related Macular Degeneration (2014) (0)

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