Anand Swaroop - Publications

Affiliations: 
University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Genetics, Molecular Biology, Biostatistics Biology

248 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
2019 Chen HY, Welby E, Li T, Swaroop A. Retinal disease in ciliopathies: Recent advances with a focus on stem cell-based therapies. Translational Science of Rare Diseases. 4: 97-115. PMID 31763178 DOI: 10.3233/TRD-190038  0.6
2019 Brooks MJ, Chen HY, Kelley RA, Mondal AK, Nagashima K, De Val N, Li T, Chaitankar V, Swaroop A. Improved Retinal Organoid Differentiation by Modulating Signaling Pathways Revealed by Comparative Transcriptome Analyses with Development In Vivo. Stem Cell Reports. PMID 31631019 DOI: 10.1016/j.stemcr.2019.09.009  0.6
2019 van Asten F, Chiu CY, Agrón E, Clemons TE, Ratnapriya R, Swaroop A, Klein ML, Fan R, Chew EY. 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. Ophthalmology. PMID 31358387 DOI: 10.1016/j.ophtha.2019.06.004  0.52
2019 Grassmann F, Harsch S, Brandl C, Kiel C, Nürnberg P, Toliat MR, Fleckenstein M, Pfau M, Schmitz-Valckenberg S, Holz FG, Chew EY, Swaroop A, Ratnapriya R, Klein ML, Mulyukov Z, et al. Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration. Jama Ophthalmology. PMID 31120506 DOI: 10.1001/jamaophthalmol.2019.1318  0.52
2019 Ratnapriya R, Sosina OA, Starostik MR, Kwicklis M, Kapphahn RJ, Fritsche LG, Walton A, Arvanitis M, Gieser L, Pietraszkiewicz A, Montezuma SR, Chew EY, Battle A, Abecasis GR, Ferrington DA, ... ... Swaroop A, et al. Author Correction: Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration. Nature Genetics. PMID 31068672 DOI: 10.1038/s41588-019-0430-y  0.52
2019 Rohrer B, Frazer-Abel A, Leonard A, Ratnapriya R, Ward T, Pietraszkiewicz A, O'Quinn E, Adams K, Swaroop A, Wolf BJ. Association of age-related macular degeneration with complement activation products, smoking, and single nucleotide polymorphisms in South Carolinians of European and African descent. Molecular Vision. 25: 79-92. PMID 30820144  0.52
2019 Ratnapriya R, Sosina OA, Starostik MR, Kwicklis M, Kapphahn RJ, Fritsche LG, Walton A, Arvanitis M, Gieser L, Pietraszkiewicz A, Montezuma SR, Chew EY, Battle A, Abecasis GR, Ferrington DA, ... ... Swaroop A, et al. Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration. Nature Genetics. PMID 30742112 DOI: 10.1038/s41588-019-0351-9  0.52
2018 Sivakumaran TA, Igo RP, Kidd JM, Itsara A, Kopplin LJ, Chen W, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, Chew EY, Ramprasad VL, Tay WT, Mitchell P, Seielstad M, ... ... Swaroop A, et al. Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration. Plos One. 13: e0209943. PMID 30571798 DOI: 10.1371/journal.pone.0209943  0.52
2018 Mookherjee S, Chen HY, Isgrig K, Yu W, Hiriyanna S, Levron R, Li T, Colosi P, Chien W, Swaroop A, Wu Z. A CEP290 C-Terminal Domain Complements the Mutant CEP290 of Rd16 Mice In Trans and Rescues Retinal Degeneration. Cell Reports. 25: 611-623.e6. PMID 30332642 DOI: 10.1016/j.celrep.2018.09.043  0.6
2018 Keenan TD, Agrón E, Domalpally A, Clemons TE, van Asten F, Wong WT, Danis RG, Sadda S, Rosenfeld PJ, Klein ML, Ratnapriya R, Swaroop A, Ferris FL, Chew EY. Progression of Geographic Atrophy in Age-related Macular Degeneration: AREDS2 Report Number 16. Ophthalmology. PMID 30060980 DOI: 10.1016/j.ophtha.2018.05.028  0.52
2018 Yan Q, Ding Y, Liu Y, Sun T, Fritsche LG, Clemons T, Ratnapriya R, Klein ML, Cook RJ, Liu Y, Fan R, Wei L, Abecasis GR, Swaroop A, Chew EY, et al. Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration. Human Molecular Genetics. PMID 29346644 DOI: 10.1093/hmg/ddy002  0.52
2017 Hoshino A, Ratnapriya R, Brooks MJ, Chaitankar V, Wilken MS, Zhang C, Starostik MR, Gieser L, La Torre A, Nishio M, Bates O, Walton A, Bermingham-McDonogh O, Glass IA, Wong ROL, ... Swaroop A, et al. Molecular Anatomy of the Developing Human Retina. Developmental Cell. PMID 29233477 DOI: 10.1016/j.devcel.2017.10.029  0.52
2017 Pietraszkiewicz A, van Asten F, Kwong A, Ratnapriya R, Abecasis G, Swaroop A, Chew EY. Association of Rare Predicted Loss-of-Function Variants in Cellular Pathways with Sub-Phenotypes in Age-Related Macular Degeneration. Ophthalmology. PMID 29224928 DOI: 10.1016/j.ophtha.2017.10.027  0.52
2017 van Asten F, Simmons M, Singhal A, Keenan TD, Ratnapriya R, Agrón E, Clemons TE, Swaroop A, Lu Z, Chew EY. 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. Ophthalmology. PMID 29096998 DOI: 10.1016/j.ophtha.2017.09.023  0.52
2017 Zelinger L, Karakülah G, Chaitankar V, Kim JW, Yang HJ, Brooks MJ, Swaroop A. Regulation of Noncoding Transcriptome in Developing Photoreceptors by Rod Differentiation Factor NRL. Investigative Ophthalmology & Visual Science. 58: 4422-4435. PMID 28863214 DOI: 10.1167/iovs.17-21805  0.52
2017 McGuigan DB, Heon E, Cideciyan AV, Ratnapriya R, Lu M, Sumaroka A, Roman AJ, Batmanabane V, Garafalo AV, Stone EM, Swaroop A, Jacobson SG. EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression. Genes. 8. PMID 28704921 DOI: 10.3390/genes8070178  0.52
2017 Shimada H, Lu Q, Insinna-Kettenhofen C, Nagashima K, English MA, Semler EM, Mahgerefteh J, Cideciyan AV, Li T, Brooks BP, Gunay-Aygun M, Jacobson SG, Cogliati T, Westlake CJ, Swaroop A. In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations. Cell Reports. 20: 384-396. PMID 28700940 DOI: 10.1016/j.celrep.2017.06.045  0.6
2017 Pierrache LHM, Kimchi A, Ratnapriya R, Roberts L, Astuti GDN, Obolensky A, Beryozkin A, Tjon-Fo-Sang MJH, Schuil J, Klaver CCW, Bongers EMHF, Haer-Wigman L, Schalij N, Breuning MH, Fischer GM, ... ... Swaroop A, et al. Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma. Ophthalmology. PMID 28412069 DOI: 10.1016/j.ophtha.2017.03.010  0.52
2017 Veleri S, Nellissery J, Mishra B, Manjunath SH, Brooks MJ, Dong L, Nagashima K, Qian H, Gao C, Sergeev YV, Huang XF, Qu J, Lu F, Cideciyan AV, Li T, ... ... Swaroop A, et al. REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival. Human Molecular Genetics. PMID 28369466 DOI: 10.1093/hmg/ddx111  0.6
2017 Ding Y, Liu Y, Yan Q, Fritsche LG, Cook RJ, Clemons T, Ratnapriya R, Klein ML, Abecasis GR, Swaroop A, Chew EY, Weeks DE, Chen W. Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk Scores. Genetics. PMID 28341650 DOI: 10.1534/genetics.116.196998  0.52
2017 Yu W, Mookherjee S, Chaitankar V, Hiriyanna S, Kim JW, Brooks M, Ataeijannati Y, Sun X, Dong L, Li T, Swaroop A, Wu Z. Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice. Nature Communications. 8: 14716. PMID 28291770 DOI: 10.1038/ncomms14716  0.6
2016 Roberts L, Ratnapriya R, du Plessis M, Chaitankar V, Ramesar RS, Swaroop A. Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing. Investigative Ophthalmology & Visual Science. 57: 6374-6381. PMID 27898983 DOI: 10.1167/iovs.16-19785  0.52
2016 Kim JW, Yang HJ, Brooks MJ, Zelinger L, Karakülah G, Gotoh N, Boleda A, Gieser L, Giuste F, Whitaker DT, Walton A, Villasmil R, Barb JJ, Munson PJ, Kaya KD, ... ... Swaroop A, et al. NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors. Cell Reports. 17: 2460-2473. PMID 27880916 DOI: 10.1016/j.celrep.2016.10.074  0.52
2016 Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D. Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. American Journal of Human Genetics. 99: 1222-1223. PMID 27814526 DOI: 10.1016/j.ajhg.2016.09.012  0.52
2016 Sifuentes CJ, Kim JW, Swaroop A, Raymond PA. Rapid, Dynamic Activation of Müller Glial Stem Cell Responses in Zebrafish. Investigative Ophthalmology & Visual Science. 57: 5148-5160. PMID 27699411 DOI: 10.1167/iovs.16-19973  0.52
2016 Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D. Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. American Journal of Human Genetics. 99: 777-84. PMID 27588452 DOI: 10.1016/j.ajhg.2016.07.010  0.52
2016 Das S, Forer L, Schönherr S, Sidore C, Locke AE, Kwong A, Vrieze SI, Chew EY, Levy S, McGue M, Schlessinger D, Stambolian D, Loh PR, Iacono WG, Swaroop A, et al. Next-generation genotype imputation service and methods. Nature Genetics. PMID 27571263 DOI: 10.1038/ng.3656  0.92
2016 Rueda EM, Johnson JE, Giddabasappa A, Swaroop A, Brooks MJ, Sigel I, Chaney SY, Fox DA. The cellular and compartmental profile of mouse retinal glycolysis, tricarboxylic acid cycle, oxidative phosphorylation, and ~P transferring kinases. Molecular Vision. 22: 847-85. PMID 27499608  0.92
2016 Kim JW, Yang HJ, Oel AP, Brooks MJ, Jia L, Plachetzki DC, Li W, Allison WT, Swaroop A. Recruitment of Rod Photoreceptors from Short-Wavelength-Sensitive Cones during the Evolution of Nocturnal Vision in Mammals. Developmental Cell. 37: 520-532. PMID 27326930 DOI: 10.1016/j.devcel.2016.05.023  0.92
2016 Chaitankar V, Karakülah G, Ratnapriya R, Giuste FO, Brooks MJ, Swaroop A. Next generation sequencing technology and genomewide data analysis: Perspectives for retinal research. Progress in Retinal and Eye Research. PMID 27297499 DOI: 10.1016/j.preteyeres.2016.06.001  0.92
2016 Sun X, Park JH, Gumerson J, Wu Z, Swaroop A, Qian H, Roll-Mecak A, Li T. Loss of RPGR glutamylation underlies the pathogenic mechanism of retinal dystrophy caused by TTLL5 mutations. Proceedings of the National Academy of Sciences of the United States of America. PMID 27162334 DOI: 10.1073/pnas.1523201113  0.6
2016 Kaewkhaw R, Swaroop M, Homma K, Nakamura J, Brooks M, Kaya KD, Chaitankar V, Michael S, Tawa G, Zou J, Rao M, Zheng W, Cogliati T, Swaroop A. Treatment Paradigms for Retinal and Macular Diseases Using 3-D Retina Cultures Derived From Human Reporter Pluripotent Stem Cell Lines. Investigative Ophthalmology & Visual Science. 57: ORSFl1-ORSFl11. PMID 27116668 DOI: 10.1167/iovs.15-17639  0.92
2016 Yadav SP, Sharma NK, Liu C, Dong L, Li T, Swaroop A. Centrosomal protein CP110 controls maturation of mother centriole during cilia biogenesis. Development (Cambridge, England). PMID 26965371 DOI: 10.1242/dev.130120  0.6
2016 Beryozkin A, Levy G, Blumenfeld A, Meyer S, Namburi P, Morad Y, Gradstein L, Swaroop A, Banin E, Sharon D. Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual. Investigative Ophthalmology & Visual Science. 57: 940-7. PMID 26962691 DOI: 10.1167/iovs.15-18702  0.92
2016 Mishra B, Swaroop A, Kandpal RP. Genetic components in diabetic retinopathy. Indian Journal of Ophthalmology. 64: 55-61. PMID 26953025 DOI: 10.4103/0301-4738.178153  0.92
2016 Liu C, Widen SA, Williamson KA, Ratnapriya R, Gerth-Kahlert C, Rainger J, Alur RP, Strachan E, Manjunath SH, Balakrishnan A, Floyd JA, Li T, Waskiewicz A, Brooks BP, ... ... Swaroop A, et al. A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma. Human Molecular Genetics. PMID 26908622 DOI: 10.1093/hmg/ddw020  0.92
2016 Ferrington DA, Kapphahn RJ, Leary MM, Atilano SR, Terluk MR, Karunadharma P, Chen GK, Ratnapriya R, Swaroop A, Montezuma SR, Kenney MC. Increased retinal mtDNA damage in the CFH variant associated with age-related macular degeneration. Experimental Eye Research. 145: 269-277. PMID 26854823 DOI: 10.1016/j.exer.2016.01.018  0.52
2016 Fan R, Wang Y, Yan Q, Ding Y, Weeks DE, Lu Z, Ren H, Cook RJ, Xiong M, Swaroop A, Chew EY, Chen W. Gene-Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions. Genetic Epidemiology. PMID 26782979 DOI: 10.1002/gepi.21947  0.32
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, ... ... Swaroop A, 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  0.52
2015 Kooragayala K, Gotoh N, Cogliati T, Nellissery J, Kaden TR, French S, Balaban R, Li W, Covian R, Swaroop A. Quantification of Oxygen Consumption in Retina Ex Vivo Demonstrates Limited Reserve Capacity of Photoreceptor Mitochondria. Investigative Ophthalmology & Visual Science. 56: 8428-8436. PMID 26747773 DOI: 10.1167/iovs.15-17901  0.92
2015 Mookherjee S, Hiriyanna S, Kaneshiro K, Li L, Li Y, Li W, Qian H, Li T, Khanna H, Colosi P, Swaroop A, Wu Z. Long-Term Rescue of Cone Photoreceptor Degeneration in Retinitis Pigmentosa 2 (RP2) Knockout Mice by Gene Replacement Therapy. Human Molecular Genetics. PMID 26358772 DOI: 10.1093/hmg/ddv354  0.92
2015 Beryozkin A, Shevah E, Kimchi A, Mizrahi-Meissonnier L, Khateb S, Ratnapriya R, Lazar CH, Blumenfeld A, Ben-Yosef T, Hemo Y, Pe'er J, Averbuch E, Sagi M, Boleda A, Gieser L, ... ... Swaroop A, et al. Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies. Scientific Reports. 5: 13187. PMID 26306921 DOI: 10.1038/srep13187  0.92
2015 Kaewkhaw R, Kaya KD, Brooks M, Homma K, Zou J, Chaitankar V, Rao M, Swaroop A. 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. Stem Cells (Dayton, Ohio). PMID 26235913 DOI: 10.1002/stem.2122  0.92
2015 Lazar CH, Kimchi A, Namburi P, Mutsuddi M, Zelinger L, Beryozkin A, Ben-Simhon S, Obolensky A, Ben-Neriah Z, Argov Z, Pikarsky E, Fellig Y, Marks-Ohana D, Ratnapriya R, Banin E, ... ... Swaroop A, et al. 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. Human Mutation. PMID 26077327 DOI: 10.1002/humu.22822  0.92
2015 Oliver V, Jaffe AE, Song J, Wang G, Zhang P, Branham KE, Swaroop A, Eberhart CG, Zack DJ, Qian J, Merbs SL. Differential DNA Methylation Identified in the Blood and Retina of AMD Patients. Epigenetics : Official Journal of the Dna Methylation Society. 0. PMID 26067391 DOI: 10.1080/15592294.2015.1060388  0.32
2015 Grassmann F, Fleckenstein M, Chew EY, Strunz T, Schmitz-Valckenberg S, Göbel AP, Klein ML, Ratnapriya R, Swaroop A, Holz FG, Weber BH. Clinical and genetic factors associated with progression of geographic atrophy lesions in age-related macular degeneration. Plos One. 10: e0126636. PMID 25962167 DOI: 10.1371/journal.pone.0126636  0.52
2015 Wu Z, Hiriyanna S, Qian H, Mookherjee S, Campos MM, Gao C, Fariss R, Sieving PA, Li T, Colosi P, Swaroop A. A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degeneration. Human Molecular Genetics. 24: 3956-70. PMID 25877300 DOI: 10.1093/hmg/ddv134  0.92
2015 Rachel RA, Yamamoto EA, Dewanjee MK, May-Simera HL, Sergeev YV, Hackett AN, Pohida K, Munasinghe J, Gotoh N, Wickstead B, Fariss RN, Dong L, Li T, Swaroop A. CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies. Human Molecular Genetics. 24: 3775-91. PMID 25859007 DOI: 10.1093/hmg/ddv123  0.92
2015 Yang HJ, Ratnapriya R, Cogliati T, Kim JW, Swaroop A. Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease. Progress in Retinal and Eye Research. 46: 1-30. PMID 25668385 DOI: 10.1016/j.preteyeres.2015.01.005  0.92
2015 Veleri S, Lazar CH, Chang B, Sieving PA, Banin E, Swaroop A. Biology and therapy of inherited retinal degenerative disease: insights from mouse models. Disease Models & Mechanisms. 8: 109-29. PMID 25650393 DOI: 10.1242/dmm.017913  0.92
2015 Lazar CH, Mutsuddi M, Kimchi A, Zelinger L, Mizrahi-Meissonnier L, Marks-Ohana D, Boleda A, Ratnapriya R, Sharon D, Swaroop A, Banin E. Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in Israel. Investigative Ophthalmology & Visual Science. 56: 420-30. PMID 25515582 DOI: 10.1167/iovs.14-15647  0.92
2015 Fleury G, Hero A, Yoshida S, Carter T, Barlow C, Swaroop A. Pareto analysis for gene filtering in microarray experiments European Signal Processing Conference. 2015.  0.44
2014 Masuda T, Zhang X, Berlinicke C, Wan J, Yerrabelli A, Conner EA, Kjellstrom S, Bush R, Thorgeirsson SS, Swaroop A, Chen S, Zack DJ. The transcription factor GTF2IRD1 regulates the topology and function of photoreceptors by modulating photoreceptor gene expression across the retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 15356-68. PMID 25392503 DOI: 10.1523/JNEUROSCI.2089-14.2014  0.92
2014 Fu Y, Liu H, Ng L, Kim JW, Hao H, Swaroop A, Forrest D. Feedback induction of a photoreceptor-specific isoform of retinoid-related orphan nuclear receptor β by the rod transcription factor NRL. The Journal of Biological Chemistry. 289: 32469-80. PMID 25296752 DOI: 10.1074/jbc.M114.605774  0.92
2014 Liu C, Lin C, Gao C, May-Simera H, Swaroop A, Li T. Null and hypomorph Prickle1 alleles in mice phenocopy human Robinow syndrome and disrupt signaling downstream of Wnt5a. Biology Open. 3: 861-70. PMID 25190059 DOI: 10.1242/bio.20148375  0.6
2014 Kim SY, Yang HJ, Chang YS, Kim JW, Brooks M, Chew EY, Wong WT, Fariss RN, Rachel RA, Cogliati T, Qian H, Swaroop A. Deletion of aryl hydrocarbon receptor AHR in mice leads to subretinal accumulation of microglia and RPE atrophy. Investigative Ophthalmology & Visual Science. 55: 6031-40. PMID 25159211 DOI: 10.1167/iovs.14-15091  0.92
2014 Swaroop A, Bagchi M, Kumar P, Preuss HG, Tiwari K, Marone PA, Bagchi D. Safety, efficacy and toxicological evaluation of a novel, patented anti-diabetic extract of Trigonella Foenum-Graecum seed extract (Fenfuro). Toxicology Mechanisms and Methods. 24: 495-503. PMID 25045923 DOI: 10.3109/15376516.2014.943443  0.92
2014 Chew EY, Klein ML, Clemons TE, Agrón E, Ratnapriya R, Edwards AO, Fritsche LG, Swaroop A, Abecasis GR. No clinically significant association between CFH and ARMS2 genotypes and response to nutritional supplements: AREDS report number 38. Ophthalmology. 121: 2173-80. PMID 24974817 DOI: 10.1016/j.ophtha.2014.05.008  0.92
2014 Veleri S, Manjunath SH, Fariss RN, May-Simera H, Brooks M, Foskett TA, Gao C, Longo TA, Liu P, Nagashima K, Rachel RA, Li T, Dong L, Swaroop A. Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesis. Nature Communications. 5: 4207. PMID 24947469 DOI: 10.1038/ncomms5207  0.6
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, ... ... Swaroop A, 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  0.92
2014 Fritsche LG, Fariss RN, Stambolian D, Abecasis GR, Curcio CA, Swaroop A. Age-related macular degeneration: genetics and biology coming together. Annual Review of Genomics and Human Genetics. 15: 151-71. PMID 24773320 DOI: 10.1146/annurev-genom-090413-025610  0.92
2014 Bagchi D, Swaroop A, Preuss HG, Bagchi M. Free radical scavenging, antioxidant and cancer chemoprevention by grape seed proanthocyanidin: an overview. Mutation Research. 768: 69-73. PMID 24751946 DOI: 10.1016/j.mrfmmm.2014.04.004  0.92
2014 Hao H, Veleri S, Sun B, Kim DS, Keeley PW, Kim JW, Yang HJ, Yadav SP, Manjunath SH, Sood R, Liu P, Reese BE, Swaroop A. Regulation of a novel isoform of Receptor Expression Enhancing Protein REEP6 in rod photoreceptors by bZIP transcription factor NRL. Human Molecular Genetics. 23: 4260-71. PMID 24691551 DOI: 10.1093/hmg/ddu143  0.92
2014 Boye SE, Huang WC, Roman AJ, Sumaroka A, Boye SL, Ryals RC, Olivares MB, Ruan Q, Tucker BA, Stone EM, Swaroop A, Cideciyan AV, Hauswirth WW, Jacobson SG. Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy. Plos One. 9: e92928. PMID 24671090 DOI: 10.1371/journal.pone.0092928  0.92
2014 Wang C, Zhan X, Bragg-Gresham J, Kang HM, Stambolian D, Chew EY, Branham KE, Heckenlively J, Fulton R, Wilson RK, Mardis ER, Lin X, Swaroop A, Zöllner S, Abecasis GR. Ancestry estimation and control of population stratification for sequence-based association studies Nature Genetics. 46: 409-415. PMID 24633160 DOI: 10.1038/ng.2924  0.92
2014 Roger JE, Hiriyanna A, Gotoh N, Hao H, Cheng DF, Ratnapriya R, Kautzmann MA, Chang B, Swaroop A. OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness. The Journal of Clinical Investigation. 124: 631-43. PMID 24382353 DOI: 10.1172/JCI72722  0.92
2014 Yadav SP, Hao H, Yang HJ, Kautzmann MA, Brooks M, Nellissery J, Klocke B, Seifert M, Swaroop A. The transcription-splicing protein NonO/p54nrb and three NonO-interacting proteins bind to distal enhancer region and augment rhodopsin expression. Human Molecular Genetics. 23: 2132-44. PMID 24301678 DOI: 10.1093/hmg/ddt609  0.92
2014 Ozel AB, Moroi SE, Reed DM, Nika M, Schmidt CM, Akbari S, Scott K, Rozsa F, Pawar H, Musch DC, Lichter PR, Gaasterland D, Branham K, Gilbert J, Garnai SJ, ... ... Swaroop A, et al. Genome-wide association study and meta-analysis of intraocular pressure. Human Genetics. 133: 41-57. PMID 24002674 DOI: 10.1007/s00439-013-1349-5  0.92
2014 Roger JE, Swaroop A. Photoreceptor degeneration: Molecular mechanisms of photoreceptor degeneration Vertebrate Photoreceptors: Functional Molecular Bases. 275-308. DOI: 10.1007/978-4-431-54880-5_11  0.92
2013 Oliver VF, Franchina M, Jaffe AE, Branham KE, Othman M, Heckenlively JR, Swaroop A, Campochiaro B, Vote BJ, Craig JE, Saffery R, Mackey DA, Qian J, Zack DJ, Hewitt AW, et al. Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degeneration. Cell Reports. 5: 1527-35. PMID 24373284 DOI: 10.1016/j.celrep.2013.11.042  0.92
2013 Keeley PW, Luna G, Fariss RN, Skyles KA, Madsen NR, Raven MA, Poché RA, Swindell EC, Jamrich M, Oh EC, Swaroop A, Fisher SK, Reese BE. Development and plasticity of outer retinal circuitry following genetic removal of horizontal cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 17847-62. PMID 24198374 DOI: 10.1523/JNEUROSCI.1373-13.2013  0.92
2013 Ratnapriya R, Swaroop A. Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing. Genome Medicine. 5: 84. PMID 24112618 DOI: 10.1186/gm488  0.92
2013 Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, ... ... Swaroop A, et al. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature Genetics. 45: 1375-9. PMID 24036949 DOI: 10.1038/ng.2758  0.92
2013 Li L, Khan N, Hurd T, Ghosh AK, Cheng C, Molday R, Heckenlively JR, Swaroop A, Khanna H. Ablation of the X-linked retinitis pigmentosa 2 (Rp2) gene in mice results in opsin mislocalization and photoreceptor degeneration. Investigative Ophthalmology & Visual Science. 54: 4503-11. PMID 23745007 DOI: 10.1167/iovs.13-12140  0.92
2013 Swaroop A, Sieving PA. The golden era of ocular disease gene discovery: Race to the finish Clinical Genetics. 84: 99-101. PMID 23713688 DOI: 10.1111/cge.12204  0.92
2013 Zahid S, Khan N, Branham K, Othman M, Karoukis AJ, Sharma N, Moncrief A, Mahmood MN, Sieving PA, Swaroop A, Heckenlively JR, Jayasundera T. Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutations. Jama Ophthalmology. 131: 1016-25. PMID 23681342 DOI: 10.1001/jamaophthalmol.2013.120  0.92
2013 Liu H, Kim SY, Fu Y, Wu X, Ng L, Swaroop A, Forrest D. An isoform of retinoid-related orphan receptor β directs differentiation of retinal amacrine and horizontal interneurons. Nature Communications. 4: 1813. PMID 23652001 DOI: 10.1038/ncomms2793  0.92
2013 Ma W, Cojocaru R, Gotoh N, Gieser L, Villasmil R, Cogliati T, Swaroop A, Wong WT. Gene expression changes in aging retinal microglia: relationship to microglial support functions and regulation of activation. Neurobiology of Aging. 34: 2310-21. PMID 23608111 DOI: 10.1016/j.neurobiolaging.2013.03.022  0.92
2013 Homma K, Okamoto S, Mandai M, Gotoh N, Rajasimha HK, Chang YS, Chen S, Li W, Cogliati T, Swaroop A, Takahashi M. Developing rods transplanted into the degenerating retina of Crx-knockout mice exhibit neural activity similar to native photoreceptors. Stem Cells (Dayton, Ohio). 31: 1149-59. PMID 23495178 DOI: 10.1002/stem.1372  0.92
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, ... ... Swaroop A, 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  0.52
2013 Swaroop A. What's in a name? RPGR mutations redefine the genetic and phenotypic landscape in retinal degenerative diseases. Investigative Ophthalmology & Visual Science. 54: 1417. PMID 23423174 DOI: 10.1167/iovs.13-11750  0.92
2013 Liu C, Lin C, Whitaker DT, Bakeri H, Bulgakov OV, Liu P, Lei J, Dong L, Li T, Swaroop A. Prickle1 is expressed in distinct cell populations of the central nervous system and contributes to neuronal morphogenesis. Human Molecular Genetics. 22: 2234-46. PMID 23420014 DOI: 10.1093/hmg/ddt075  0.92
2013 Nasonkin IO, Merbs SL, Lazo K, Oliver VF, Brooks M, Patel K, Enke RA, Nellissery J, Jamrich M, Le YZ, Bharti K, Fariss RN, Rachel RA, Zack DJ, Rodriguez-Boulan EJ, ... Swaroop A, et al. Conditional knockdown of DNA methyltransferase 1 reveals a key role of retinal pigment epithelium integrity in photoreceptor outer segment morphogenesis. Development (Cambridge, England). 140: 1330-41. PMID 23406904 DOI: 10.1242/dev.086603  0.92
2012 Rachel RA, Li T, Swaroop A. Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins. Cilia. 1: 22. PMID 23351659 DOI: 10.1186/2046-2530-1-22  0.92
2012 Dickison VM, Richmond AM, Abu Irqeba A, Martak JG, Hoge SC, Brooks MJ, Othman MI, Khanna R, Mears AJ, Chowdhury AY, Swaroop A, Ogilvie JM. A role for prenylated rab acceptor 1 in vertebrate photoreceptor development. Bmc Neuroscience. 13: 152. PMID 23241222 DOI: 10.1186/1471-2202-13-152  0.92
2012 Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, ... ... Swaroop A, et al. Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. Investigative Ophthalmology & Visual Science. 53: 8232-7. PMID 23150612 DOI: 10.1167/iovs.12-11025  0.92
2012 Priya RR, Chew EY, Swaroop A. Genetic studies of age-related macular degeneration: lessons, challenges, and opportunities for disease management. Ophthalmology. 119: 2526-36. PMID 23009893 DOI: 10.1016/j.ophtha.2012.06.042  0.92
2012 Huang WC, Wright AF, Roman AJ, Cideciyan AV, Manson FD, Gewaily DY, Schwartz SB, Sadigh S, Limberis MP, Bell P, Wilson JM, Swaroop A, Jacobson SG. RPGR-associated retinal degeneration in human X-linked RP and a murine model. Investigative Ophthalmology & Visual Science. 53: 5594-608. PMID 22807293 DOI: 10.1167/iovs.12-10070  0.92
2012 Roger JE, Nellissery J, Swaroop A. Determination of posttranslational modifications of photoreceptor differentiation factor NRL: focus on SUMOylation. Methods in Molecular Biology (Clifton, N.J.). 884: 353-61. PMID 22688719 DOI: 10.1007/978-1-61779-848-1_25  0.92
2012 Priya RR, Rajasimha HK, Brooks MJ, Swaroop A. Exome sequencing: capture and sequencing of all human coding regions for disease gene discovery. Methods in Molecular Biology (Clifton, N.J.). 884: 335-51. PMID 22688718 DOI: 10.1007/978-1-61779-848-1_24  0.92
2012 Brooks MJ, Rajasimha HK, Swaroop A. Retinal transcriptome profiling by directional next-generation sequencing using 100 ng of total RNA. Methods in Molecular Biology (Clifton, N.J.). 884: 319-34. PMID 22688717 DOI: 10.1007/978-1-61779-848-1_23  0.92
2012 Thompson DA, Khan NW, Othman MI, Chang B, Jia L, Grahek G, Wu Z, Hiriyanna S, Nellissery J, Li T, Khanna H, Colosi P, Swaroop A, Heckenlively JR. Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15. Plos One. 7: e35865. PMID 22563472 DOI: 10.1371/journal.pone.0035865  0.92
2012 Forrest D, Swaroop A. Minireview: the role of nuclear receptors in photoreceptor differentiation and disease. Molecular Endocrinology (Baltimore, Md.). 26: 905-15. PMID 22556342 DOI: 10.1210/me.2012-1010  0.92
2012 Hambright D, Park KY, Brooks M, McKay R, Swaroop A, Nasonkin IO. Long-term survival and differentiation of retinal neurons derived from human embryonic stem cell lines in un-immunosuppressed mouse retina. Molecular Vision. 18: 920-36. PMID 22539871  0.92
2012 Hao H, Kim DS, Klocke B, Johnson KR, Cui K, Gotoh N, Zang C, Gregorski J, Gieser L, Peng W, Fann Y, Seifert M, Zhao K, Swaroop A. Transcriptional regulation of rod photoreceptor homeostasis revealed by in vivo NRL targetome analysis. Plos Genetics. 8: e1002649. PMID 22511886 DOI: 10.1371/journal.pgen.1002649  0.92
2012 Veleri S, Bishop K, Dalle Nogare DE, English MA, Foskett TJ, Chitnis A, Sood R, Liu P, Swaroop A. Knockdown of Bardet-Biedl syndrome gene BBS9/PTHB1 leads to cilia defects. Plos One. 7: e34389. PMID 22479622 DOI: 10.1371/journal.pone.0034389  0.92
2012 Rachel RA, May-Simera HL, Veleri S, Gotoh N, Choi BY, Murga-Zamalloa C, McIntyre JC, Marek J, Lopez I, Hackett AN, Zhang J, Brooks M, den Hollander AI, Beales PL, Li T, ... ... Swaroop A, et al. Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis. The Journal of Clinical Investigation. 122: 1233-45. PMID 22446187 DOI: 10.1172/JCI60981  0.92
2012 Sharma YV, Cojocaru RI, Ritter LM, Khattree N, Brooks M, Scott A, Swaroop A, Goldberg AF. Protective gene expression changes elicited by an inherited defect in photoreceptor structure. Plos One. 7: e31371. PMID 22363631 DOI: 10.1371/journal.pone.0031371  0.92
2012 Beltran WA, Cideciyan AV, Lewin AS, Iwabe S, Khanna H, Sumaroka A, Chiodo VA, Fajardo DS, Román AJ, Deng WT, Swider M, Alemán TS, Boye SL, Genini S, Swaroop A, et al. Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa. Proceedings of the National Academy of Sciences of the United States of America. 109: 2132-7. PMID 22308428 DOI: 10.1073/pnas.1118847109  0.92
2012 Sofat R, Casas JP, Webster AR, Bird AC, Mann SS, Yates JR, Moore AT, Sepp T, Cipriani V, Bunce C, Khan JC, Shahid H, Swaroop A, Abecasis G, Branham KE, et al. Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. International Journal of Epidemiology. 41: 250-62. PMID 22253316 DOI: 10.1093/ije/dyr204  0.92
2012 Roger JE, Ranganath K, Zhao L, Cojocaru RI, Brooks M, Gotoh N, Veleri S, Hiriyanna A, Rachel RA, Campos MM, Fariss RN, Wong WT, Swaroop A. Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 528-41. PMID 22238088 DOI: 10.1523/JNEUROSCI.3591-11.2012  0.92
2012 Liu C, Bakeri H, Li T, Swaroop A. Regulation of retinal progenitor expansion by Frizzled receptors: implications for microphthalmia and retinal coloboma. Human Molecular Genetics. 21: 1848-60. PMID 22228100 DOI: 10.1093/hmg/ddr616  0.92
2012 Swaroop A. Construction of Directional cDNA Libraries Automated Dna Sequencing and Analysis. 115-119. DOI: 10.1016/B978-0-08-092639-1.50021-6  0.92
2011 Brooks MJ, Rajasimha HK, Roger JE, Swaroop A. Next-generation sequencing facilitates quantitative analysis of wild-type and Nrl(-/-) retinal transcriptomes. Molecular Vision. 17: 3034-54. PMID 22162623  0.92
2011 Sivakumaran TA, Igo RP, Kidd JM, Itsara A, Kopplin LJ, Chen W, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, Chew EY, Ramprasad VL, Tay WT, Mitchell P, Seielstad M, ... ... Swaroop A, et al. A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. Plos One. 6: e25598. PMID 22022419 DOI: 10.1371/journal.pone.0025598  0.92
2011 Stanton CM, Yates JR, den Hollander AI, Seddon JM, Swaroop A, Stambolian D, Fauser S, Hoyng C, Yu Y, Atsuhiro K, Branham K, Othman M, Chen W, Kortvely E, Chalmers K, et al. Complement factor D in age-related macular degeneration. Investigative Ophthalmology & Visual Science. 52: 8828-34. PMID 22003108 DOI: 10.1167/iovs.11-7933  0.92
2011 McKay GJ, Patterson CC, Chakravarthy U, Dasari S, Klaver CC, Vingerling JR, Ho L, de Jong PT, Fletcher AE, Young IS, Seland JH, Rahu M, Soubrane G, Tomazzoli L, Topouzis F, ... ... Swaroop A, et al. Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies. Human Mutation. 32: 1407-16. PMID 21882290 DOI: 10.1002/humu.21577  0.92
2011 Sobrin L, Green T, Sim X, Jensen RA, Tai ES, Tay WT, Wang JJ, Mitchell P, Sandholm N, Liu Y, Hietala K, Iyengar SK, Brooks M, Buraczynska M, ... ... Swaroop A, et al. Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Investigative Ophthalmology & Visual Science. 52: 7593-602. PMID 21873659 DOI: 10.1167/iovs.11-7510  0.92
2011 Hao H, Tummala P, Guzman E, Mali RS, Gregorski J, Swaroop A, Mitton KP. The transcription factor neural retina leucine zipper (NRL) controls photoreceptor-specific expression of myocyte enhancer factor Mef2c from an alternative promoter. The Journal of Biological Chemistry. 286: 34893-902. PMID 21849497 DOI: 10.1074/jbc.M111.271072  0.92
2011 Ng L, Lu A, Swaroop A, Sharlin DS, Swaroop A, Forrest D. Two transcription factors can direct three photoreceptor outcomes from rod precursor cells in mouse retinal development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 11118-25. PMID 21813673 DOI: 10.1523/JNEUROSCI.1709-11.2011  0.32
2011 Cheng H, Khan NW, Roger JE, Swaroop A. 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. Human Molecular Genetics. 20: 4102-15. PMID 21813656 DOI: 10.1093/hmg/ddr334  0.92
2011 Kautzmann MA, Kim DS, Felder-Schmittbuhl MP, Swaroop A. Combinatorial regulation of photoreceptor differentiation factor, neural retina leucine zipper gene NRL, revealed by in vivo promoter analysis. The Journal of Biological Chemistry. 286: 28247-55. PMID 21673114 DOI: 10.1074/jbc.M111.257246  0.92
2011 Xue W, Cojocaru RI, Dudley VJ, Brooks M, Swaroop A, Sarthy VP. Ciliary neurotrophic factor induces genes associated with inflammation and gliosis in the retina: a gene profiling study of flow-sorted, Müller cells. Plos One. 6: e20326. PMID 21637858 DOI: 10.1371/journal.pone.0020326  0.92
2011 McKay GJ, Silvestri G, Chakravarthy U, Dasari S, Fritsche LG, Weber BH, Keilhauer CN, Klein ML, Francis PJ, Klaver CC, Vingerling JR, Ho L, De Jong PT, Dean M, Sawitzke J, ... ... Swaroop A, et al. Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. American Journal of Epidemiology. 173: 1357-64. PMID 21498624 DOI: 10.1093/aje/kwr015  0.92
2011 Nasonkin IO, Lazo K, Hambright D, Brooks M, Fariss R, Swaroop A. Distinct nuclear localization patterns of DNA methyltransferases in developing and mature mammalian retina. The Journal of Comparative Neurology. 519: 1914-30. PMID 21452232 DOI: 10.1002/cne.22613  0.92
2011 Cideciyan AV, Rachel RA, Aleman TS, Swider M, Schwartz SB, Sumaroka A, Roman AJ, Stone EM, Jacobson SG, Swaroop A. 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. Human Molecular Genetics. 20: 1411-23. PMID 21245082 DOI: 10.1093/hmg/ddr022  0.92
2011 Chakarova CF, Khanna H, Shah AZ, Patil SB, Sedmak T, Murga-Zamalloa CA, Papaioannou MG, Nagel-Wolfrum K, Lopez I, Munro P, Cheetham M, Koenekoop RK, Rios RM, Matter K, Wolfrum U, ... Swaroop A, et al. TOPORS, implicated in retinal degeneration, is a cilia-centrosomal protein. Human Molecular Genetics. 20: 975-87. PMID 21159800 DOI: 10.1093/hmg/ddq543  0.92
2011 Brión M, Sanchez-Salorio M, Cortón M, de la Fuente M, Pazos B, Othman M, Swaroop A, Abecasis G, Sobrino B, Carracedo A. Genetic association study of age-related macular degeneration in the Spanish population. Acta Ophthalmologica. 89: e12-22. PMID 21106043 DOI: 10.1111/j.1755-3768.2010.02040.x  0.92
2011 Yao J, Feathers KL, Khanna H, Thompson D, Tsilfidis C, Hauswirth WW, Heckenlively JR, Swaroop A, Zacks DN. XIAP therapy increases survival of transplanted rod precursors in a degenerating host retina. Investigative Ophthalmology & Visual Science. 52: 1567-72. PMID 20926819 DOI: 10.1167/iovs.10-5998  0.92
2010 Parapuram SK, Cojocaru RI, Chang JR, Khanna R, Brooks M, Othman M, Zareparsi S, Khan NW, Gotoh N, Cogliati T, Swaroop A. Distinct signature of altered homeostasis in aging rod photoreceptors: implications for retinal diseases. Plos One. 5: e13885. PMID 21079736 DOI: 10.1371/journal.pone.0013885  0.92
2010 Baratz KH, Tosakulwong N, Ryu E, Brown WL, Branham K, Chen W, Tran KD, Schmid-Kubista KE, Heckenlively JR, Swaroop A, Abecasis G, Bailey KR, Edwards AO. E2-2 protein and Fuchs's corneal dystrophy. The New England Journal of Medicine. 363: 1016-24. PMID 20825314 DOI: 10.1056/NEJMoa1007064  0.92
2010 Hurd T, Zhou W, Jenkins P, Liu CJ, Swaroop A, Khanna H, Martens J, Hildebrandt F, Margolis B. The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development. Human Molecular Genetics. 19: 4330-44. PMID 20729296 DOI: 10.1093/hmg/ddq355  0.92
2010 Friedman JS, Chang B, Krauth DS, Lopez I, Waseem NH, Hurd RE, Feathers KL, Branham KE, Shaw M, Thomas GE, Brooks MJ, Liu C, Bakeri HA, Campos MM, Maubaret C, ... ... Swaroop A, et al. Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 mice. Proceedings of the National Academy of Sciences of the United States of America. 107: 15523-8. PMID 20713727 DOI: 10.1073/pnas.1002897107  0.92
2010 Kanda A, Stambolian D, Chen W, Curcio CA, Abecasis GR, Swaroop A. Age-related macular degeneration-associated variants at chromosome 10q26 do not significantly alter ARMS2 and HTRA1 transcript levels in the human retina. Molecular Vision. 16: 1317-23. PMID 20664794  0.92
2010 Swaroop A, Kim D, Forrest D. Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina. Nature Reviews. Neuroscience. 11: 563-76. PMID 20648062 DOI: 10.1038/nrn2880  0.92
2010 Murga-Zamalloa CA, Atkins SJ, Peranen J, Swaroop A, Khanna H. Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration. Human Molecular Genetics. 19: 3591-8. PMID 20631154 DOI: 10.1093/hmg/ddq275  0.92
2010 Jayasundera T, Branham KE, Othman M, Rhoades WR, Karoukis AJ, Khanna H, Swaroop A, Heckenlively JR. RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 915-23. PMID 20625056 DOI: 10.1001/archophthalmol.2010.122  0.92
2010 Raychaudhuri S, Ripke S, Li M, Neale BM, Fagerness J, Reynolds R, Sobrin L, Swaroop A, Abecasis G, Seddon JM, Daly MJ. Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent. Nature Genetics. 42: 553-5; author reply . PMID 20581873 DOI: 10.1038/ng0710-553  0.92
2010 Roger JE, Nellissery J, Kim DS, Swaroop A. Sumoylation of bZIP transcription factor NRL modulates target gene expression during photoreceptor differentiation. The Journal of Biological Chemistry. 285: 25637-44. PMID 20551322 DOI: 10.1074/jbc.M110.142810  0.92
2010 Hugosson T, Friedman JS, Ponjavic V, Abrahamson M, Swaroop A, Andréasson S. Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 772-8. PMID 20547956 DOI: 10.1001/archophthalmol.2010.98  0.92
2010 Nichols LL, Alur RP, Boobalan E, Sergeev YV, Caruso RC, Stone EM, Swaroop A, Johnson MA, Brooks BP. Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL. Human Mutation. 31: E1472-83. PMID 20513135 DOI: 10.1002/humu.21268  0.92
2010 Chen W, Stambolian D, Edwards AO, Branham KE, Othman M, Jakobsdottir J, Tosakulwong N, Pericak-Vance MA, Campochiaro PA, Klein ML, Tan PL, Conley YP, Kanda A, Kopplin L, Li Y, ... ... Swaroop A, et al. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 107: 7401-6. PMID 20385819 DOI: 10.1073/pnas.0912702107  0.32
2010 Murga-Zamalloa C, Swaroop A, Khanna H. Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP). Advances in Experimental Medicine and Biology. 664: 105-14. PMID 20238008 DOI: 10.1007/978-1-4419-1399-9_13  0.92
2010 Hackler L, Wan J, Swaroop A, Qian J, Zack DJ. MicroRNA profile of the developing mouse retina. Investigative Ophthalmology & Visual Science. 51: 1823-31. PMID 19933188 DOI: 10.1167/iovs.09-4657  0.92
2010 Ghosh AK, Murga-Zamalloa CA, Chan L, Hitchcock PF, Swaroop A, Khanna H. Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development. Human Molecular Genetics. 19: 90-8. PMID 19815619 DOI: 10.1093/hmg/ddp469  0.92
2009 Murga-Zamalloa CA, Swaroop A, Khanna H. RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction. Journal of Genetics. 88: 399-407. PMID 20090203 DOI: 10.1007/s12041-009-0061-7  0.92
2009 Kanda A, Swaroop A. A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3 Molecular Vision. 15: 2174-2184. PMID 19898638  0.92
2009 Jia L, Oh EC, Ng L, Srinivas M, Brooks M, Swaroop A, Forrest D. Retinoid-related orphan nuclear receptor RORbeta is an early-acting factor in rod photoreceptor development. Proceedings of the National Academy of Sciences of the United States of America. 106: 17534-9. PMID 19805139 DOI: 10.1073/pnas.0902425106  0.92
2009 Edwards AO, Swaroop A, Seddon JM. Geographic atrophy in age-related macular degeneration and TLR3 New England Journal of Medicine. 360: 2254-2255. PMID 19469037  0.92
2009 Swaroop A, Chew EY, Rickman CB, Abecasis GR. Unraveling a multifactorial late-onset disease: from genetic susceptibility to disease mechanisms for age-related macular degeneration. Annual Review of Genomics and Human Genetics. 10: 19-43. PMID 19405847 DOI: 10.1146/annurev.genom.9.081307.164350  0.92
2009 Layman WS, McEwen DP, Beyer LA, Lalani SR, Fernbach SD, Oh E, Swaroop A, Hegg CC, Raphael Y, Martens JR, Martin DM. Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome. Human Molecular Genetics. 18: 1909-23. PMID 19279158 DOI: 10.1093/hmg/ddp112  0.92
2008 Tsang WY, Bossard C, Khanna H, Peränen J, Swaroop A, Malhotra V, Dynlacht BD. CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease. Developmental Cell. 15: 187-97. PMID 18694559 DOI: 10.1016/j.devcel.2008.07.004  0.92
2008 Siffroi-Fernandez S, Felder-Schmittbuhl MP, Khanna H, Swaroop A, Hicks D. FGF19 exhibits neuroprotective effects on adult mammalian photoreceptors in vitro. Investigative Ophthalmology & Visual Science. 49: 1696-704. PMID 18385093 DOI: 10.1167/iovs.07-1272  0.92
2008 Kanda A, Abecasis G, Swaroop A. Inflammation in the pathogenesis of age-related macular degeneration British Journal of Ophthalmology. 92: 448-450. PMID 18369057 DOI: 10.1136/bjo.2007.131581  0.92
2008 Walia S, Fishman GA, Swaroop A, Branham KEH, Lindeman M, Othman M, Weleber RG. Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene Archives of Ophthalmology. 126: 379-384. PMID 18332319 DOI: 10.1001/archophthalmol.2007.72  0.92
2008 Oh ECT, Cheng H, Hao H, Jia L, Khan NW, Swaroop A. Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors Brain Research. 1236: 16-29. PMID 18294621 DOI: 10.1016/j.brainres.2008.01.028  0.92
2008 Iannaccone A, Othman MI, Cantrell AD, Jennings BJ, Branham K, Swaroop A. Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene. Advances in Experimental Medicine and Biology. 613: 221-7. PMID 18188948 DOI: 10.1007/978-0-387-74904-4_25  0.92
2008 He S, Parapuram SK, Hurd TW, Behnam B, Margolis B, Swaroop A, Khanna H. Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: insights into X-linked Retinitis Pigmentosa and associated ciliopathies. Vision Research. 48: 366-76. PMID 17904189 DOI: 10.1016/j.visres.2007.08.005  0.92
2007 Swaroop A, Branham KEH, Chen W, Abecasis G. Genetic susceptibility to age-related macular degeneration: A paradigm for dissecting complex disease traits Human Molecular Genetics. 16. PMID 17911160 DOI: 10.1093/hmg/ddm212  0.92
2007 Swain P, Kumar S, Patel D, Richong S, Oberoi P, Ghosh M, Swaroop A. Mutations associated with retinopathies alter mitogen-activated protein kinase-induced phosphorylation of neural retina leucine-zipper. Molecular Vision. 13: 1114-20. PMID 17653056  0.92
2007 Trager EH, Khanna R, Marrs A, Siden L, Branham KE, Swaroop A, Richards JE. Madeline 2.0 PDE: a new program for local and web-based pedigree drawing. Bioinformatics (Oxford, England). 23: 1854-6. PMID 17488757 DOI: 10.1093/bioinformatics/btm242  0.92
2007 Raven MA, Oh EC, Swaroop A, Reese BE. Afferent control of horizontal cell morphology revealed by genetic respecification of rods and cones. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 3540-7. PMID 17392470 DOI: 10.1523/JNEUROSCI.0372-07.2007  0.92
2007 Kanda A, Friedman JS, Nishiguchi KM, Swaroop A. Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity. Human Mutation. 28: 589-98. PMID 17335001 DOI: 10.1002/humu.20488  0.92
2007 Oh EC, Khan N, Novelli E, Khanna H, Strettoi E, Swaroop A. Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL. Proceedings of the National Academy of Sciences of the United States of America. 104: 1679-84. PMID 17242361 DOI: 10.1073/pnas.0605934104  0.92
2007 Sinha AK, Sharma A, Swaroop A, Kumar V. An efficient chemoselective strategy for the preparation of (E)-cinnamic esters from cinnamaldehydes using heterogeneous catalyst and DDQ Tetrahedron. 63: 1000-1007. DOI: 10.1016/j.tet.2006.11.011  0.92
2007 Agarwal A, Tehranian S, Swaroop A, Mckenzie K. A robust framework for distributed processing of GIFTS hyperspectral data 87th Ams Annual Meeting 0.92
2007 Tehranian S, Carr JL, Yang S, Swaroop A, McKenzie K. XGOHI, extended GOES high-inclination mission for South-American coverage 87th Ams Annual Meeting 0.92
2006 Ronan S, Nusinowitz S, Swaroop A, Heckenlively JR. Senile panretinal cone dysfunction in age-related macular degeneration (AMD): A report of 52 AMD patients compared to age-matched controls Transactions of the American Ophthalmological Society. 104: 232-239. PMID 17471344  0.92
2006 Cheng H, Aleman TS, Cideciyan AV, Khanna R, Jacobson SG, Swaroop A. In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development Human Molecular Genetics. 15: 2588-2602. PMID 16868010 DOI: 10.1093/hmg/ddl185  0.92
2006 Khanna H, Akimoto M, Siffroi-Fernandez S, Friedman JS, Hicks D, Swaroop A. Retinoic acid regulates the expression of photoreceptor transcription factor NRL. The Journal of Biological Chemistry. 281: 27327-34. PMID 16854989 DOI: 10.1074/jbc.M605500200  0.92
2006 Zacks DN, Han Y, Zeng Y, Swaroop A. Activation of signaling pathways and stress-response genes in an experimental model of retinal detachment Investigative Ophthalmology and Visual Science. 47: 1691-1695. PMID 16565410 DOI: 10.1167/iovs.05-1209  0.92
2006 Akimoto M, Cheng H, Zhu D, Brzezinski JA, Khanna R, Filippova E, Oh EC, Jing Y, Linares JL, Brooks M, Zareparsi S, Mears AJ, Hero A, Glaser T, Swaroop A. Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors. Proceedings of the National Academy of Sciences of the United States of America. 103: 3890-5. PMID 16505381 DOI: 10.1073/pnas.0508214103  0.92
2006 Tata S, Patel JM, Friedman JS, Swaroop A. Declarative querying for biological sequences Proceedings - International Conference On Data Engineering. 2006: 87. DOI: 10.1109/ICDE.2006.47  0.92
2006 Tehranian S, Zhao Y, Harvey T, Swaroop A, McKenzie K. A robust framework for real-time distributed processing of satellite data Journal of Parallel and Distributed Computing. 66: 403-418. DOI: 10.1016/j.jpdc.2005.12.001  0.92
2005 Vine AK, Stader J, Branham K, Musch DC, Swaroop A. Biomarkers of cardiovascular disease as risk factors for age-related macular degeneration Ophthalmology. 112: 2076-2080. PMID 16225921 DOI: 10.1016/j.ophtha.2005.07.004  0.92
2005 Zhu D, Hero AO, Qin ZS, Swaroop A. High throughput screening of co-expressed gene pairs with controlled false discovery rate (FDR) and minimum acceptable strength (MAS). Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 12: 1029-45. PMID 16201920 DOI: 10.1089/cmb.2005.12.1029  0.92
2005 Swaroop A, Sinha AK, Chawla R, Arora R, Sharma RK, Kumara JK. Isolation and characterization of 1,3-dicapryloyl-2-linoleoylglycerol: A novel triglyceride from berries of Hippophae rhamnoides Chemical and Pharmaceutical Bulletin. 53: 1021-1024. PMID 16079540 DOI: 10.1248/cpb.53.1021  0.92
2005 Nikonov SS, Daniele LL, Zhu X, Craft CM, Swaroop A, Pugh EN. Photoreceptors of Nrl -/- mice coexpress functional S- and M-cone opsins having distinct inactivation mechanisms. The Journal of General Physiology. 125: 287-304. PMID 15738050 DOI: 10.1085/jgp.200409208  0.92
2004 Nishiguchi KM, Friedman JS, Sandberg MA, Swaroop A, Berson EL, Dryja TP. Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function. Proceedings of the National Academy of Sciences of the United States of America. 101: 17819-24. PMID 15591106 DOI: 10.1073/pnas.0408183101  0.92
2004 Strettoi E, Mears AJ, Swaroop A. Recruitment of the rod pathway by cones in the absence of rods. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 7576-82. PMID 15329405 DOI: 10.1523/JNEUROSCI.2245-04.2004  0.92
2004 Lord-Grignon J, Tétreault N, Mears AJ, Swaroop A, Bernier G. Characterization of new transcripts enriched in the mouse retina and identification of candidate retinal disease genes. Investigative Ophthalmology & Visual Science. 45: 3313-9. PMID 15326156 DOI: 10.1167/iovs.03-1350  0.92
2004 Yu J, He S, Friedman JS, Akimoto M, Ghosh D, Mears AJ, Hicks D, Swaroop A. 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. The Journal of Biological Chemistry. 279: 42211-20. PMID 15292180 DOI: 10.1074/jbc.M408223200  0.92
2004 Bumsted O'Brien KM, Cheng H, Jiang Y, Schulte D, Swaroop A, Hendrickson AE. Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina. Investigative Ophthalmology & Visual Science. 45: 2807-12. PMID 15277507 DOI: 10.1167/iovs.03-1317  0.92
2004 Zareparsi S, Hero A, Zack DJ, Williams RW, Swaroop A. Seeing the unseen: Microarray-based gene expression profiling in vision. Investigative Ophthalmology & Visual Science. 45: 2457-62. PMID 15277464 DOI: 10.1167/iovs.04-0183  0.92
2004 Cheng H, Khanna H, Oh EC, Hicks D, Mitton KP, Swaroop A. Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors. Human Molecular Genetics. 13: 1563-75. PMID 15190009 DOI: 10.1093/hmg/ddh173  0.92
2004 Yoshida S, Mears AJ, Friedman JS, Carter T, He S, Oh E, Jing Y, Farjo R, Fleury G, Barlow C, Hero AO, Swaroop A. Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl. Human Molecular Genetics. 13: 1487-503. PMID 15163632 DOI: 10.1093/hmg/ddh160  0.92
2004 Dang L, Pulukuri S, Mears AJ, Swaroop A, Reese BE, Sitaramayya A. Connexin 36 in photoreceptor cells: studies on transgenic rod-less and cone-less mouse retinas. Molecular Vision. 10: 323-7. PMID 15152186  0.92
2004 Yu J, Mears AJ, Yoshida S, Farjo R, Carter TA, Ghosh D, Hero A, Barlow C, Swaroop A. From disease genes to cellular pathways: a progress report. Novartis Foundation Symposium. 255: 147-60; discussion 1. PMID 14750602  0.92
2004 Akimoto M, Filippova E, Gage PJ, Zhu X, Craft CM, Swaroop A. Transgenic mice expressing Cre-recombinase specifically in M- or S-cone photoreceptors. Investigative Ophthalmology & Visual Science. 45: 42-7. PMID 14691152 DOI: 10.1167/iovs.03-0804  0.92
2004 Hero AO, Fleury G, Mears AJ, Swaroop A. Multicriteria Gene Screening for Analysis of Differential Expression with DNA Microarrays Eurasip Journal On Applied Signal Processing. 2004: 43-52. DOI: 10.1155/S1110865704310036  0.92
2004 Fleury G, Hero A, Zareparsi S, Swaroop A. Gene discovery using Pareto depth sampling distributions Journal of the Franklin Institute. 341: 55-75. DOI: 10.1016/j.jfranklin.2003.12.007  0.92
2004 Fleury G, Hero A, Zareparsi S, Swaroop A. Pareto depth sampling distributions for gene ranking 2004 2nd Ieee International Symposium On Biomedical Imaging: Macro to Nano. 1: 65-68.  0.92
2003 Iannaccone A, Breuer DK, Wang XF, Kuo SF, Normando EM, Filippova E, Baldi A, Hiriyanna S, MacDonald CB, Baldi F, Cosgrove D, Morton CC, Swaroop A, Jablonski MM. Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation. Journal of Medical Genetics. 40: e118. PMID 14627685  0.92
2003 Andréasson S, Breuer DK, Eksandh L, Ponjavic V, Frennesson C, Hiriyanna S, Filippova E, Yashar BM, Swaroop A. Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes. Ophthalmic Genetics. 24: 215-23. PMID 14566651 DOI: 10.1076/opge.24.4.215.17228  0.92
2003 Yu J, Farjo R, MacNee SP, Baehr W, Stambolian DE, Swaroop A. Annotation and analysis of 10,000 expressed sequence tags from developing mouse eye and adult retina. Genome Biology. 4: R65. PMID 14519200 DOI: 10.1186/gb-2003-4-10-r65  0.92
2003 Xi J, Farjo R, Yoshida S, Kern TS, Swaroop A, Andley UP. A comprehensive analysis of the expression of crystallins in mouse retina Molecular Vision. 9: 410-419. PMID 12949468  0.92
2003 Schwartz SB, Aleman TS, Cideciyan AV, Swaroop A, Jacobson SG, Stone EM. De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 44: 3593-7. PMID 12882812 DOI: 10.1167/iovs.03-0155  0.92
2003 Zhu X, Brown B, Li A, Mears AJ, Swaroop A, Craft CM. GRK1-dependent phosphorylation of S and M opsins and their binding to cone arrestin during cone phototransduction in the mouse retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 6152-60. PMID 12853434  0.92
2003 Mitton KP, Swain PK, Khanna H, Dowd M, Apel IJ, Swaroop A. Interaction of retinal bZIP transcription factor NRL with Flt3-interacting zinc-finger protein Fiz1: possible role of Fiz1 as a transcriptional repressor. Human Molecular Genetics. 12: 365-73. PMID 12566383 DOI: 10.1093/hmg/ddg035  0.92
2002 Aguirre GD, Yashar BM, John SK, Smith JE, Breuer DK, Hiriyanna S, Swaroop A, Milam AH. Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15. Experimental Eye Research. 75: 431-43. PMID 12387791 DOI: 10.1016/S0014-4835(02)92037-3  0.92
2002 Swaroop A, Zack DJ. Transcriptome analysis of the retina. Genome Biology. 3: REVIEWS1022. PMID 12186651  0.92
2002 Yoshida S, Yashar BM, Hiriyanna S, Swaroop A. Microarray analysis of gene expression in the aging human retina Investigative Ophthalmology and Visual Science. 43: 2554-2560. PMID 12147584  0.92
2002 Yu J, Othman MI, Farjo R, Zareparsi S, MacNee SP, Yoshida S, Swaroop A. Evaluation and optimization of procedures for target labeling and hybridization of cDNA microarrays. Molecular Vision. 8: 130-7. PMID 12011805  0.52
2002 Breuer DK, Yashar BM, Filippova E, Hiriyanna S, Lyons RH, Mears AJ, Asaye B, Acar C, Vervoort R, Wright AF, Musarella MA, Wheeler P, MacDonald I, Iannaccone A, Birch D, ... ... Swaroop A, et al. A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa. American Journal of Human Genetics. 70: 1545-54. PMID 11992260 DOI: 10.1086/340848  0.92
2002 Farjo R, Yu J, Othman MI, Yoshida S, Sheth S, Glaser T, Baehr W, Swaroop A. Mouse eye gene microarrays for investigating ocular development and disease. Vision Research. 42: 463-70. PMID 11853762 DOI: 10.1016/S0042-6989(01)00219-X  0.92
2002 Fleury G, Hero A, Yoshida S, Carter T, Barlow C, Swaroop A. Clustering gene expression signals from retinal microarray data Icassp, Ieee International Conference On Acoustics, Speech and Signal Processing - Proceedings. 4.  0.92
2000 Bessant DAR, Payne AM, Plant C, Bird AC, Swaroop A, Bhattacharya SS. NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies European Journal of Human Genetics. 8: 783-787. PMID 11039579 DOI: 10.1038/sj.ejhg.5200538  0.92
2000 Mitton KP, Swain PK, Chen S, Xu S, Zack DJ, Swaroop A. The leucine zipper of NRL interacts with the CRX homeodomain. A possible mechanism of transcriptional synergy in rhodopsin regulation. The Journal of Biological Chemistry. 275: 29794-9. PMID 10887186 DOI: 10.1074/jbc.M003658200  0.92
2000 Sinha S, Sharma A, Agarwal N, Swaroop A, Yang-Feng TL. Expression profile and chromosomal location of cDNA clones, identified from an enriched adult human retina library Investigative Ophthalmology and Visual Science. 41: 24-28. PMID 10634596  0.92
1999 Bessant DA, Payne AM, Mitton KP, Wang QL, Swain PK, Plant C, Bird AC, Zack DJ, Swaroop A, Bhattacharya SS. A mutation in NRL is associated with autosomal dominant retinitis pigmentosa. Nature Genetics. 21: 355-6. PMID 10192380 DOI: 10.1038/7678  0.92
1998 Ponjavic V, Andréasson S, Abrahamson M, Ehinger B, Gieser L, Fujita R, Swaroop A. Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype Ophthalmic Genetics. 19: 187-196. PMID 9895243  0.92
1998 He L, Campbell ML, Srivastava D, Blocker YS, Harris JR, Swaroop A, Fox DA. Spatial and temporal expression of AP-1 responsive rod photoreceptor genes and bZIP transcription factors during development of the rat retina. Molecular Vision. 4: 32. PMID 9873070  0.92
1998 Fishman GA, Graver S, Buraczynska M, Wu W, Swaroop A. A new 2-base pair deletion in the RPGR gene in a black family with X- linked retinitis pigmentosa Archives of Ophthalmology. 116: 213-218. PMID 9488274  0.92
1997 Forsythe P, Maguire A, Fujita R, Moen C, Swaroop A, Bennett J. A carboxy-terminal truncation of 99 amino acids resulting from a novel mutation (Arg555-->stop) in the CHM gene leads to choroideremia Experimental Eye Research. 64: 487-490. PMID 9196401  0.92
1997 Swaroop A. cDNA library Investigative Ophthalmology &Amp; Visual Science. 38: 1053. PMID 9152223  0.92
1996 Fujita R, Swaroop A. RPGR: part one of the X-linked retinitis pigmentosa story Molecular Vision. 2: 4. PMID 9233985  0.92
1996 Rehemtulla A, Warwar R, Kumar R, Ji X, Zack DJ, Swaroop A. The basic motif-leucine zipper transcription factor Nrl can positively regulate rhodopsin gene expression. Proceedings of the National Academy of Sciences of the United States of America. 93: 191-5. PMID 8552602 DOI: 10.1073/pnas.93.1.191  0.92
1996 Liu Q, Ji X, Breitman ML, Hitchcock PF, Swaroop A. Expression of the bZIP transcription factor gene Nrl in the developing nervous system. Oncogene. 12: 207-11. PMID 8552394  0.92
1996 Yan D, Fujita R, Swaroop A. [11]Isolation of candidate genes for inherited diseases: Application to X-linked retinal degenerations Methods in Molecular Genetics. 8: 207-228. DOI: 10.1016/S1067-2389(96)80044-6  0.92
1996 Hsieh F, Kido M, Swaroop A, Blanks JC, Rich KA. In situ localization of bZIP transcription factor NRL during mouse retinal development demonstrates a temporal correlation with rod photoreceptor differentiation Investigative Ophthalmology and Visual Science. 37: S624.  0.92
1996 Warwar R, Farjo Q, Lee C, Sadri E, Forsythe P, Swaroop A. Organization of the human bZIP transcription factor gene NRL and characterization of its promoter region Investigative Ophthalmology and Visual Science. 37.  0.92
1996 Forsythe P, Fujita R, Buraczynska M, Hoffman D, Jacobson S, Sieving P, Swaroop A. Genetic analysis of the X-linked retinitis pigmentosa locus RP3 Investigative Ophthalmology and Visual Science. 37.  0.92
1995 Shaywitz DA, Orci L, Ravazzola M, Swaroop A, Kaiser CA. Human SEC13Rp functions in yeast and is located on transport vesicles budding from the endoplasmic reticulum Journal of Cell Biology. 128: 769-777. PMID 7876304 DOI: 10.1083/jcb.128.5.769  0.92
1995 Fujita R, Skolnick C, Pakstis AJ, Yang-Feng TL, Swaroop A. Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13 Human Genetics. 95: 467-468. PMID 7705848 DOI: 10.1007/BF00208981  0.92
1995 Fujita R, Swaroop A. Alu-vector PCR with biotinylated primers to isolate YAC ends ready for sequencing Biotechniques. 18. PMID 7619480  0.92
1994 Saikumar P, Swaroop A, Ramakrishna Kurup CK, Ramasarma T. Competing peroxidase and oxidase reactions in scopoletin-dependent H2O2-initiated oxidation of NADH by horseradish peroxidase Biochimica Et Biophysica Acta (Bba)/Protein Structure and Molecular. 1204: 117-123. PMID 8305468 DOI: 10.1016/0167-4838(94)90040-X  0.92
1994 Hernando N, Martin-Vasallo P, Ghosh S, Ghosh PK, Swaroop A, Coca-Prados M. Nucleotide sequence of a cDNA for the beta 2 subunit isoform of Na+,K(+)-ATPase from human retina. Biochimica Et Biophysica Acta. 1189: 109-11. PMID 8305453 DOI: 10.1016/0005-2736(94)90287-9  0.92
1994 Tombran-Tink J, Pawar H, Swaroop A, Rodriguez I, Chader GJ. Localization of the Gene for Pigment Epithelium-Derived Factor (PEDF) to Chromosome 17p13.1 and Expression in Cultured Human Retinoblastoma Cells Genomics. 19: 266-272. PMID 8188257 DOI: 10.1006/geno.1994.1057  0.92
1993 Swaroop A, Ganguly S, Sarkar SN, Vasavada HA. λSHK and λAASV: phage vectors for efficient cDNA cloning and expression in mammalian cells Gene. 123: 287-288. PMID 8428673 DOI: 10.1016/0378-1119(93)90140-X  0.92
1993 Swaroop A, Xu J. cDNA libraries from human tissues and cell lines Cytogenetics and Cell Genetics. 64: 292-294. PMID 8404057  0.92
1993 Farjo Q, Jackson AU, Xu J, Gryzenia M, Skolnick C, Agarwal N, Swaroop A. Molecular characterization of the murine neural retina leucine zipper gene, Nrl. Genomics. 18: 216-22. PMID 8288222 DOI: 10.1006/geno.1993.1458  0.92
1993 Bespalova IN, Farjo Q, Mortlock DP, Jackson AU, Meisler MH, Swaroop A, Burmeister M. Mapping of the neural retina leucine zipper gene, Nrl, to mouse chromosome 14. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 618-20. PMID 8268663 DOI: 10.1007/BF00361397  0.92
1992 Swaroop A, Xu J, Pawar H, Jackson A, Skolnick C, Agarwal N. A conserved retina-specific gene encodes a basic motif/leucine zipper domain Proceedings of the National Academy of Sciences of the United States of America. 89: 266-270. PMID 1729696  0.92
1992 Gieser L, Swaroop A. Expressed sequence tags and chromosomal localization of cDNA clones from a subtracted retinal pigment epithelium library Genomics. 13: 873-876. PMID 1639417 DOI: 10.1016/0888-7543(92)90173-P  0.92
1992 Yang-Feng TL, Swaroop A. Neural retina-specific leucine zipper gene NRL (D14S46E) maps to human chromosome 14q11.1-q11.2 Genomics. 14: 491-492. PMID 1427865 DOI: 10.1016/S0888-7543(05)80248-4  0.92
1991 Swaroop A, Xu JZ, Agarwal N, Weissman SM. A simple and efficient cDNA library subtraction procedure: isolation of human retina-specific cDNA clones. Nucleic Acids Research. 19: 1954. PMID 2030979 DOI: 10.1093/nar/19.8.1954  0.92
1991 Swaroop A, Agarwal N, Gruen JR, Bick D, Weissman SM. Differential expression of novel Gs alpha signal transduction protein cDNA species. Nucleic Acids Research. 19: 4725-9. PMID 1716359 DOI: 10.1093/nar/19.17.4725  0.92
1991 Agarwal N, Hsieh CL, Sills D, Swaroop M, Desai B, Francke U, Swaroop A. 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). Experimental Eye Research. 52: 549-61. PMID 1712312 DOI: 10.1016/0014-4835(91)90056-K  0.92
1990 Vasavada HA, Ganguly S, Chorney M, Mathur R, Shukla H, Swaroop A, Weissman SM. pSH4: a mammalian cDNA expression vector. Nucleic Acids Research. 18: 3668. PMID 2362830 DOI: 10.1093/nar/18.12.3668  0.92
1990 Shukla H, Swaroop A, Srivastava R, Weissman SM. The mRNA of a human class I gene HLA G/HLA 6.0 exhibits a restricted pattern of expression. Nucleic Acids Research. 18: 2189. PMID 2336406 DOI: 10.1093/nar/18.8.2189  0.92
1990 Barjatiya MK, Mathur RN, Swaroop A. Byssinosis in cotton textile workers of Kishangarh The Indian Journal of Chest Diseases &Amp; Allied Sciences. 32: 215-223. PMID 2134233  0.92
1990 Hsieh CL, Swaroop A, Francke U. Chromosomal localization and cDNA sequence of human ralB, a GTP binding protein Somatic Cell and Molecular Genetics. 16: 407-410. PMID 2120779 DOI: 10.1007/BF01232469  0.92
1990 Francke U, Ochs HD, Darras BT, Swaroop A. Origin of mutations in two families with X-linked chronic granulomatous disease Blood. 76: 602-606. PMID 1974155  0.92
1989 Swaroop A. CK isoenzyme variants in electrophoresis Laboratory Medicine. 20: 305-310.  0.92
1988 Swaroop A, Weissman SM. Charon BS (+) and (-), versatile λ phage vectors for constructing directional cDNA libraries and their efficient transfer to plasmids Nucleic Acids Research. 16: 8739. PMID 2971160 DOI: 10.1093/nar/16.17.8739  0.92
1988 Swaroop A, Hogan BLM, Francke U. Molecular analysis of the cDNA for human SPARC/osteonectin/BM-40: Sequence, expression, and localization of the gene to chromosome 5q31-q33 Genomics. 2: 37-47. PMID 2838412 DOI: 10.1016/0888-7543(88)90107-3  0.92
1987 Swaroop A, Swaroop M, Garen A. Sequence analysis of the complete cDNA and encoded polypeptide for the Glued gene of Drosophila melanogaster. Proceedings of the National Academy of Sciences of the United States of America. 84: 6501-5. PMID 2819881  0.92
1986 Patole MS, Swaroop A, Ramasarma T. Generation of H2O2 in brain mitochondria Journal of Neurochemistry. 47: 1-8. PMID 3711892  0.92
1986 Swaroop A, Sun JW, Paco-Larson ML, Garen A. Molecular organization and expression of the genetic locus glued in Drosophila melanogaster. Molecular and Cellular Biology. 6: 833-41. PMID 3022132  0.92
1985 Swaroop A, Ramasarma T. Heat exposure and hypothyroid conditions decrease hydrogen peroxide generation in liver mitochondria Biochemical Journal. 226: 403-408. PMID 3994666  0.92
1985 Swaroop A, Paco-Larson ML, Garen A. Molecular genetics of a transposon-induced dominant mutation in the Drosophila locus Glued. Proceedings of the National Academy of Sciences of the United States of America. 82: 1751-5. PMID 2984667  0.92
1983 Swaroop A, Patole MS, Puranam RS, Ramasarma T. Noradrenaline treatment of rats stimulates H2O2 generation in liver mitochondria Biochemical Journal. 214: 745-750. PMID 6312963  0.92
1982 Swaroop A, Ramasarma T. Changes in mitochondrial oxidative metabolism under conditions of heat stress Indian Journal of Biochemistry and Biophysics. 19: 382-387. PMID 7184857  0.92
1981 Ramasarma T, Swaroop A, MacKellar W, Crane FL. Generation of hydrogen peroxide on oxidation of NADH by hepatic plasma membranes Journal of Bioenergetics and Biomembranes. 13: 241-253. PMID 7334020 DOI: 10.1007/BF00743203  0.92
1981 Swaroop A, Ramasarma T. Inhibition of H2O2 generation in rat liver mitochondria by radical quenchers and phenolic compounds Biochemical Journal. 194: 657-665. PMID 7306014  0.92
1981 Swaroop A, Ramasarma T. Choline-dependent H2O2 generation in mitochondria responds to altered status of thyroxine and thermogenesis Biochemistry International. 2: 85-93.  0.92
1979 Singh Y, Swaroop A, Misra UK. Kidney lipids of weanling rats fed lysine threonine deficient rice diets Nutrition Reports International. 20: 75-77.  0.92
1979 Swaroop A, Singh Y, Misra UK. Liver lipids on weanling rats fed lysine threonine deficient rice diets Nutrition Reports International. 20: 79-81.  0.92
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