| Year |
Citation |
Score |
| 2024 |
McNamee SM, Chan NP, Akula M, Avola MO, Whalen M, Nystuen K, Singh P, Upadhyay AK, DeAngelis MM, Haider NB. Preclinical dose response study shows NR2E3 can attenuate retinal degeneration in the retinitis pigmentosa mouse model Rho. Gene Therapy. PMID 38273095 DOI: 10.1038/s41434-024-00440-6 |
0.362 |
|
| 2020 |
Li S, Datta S, Brabbit E, Love Z, Woytowicz V, Flattery K, Capri J, Yao K, Wu S, Imboden M, Upadhyay A, Arumugham R, Thoreson WB, DeAngelis MM, Haider NB. Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa. Gene Therapy. PMID 32123325 DOI: 10.1038/S41434-020-0134-Z |
0.478 |
|
| 2017 |
Olivares AM, Han Y, Soto D, Flattery K, Marini J, Molemma N, Haider A, Escher P, DeAngelis MM, Haider NB. Corrigendum to "The Nuclear Hormone Receptor Nr2c1 (Tr2) is a critical regulator of early retina cell pattering" [Dev. Biol. 16 (2017) 30797-7]. Developmental Biology. PMID 28743516 DOI: 10.1016/J.Ydbio.2017.07.009 |
0.387 |
|
| 2017 |
Olivares AM, Han Y, Soto D, Flattery K, Marini J, Molemma N, Haider A, Escher P, DeAngelis MM, Haider NB. The Nuclear Hormone Receptor Gene Nr2c1 (Tr2) is a Critical Regulator of Early Retina Cell Patterning. Developmental Biology. PMID 28551284 DOI: 10.1016/J.Ydbio.2017.05.021 |
0.47 |
|
| 2017 |
Olivares AM, Jelcick AS, Reinecke J, Leehy B, Haider A, Morrison MA, Cheng L, Chen DF, DeAngelis MM, Haider NB. Multimodal Regulation Orchestrates Normal and Complex Disease States in the Retina. Scientific Reports. 7: 690. PMID 28386079 DOI: 10.1038/S41598-017-00788-3 |
0.338 |
|
| 2015 |
Olivares AM, Moreno-Ramos OA, Haider NB. Role of Nuclear Receptors in Central Nervous System Development and Associated Diseases. Journal of Experimental Neuroscience. 9: 93-121. PMID 27168725 DOI: 10.4137/Jen.S25480 |
0.459 |
|
| 2015 |
Grishchuk Y, Stember KG, Matsunaga A, Olivares AM, Cruz NM, King VE, Humphrey DM, Wang SL, Muzikansky A, Betensky RA, Thoreson WB, Haider N, Slaugenhaupt SA. Retinal Dystrophy and Optic Nerve Pathology in the Mouse Model of Mucolipidosis IV. The American Journal of Pathology. PMID 26608452 DOI: 10.1016/J.Ajpath.2015.09.017 |
0.394 |
|
| 2015 |
Moreno-Ramos OA, Olivares AM, Haider NB, de Autismo LC, Lattig MC. Whole-Exome Sequencing in a South American Cohort Links ALDH1A3, FOXN1 and Retinoic Acid Regulation Pathways to Autism Spectrum Disorders. Plos One. 10: e0135927. PMID 26352270 DOI: 10.1371/Journal.Pone.0135927 |
0.34 |
|
| 2015 |
von Alpen D, Tran HV, Guex N, Venturini G, Munier FL, Schorderet DF, Haider NB, Escher P. Differential dimerization of variants linked to enhanced S-cone sensitivity syndrome (ESCS) located in the NR2E3 ligand-binding domain. Human Mutation. 36: 599-610. PMID 25703721 DOI: 10.1002/Humu.22775 |
0.39 |
|
| 2014 |
Hasegawa E, Sweigard H, Husain D, Olivares AM, Chang B, Smith KE, Birsner AE, D'Amato RJ, Michaud NA, Han Y, Vavvas DG, Miller JW, Haider NB, Connor KM. Characterization of a spontaneous retinal neovascular mouse model. Plos One. 9: e106507. PMID 25188381 DOI: 10.1371/Journal.Pone.0106507 |
0.397 |
|
| 2014 |
Owen LA, Morrison MA, Ahn J, Woo SJ, Sato H, Robinson R, Morgan DJ, Zacharaki F, Simeonova M, Uehara H, Chakravarthy U, Hogg RE, Ambati BK, Kotoula M, Baehr W, ... Haider NB, et al. FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression. Investigative Ophthalmology & Visual Science. 55: 3543-54. PMID 24812550 DOI: 10.1167/Iovs.14-14047 |
0.374 |
|
| 2014 |
Cruz NM, Yuan Y, Leehy BD, Baid R, Kompella U, DeAngelis MM, Escher P, Haider NB. Modifier genes as therapeutics: the nuclear hormone receptor Rev Erb alpha (Nr1d1) rescues Nr2e3 associated retinal disease. Plos One. 9: e87942. PMID 24498227 DOI: 10.1371/Journal.Pone.0087942 |
0.539 |
|
| 2012 |
Kador PF, Zhang P, Makita J, Zhang Z, Guo C, Randazzo J, Kawada H, Haider N, Blessing K. Novel diabetic mouse models as tools for investigating diabetic retinopathy. Plos One. 7: e49422. PMID 23251343 DOI: 10.1371/Journal.Pone.0049422 |
0.336 |
|
| 2011 |
Morrison MA, Silveira AC, Huynh N, Jun G, Smith SE, Zacharaki F, Sato H, Loomis S, Andreoli MT, Adams SM, Radeke MJ, Jelcick AS, Yuan Y, Tsiloulis AN, Chatzoulis DZ, ... ... Haider NB, et al. Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration. Human Genomics. 5: 538-68. PMID 22155603 DOI: 10.1186/1479-7364-5-6-538 |
0.728 |
|
| 2011 |
Jun G, Nicolaou M, Morrison MA, Buros J, Morgan DJ, Radeke MJ, Yonekawa Y, Tsironi EE, Kotoula MG, Zacharaki F, Mollema N, Yuan Y, Miller JW, Haider NB, Hageman GS, et al. Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology. Plos One. 6: e25775. PMID 21998696 DOI: 10.1371/Journal.Pone.0025775 |
0.741 |
|
| 2011 |
Randazzo J, Zhang Z, Hoff M, Kawada H, Sachs A, Yuan Y, Haider N, Kador P. Orally active multi-functional antioxidants are neuroprotective in a rat model of light-induced retinal damage. Plos One. 6: e21926. PMID 21779355 DOI: 10.1371/Journal.Pone.0021926 |
0.367 |
|
| 2011 |
Jelcick AS, Yuan Y, Leehy BD, Cox LC, Silveira AC, Qiu F, Schenk S, Sachs AJ, Morrison MA, Nystuen AM, DeAngelis MM, Haider NB. Genetic variations strongly influence phenotypic outcome in the mouse retina. Plos One. 6: e21858. PMID 21779340 DOI: 10.1371/Journal.Pone.0021858 |
0.763 |
|
| 2011 |
Mollema NJ, Yuan Y, Jelcick AS, Sachs AJ, von Alpen D, Schorderet D, Escher P, Haider NB. Nuclear receptor Rev-erb alpha (Nr1d1) functions in concert with Nr2e3 to regulate transcriptional networks in the retina. Plos One. 6: e17494. PMID 21408158 DOI: 10.1371/Journal.Pone.0017494 |
0.701 |
|
| 2010 |
Mollema N, Haider NB. Focus on molecules: nuclear hormone receptor Nr2e3: impact on retinal development and disease. Experimental Eye Research. 91: 116-7. PMID 20450910 DOI: 10.1016/J.Exer.2010.04.013 |
0.748 |
|
| 2010 |
Silveira AC, Morrison MA, Ji F, Xu H, Reinecke JB, Adams SM, Arneberg TM, Janssian M, Lee JE, Yuan Y, Schaumberg DA, Kotoula MG, Tsironi EE, Tsiloulis AN, Chatzoulis DZ, ... ... Haider NB, et al. Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: a systems biology based approach. Vision Research. 50: 698-715. PMID 19786043 DOI: 10.1016/J.Visres.2009.09.016 |
0.43 |
|
| 2009 |
Sachs AJ, David SA, Haider NB, Nystuen AM. Patterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4. Plos One. 4: e8270. PMID 20011524 DOI: 10.1371/Journal.Pone.0008270 |
0.338 |
|
| 2009 |
Haider NB, Mollema N, Gaule M, Yuan Y, Sachs AJ, Nystuen AM, Naggert JK, Nishina PM. Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction. Experimental Eye Research. 89: 365-72. PMID 19379737 DOI: 10.1016/J.Exer.2009.04.006 |
0.768 |
|
| 2008 |
Nystuen AM, Sachs AJ, Yuan Y, Heuermann L, Haider NB. A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 19: 623-33. PMID 18763016 DOI: 10.1007/S00335-008-9138-5 |
0.451 |
|
| 2008 |
Haider NB, Zhang W, Hurd R, Ikeda A, Nystuen AM, Naggert JK, Nishina PM. Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 19: 145-54. PMID 18286335 DOI: 10.1007/S00335-008-9092-2 |
0.45 |
|
| 2007 |
Sachs AJ, Schwendinger JK, Yang AW, Haider NB, Nystuen AM. The mouse mutants recoil wobbler and nmf373 represent a series of Grm1 mutations. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 749-56. PMID 17934773 DOI: 10.1007/S00335-007-9064-Y |
0.756 |
|
| 2007 |
Nystuen AM, Schwendinger JK, Sachs AJ, Yang AW, Haider NB. A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutant. Neurogenetics. 8: 1-10. PMID 17102983 DOI: 10.1007/S10048-006-0068-7 |
0.76 |
|
| 2006 |
Haider NB, Demarco P, Nystuen AM, Huang X, Smith RS, McCall MA, Naggert JK, Nishina PM. The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation. Visual Neuroscience. 23: 917-29. PMID 17266784 DOI: 10.1017/S095252380623027X |
0.472 |
|
| 2003 |
Mehalow AK, Kameya S, Smith RS, Hawes NL, Denegre JM, Young JA, Bechtold L, Haider NB, Tepass U, Heckenlively JR, Chang B, Naggert JK, Nishina PM. CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina. Human Molecular Genetics. 12: 2179-89. PMID 12915475 DOI: 10.1093/Hmg/Ddg232 |
0.489 |
|
| 2002 |
Haider NB, Ikeda A, Naggert JK, Nishina PM. Genetic modifiers of vision and hearing. Human Molecular Genetics. 11: 1195-206. PMID 12015279 DOI: 10.1093/Hmg/11.10.1195 |
0.43 |
|
| 2001 |
Haider NB, Naggert JK, Nishina PM. Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice. Human Molecular Genetics. 10: 1619-26. PMID 11487564 DOI: 10.1093/Hmg/10.16.1619 |
0.477 |
|
| 2001 |
Mykytyn K, Braun T, Carmi R, Haider NB, Searby CC, Shastri M, Beck G, Wright AF, Iannaccone A, Elbedour K, Riise R, Baldi A, Raas-Rothschild A, Gorman SW, Duhl DM, et al. Identification of the gene that, when mutated, causes the human obesity syndrome BBS4. Nature Genetics. 28: 188-91. PMID 11381270 DOI: 10.1038/88925 |
0.366 |
|
| 2001 |
Nishimura DY, Searby CC, Carmi R, Elbedour K, Van Maldergem L, Fulton AB, Lam BL, Powell BR, Swiderski RE, Bugge KE, Haider NB, Kwitek-Black AE, Ying L, Duhl DM, Gorman SW, et al. Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2). Human Molecular Genetics. 10: 865-74. PMID 11285252 DOI: 10.1093/Hmg/10.8.865 |
0.34 |
|
| 2000 |
Miano MG, Jacobson SG, Carothers A, Hanson I, Teague P, Lovell J, Cideciyan AV, Haider N, Stone EM, Sheffield VC, Wright AF. Pitfalls in homozygosity mapping. American Journal of Human Genetics. 67: 1348-51. PMID 11007652 DOI: 10.1016/S0002-9297(07)62966-8 |
0.307 |
|
| 2000 |
Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, et al. Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. Nature Genetics. 24: 127-31. PMID 10655056 DOI: 10.1038/72777 |
0.468 |
|
| 2000 |
Ventura-Holman T, Haider NB, Maher JF. Rapid Communication: The Human FEMI B Gene Maps to Chromosome lSq22 and Is Excluded as the Gene for Bardet-Biedl Syndrome, Type 4 The American Journal of the Medical Sciences. 319: 268-270. DOI: 10.1016/S0002-9629(15)40743-8 |
0.315 |
|
| 1999 |
Ying L, Katz Y, Schlesinger M, Carmi R, Shalev H, Haider N, Beck G, Sheffield VC, Landau D. Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome. American Journal of Human Genetics. 65: 1538-46. PMID 10577907 DOI: 10.1086/302673 |
0.388 |
|
| 1999 |
Haider NB, Searby C, Galperin E, Mintz L, Horowitz M, Stone EM, Sheffield VC. Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1). Gene. 240: 227-32. PMID 10564830 DOI: 10.1016/S0378-1119(99)00395-9 |
0.403 |
|
| 1999 |
Gorman SW, Haider NB, Grieshammer U, Swiderski RE, Kim E, Welch JW, Searby C, Leng S, Carmi R, Sheffield VC, Duhl DM. The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23. Genomics. 59: 150-60. PMID 10409426 DOI: 10.1006/Geno.1999.5867 |
0.411 |
|
| 1997 |
Nystuen A, Costeff H, Elpeleg ON, Apter N, Bonné-Tamir B, Mohrenweiser H, Haider N, Stone EM, Sheffield VC. Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene. Human Molecular Genetics. 6: 563-9. PMID 9097959 DOI: 10.1093/Hmg/6.4.563 |
0.335 |
|
| 1995 |
Bhol K, Udell I, Haider N, Yunis JJ, Mohimen A, Neuman R, Grasso C, Ahmed AR, Foster S. Ocular cicatricial pemphigoid. A case report of monozygotic twins discordant for the disease. Archives of Ophthalmology (Chicago, Ill. : 1960). 113: 202-7. PMID 7864752 DOI: 10.1001/Archopht.1995.01100020086034 |
0.35 |
|
| 1992 |
Haider N, Neuman R, Foster CS, Ahmed AR. Report on the sequence of DQB1*0301 gene in ocular cicatricial pemphigoid patients. Current Eye Research. 11: 1233-8. PMID 1490342 DOI: 10.3109/02713689208999549 |
0.368 |
|
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