Neena B. Haider - Publications

Affiliations: 
University of Nebraska Medical Center, Omaha, NE, United States 
Area:
Cell Biology, Genetics, Neuroscience Biology

22 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
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  0.4
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  0.4
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2010 Duke SL, Kump LI, Yuan Y, West WW, Sachs AJ, Haider NB, Margalit E. The safety of intraocular linezolid in rabbits. Investigative Ophthalmology & Visual Science. 51: 3115-9. PMID 20042664 DOI: 10.1167/iovs.09-4244  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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