Jessica Gardner, Ph.D - Publications

Pharmacology & Experimental Neuroscience University of Nebraska Medical Center, Omaha, NE, United States 
neuroinflammation, astrocytes, glia

34 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
2016 Gardner JC, Michaelides M, Hardcastle AJ. Cone opsins, colour blindness and cone dystrophy: Genotype-phenotype correlations South African Medical Journal. 106: S75-S78. DOI: 10.7196/SAMJ.2016.v106i6.11001  1
2014 Gardner JC, Liew G, Quan YH, Ermetal B, Ueyama H, Davidson AE, Schwarz N, Kanuga N, Chana R, Maher ER, Webster AR, Holder GE, Robson AG, Cheetham ME, Liebelt J, et al. Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variants. Human Mutation. 35: 1354-62. PMID 25168334 DOI: 10.1002/humu.22679  1
2014 Davidson AE, Cheong SS, Hysi PG, Venturini C, Plagnol V, Ruddle JB, Ali H, Carnt N, Gardner JC, Hassan H, Gade E, Kearns L, Jelsig AM, Restori M, Webb TR, et al. Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness. Plos One. 9: e104163. PMID 25093588 DOI: 10.1371/Journal.Pone.0104163  1
2013 Cideciyan AV, Hufnagel RB, Carroll J, Sumaroka A, Luo X, Schwartz SB, Dubra A, Land M, Michaelides M, Gardner JC, Hardcastle AJ, Moore AT, Sisk RA, Ahmed ZM, Kohl S, et al. Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy. Human Gene Therapy. 24: 993-1006. PMID 24067079 DOI: 10.1089/Hum.2013.153  1
2013 Karampelas M, Gardner J, Holder G, Hardcastle A, Webster A. Retinal dysfunction and high myopia in association with 48,XXYY syndrome. Documenta Ophthalmologica. Advances in Ophthalmology. 127: 245-7. PMID 24048723 DOI: 10.1007/s10633-013-9406-x  1
2012 Carroll J, Dubra A, Gardner JC, Mizrahi-Meissonnier L, Cooper RF, Dubis AM, Nordgren R, Genead M, Connor TB, Stepien KE, Sharon D, Hunt DM, Banin E, Hardcastle AJ, Moore AT, et al. The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic. Investigative Ophthalmology & Visual Science. 53: 8006-15. PMID 23139274 DOI: 10.1167/Iovs.12-11087  1
2012 Webb TR, Parfitt DA, Gardner JC, Martinez A, Bevilacqua D, Davidson AE, Zito I, Thiselton DL, Ressa JH, Apergi M, Schwarz N, Kanuga N, Michaelides M, Cheetham ME, Gorin MB, et al. Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23). Human Molecular Genetics. 21: 3647-54. PMID 22619378 DOI: 10.1093/hmg/dds194  1
2012 Webb TR, Matarin M, Gardner JC, Kelberman D, Hassan H, Ang W, Michaelides M, Ruddle JB, Pennell CE, Yazar S, Khor CC, Aung T, Yogarajah M, Robson AG, Holder GE, et al. X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development. American Journal of Human Genetics. 90: 247-59. PMID 22284829 DOI: 10.1016/j.ajhg.2011.12.019  1
2012 Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, et al. A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5). Advances in Experimental Medicine and Biology. 723: 595-601. PMID 22183383 DOI: 10.1007/978-1-4614-0631-0_76  1
2011 Slee M, Finkemeyer J, Krupa M, Raghupathi R, Gardner J, Blumbergs P, Agzarian M, Thyagarajan D. A novel mitochondrial DNA deletion producing progressive external ophthalmoplegia associated with multiple sclerosis. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 18: 1318-24. PMID 21795050 DOI: 10.1016/j.jocn.2011.02.019  1
2010 Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, et al. X-linked cone dystrophy caused by mutation of the red and green cone opsins. American Journal of Human Genetics. 87: 26-39. PMID 20579627 DOI: 10.1016/J.Ajhg.2010.05.019  1
2009 Gardner JC, Michaelides M, Holder GE, Kanuga N, Webb TR, Mollon JD, Moore AT, Hardcastle AJ. Blue cone monochromacy: causative mutations and associated phenotypes. Molecular Vision. 15: 876-84. PMID 19421413  1
2006 Gardner J, Borgmann K, Deshpande MS, Dhar A, Wu L, Persidsky R, Ghorpade A. Potential mechanisms for astrocyte-TIMP-1 downregulation in chronic inflammatory diseases. Journal of Neuroscience Research. 83: 1281-92. PMID 16555295 DOI: 10.1002/Jnr.20823  1
2006 Dhar A, Gardner J, Borgmann K, Wu L, Ghorpade A. Novel role of TGF-beta in differential astrocyte-TIMP-1 regulation: implications for HIV-1-dementia and neuroinflammation. Journal of Neuroscience Research. 83: 1271-80. PMID 16496359 DOI: 10.1002/Jnr.20787  1
2005 Gardner JC, van Bezooijen RL, Mervis B, Hamdy NA, Löwik CW, Hamersma H, Beighton P, Papapoulos SE. Bone mineral density in sclerosteosis; affected individuals and gene carriers. The Journal of Clinical Endocrinology and Metabolism. 90: 6392-5. PMID 16189254 DOI: 10.1210/jc.2005-1235  1
2003 Gardner J, Ghorpade A. Tissue inhibitor of metalloproteinase (TIMP)-1: the TIMPed balance of matrix metalloproteinases in the central nervous system. Journal of Neuroscience Research. 74: 801-6. PMID 14648584 DOI: 10.1002/Jnr.10835  1
2003 Hamersma H, Gardner J, Beighton P. The natural history of sclerosteosis Clinical Genetics. 63: 192-197. PMID 12694228 DOI: 10.1034/j.1399-0004.2003.00036.x  1
2002 Staehling-Hampton K, Proll S, Paeper BW, Zhao L, Charmley P, Brown A, Gardner JC, Galas D, Schatzman RC, Beighton P, Papapoulos S, Hamersma H, Brunkow ME. A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population. American Journal of Medical Genetics. 110: 144-52. PMID 12116252 DOI: 10.1002/ajmg.10401  1
2002 Kozlowski K, Godlonton J, Gardner J, Beighton P. Lethal non-rhizomelic dysplasia epiphysealis punctata. Clinical Dysmorphology. 11: 203-8. PMID 12072802  1
2001 Stephen LXG, Hamersma H, Gardner J, Beighton P. Dental and oral manifestations of Sclerosteosis International Dental Journal. 51: 287-290. PMID 11570544  1
2001 Reichenberger E, Tiziani V, Watanabe S, Park L, Ueki Y, Santanna C, Baur ST, Shiang R, Grange DK, Beighton P, Gardner J, Hamersma H, Sellars S, Ramesar R, Lidral AC, et al. Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK. American Journal of Human Genetics. 68: 1321-6. PMID 11326338 DOI: 10.1086/320612  1
2001 Brunkow ME, Gardner JC, Van Ness J, Paeper BW, Kovacevich BR, Proll S, Skonier JE, Zhao L, Sabo PJ, Fu YH, Alisch RS, Gillett L, Colbert T, Tacconi P, Galas D, et al. Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein American Journal of Human Genetics. 68: 577-589. PMID 11179006 DOI: 10.1086/318811  1
2000 Basel D, Sobey G, Gardner J, Beighton P. The Gordon syndrome revisited South African Medical Journal. 90: 864-867. PMID 11081133  1
1999 Gardner J, Woods D, Williamson D. Management of double-layered patellae by compression screw fixation Journal of Pediatric Orthopaedics Part B. 8: 39-41. PMID 10709596  1
1999 Beighton P, Gardner J, Smart R, Kozlowski KS. Broad clavicles in trisomy 8 mosaicism: A new sign Skeletal Radiology. 28: 359-361. PMID 10450886 DOI: 10.1007/s002560050532  1
1999 Kozlowski K, Bieganski T, Gardner J, Beighton P. Osteochondrodystrophies with marked platyspondyly and distinctive peripheral anomalies Pediatric Radiology. 29: 1-5. PMID 9880606 DOI: 10.1007/s002470050522  1
1997 Gardner J, Beighton P, Sellars SL. The genetics of childhood deafness South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 87: 1661-1662. PMID 9497826  1
1997 Gardner JC, Goliath R, Viljoen D, Sellars S, Cortopassi G, Hutchin T, Greenberg J, Beighton P. Familial streptomycin ototoxicity in a South African family: A mitochondrial disorder Journal of Medical Genetics. 34: 904-906. PMID 9391883  1
1996 Samson G, Gardner JC. Craniosynostosis, microcephaly, hydrancephaly, humero-radial synostosis, and thumb aplasia: A new syndrome? American Journal of Medical Genetics. 61: 174-177. PMID 8669448 DOI: 10.1002/(SICI)1096-8628(19960111)61:2<174::AID-AJMG15>3.0.CO;2-R  1
1994 Gardner J, Beighton P. Brachyolmia: An autosomal dominant form American Journal of Medical Genetics. 49: 308-312. PMID 8209891  1
1994 Gardner J, Viljoen D. Aplasia cutis congenita with epibulbar dermoids: Further evidence for syndromic identity of the ocular ectodermal syndrome American Journal of Medical Genetics. 53: 317-320. PMID 7864039 DOI: 10.1002/ajmg.1320530403  1
1989 Wolff PH, Gardner J, Paccla J, Lappen J. The greeting behavior of fragile X males. American Journal of Mental Retardation : Ajmr. 93: 406-11. PMID 2522786  1
1988 Wolff PH, Gardner J, Lappen J, Paccia J, Meryash D. Variable expression of the fragile X syndrome in heterozygous females of normal intelligence. American Journal of Medical Genetics. 30: 213-25. PMID 3177447  1
1983 Gardner J, Zorfass J. From sign to speech: The language development of a hearing-impaired child American Annals of the Deaf. 128: 20-24. PMID 6837384  1
Show low-probability matches.