| Year |
Citation |
Score |
| 2013 |
Gibbs EM, Davidson AE, Trickey-Glassman A, Backus C, Hong Y, Sakowski SA, Dowling JJ, Feldman EL. Two dynamin-2 genes are required for normal zebrafish development. Plos One. 8: e55888. PMID 23418470 DOI: 10.1371/Journal.Pone.0055888 |
0.324 |
|
| 2009 |
Davidson AE, Gratsch TE, Morell MH, O'Shea KS, Krull CE. Use of the Sleeping Beauty transposon system for stable gene expression in mouse embryonic stem cells. Cold Spring Harbor Protocols. 2009: pdb.prot5270. PMID 20147246 DOI: 10.1101/pdb.prot5270 |
0.398 |
|
| 2006 |
Sivasubbu S, Balciunas D, Davidson AE, Pickart MA, Hermanson SB, Wangensteen KJ, Wolbrink DC, Ekker SC. Gene-breaking transposon mutagenesis reveals an essential role for histone H2afza in zebrafish larval development. Mechanisms of Development. 123: 513-29. PMID 16859902 DOI: 10.1016/J.Mod.2006.06.002 |
0.584 |
|
| 2004 |
Hermanson S, Davidson AE, Sivasubbu S, Balciunas D, Ekker SC. Sleeping Beauty transposon for efficient gene delivery. Methods in Cell Biology. 77: 349-62. PMID 15602921 DOI: 10.1016/S0091-679X(04)77019-3 |
0.639 |
|
| 2004 |
Balciunas D, Davidson AE, Sivasubbu S, Hermanson SB, Welle Z, Ekker SC. Enhancer trapping in zebrafish using the Sleeping Beauty transposon. Bmc Genomics. 5: 62. PMID 15347431 DOI: 10.1186/1471-2164-5-62 |
0.627 |
|
| 2003 |
Davidson AE, Balciunas D, Mohn D, Shaffer J, Hermanson S, Sivasubbu S, Cliff MP, Hackett PB, Ekker SC. Efficient gene delivery and gene expression in zebrafish using the Sleeping Beauty transposon. Developmental Biology. 263: 191-202. PMID 14597195 DOI: 10.1016/J.Ydbio.2003.07.013 |
0.648 |
|
| 2002 |
Dupuy AJ, Clark K, Carlson CM, Fritz S, Davidson AE, Markley KM, Finley K, Fletcher CF, Ekker SC, Hackett PB, Horn S, Largaespada DA. Mammalian germ-line transgenesis by transposition. Proceedings of the National Academy of Sciences of the United States of America. 99: 4495-9. PMID 11904379 DOI: 10.1073/Pnas.062630599 |
0.603 |
|
| 2001 |
Finley KR, Davidson AE, Ekker SC. Three-color imaging using fluorescent proteins in living zebrafish embryos. Biotechniques. 31: 66-70, 72. PMID 11464522 DOI: 10.2144/01311St02 |
0.503 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2022 |
Bandla A, Melancon E, Taylor CR, Davidson AE, Eisen JS, Ganz J. A New Transgenic Tool to Study the Ret Signaling Pathway in the Enteric Nervous System. International Journal of Molecular Sciences. 23. PMID 36555308 DOI: 10.3390/ijms232415667 |
0.286 |
|
| 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 |
0.285 |
|
| 2012 |
Davidson A, Majczenko K, Camelo-Piragua S, Li X, Joshi S, Xu J, Peng W, Li J, Burmeister M, Dowling J. C.O.4 Dominant mutation in CCDC78 in a unique congenital myopathy with central nuclei and atypical cores Neuromuscular Disorders. 22: 840. DOI: 10.1016/J.Nmd.2012.06.126 |
0.283 |
|
| 2015 |
Davidson AE, Liskova P, Evans CJ, Dudakova L, Nosková L, Pontikos N, Hartmannová H, Hodaňová K, Stránecký V, Kozmík Z, Levis HJ, Idigo N, Sasai N, Maher GJ, Bellingham J, et al. Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2. American Journal of Human Genetics. PMID 26749309 DOI: 10.1016/J.Ajhg.2015.11.018 |
0.28 |
|
| 2015 |
Liskova P, Evans CJ, Davidson AE, Zaliova M, Dudakova L, Trkova M, Stranecky V, Carnt N, Plagnol V, Vincent AL, Tuft SJ, Hardcastle AJ. Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3. European Journal of Human Genetics : Ejhg. PMID 26508574 DOI: 10.1038/Ejhg.2015.232 |
0.249 |
|
| 2014 |
Yuen M, Sandaradura SA, Dowling JJ, Kostyukova AS, Moroz N, Quinlan KG, Lehtokari VL, Ravenscroft G, Todd EJ, Ceyhan-Birsoy O, Gokhin DS, Maluenda J, Lek M, Nolent F, Pappas CT, ... ... Davidson AE, et al. Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy. The Journal of Clinical Investigation. 124: 4693-708. PMID 25250574 DOI: 10.1172/Jci75199 |
0.234 |
|
| 2011 |
Sergouniotis PI, Davidson AE, Sehmi K, Webster AR, Robson AG, Moore AT. Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene. Eye (London, England). 25: 1098-101. PMID 21494281 DOI: 10.1038/eye.2011.88 |
0.229 |
|
| 2012 |
Majczenko K, Davidson AE, Camelo-Piragua S, Agrawal PB, Manfready RA, Li X, Joshi S, Xu J, Peng W, Beggs AH, Li JZ, Burmeister M, Dowling JJ. Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical cores. American Journal of Human Genetics. 91: 365-71. PMID 22818856 DOI: 10.1016/J.Ajhg.2012.06.012 |
0.226 |
|
| 2010 |
Davidson AE, Sergouniotis PI, Burgess-Mullan R, Hart-Holden N, Low S, Foster PJ, Manson FD, Black GC, Webster AR. A synonymous codon variant in two patients with autosomal recessive bestrophinopathy alters in vitro splicing of BEST1. Molecular Vision. 16: 2916-22. PMID 21203346 |
0.225 |
|
| 2013 |
Davidson AE, Siddiqui FM, Lopez MA, Lunt P, Carlson HA, Moore BE, Love S, Born DE, Roper H, Majumdar A, Jayadev S, Underhill HR, Smith CO, von der Hagen M, Hubner A, et al. Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies. Brain : a Journal of Neurology. 136: 508-21. PMID 23413262 DOI: 10.1093/Brain/Aws344 |
0.221 |
|
| 2014 |
Gibbs EM, Davidson AE, Telfer WR, Feldman EL, Dowling JJ. The myopathy-causing mutation DNM2-S619L leads to defective tubulation in vitro and in developing zebrafish. Disease Models & Mechanisms. 7: 157-61. PMID 24135484 DOI: 10.1242/Dmm.012286 |
0.22 |
|
| 2012 |
Ramsden SC, Davidson AE, Leroy BP, Moore AT, Webster AR, Black GC, Manson FD. Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies). European Journal of Human Genetics : Ejhg. 20. PMID 22234150 DOI: 10.1038/ejhg.2011.251 |
0.215 |
|
| 2013 |
Davidson AE, Sergouniotis PI, Mackay DS, Wright GA, Waseem NH, Michaelides M, Holder GE, Robson AG, Moore AT, Plagnol V, Webster AR. RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy. Human Mutation. 34: 506-14. PMID 23281133 DOI: 10.1002/Humu.22264 |
0.214 |
|
| 2013 |
Davidson A, Li X, Dowling J. P9.17 Function of CCDC78 in muscle development and muscle disease Neuromuscular Disorders. 23: 788-789. DOI: 10.1016/J.Nmd.2013.06.530 |
0.214 |
|
| 2013 |
Mackay DS, Borman AD, Sui R, van den Born LI, Berson EL, Ocaka LA, Davidson AE, Heckenlively JR, Branham K, Ren H, Lopez I, Maria M, Azam M, Henkes A, Blokland E, et al. Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations. Human Mutation. 34: 1537-46. PMID 23946133 DOI: 10.1002/Humu.22398 |
0.21 |
|
| 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 |
0.206 |
|
| 2012 |
Dowling J, Davidson A, Lopez M, Siddiqui F, Lunt P, Li J, Jungbluth H, Love S, Moore S. D.P.8 Expanding the clinical and genetic phenotype of TPM2-related myopathies Neuromuscular Disorders. 22: 810. DOI: 10.1016/J.Nmd.2012.06.028 |
0.205 |
|
| 2015 |
Davidson AE, Borasio E, Liskova P, Khan AO, Hassan H, Cheetham ME, Plagnol V, Alkuraya FS, Tuft SJ, Hardcastle AJ. Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus. Investigative Ophthalmology & Visual Science. 56: 578-86. PMID 25564447 DOI: 10.1167/Iovs.14-15792 |
0.203 |
|
| 2011 |
Sergouniotis PI, Davidson AE, Mackay DS, Li Z, Yang X, Plagnol V, Moore AT, Webster AR. Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosis. American Journal of Human Genetics. 89: 183-90. PMID 21763485 DOI: 10.1016/J.Ajhg.2011.06.002 |
0.196 |
|
| 2016 |
Sabha N, Volpatti JR, Gonorazky H, Reifler A, Davidson AE, Li X, Eltayeb NM, Dall'Armi C, Di Paolo G, Brooks SV, Buj-Bello A, Feldman EL, Dowling JJ. PIK3C2B inhibition improves function and prolongs survival in myotubular myopathy animal models. The Journal of Clinical Investigation. PMID 27548528 DOI: 10.1172/Jci86841 |
0.185 |
|
| 2014 |
Volpatti J, Burns A, Davidson A, Roy P, Dowling J. G.P.46 Neuromuscular Disorders. 24: 808. DOI: 10.1016/J.Nmd.2014.06.060 |
0.185 |
|
| 2013 |
Davidson AE, Schwarz N, Zelinger L, Stern-Schneider G, Shoemark A, Spitzbarth B, Gross M, Laxer U, Sosna J, Sergouniotis PI, Waseem NH, Wilson R, Kahn RA, Plagnol V, Wolfrum U, et al. Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosa. American Journal of Human Genetics. 93: 321-9. PMID 23849777 DOI: 10.1016/J.Ajhg.2013.06.003 |
0.18 |
|
| 2009 |
Burgess R, MacLaren RE, Davidson AE, Urquhart JE, Holder GE, Robson AG, Moore AT, Keefe RO, Black GC, Manson FD. ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing. Journal of Medical Genetics. 46: 620-5. PMID 18611979 DOI: 10.1136/Jmg.2008.059881 |
0.18 |
|
| 2012 |
Poulter JA, Davidson AE, Ali M, Gilmour DF, Parry DA, Mintz-Hittner HA, Carr IM, Bottomley HM, Long VW, Downey LM, Sergouniotis PI, Wright GA, MacLaren RE, Moore AT, Webster AR, et al. Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR). Investigative Ophthalmology & Visual Science. 53: 2873-9. PMID 22427576 DOI: 10.1167/iovs.11-8629 |
0.176 |
|
| 2014 |
Waugh TA, Horstick E, Hur J, Jackson SW, Davidson AE, Li X, Dowling JJ. Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy. Human Molecular Genetics. 23: 4651-62. PMID 24760771 DOI: 10.1093/Hmg/Ddu185 |
0.173 |
|
| 2009 |
Davidson AE, Gratsch TE, Colvin AM, O'Shea KS, Krull CE. Targeting CNS integration of mouse ES cells using Eph/ephrins Developmental Biology. 331: 501. DOI: 10.1016/j.ydbio.2009.05.431 |
0.17 |
|
| 2011 |
Sergouniotis PI, Davidson AE, Mackay DS, Lenassi E, Li Z, Robson AG, Yang X, Kam JH, Isaacs TW, Holder GE, Jeffery G, Beck JA, Moore AT, Plagnol V, Webster AR. Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retina. American Journal of Human Genetics. 89: 782-91. PMID 22137173 DOI: 10.1016/J.Ajhg.2011.11.004 |
0.169 |
|
| 2009 |
Davidson AE, Millar ID, Urquhart JE, Burgess-Mullan R, Shweikh Y, Parry N, O'Sullivan J, Maher GJ, McKibbin M, Downes SM, Lotery AJ, Jacobson SG, Brown PD, Black GC, Manson FD. Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa. American Journal of Human Genetics. 85: 581-92. PMID 19853238 DOI: 10.1016/J.Ajhg.2009.09.015 |
0.163 |
|
| 2014 |
Borman AD, Pearce LR, Mackay DS, Nagel-Wolfrum K, Davidson AE, Henderson R, Garg S, Waseem NH, Webster AR, Plagnol V, Wolfrum U, Farooqi IS, Moore AT. A homozygous mutation in the TUB gene associated with retinal dystrophy and obesity. Human Mutation. 35: 289-93. PMID 24375934 DOI: 10.1002/Humu.22482 |
0.154 |
|
| 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 |
0.148 |
|
| 2015 |
Smith SJ, Horstick EJ, Davidson AE, Dowling J. Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye. Journal of Visualized Experiments : Jove. PMID 26649573 DOI: 10.3791/53183 |
0.143 |
|
| 2014 |
Mackay DS, Borman AD, Sui R, van den Born LI, Berson EL, Ocaka LA, Davidson AE, Heckenlively JR, Branham K, Ren H, Lopez I, Maria M, Azam M, Henkes A, Blokland E, et al. Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype-Phenotype Correlations. [34, 11, 1537-1546, 10.1002/humu.22398] Human Mutation. 35: 150-150. DOI: 10.1002/Humu.22467 |
0.141 |
|
| 2011 |
Maher GJ, Hilton EN, Urquhart JE, Davidson AE, Spencer HL, Black GC, Manson FD. The cataract-associated protein TMEM114, and TMEM235, are glycosylated transmembrane proteins that are distinct from claudin family members. Febs Letters. 585: 2187-92. PMID 21689651 DOI: 10.1016/j.febslet.2011.05.060 |
0.124 |
|
| 2011 |
Davidson AE, Millar ID, Burgess-Mullan R, Maher GJ, Urquhart JE, Brown PD, Black GC, Manson FD. Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathy. Investigative Ophthalmology & Visual Science. 52: 3730-6. PMID 21330666 DOI: 10.1167/iovs.10-6707 |
0.12 |
|
| 2014 |
Davidson AE, Hayes S, Hardcastle AJ, Tuft SJ. The pathogenesis of keratoconus. Eye (London, England). 28: 189-95. PMID 24357835 DOI: 10.1038/eye.2013.278 |
0.118 |
|
| 2013 |
Horstick EJ, Gibbs EM, Li X, Davidson AE, Dowling JJ. Analysis of embryonic and larval zebrafish skeletal myofibers from dissociated preparations. Journal of Visualized Experiments : Jove. e50259. PMID 24300240 DOI: 10.3791/50259 |
0.115 |
|
| 2015 |
Bellingham J, Davidson AE, Aboshiha J, Simonelli F, Bainbridge JW, Michaelides M, van der Spuy J. Investigation of Aberrant Splicing Induced by AIPL1 Variations as a Cause of Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 56: 7784-7793. PMID 26650897 DOI: 10.1167/iovs.15-18092 |
0.113 |
|
| 2015 |
Evans CJ, Liskova P, Dudakova L, Hrabcikova P, Horinek A, Jirsova K, Filipec M, Hardcastle AJ, Davidson AE, Tuft SJ. Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3. Annals of Human Genetics. 79: 1-9. PMID 25441224 DOI: 10.1111/ahg.12090 |
0.112 |
|
| 2008 |
Davidson A, Traub-Dargatz JL, Magnuson R, Hill A, Irwin V, Newton R, Waller A, Smith K, Callan RJ, Meehan M, Owen P, Salman M. Lack of correlation between antibody titers to fibrinogen-binding protein of Streptococcus equi and persistent carriers of strangles Journal of Veterinary Diagnostic Investigation. 20: 457-462. PMID 18599850 DOI: 10.1177/104063870802000407 |
0.107 |
|
| 2012 |
Sergouniotis PI, Davidson AE, Lenassi E, Devery SR, Moore AT, Webster AR. Retinal structure, function, and molecular pathologic features in gyrate atrophy. Ophthalmology. 119: 596-605. PMID 22182799 DOI: 10.1016/j.ophtha.2011.09.017 |
0.106 |
|
| 2013 |
Fujinami K, Sergouniotis PI, Davidson AE, Mackay DS, Tsunoda K, Tsubota K, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR. The clinical effect of homozygous ABCA4 alleles in 18 patients. Ophthalmology. 120: 2324-31. PMID 23769331 DOI: 10.1016/j.ophtha.2013.04.016 |
0.104 |
|
| 2015 |
Liskova P, Dudakova L, Tesar V, Bednarova V, Kidorova J, Jirsova K, Davidson AE, Hardcastle AJ. Detailed assessment of renal function in a proband with Harboyan syndrome caused by a novel homozygous SLC4A11 nonsense mutation. Ophthalmic Research. 53: 30-5. PMID 25500497 DOI: 10.1159/000365109 |
0.093 |
|
| 2014 |
Sundaram V, Wilde C, Aboshiha J, Cowing J, Han C, Langlo CS, Chana R, Davidson AE, Sergouniotis PI, Bainbridge JW, Ali RR, Dubra A, Rubin G, Webster AR, Moore AT, et al. Retinal structure and function in achromatopsia: implications for gene therapy. Ophthalmology. 121: 234-45. PMID 24148654 DOI: 10.1016/J.Ophtha.2013.08.017 |
0.09 |
|
| 1967 |
Stuart AE, Davidson AE, Cumming RA. Sensitivity and methodology of erythrophagocytosis for the detection of heteroantibodies and natural isoantibodies to human red cells. Journal of the Reticuloendothelial Society. 4: 109-21. PMID 6072613 |
0.088 |
|
| 2011 |
Low S, Davidson AE, Holder GE, Hogg CR, Bhattacharya SS, Black GC, Foster PJ, Webster AR. Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study. Molecular Vision. 17: 2272-82. PMID 21921978 |
0.086 |
|
| 1971 |
Stuart AE, Davidson AE. The human reticular cell: morphology and cytochemistry. The Journal of Pathology. 103: 41-7. PMID 4105879 DOI: 10.1002/path.1711030106 |
0.086 |
|
| 1964 |
STUART AE, DAVIDSON AE. EFFECT OF SIMPLE LIPIDS ON ANTIBODY FORMATION AFTER INJECTION OF FOREIGN RED CELLS. The Journal of Pathology and Bacteriology. 87: 305-16. PMID 14137690 |
0.082 |
|
| 1970 |
Davidson AE, Stuart AE. Properties of the human reticular cell. Journal of Medical Microbiology. 3: P7-8. PMID 5448885 |
0.078 |
|
| 2011 |
Borman AD, Davidson AE, O'Sullivan J, Thompson DA, Robson AG, De Baere E, Black GC, Webster AR, Holder GE, Leroy BP, Manson FD, Moore AT. Childhood-onset autosomal recessive bestrophinopathy. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 1088-93. PMID 21825197 DOI: 10.1001/archophthalmol.2011.197 |
0.078 |
|
| 2013 |
Fujinami K, Sergouniotis PI, Davidson AE, Wright G, Chana RK, Tsunoda K, Tsubota K, Egan CA, Robson AG, Moore AT, Holder GE, Michaelides M, Webster AR. Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function. American Journal of Ophthalmology. 156: 487-501.e1. PMID 23953153 DOI: 10.1016/j.ajo.2013.05.003 |
0.072 |
|
| 1971 |
Stuart AE, Davidson AE. The human reticular cell: reactions to vital dyes and particulate substances. The Journal of Pathology. 103: 194-8. PMID 4105391 DOI: 10.1002/path.1711030309 |
0.063 |
|
| 2015 |
Jonsson F, Byström B, Davidson AE, Backman LJ, Kellgren TG, Tuft SJ, Koskela T, Rydén P, Sandgren O, Danielson P, Hardcastle AJ, Golovleva I. Mutations in collagen, type XVII, alpha 1 (COL17A1) cause epithelial recurrent erosion dystrophy (ERED). Human Mutation. 36: 463-73. PMID 25676728 DOI: 10.1002/humu.22764 |
0.056 |
|
| 1992 |
Davidson AE, Passero MA, Settipane GA. Buckwheat-induced anaphylaxis: a case report. Annals of Allergy. 69: 158-9. PMID 1510289 |
0.042 |
|
| 1992 |
Davidson AE, Passero MA, Settipane GA. Buckwheat-induced anaphylaxis: a case report. Annals of Allergy. 69: 439-40. PMID 1456486 |
0.042 |
|
| 1971 |
Stuart AE, Davidson AE. The handling of antigen-antibody complexes and of antigen by human peritoneal cells in vitro. The Journal of Pathology. 104: 37-43. PMID 4936193 DOI: 10.1002/path.1711040105 |
0.041 |
|
| 1992 |
Davidson AE, Miller SD, Settipane G, Klein D. Urticaria and angioedema. Cleveland Clinic Journal of Medicine. 59: 529-34. PMID 1361426 |
0.04 |
|
| 2013 |
Fujinami K, Lois N, Davidson AE, Mackay DS, Hogg CR, Stone EM, Tsunoda K, Tsubota K, Bunce C, Robson AG, Moore AT, Webster AR, Holder GE, Michaelides M. A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations. American Journal of Ophthalmology. 155: 1075-1088.e13. PMID 23499370 DOI: 10.1016/J.Ajo.2013.01.018 |
0.038 |
|
| 1992 |
Weltman JK, Melucci CL, Chen J, Davidson AE. Internalization of monoclonal antibodies selected for immunotoxin activity against small-cell lung cancer. Hybridoma. 11: 547-59. PMID 1334041 |
0.038 |
|
| 1992 |
Ber DJ, Davidson AE, Klein DE, Settipane GA. Latex hypersensitivity: two case reports. Allergy Proceedings : the Official Journal of Regional and State Allergy Societies. 13: 71-3. PMID 1587467 |
0.037 |
|
| 2015 |
Yuen M, Sandaradura SA, Dowling JJ, Kostyukova AS, Moroz N, Quinlan KG, Lehtokari VL, Ravenscroft G, Todd EJ, Ceyhan-Birsoy O, Gokhin DS, Maluenda J, Lek M, Nolent F, Pappas CT, ... ... Davidson AE, et al. Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy. The Journal of Clinical Investigation. 125: 456-7. PMID 25654555 DOI: 10.1172/Jci80057 |
0.033 |
|
| 1963 |
STUART AE, DAVIDSON AE. The effect of intravenous cholesterol oleate on the phagocytic function of the reticulo-endothelial system. British Journal of Experimental Pathology. 44: 24-30. PMID 13993234 |
0.031 |
|
| 2019 |
Woodfield J, Deo P, Davidson A, Chen TY, van Rij A. Patient reporting of complications after surgery: what impact does documenting postoperative problems from the perspective of the patient using telephone interview and postal questionnaires have on the identification of complications after surgery? Bmj Open. 9: e028561. PMID 31289081 DOI: 10.1136/bmjopen-2018-028561 |
0.028 |
|
| 1992 |
Davidson AE, Miller SD, Settipane RJ, Ricci AR, Klein DE, Settipane GA. Delayed nasal mucociliary clearance in patients with nonallergic rhinitis and nasal eosinophilia. Allergy Proceedings : the Official Journal of Regional and State Allergy Societies. 13: 81-4. PMID 1587470 DOI: 10.2500/108854192778878854 |
0.026 |
|
| 1994 |
Davidson AE, Klein DE, Settipane GA, Alario AJ. Access to care among children visiting the emergency room with acute exacerbations of asthma. Annals of Allergy. 72: 469-73. PMID 8179236 |
0.026 |
|
| 2007 |
Davidson A. Preventing adverse drug events [7] Cmaj. 176: 67-68. PMID 17200399 DOI: 10.1503/cmaj.060801 |
0.025 |
|
| 2004 |
Davidson AE, Wallack L. A content analysis of sexually transmitted diseases in the print news media. Journal of Health Communication. 9: 111-7. PMID 15204822 DOI: 10.1080/10810730490425268 |
0.023 |
|
| 1948 |
DAVIDSON AE. Prefrontal leucotomy; selection of patients. Northwest Medicine. 47: 417-9. PMID 18868348 |
0.021 |
|
| 2020 |
Yu J, Wang G, Davidson A, Chow I, Chiu A. Antibiotics Utilization for Community Acquired Pneumonia in a Community Hospital Emergency Department. Journal of Pharmacy Practice. 897190020953032. PMID 32912068 DOI: 10.1177/0897190020953032 |
0.021 |
|
| 1971 |
Davidson AE, Clark C, Smith G. Postoperative wound infection: a computer analysis. The British Journal of Surgery. 58: 333-7. PMID 5574716 |
0.01 |
|
| 1967 |
Davidson AE. Planning psychiatric services. Medical Services Journal, Canada. 23: 1261-2. PMID 5627853 |
0.01 |
|
| Hide low-probability matches. |