| Year |
Citation |
Score |
| 2019 |
Lee AJ, Jones KA, Butterfield RJ, Cox MO, Konersman CG, Grosmann C, Abdenur JE, Boyer M, Beson B, Wang C, Dowling JJ, Gibbons MA, Ballard A, Janas JS, Leshner RT, et al. Clinical, genetic, and pathologic characterization of Mexican founder mutation c.1387A>G. Neurology. Genetics. 5: e315. PMID 31041397 DOI: 10.1212/Nxg.0000000000000315 |
0.311 |
|
| 2018 |
Ostrander BEP, Butterfield RJ, Pedersen BS, Farrell AJ, Layer RM, Ward A, Miller C, DiSera T, Filloux FM, Candee MS, Newcomb T, Bonkowsky JL, Marth GT, Quinlan AR. Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy. Npj Genomic Medicine. 3: 22. PMID 30109124 DOI: 10.1038/S41525-018-0061-8 |
0.309 |
|
| 2017 |
Butterfield RJ, Dunn DM, Hu Y, Johnson K, Bönnemann CG, Weiss RB. Transcriptome profiling identifies regulators of pathogenesis in collagen VI related muscular dystrophy. Plos One. 12: e0189664. PMID 29244830 DOI: 10.1371/Journal.Pone.0189664 |
0.315 |
|
| 2015 |
Donkervoort S, Hu Y, Stojkovic T, Voermans NC, Foley AR, Leach ME, Dastgir J, Bolduc V, Cullup T, de Becdelièvre A, Yang L, Su H, Meilleur K, Schindler AB, Kamsteeg EJ, ... ... Butterfield RJ, et al. Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variability. Human Mutation. 36: 48-56. PMID 25204870 DOI: 10.1002/Humu.22691 |
0.328 |
|
| 2014 |
Hu Y, Donkervoot S, Stojkovic T, Voermans N, Foley AR, Leach M, Dastgir J, Bolduc V, Cullup T, Becdelièvre A, Yang L, Su H, Meilleur K, Schindler A, Kamsteeg E, ... ... Butterfield R, et al. G.P.214 Neuromuscular Disorders. 24: 881. DOI: 10.1016/J.Nmd.2014.06.290 |
0.324 |
|
| 2011 |
Blankenhorn EP, Butterfield R, Case LK, Wall EH, del Rio R, Diehl SA, Krementsov DN, Saligrama N, Teuscher C. Genetics of experimental allergic encephalomyelitis supports the role of T helper cells in multiple sclerosis pathogenesis. Annals of Neurology. 70: 887-96. PMID 22190363 DOI: 10.1002/Ana.22642 |
0.375 |
|
| 2010 |
Butterfield RJ, Swoboda K, Flanigan KM, Bonnemann CG, Weiss RB. P1.12 Frequency of genomic deletion mutations in collagen VI myopathies Neuromuscular Disorders. 20: 603-603. DOI: 10.1016/J.Nmd.2010.07.027 |
0.367 |
|
| 2009 |
Butterfield RJ, Ramachandran D, Hasstedt SJ, Otterud BE, Leppert MF, Swoboda KJ, Flanigan KM. A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22. Neuromuscular Disorders : Nmd. 19: 279-87. PMID 19318250 DOI: 10.1016/J.Nmd.2009.02.006 |
0.365 |
|
| 2004 |
Teuscher C, Bunn JY, Fillmore PD, Butterfield RJ, Zachary JF, Blankenhorn EP. Gender, age, and season at immunization uniquely influence the genetic control of susceptibility to histopathological lesions and clinical signs of experimental allergic encephalomyelitis: implications for the genetics of multiple sclerosis. The American Journal of Pathology. 165: 1593-602. PMID 15509529 DOI: 10.1016/S0002-9440(10)63416-5 |
0.403 |
|
| 2003 |
Butterfield RJ, Roper RJ, Rhein DM, Melvold RW, Haynes L, Ma RZ, Doerge RW, Teuscher C. Sex-specific quantitative trait loci govern susceptibility to Theiler's murine encephalomyelitis virus-induced demyelination. Genetics. 163: 1041-6. PMID 12663542 |
0.645 |
|
| 2002 |
Roper RJ, Ma RZ, Biggins JE, Butterfield RJ, Michael SD, Tung KS, Doerge RW, Teuscher C. Interacting quantitative trait loci control loss of peripheral tolerance and susceptibility to autoimmune ovarian dysgenesis after day 3 thymectomy in mice. Journal of Immunology (Baltimore, Md. : 1950). 169: 1640-6. PMID 12133995 DOI: 10.4049/Jimmunol.169.3.1640 |
0.646 |
|
| 2001 |
Roper RJ, Weis JJ, McCracken BA, Green CB, Ma Y, Weber KS, Fairbairn D, Butterfield RJ, Potter MR, Zachary JF, Doerge RW, Teuscher C. Genetic control of susceptibility to experimental Lyme arthritis is polygenic and exhibits consistent linkage to multiple loci on chromosome 5 in four independent mouse crosses. Genes and Immunity. 2: 388-97. PMID 11704805 DOI: 10.1038/sj.gene.6363801 |
0.638 |
|
| 2000 |
Butterfield RJ, Blankenhorn EP, Roper RJ, Zachary JF, Doerge RW, Teuscher C. Identification of genetic loci controlling the characteristics and severity of brain and spinal cord lesions in experimental allergic encephalomyelitis American Journal of Pathology. 157: 637-645. PMID 10934166 DOI: 10.1016/S0002-9440(10)64574-9 |
0.653 |
|
| 2000 |
Blankenhorn EP, Butterfield RJ, Rigby R, Cort L, Giambrone D, McDermott P, McEntee K, Solowski N, Meeker ND, Zachary JF, Doerge RW, Teuscher C. Genetic analysis of the influence of pertussis toxin on experimental allergic encephalomyelitis susceptibility: An environmental agent can override genetic checkpoints Journal of Immunology. 164: 3420-3425. PMID 10706738 DOI: 10.4049/Jimmunol.164.6.3420 |
0.443 |
|
| 1999 |
Teuscher C, Butterfield RJ, Ma RZ, Zachary JF, Doerge RW, Blankenhorn EP. Sequence polymorphisms in the chemokines Scya1 (TCA-3), Scya2 (monocyte chemoattractant protein (MCP)-1), and Scya12 (MCP-5) are candidates for eae7, a locus controlling susceptibility to monophasic remitting/nonrelapsing experimental allergic encephalomyelitis Journal of Immunology. 163: 2262-2266. PMID 10438970 |
0.331 |
|
| 1999 |
Butterfield RJ, Blankenhorn EP, Roper RJ, Zachary JF, Doerge RW, Sudweeks J, Rose J, Teuscher C. Genetic analysis of disease subtypes and sexual dimorphisms in mouse experimental allergic encephalomyelitis (EAE): Relapsing/remitting and monophasic remitting/nonrelapsing EAE are immunogenetically distinct Journal of Immunology. 162: 3096-3102. PMID 10072563 |
0.639 |
|
| 1998 |
Butterfield RJ, Sudweeks JD, Blankenhorn EP, Korngold R, Marini JC, Todd JA, Roper RJ, Teuscher C. New genetic loci that control susceptibility and symptoms of experimental allergic encephalomyelitis in inbred mice Journal of Immunology. 161: 1860-1867. PMID 9712054 |
0.657 |
|
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