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Page 1
American Academy of Neurology qualifications and guidelines for the physician expert witness.
Williams MA, Mackin GA, Beresford HR, Gordon J, Jacobson PL, McQuillen MP, Reimschisel TE, Taylor RM, Bernat JL, Rizzo M, Snyder RD, Sagsveen MG, Amery M, Brannon WL Jr; American Academy of Neurology. Williams MA, et al. Among authors: reimschisel te. Neurology. 2006 Jan 10;66(1):13-4. doi: 10.1212/01.wnl.0000190568.69950.11. Neurology. 2006. PMID: 16401838 No abstract available.
Heart Transplantation in Children with Mitochondrial Disease.
Weiner JG, Lambert AN, Thurm C, Hall M, Soslow JH, Reimschisel TE, Bearl DW, Dodd DA, Feingold B, Godown J. Weiner JG, et al. Among authors: reimschisel te. J Pediatr. 2020 Feb;217:46-51.e4. doi: 10.1016/j.jpeds.2019.10.016. Epub 2019 Nov 8. J Pediatr. 2020. PMID: 31711761 Free PMC article.
Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance.
Barber JC, Rosenfeld JA, Graham JM, Kramer N, Lachlan KL, Bateman MS, Collinson MN, Stadheim BF, Turner CL, Gauthier JN, Reimschisel TE, Qureshi AM, Dabir TA, Humphreys MW, Marble M, Huang T, Beal SJ, Massiah J, Taylor EJ, Wynn SL. Barber JC, et al. Among authors: reimschisel te. Am J Med Genet A. 2015 Sep;167A(9):2052-64. doi: 10.1002/ajmg.a.37120. Epub 2015 Jun 11. Am J Med Genet A. 2015. PMID: 26097203
Comprehensive assessment of serious adverse events following immunization by health care providers.
Williams SE, Edwards KM, Baxter RP, LaRussa PS, Halsey NA, Dekker CL, Vellozzi C, Marchant CD, Donofrio PD, Reimschisel TE, Berger M, Gidudu JF, Klein NP. Williams SE, et al. Among authors: reimschisel te. J Pediatr. 2013 Jun;162(6):1276-81, 1281.e1. doi: 10.1016/j.jpeds.2013.01.028. Epub 2013 Feb 26. J Pediatr. 2013. PMID: 23452584 Free PMC article. No abstract available.
Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148.
Dharmadhikari AV, Kang SH, Szafranski P, Person RE, Sampath S, Prakash SK, Bader PI, Phillips JA 3rd, Hannig V, Williams M, Vinson SS, Wilfong AA, Reimschisel TE, Craigen WJ, Patel A, Bi W, Lupski JR, Belmont J, Cheung SW, Stankiewicz P. Dharmadhikari AV, et al. Among authors: reimschisel te. Hum Mol Genet. 2012 Aug 1;21(15):3345-55. doi: 10.1093/hmg/dds166. Epub 2012 Apr 27. Hum Mol Genet. 2012. PMID: 22543972 Free PMC article.
Detection of clinically relevant exonic copy-number changes by array CGH.
Boone PM, Bacino CA, Shaw CA, Eng PA, Hixson PM, Pursley AN, Kang SH, Yang Y, Wiszniewska J, Nowakowska BA, del Gaudio D, Xia Z, Simpson-Patel G, Immken LL, Gibson JB, Tsai AC, Bowers JA, Reimschisel TE, Schaaf CP, Potocki L, Scaglia F, Gambin T, Sykulski M, Bartnik M, Derwinska K, Wisniowiecka-Kowalnik B, Lalani SR, Probst FJ, Bi W, Beaudet AL, Patel A, Lupski JR, Cheung SW, Stankiewicz P. Boone PM, et al. Among authors: reimschisel te. Hum Mutat. 2010 Dec;31(12):1326-42. doi: 10.1002/humu.21360. Epub 2010 Nov 2. Hum Mutat. 2010. PMID: 20848651 Free PMC article.