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Journal of the American Medical Informatics Association : JAMIA|March 16, 2013
Paper- and computer-based workarounds to electronic health record use at three benchmark institutionsMindy E Flanagan, Jason J Saleem, Laura G Millitello, et al.Journal of Clinical Research in Pediatric Endocrinology|June 11, 2013
Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 geneMehmet Boyraz, Korkut Ulucan, Necati Taşkın, et al.Applied Ergonomics|August 13, 2018
Comparative usability evaluation of consultation order templates in a simulated primary care environmentApril Savoy, Himalaya Patel, Mindy E Flanagan, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 23, 2017
Clinical presentation and treatment response to diazoxide in two siblings with congenital hyperinsulinism as a result of a novel compound heterozygous ABCC8 missense mutationSonya Galcheva, Violeta Iotova, Sian Ellard, et al.BMJ Quality & Safety|July 29, 2015
"Anybody on this list that you're more worried about?" Qualitative analysis exploring the functions of questions during end of shift handoffsColleen M O'Brien, Mindy E Flanagan, Alicia A Bergman, et al.Clinical Genetics|November 27, 2024
The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal CommunityVandana Jain, Venkatesan Radha, Viswanathan Mohan, et al.European Journal of Endocrinology|March 23, 2011
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinismSo Eun Park, Sarah E Flanagan, Khalid Hussain, et al.Diabetes|October 19, 2007
An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinismKhalid Hussain, Sarah E Flanagan, Virpi V Smith, et al.European Journal of Endocrinology|January 25, 2013
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinismRitika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, et al.Cerebellum (London, England)|September 10, 2017
Psychosis in Spinocerebellar Ataxias: a Case Series and Study of Tyrosine Hydroxylase in Substantia NigraKatherine W Turk, Margaret E Flanagan, Samuel Josephson, et al.Pageof 51