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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 28, 2023
Applications of artificial intelligence in clinical laboratory genomicsSwaroop Aradhya, Flavia M Facio, Hillery Metz, et al.Journal of Nutrition Education and Behavior|March 12, 2013
Expanding children's food experiences: the impact of a school-based kitchen garden programLisa Gibbs, Petra K Staiger, Britt Johnson, et al.Plos One|September 15, 2015
Treatment with a Small Molecule Mutant IDH1 Inhibitor Suppresses Tumorigenic Activity and Decreases Production of the Oncometabolite 2-Hydroxyglutarate in Human Chondrosarcoma CellsLuyuan Li, Ana C Paz, Breelyn A Wilky, et al.Annals of Laboratory Medicine|July 5, 2013
Analysis of lyso-globotriaosylsphingosine in dried blood spotsBritt Johnson, Hermann Mascher, Daniel Mascher, et al.European Journal of Human Genetics : EJHG|February 20, 2014
Subfertility and growth restriction in a new galactose-1 phosphate uridylyltransferase (GALT) - deficient mouse modelManshu Tang, Anwer Siddiqi, Benjamin Witt, et al.Arthritis Care & Research|November 8, 2015
When Patients Write the Guidelines: Patient Panel Recommendations for the Treatment of Rheumatoid ArthritisLiana Fraenkel, Amy S Miller, Kelly Clayton, et al.American Journal of Medical Genetics. Part A|April 17, 2020
Severe SOPH syndrome due to a novel NBAS mutation in a 27-year-old woman-Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decadesYves Lacassie, Britt Johnson, Guillermo Lay-Son, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 11, 2021
Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing ProgramEric T Rush, Britt Johnson, Swaroop Aradhya, et al.JAMA Cardiology|August 10, 2022
Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic TestingLisa M Dellefave-Castillo, Allison L Cirino, Thomas E Callis, et al.Epilepsia|April 27, 2022
Value of genetic testing for pediatric epilepsy: Driving earlier diagnosis of ceroid lipofuscinosis type 2 Batten diseaseFernanda Leal-Pardinas, Rebecca Truty, Dianalee A McKnight, et al.Pageof 4