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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex developmentDorien Baetens, Tülay Güran, Berenice B Mendonca, et al.
JAMA|August 29, 2013
Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetesLu Qi, Qibin Qi, Sabrina Prudente, et al.
Cancers|March 11, 2023
Interpretable and Reliable Oral Cancer Classifier with Attention Mechanism and Expert Knowledge Embedding via Attention MapBofan Song, Chicheng Zhang, Sumsum Sunny, et al.
ERJ Open Research|June 1, 2023
Asthma innovations from the first International Collaborative Asthma Network forumBenjamin Gaston, Donna D Gardner, Kenzie Mahan, et al.
Journal of Biomedical Optics|January 13, 2022
Interpretable deep learning approach for oral cancer classification using guided attention inference networkKevin Chew Figueroa, Bofan Song, Sumsum Sunny, et al.
Hormone Research in Paediatrics|April 11, 2017
Triple A Syndrome: Preliminary Response to the Antioxidant N-Acetylcysteine Treatment in a ChildMaria Candida Barisson Villares Fragoso, Edoarda Vasco de Albuquerque Albuquerque, Ana Luiza de Almeida Cardoso, et al.
European Journal of Endocrinology|November 4, 2011
Combined expression of BUB1B, DLGAP5, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patientsMaria Candida B V Fragoso, Madson Queiroz Almeida, Tania L Mazzuco, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2014
ARMC5 mutations are a frequent cause of primary macronodular adrenal HyperplasiaGuilherme Asmar Alencar, Antonio Marcondes Lerario, Mirian Yumie Nishi, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 25, 2015
Effects of Emtricitabine/Tenofovir on Bone Mineral Density in HIV-Negative Persons in a Randomized, Double-Blind, Placebo-Controlled TrialKathleen Mulligan, David V Glidden, Peter L Anderson, et al.
Endocrine Connections|March 12, 2015
FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficienciesFernanda A Correa, Ericka B Trarbach, Cintia Tusset, et al.
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