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Parasites & Vectors|December 15, 2015
Quantitative analyses and modelling to support achievement of the 2020 goals for nine neglected tropical diseasesT Déirdre Hollingsworth, Emily R Adams, Roy M Anderson, et al.
Rare (Amsterdam, Netherlands)|October 18, 2024
Dual diagnosis of <i>UQCRFS1</i>-related mitochondrial complex III deficiency and recessive <i>GJA8</i>-related cataractsElizabeth E Blue, Samuel J Huang, Alyna Khan, et al.
Medrxiv : the Preprint Server for Health Sciences|July 2, 2026
A class of deep intronic <i>IGHMBP2</i> variants activate a shared cryptic splice donor, enabling correction of select variants with a single antisense oligonucleotideSarah Silverstein, Andrew D Nguyen, Rotem Orbach, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|September 28, 2020
Predicted Impact of COVID-19 on Neglected Tropical Disease Programs and the Opportunity for InnovationJaspreet Toor, Emily R Adams, Maryam Aliee, et al.
Frontiers in Medicine|June 13, 2017
Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program ExperienceTimothy Gall, Elise Valkanas, Christofer Bello, et al.
JAMA Network Open|September 25, 2025
Olfactory Dysfunction After SARS-CoV-2 Infection in the RECOVER Adult CohortLeora I Horwitz, Jacqueline H Becker, Weixing Huang, et al.
Neuron|November 6, 2015
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic DiseaseEnder Karaca, Tamar Harel, Davut Pehlivan, et al.
Nature|February 22, 2013
A sub-Mercury-sized exoplanetThomas Barclay, Jason F Rowe, Jack J Lissauer, et al.
Wellcome Open Research|March 22, 2021
Antibody testing for COVID-19: A report from the National COVID Scientific Advisory PanelEmily R Adams, Mark Ainsworth, Rekha Anand, et al.
Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disordersYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
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