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Msystems|November 2, 2021
Identification and Development of Therapeutics for COVID-19Halie M Rando, Nils Wellhausen, Soumita Ghosh, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 30, 2025
Unbiased DNA Pathogen Detection in Tissues: Real-World Experience With Metagenomic Sequencing in PathologyBaptiste Hamelin, Salome Hosch, Claudio Neidhöfer, et al.
Royal Society Open Science|February 9, 2023
The process of replication target selection in psychology: what to consider?Merle-Marie Pittelkow, Sarahanne M Field, Peder M Isager, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Journal of Biomedical Optics|January 19, 2022
Kernel Flow: a high channel count scalable time-domain functional near-infrared spectroscopy systemHan Y Ban, Geoffrey M Barrett, Alex Borisevich, et al.
Molecular Biology of the Cell|December 12, 2002
Mammalian septins nomenclatureIan G Macara, Richard Baldarelli, Christine M Field, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
Circulation|October 20, 2010
Part 1: executive summary: 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular CareJohn M Field, Mary Fran Hazinski, Michael R Sayre, et al.
Cell|November 16, 2019
Gene Expression Changes and Community Turnover Differentially Shape the Global Ocean MetatranscriptomeGuillem Salazar, Lucas Paoli, Adriana Alberti, et al.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
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