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Genome Medicine|March 23, 2017
Lessons learned from additional research analyses of unsolved clinical exome casesMohammad K Eldomery, Zeynep Coban-Akdemir, Tamar Harel, et al.Nature Communications|June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traitsNatasha A Karp, Jeremy Mason, Arthur L Beaudet, et al.Global Heart|May 3, 2018
Implementation Research to Address the United States Health Disadvantage: Report of a National Heart, Lung, and Blood Institute WorkshopMichael M Engelgau, K M Venkat Narayan, Majid Ezzati, et al.Science Advances|October 21, 2022
Frontal sinuses and human evolutionAntoine Balzeau, Lou Albessard-Ball, Anna Maria Kubicka, et al.Nature Communications|February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discoveryPilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.American Journal of Human Genetics|January 26, 2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 MutationsSeema R Lalani, Pengfei Liu, Jill A Rosenfeld, et al.Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.JAMA Pediatrics|October 4, 2017
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical ManagementLinyan Meng, Mohan Pammi, Anirudh Saronwala, et al.Journal of Physics. Condensed Matter : an Institute of Physics Journal|March 28, 2018
QMCPACK: an open source ab initio quantum Monte Carlo package for the electronic structure of atoms, molecules and solidsJeongnim Kim, Andrew T Baczewski, Todd D Beaudet, et al.Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.Pageof 105