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Cardiovascular and Interventional Radiology|October 30, 2024
Beyond MELD Score: Association of Machine Learning-derived CT Body Composition with 90-Day Mortality Post Transjugular Intrahepatic Portosystemic Shunt PlacementTarig Elhakim, Arian Mansur, Jordan Kondo, et al.
Neurosurgery|May 12, 2023
Flow Diverter Performance in Aneurysms Arising From the Posterior Communicating Artery: A Systematic Review and Meta-AnalysisJuan Vivanco-Suarez, Aaron Rodriguez-Calienes, Peter T Kan, et al.
Mbio|September 19, 2022
Genome Capture Sequencing Selectively Enriches Bacterial DNA and Enables Genome-Wide Measurement of Intrastrain Genetic Diversity in Human InfectionsHillary S Hayden, Snehal Joshi, Matthew C Radey, et al.
Clinical Genetics|July 21, 2022
Expanding the phenotype of DNAJC30-associated Leigh syndromeMarta Zawadzka, Magdalena Krygier, Małgorzata Pawłowicz, et al.
BMC Genomics|November 18, 2009
3' tag digital gene expression profiling of human brain and universal reference RNA using Illumina Genome AnalyzerYan W Asmann, Eric W Klee, E Aubrey Thompson, et al.
Nano Letters|April 25, 2015
Toward Ferroelectric Control of Monolayer MoS2Ariana Nguyen, Pankaj Sharma, Thomas Scott, et al.
Journal of Asthma and Allergy|March 25, 2024
Level of Education Modifies Asthma Mortality in Norway and Sweden. The Nordic EpiLung StudyHelena Backman, Laxmi Bhatta, Linnea Hedman, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2022
A flavin-dependent monooxygenase produces nitrogenous tomato aroma volatiles using cysteine as a nitrogen sourceDavid K Liscombe, Yusuke Kamiyoshihara, Jérémie Ghironzi, et al.
Mayo Clinic Proceedings|October 10, 2024
Prevalence, Penetrance, and Phenotypic Manifestation of Cardiomyopathy-Associated Genetic Variants in the General Population: Insights from a Mayo Clinic Biobank StudyMarta Figueiral, Alessia Paldino, Matheus Vernet Machado Bressan Wilke, et al.
BMC Genomics|April 16, 2024
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic diseaseNumrah Fadra, Laura E Schultz-Rogers, Pritha Chanana, et al.
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