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Nature Neuroscience|January 15, 2020
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophreniaElliott Rees, Jun Han, Joanne Morgan, et al.
BMJ Open|November 10, 2022
Studying the Long-term Impact of COVID-19 in Kids (SLICK). Healthcare use and costs in children and young people following community-acquired SARS-CoV-2 infection: protocol for an observational study using linked primary and secondary routinely collected healthcare data from England, Scotland and WalesOlivia V Swann, Nazir I Lone, Ewen M Harrison, et al.
International Journal for Parasitology|June 20, 2025
Comparative genomic analysis of necrophagous and parasitic subspecies of Lucilia cuprina (Diptera: Calliphoridae) provides important insight into their divergent biologiesShilpa Kapoor, Paul V Hickner, Allison N Dickey, et al.
Magnetic Resonance in Medicine|September 3, 2021
Protocols for multi-site trials using hyperpolarized <sup>129</sup> Xe MRI for imaging of ventilation, alveolar-airspace size, and gas exchange: A position paper from the <sup>129</sup> Xe MRI clinical trials consortiumPeter J Niedbalski, Chase S Hall, Mario Castro, et al.
Global Change Biology|January 26, 2024
Global dominance of lianas over trees is driven by forest disturbance, climate and topographyAlain Senghor K Ngute, David S Schoeman, Marion Pfeifer, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 21, 2012
Preferences for place of death if faced with advanced cancer: a population survey in England, Flanders, Germany, Italy, the Netherlands, Portugal and SpainB Gomes, I J Higginson, N Calanzani, et al.
The Pharmacogenomics Journal|February 1, 2019
Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEPEleanor M Wigmore, Jonathan D Hafferty, Lynsey S Hall, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 2, 2008
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarctionWolfgang Lieb, Tanja Zeller, Massimo Mangino, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 10, 2022
Combination Nivolumab, CD137 Agonism, and Adoptive Cell Therapy with Tumor-Infiltrating Lymphocytes for Patients with Metastatic MelanomaMacLean S Hall, John E Mullinax, Cheryl A Cox, et al.
Plos Medicine|August 17, 2016
Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model AnalysisAndrew M McIntosh, Lynsey S Hall, Yanni Zeng, et al.
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