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Neuron|September 15, 2020
A Systematic Nomenclature for the Drosophila Ventral Nerve CordRobert Court, Shigehiro Namiki, J Douglas Armstrong, et al.Developmental Medicine and Child Neurology|October 15, 2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaNuala H Simpson, Laura Addis, William M Brandler, et al.The Lancet. Infectious Diseases|July 24, 2015
Clinical features and viral kinetics in a rapidly cured patient with Ebola virus disease: a case reportManuel Schibler, Pauline Vetter, Pascal Cherpillod, et al.Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.Disease Models & Mechanisms|September 20, 2022
Promoting validation and cross-phylogenetic integration in model organism researchKeith C Cheng, Rebecca D Burdine, Mary E Dickinson, et al.International Journal of Antimicrobial Agents|August 21, 2022
Apramycin susceptibility of multidrug-resistant Gram-negative blood culture isolates in five countries in Southeast AsiaMarina Gysin, Pei Yun Hon, Pisey Tan, et al.The Lancet. Planetary Health|September 7, 2024
Expert judgement reveals current and emerging UK climate-mortality burdenDann Mitchell, Y T Eunice Lo, Emily Ball, et al.Cancer|October 15, 2014
Clinical and pathologic features of familial pancreatic cancerJeremy L Humphris, Amber L Johns, Skye H Simpson, et al.Plos Genetics|March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.Nature Communications|October 25, 2017
αv integrins on mesenchymal cells regulate skeletal and cardiac muscle fibrosisI R Murray, Z N Gonzalez, J Baily, et al.Pageof 74