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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.
ESMO Open|January 4, 2025
Unraveling the complexity of HRD assessment in ovarian cancer by combining genomic and functional approaches: translational analyses of MITO16-MaNGO-OV-2 trialB Pellegrino, E D Capoluongo, M Bagnoli, et al.
ESMO Open|May 20, 2025
HR-SC-an academic-developed machine learning framework to classify HRD-positive ovarian cancer patients and predict sensitivity to olaparibL Beltrame, L Mannarino, A Sergi, et al.
Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.
Scientific Reports|November 23, 2021
Long-term sequelae are highly prevalent one year after hospitalization for severe COVID-19Mattia Bellan, Alessio Baricich, Filippo Patrucco, et al.
Nature Genetics|October 20, 2022
Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
F1000Research|July 20, 2022
A roadmap for the generation of benchmarking resources for antimicrobial resistance detection using next generation sequencingMauro Petrillo, Marco Fabbri, Dafni Maria Kagkli, et al.
American Journal of Human Genetics|August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairmentDianne F Newbury, Laura Winchester, Laura Addis, et al.
Child Development|February 13, 2023
Language and reading impairments are associated with increased prevalence of non-right-handednessFilippo Abbondanza, Philip S Dale, Carol A Wang, et al.
European Journal of Human Genetics : EJHG|September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohortJessica Becker, Darina Czamara, Tom S Scerri, et al.
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