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Proceedings of the National Academy of Sciences of the United States of America|November 18, 2024
The global spread of Oriental Horses in the past 1,500 years through the lens of the Y chromosomeLara Radovic, Viktoria Remer, Doris Rigler, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 26, 2025
BiomarkersMarianna Rizzo, Charlotte E Teunissen, Frederic Brosseron, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Basic Science and PathogenesisAurore Delvenne, Marianna Rizzo, Bailin Zhang, et al.Diagnostic Microbiology and Infectious Disease|June 8, 2025
Non-Invasive molecular dengue virus 1 diagnosis in saliva is possibleCarolina Gracia Poitevin, Carla Adriane Royer, Ana Claudia Bonatto, et al.NPJ Parkinson'S Disease|September 25, 2025
Genome-wide association study of REM sleep behavior disorder in Parkinson's diseaseYuri L Sosero, Karl Heilbron, Pierre Fontanillas, et al.The Lancet. Neurology|November 22, 2024
Sensitivity and specificity of a seed amplification assay for diagnosis of multiple system atrophy: a multicentre cohort studyYihua Ma, Carly M Farris, Sandrina Weber, et al.American Journal of Respiratory and Critical Care Medicine|August 1, 2017
Nocturnal Oximetry-based Evaluation of Habitually Snoring ChildrenRoberto Hornero, Leila Kheirandish-Gozal, Gonzalo C Gutiérrez-Tobal, et al.Transplantation Proceedings|November 18, 2008
Liver transplantation for hilar cholangiocarcinoma: a German surveyG M Kaiser, G C Sotiropoulos, K W Jauch, et al.Human Mutation|May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizuresJulian Schubert, Roberta Paravidino, Felicitas Becker, et al.The Journal of Clinical Investigation|February 4, 2021
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystoniaNiccolò E Mencacci, Marisa M Brockmann, Jinye Dai, et al.Pageof 176