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American Journal of Human Genetics|October 29, 2024
Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemiaScott Barish, Sheng-Jia Lin, Reza Maroofian, et al.
Behavioural Brain Research|April 28, 2023
Potential Biomarkers of impulsivity in mild traumatic brain injury: A pilot studyMaíra Glória de Freitas Cardoso, João Luís Vieira Monteiro de Barros, Rafael Alves Bonfim de Queiroz, et al.
Surgery|November 25, 2022
Use of fluorescence imaging and indocyanine green during colorectal surgery: Results of an intercontinental Delphi surveySteven Wexner, Mahmoud Abu-Gazala, Luigi Boni, et al.
Scientific Reports|August 19, 2021
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of deathStefano Bonassi, Marcello Ceppi, Peter Møller, et al.
Brain : a Journal of Neurology|January 27, 2025
Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genesFahri Küçükali, Elizabeth Hill, Tijs Watzeels, et al.
Plos One|July 30, 2024
Genome wide association study of clinical duration and age at onset of sporadic CJDHolger Hummerich, Helen Speedy, Tracy Campbell, et al.
The World Journal of Men'S Health|July 19, 2024
Regenerative Therapy in Erectile Dysfunction: A Survey on Current Global Practice Trends and GAF Expert RecommendationsManaf Al Hashimi, Germar-M Pinggera, Taymour Mostafa, et al.
NPJ Vaccines|September 2, 2022
SARS-CoV-2 mRNA-vaccine candidate; COReNAPCIN®, induces robust humoral and cellular immunity in mice and non-human primatesReza Alimohammadi, Meysam Porgoo, Mohamad Eftekhary, et al.
American Journal of Human Genetics|July 13, 2022
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcificationsErik Rosenhahn, Thomas J O'Brien, Maha S Zaki, et al.
The Lancet. Neurology|September 19, 2020
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association studyEmma Jones, Holger Hummerich, Emmanuelle Viré, et al.
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