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Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.Scientific Reports|September 1, 2016
Intron retention-dependent gene regulation in Cryptococcus neoformansSara Gonzalez-Hilarion, Damien Paulet, Kyung-Tae Lee, et al.Genome Research|September 25, 2016
Multiple major disease-associated clones of Legionella pneumophila have emerged recently and independentlySophia David, Christophe Rusniok, Massimo Mentasti, et al.Journal of Travel Medicine|May 12, 2023
Climate change and vector-borne diseases: a multi-omics approach of temperature-induced changes in the mosquitoRachel Bellone, Pierre Lechat, Laurence Mousson, et al.Plos Genetics|August 30, 2021
Multitrait GWAS to connect disease variants and biological mechanismsHanna Julienne, Vincent Laville, Zachary R McCaw, et al.The Journal of Clinical Investigation|April 26, 2016
Public T cell receptors confer high-avidity CD4 responses to HIV controllersDaniela Benati, Moran Galperin, Olivier Lambotte, et al.Biorxiv : the Preprint Server for Biology|July 9, 2025
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionDavid Porubsky, DongAhn Yoo, Philip C Dishuck, et al.Nature Communications|April 18, 2026
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionDavid Porubsky, DongAhn Yoo, Nidhi Koundinya, et al.Journal of Inherited Metabolic Disease|October 24, 2025
ATP6AP2-Related Disease Caused by Splicing Defects: Abnormal Glycosylation and the First Affected FemaleAlexandre Raynor, Jean-Madeleine de Sainte-Agathe, Merel A Post, et al.Pageof 8